Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5917 |
| ensemblid | ENSG00000113643.9 |
| hgncid | 9870 |
| symbol | RARS1 |
| name | arginyl-tRNA synthetase 1 |
| refseq_nuc | NM_002887.4 |
| refseq_prot | NP_002878.2 |
| ensembl_nuc | ENST00000231572.8 |
| ensembl_prot | ENSP00000231572.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 168486471 |
| end | 168519301 |
| strand | + |
| ver | v1.2 |
| region | chr5:168486471-168519301 |
| region5000 | chr5:168481471-168524301 |
| regionname0 | RARS1_chr5_168486471_168519301 |
| regionname5000 | RARS1_chr5_168481471_168524301 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 660 | 273 | 77 | 46 | 124 | 3 | 23 | 94 | RARS1_chr5_168481471_168524301 | RARS1 | MDILV others(655): Show |
chr5 | 168481471 | 168524301 |
| a0002 | 1/1 | 660 | 82 | 18 | 15 | 23 | 5 | 19 | 19 | RARS1_chr5_168481471_168524301 | RARS1 | MDVLV others(655): Show |
chr5 | 168481471 | 168524301 |
| a0003 | 0/0 | 660 | 34 | 1 | 9 | 18 | 2 | 4 | 15 | RARS1_chr5_168481471_168524301 | RARS1 | MDILV others(655): Show |
chr5 | 168481471 | 168524301 |
| a0004 | 0/0 | 660 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | MDILV others(655): Show |
chr5 | 168481471 | 168524301 |
| a0005 | 0/0 | 660 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | MDILV others(655): Show |
chr5 | 168481471 | 168524301 |
| a0006 | 0/0 | 627 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | MDVLV others(622): Show |
chr5 | 168481471 | 168524301 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1980 | 234 | 73 | 35 | 102 | 3 | 21 | RARS1_chr5_168481471_168524301 | RARS1 | ATGGA others(1975): Show |
chr5 | 168481471 | 168524301 | ||
| a0001c0003 | 0/0 | 1980 | 34 | 0 | 11 | 21 | 0 | 2 | RARS1_chr5_168481471_168524301 | RARS1 | ATGGA others(1975): Show |
chr5 | 168481471 | 168524301 | ||
| a0001c0007 | 0/0 | 1980 | 4 | 4 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | ATGGA others(1975): Show |
chr5 | 168481471 | 168524301 | ||
| a0001c0010 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | ATGGA others(1975): Show |
chr5 | 168481471 | 168524301 | ||
| a0002c0002 | 1/1 | 1980 | 50 | 1 | 13 | 14 | 4 | 16 | RARS1_chr5_168481471_168524301 | RARS1 | ATGGA others(1975): Show |
chr5 | 168481471 | 168524301 | ||
| a0002c0004 | 0/0 | 1980 | 32 | 17 | 2 | 9 | 1 | 3 | RARS1_chr5_168481471_168524301 | RARS1 | ATGGA others(1975): Show |
chr5 | 168481471 | 168524301 | ||
| a0003c0005 | 0/0 | 1980 | 22 | 0 | 3 | 18 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | ATGGA others(1975): Show |
chr5 | 168481471 | 168524301 | ||
| a0003c0006 | 0/0 | 1980 | 12 | 1 | 6 | 0 | 2 | 3 | RARS1_chr5_168481471_168524301 | RARS1 | ATGGA others(1975): Show |
chr5 | 168481471 | 168524301 | ||
| a0004c0008 | 0/0 | 1980 | 2 | 0 | 2 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | ATGGA others(1975): Show |
chr5 | 168481471 | 168524301 | ||
| a0005c0009 | 0/0 | 1980 | 2 | 0 | 0 | 2 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | ATGGA others(1975): Show |
chr5 | 168481471 | 168524301 | ||
| a0006c0011 | 0/0 | 1948 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | ATGGA others(1943): Show |
chr5 | 168481471 | 168524301 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2122 | 228 | 67 | 35 | 102 | 3 | 21 | RARS1_chr5_168481471_168524301 | RARS1 | ACTTG others(2117): Show |
chr5 | 168481471 | 168524301 |
| a0001c0001t0002 | 0/0 | 2122 | 4 | 4 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | ACTTG others(2117): Show |
chr5 | 168481471 | 168524301 |
| a0001c0001t0003 | 0/0 | 2122 | 2 | 2 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | ACTTG others(2117): Show |
chr5 | 168481471 | 168524301 |
| a0001c0003t0002 | 0/0 | 2122 | 34 | 0 | 11 | 21 | 0 | 2 | RARS1_chr5_168481471_168524301 | RARS1 | ACTTG others(2117): Show |
chr5 | 168481471 | 168524301 |
| a0001c0007t0001 | 0/0 | 2122 | 4 | 4 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | ACTTG others(2117): Show |
chr5 | 168481471 | 168524301 |
| a0001c0010t0001 | 0/0 | 2122 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | ACTTG others(2117): Show |
chr5 | 168481471 | 168524301 |
| a0002c0002t0001 | 1/1 | 2122 | 50 | 1 | 13 | 14 | 4 | 16 | RARS1_chr5_168481471_168524301 | RARS1 | ACTTG others(2117): Show |
chr5 | 168481471 | 168524301 |
| a0002c0004t0001 | 0/0 | 2122 | 32 | 17 | 2 | 9 | 1 | 3 | RARS1_chr5_168481471_168524301 | RARS1 | ACTTG others(2117): Show |
chr5 | 168481471 | 168524301 |
| a0003c0005t0001 | 0/0 | 2122 | 22 | 0 | 3 | 18 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | ACTTG others(2117): Show |
chr5 | 168481471 | 168524301 |
| a0003c0006t0001 | 0/0 | 2122 | 12 | 1 | 6 | 0 | 2 | 3 | RARS1_chr5_168481471_168524301 | RARS1 | ACTTG others(2117): Show |
chr5 | 168481471 | 168524301 |
| a0004c0008t0001 | 0/0 | 2122 | 2 | 0 | 2 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | ACTTG others(2117): Show |
chr5 | 168481471 | 168524301 |
| a0005c0009t0001 | 0/0 | 2122 | 2 | 0 | 0 | 2 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | ACTTG others(2117): Show |
chr5 | 168481471 | 168524301 |
| a0006c0011t0001 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | ACTTG others(2085): Show |
chr5 | 168481471 | 168524301 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0007t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0007t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0007t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0007t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0001c0010t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0004 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0132 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0001 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0004 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0002c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0005t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0006t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0006t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0006t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0006t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0006t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0006t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0006t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0006t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0006t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0006t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0003c0006t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0004c0008t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0004c0008t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0005c0009t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0005c0009t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| a0006c0011t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0364 | EUR | GBR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00140 | hp1 | a0003 | c0006 | t0001 | g0026 | EUR | GBR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00140 | hp2 | a0002 | c0004 | t0001 | g0001 | EUR | GBR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0109 | EUR | FIN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0356 | EUR | FIN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00408 | hp2 | a0001 | c0003 | t0002 | g0284 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00423 | hp2 | a0003 | c0005 | t0001 | g0008 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00438 | hp1 | a0001 | c0003 | t0002 | g0282 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00609 | hp1 | a0001 | c0003 | t0002 | g0016 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00609 | hp2 | a0002 | c0004 | t0001 | g0092 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00621 | hp1 | a0001 | c0003 | t0002 | g0283 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00639 | hp2 | a0003 | c0005 | t0001 | g0027 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0079 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00673 | hp2 | a0001 | c0003 | t0002 | g0294 | EAS | CHS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG00741 | hp2 | a0003 | c0006 | t0001 | g0040 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0358 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01070 | hp2 | a0003 | c0006 | t0001 | g0031 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01074 | hp1 | a0004 | c0008 | t0001 | g0150 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01099 | hp1 | a0004 | c0008 | t0001 | g0149 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01099 | hp2 | a0002 | c0004 | t0001 | g0001 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01106 | hp2 | a0003 | c0006 | t0001 | g0029 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01109 | hp1 | a0002 | c0004 | t0001 | g0084 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0351 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01167 | hp2 | a0003 | c0006 | t0001 | g0025 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01168 | hp1 | a0003 | c0005 | t0001 | g0020 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01169 | hp1 | a0003 | c0006 | t0001 | g0041 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01169 | hp2 | a0003 | c0005 | t0001 | g0022 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0297 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0131 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0005 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01346 | hp2 | a0001 | c0003 | t0002 | g0281 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01358 | hp2 | a0001 | c0003 | t0002 | g0285 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0293 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01496 | hp1 | a0003 | c0006 | t0001 | g0032 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0005 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0098 | EUR | IBS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0107 | EUR | IBS | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01884 | hp2 | a0002 | c0004 | t0001 | g0121 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01891 | hp2 | a0002 | c0004 | t0001 | g0010 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01928 | hp2 | a0001 | c0003 | t0002 | g0278 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01952 | hp2 | a0001 | c0003 | t0002 | g0018 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0365 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01993 | hp1 | a0001 | c0003 | t0002 | g0005 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02040 | hp2 | a0005 | c0009 | t0001 | g0202 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02055 | hp2 | a0002 | c0004 | t0001 | g0142 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02074 | hp2 | a0005 | c0009 | t0001 | g0183 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02135 | hp2 | a0006 | c0011 | t0001 | g0087 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02148 | hp1 | a0001 | c0003 | t0002 | g0016 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | CDX | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02155 | hp2 | a0003 | c0005 | t0001 | g0007 | EAS | CDX | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02165 | hp1 | a0003 | c0005 | t0001 | g0002 | EAS | CDX | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CDX | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0275 | AMR | PEL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0118 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02615 | hp2 | a0002 | c0004 | t0001 | g0096 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0090 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0099 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02698 | hp2 | a0002 | c0004 | t0001 | g0134 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02717 | hp1 | a0002 | c0004 | t0001 | g0004 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02735 | hp2 | a0003 | c0006 | t0001 | g0028 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02895 | hp2 | a0001 | c0007 | t0001 | g0050 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02896 | hp2 | a0001 | c0007 | t0001 | g0049 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02897 | hp1 | a0001 | c0007 | t0001 | g0048 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02922 | hp2 | a0002 | c0004 | t0001 | g0045 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02976 | hp2 | a0002 | c0004 | t0001 | g0088 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03017 | hp1 | a0002 | c0004 | t0001 | g0001 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03041 | hp1 | a0002 | c0004 | t0001 | g0141 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03195 | hp2 | a0002 | c0004 | t0001 | g0044 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | MSL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03209 | hp2 | a0002 | c0004 | t0001 | g0103 | AFR | MSL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03225 | hp1 | a0002 | c0004 | t0001 | g0010 | AFR | MSL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03225 | hp2 | a0002 | c0004 | t0001 | g0097 | AFR | MSL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0119 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0111 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03486 | hp1 | a0002 | c0004 | t0001 | g0095 | AFR | MSL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0299 | AFR | MSL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0081 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0124 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0129 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03579 | hp1 | a0002 | c0004 | t0001 | g0140 | AFR | MSL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0093 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0347 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0125 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | STU | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03704 | hp1 | a0003 | c0006 | t0001 | g0006 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03710 | hp2 | a0003 | c0005 | t0001 | g0030 | SAS | PJL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0114 | SAS | BEB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03927 | hp2 | a0002 | c0004 | t0001 | g0135 | SAS | BEB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03942 | hp1 | a0003 | c0006 | t0001 | g0023 | SAS | BEB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0080 | SAS | STU | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG04115 | hp2 | a0001 | c0003 | t0002 | g0288 | SAS | STU | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0312 | SAS | BEB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | STU | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0276 | SAS | STU | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0348 | SAS | STU | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | YRI | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | YRI | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | CHB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | CHB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | YRI | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18941 | hp1 | a0002 | c0004 | t0001 | g0076 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0280 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18946 | hp2 | a0001 | c0003 | t0002 | g0287 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18948 | hp2 | a0002 | c0004 | t0001 | g0104 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18949 | hp2 | a0003 | c0005 | t0001 | g0038 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18950 | hp2 | a0001 | c0003 | t0002 | g0295 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18952 | hp1 | a0001 | c0003 | t0002 | g0289 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18953 | hp1 | a0003 | c0005 | t0001 | g0008 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18954 | hp2 | a0003 | c0005 | t0001 | g0037 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18957 | hp1 | a0003 | c0005 | t0001 | g0033 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18957 | hp2 | a0001 | c0003 | t0002 | g0274 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18960 | hp2 | a0003 | c0005 | t0001 | g0035 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18961 | hp2 | a0001 | c0010 | t0001 | g0062 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18962 | hp2 | a0001 | c0003 | t0002 | g0279 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18966 | hp1 | a0003 | c0005 | t0001 | g0146 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18968 | hp2 | a0002 | c0004 | t0001 | g0110 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18969 | hp2 | a0001 | c0003 | t0002 | g0286 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18971 | hp1 | a0002 | c0004 | t0001 | g0106 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18972 | hp2 | a0003 | c0005 | t0001 | g0042 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18973 | hp2 | a0003 | c0005 | t0001 | g0036 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18979 | hp2 | a0003 | c0005 | t0001 | g0002 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18982 | hp2 | a0001 | c0003 | t0002 | g0296 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0292 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18998 | hp2 | a0002 | c0004 | t0001 | g0071 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18999 | hp1 | a0001 | c0003 | t0002 | g0017 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19002 | hp2 | a0001 | c0003 | t0002 | g0290 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19004 | hp1 | a0002 | c0004 | t0001 | g0075 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19005 | hp1 | a0001 | c0003 | t0002 | g0017 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19005 | hp2 | a0003 | c0005 | t0001 | g0034 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19012 | hp2 | a0003 | c0005 | t0001 | g0039 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | LWK | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | LWK | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19055 | hp2 | a0003 | c0005 | t0001 | g0021 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19062 | hp2 | a0003 | c0005 | t0001 | g0007 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19067 | hp2 | a0003 | c0005 | t0001 | g0043 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19068 | hp1 | a0003 | c0005 | t0001 | g0002 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19074 | hp1 | a0002 | c0004 | t0001 | g0004 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19079 | hp2 | a0001 | c0003 | t0002 | g0277 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19080 | hp2 | a0001 | c0003 | t0002 | g0018 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19081 | hp2 | a0001 | c0003 | t0002 | g0291 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19084 | hp2 | a0001 | c0003 | t0002 | g0298 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19085 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | YRI | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | YRI | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ASW | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ASW | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA20805 | hp1 | a0003 | c0006 | t0001 | g0006 | EUR | TSI | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0130 | EUR | TSI | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | GIH | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0112 | SAS | GIH | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0115 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | CLM | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02109 | hp2 | a0003 | c0006 | t0001 | g0024 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0359 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG02559 | hp2 | a0002 | c0004 | t0001 | g0128 | AFR | ACB | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03471 | hp1 | a0002 | c0004 | t0001 | g0120 | AFR | MSL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | MSL | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG06807 | hp1 | a0001 | c0007 | t0001 | g0047 | AFR | USA | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | USA | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA20300 | hp1 | a0002 | c0004 | t0001 | g0102 | AFR | USA | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | USA | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | LWK | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0132 | REF | REF | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0004 | REF | REF | RARS1_chr5_168481471_168524301 | RARS1 | chr5 | 168481471 | 168524301 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:168486505 | G | A | 4 | a0001 a0003 a0004 others(1): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
missense_variant | MODERATE | c.7G>A | p.Val3Ile | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/15 | 35/2122 | 7/1983 | 3/660 | chr5 | 168486505 | |||
| chr5:168492750 | C | T | 1 | a0005 | 2 | HG02040.hp2 HG02074.hp2 |
missense_variant | MODERATE | c.272C>T | p.Ala91Val | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/15 | 300/2122 | 272/1983 | 91/660 | chr5 | 168492750 | |||
| chr5:168506090 | T | A | 1 | a0004 | 2 | HG01074.hp1 HG01099.hp1 |
missense_variant | MODERATE | c.1127T>A | p.Val376Glu | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 10/15 | 1155/2122 | 1127/1983 | 376/660 | chr5 | 168506090 | |||
| chr5:168506153 | T | A | 1 | a0003 | 34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
missense_variant | MODERATE | c.1190T>A | p.Phe397Tyr | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 10/15 | 1218/2122 | 1190/1983 | 397/660 | chr5 | 168506153 | |||
| chr5:168518025 | TGATAGCT others(25): Show |
T | 1 | a0006 | 1 | HG02135.hp2 | frameshift_variant | HIGH | c.1839_1870delTAGCTG others(26): Show |
p.Ser614fs | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/15 | 1867/2122 | 1839/1983 | 613/660 | INFO_REALIGN_3_PRIME | chr5 | 168518025 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:168492721 | A | G | 2 | a0003c0005 a0003c0006 |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
synonymous_variant | LOW | c.243A>G | p.Gln81Gln | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/15 | 271/2122 | 243/1983 | 81/660 | chr5 | 168492721 | |||
| chr5:168492820 | G | A | 2 | a0003c0005 a0003c0006 |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
synonymous_variant | LOW | c.342G>A | p.Gln114Gln | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/15 | 370/2122 | 342/1983 | 114/660 | chr5 | 168492820 | |||
| chr5:168497255 | C | A | 2 | a0003c0005 a0003c0006 |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
synonymous_variant | LOW | c.729C>A | p.Thr243Thr | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/15 | 757/2122 | 729/1983 | 243/660 | chr5 | 168497255 | |||
| chr5:168506055 | A | G | 2 | a0003c0005 a0003c0006 |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
synonymous_variant | LOW | c.1092A>G | p.Val364Val | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 10/15 | 1120/2122 | 1092/1983 | 364/660 | chr5 | 168506055 | |||
| chr5:168506151 | A | G | 1 | a0003c0006 | 12 | HG00140.hp1 HG00741.hp2 HG01070.hp2 others(9): Show |
synonymous_variant | LOW | c.1188A>G | p.Leu396Leu | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 10/15 | 1216/2122 | 1188/1983 | 396/660 | chr5 | 168506151 | |||
| chr5:168510602 | G | A | 1 | a0001c0003 | 34 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(31): Show |
synonymous_variant | LOW | c.1368G>A | p.Ser456Ser | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/15 | 1396/2122 | 1368/1983 | 456/660 | chr5 | 168510602 | |||
| chr5:168510644 | A | T | 1 | a0001c0007 | 4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.1410A>T | p.Leu470Leu | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/15 | 1438/2122 | 1410/1983 | 470/660 | chr5 | 168510644 | |||
| chr5:168516816 | C | T | 1 | a0001c0010 | 1 | NA18961.hp2 | synonymous_variant | LOW | c.1491C>T | p.Ser497Ser | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/15 | 1519/2122 | 1491/1983 | 497/660 | chr5 | 168516816 | |||
| chr5:168516822 | G | A | 9 | a0001c0001 a0001c0003 a0001c0007 others(6): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
synonymous_variant | LOW | c.1497G>A | p.Ala499Ala | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/15 | 1525/2122 | 1497/1983 | 499/660 | chr5 | 168516822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:168519256 | C | A | 2 | a0001c0001t0002 a0001c0003t0002 |
38 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*66C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 15/15 | 66 | chr5 | 168519256 | ||||||
| chr5:168519272 | A | G | 1 | a0001c0001t0003 | 2 | HG02970.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*82A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 15/15 | 82 | chr5 | 168519272 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:168486569 | A | T | 1 | a0001c0001t0001g0366 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.45+26A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168486569 | |||||||
| chr5:168486598 | C | T | 232 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(229): Show |
243 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.45+55C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168486598 | |||||||
| chr5:168486648 | G | C | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.45+105G>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168486648 | |||||||
| chr5:168486652 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.45+109C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168486652 | |||||||
| chr5:168486656 | CAG | C | 60 | a0001c0001t0001g0019 a0001c0001t0001g0307 a0001c0001t0001g0308 others(57): Show |
61 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.45+116_45+117delAG | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 168486656 | ||||||
| chr5:168486662 | G | A | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG02258.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.45+119G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168486662 | |||||||
| chr5:168486795 | C | T | 6 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(3): Show |
6 | HG01243.hp2 HG02486.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+252C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168486795 | |||||||
| chr5:168486811 | CCTGGCAT others(40): Show |
C | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.45+269_45+315delCT others(45): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168486811 | |||||||
| chr5:168486819 | G | A | 33 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(30): Show |
38 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.45+276G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168486819 | |||||||
| chr5:168486924 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.45+381G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168486924 | |||||||
| chr5:168487042 | C | G | 1 | a0001c0001t0001g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.45+499C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168487042 | |||||||
| chr5:168487120 | T | C | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.45+577T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168487120 | |||||||
| chr5:168487229 | T | TG | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.45+694dupG | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 168487229 | ||||||
| chr5:168487229 | TG | T | 228 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(225): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.45+694delG | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 168487229 | ||||||
| chr5:168487232 | G | T | 1 | a0001c0001t0001g0365 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.45+689G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168487232 | |||||||
| chr5:168487452 | A | C | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.45+909A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168487452 | |||||||
| chr5:168487475 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.45+932A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168487475 | |||||||
| chr5:168487630 | C | T | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.46-972C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168487630 | |||||||
| chr5:168487880 | G | T | 3 | a0002c0004t0001g0140 a0002c0004t0001g0141 a0002c0004t0001g0142 |
3 | HG02055.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46-722G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168487880 | |||||||
| chr5:168487919 | AC | A | 50 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0310 others(47): Show |
50 | HG00323.hp2 HG00408.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.46-682delC | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168487919 | |||||||
| chr5:168487920 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.46-682C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168487920 | |||||||
| chr5:168488002 | T | C | 2 | a0004c0008t0001g0149 a0004c0008t0001g0150 |
2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.46-600T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168488002 | |||||||
| chr5:168488069 | T | C | 1 | a0002c0004t0001g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.46-533T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168488069 | |||||||
| chr5:168488133 | T | A | 1 | a0002c0004t0001g0045 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.46-469T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168488133 | |||||||
| chr5:168488135 | T | C | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.46-467T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168488135 | |||||||
| chr5:168488136 | C | T | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.46-466C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168488136 | |||||||
| chr5:168488138 | T | C | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.46-464T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168488138 | |||||||
| chr5:168488164 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0357 a0001c0001t0001g0358 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-438G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168488164 | |||||||
| chr5:168488168 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.46-434A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168488168 | |||||||
| chr5:168488207 | A | C | 1 | a0002c0002t0001g0139 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.46-395A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168488207 | |||||||
| chr5:168488351 | C | T | 24 | a0001c0001t0001g0148 a0001c0001t0001g0255 a0001c0001t0001g0256 others(21): Show |
24 | HG01081.hp1 HG01243.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.46-251C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168488351 | |||||||
| chr5:168488398 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.46-204G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168488398 | |||||||
| chr5:168488537 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-65C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 1/14 | chr5 | 168488537 | |||||||
| chr5:168488797 | C | G | 1 | a0001c0001t0001g0356 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.180+61C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168488797 | |||||||
| chr5:168488843 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.180+107A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168488843 | |||||||
| chr5:168488860 | A | G | 1 | a0001c0001t0001g0355 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.180+124A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168488860 | |||||||
| chr5:168488911 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.180+175G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168488911 | |||||||
| chr5:168489007 | A | C | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.180+271A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489007 | |||||||
| chr5:168489008 | G | A | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.180+272G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489008 | |||||||
| chr5:168489082 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.180+346A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489082 | |||||||
| chr5:168489186 | AT | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(58): Show |
69 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.180+462delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 168489186 | ||||||
| chr5:168489211 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0151 a0001c0001t0001g0152 |
4 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+475G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489211 | |||||||
| chr5:168489265 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.180+529C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489265 | |||||||
| chr5:168489323 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.180+587G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489323 | |||||||
| chr5:168489389 | T | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0357 a0001c0001t0001g0358 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.180+653T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489389 | |||||||
| chr5:168489567 | AT | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(26): Show |
32 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.180+834delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 168489567 | ||||||
| chr5:168489623 | G | T | 197 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(194): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.180+887G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489623 | |||||||
| chr5:168489719 | C | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0051 others(90): Show |
106 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.180+983C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489719 | |||||||
| chr5:168489812 | C | CT | 58 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(55): Show |
58 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.180+1095dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 168489812 | ||||||
| chr5:168489812 | C | CTT | 20 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0051 others(17): Show |
22 | HG00673.hp1 HG01346.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.180+1094_180+1095d others(4): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 168489812 | ||||||
| chr5:168489812 | C | CTTT | 7 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(4): Show |
8 | HG02015.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.180+1093_180+1095d others(5): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 168489812 | ||||||
| chr5:168489812 | CT | C | 40 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(37): Show |
45 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.180+1095delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 168489812 | ||||||
| chr5:168489857 | C | A | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.180+1121C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489857 | |||||||
| chr5:168489857 | C | T | 24 | a0001c0001t0001g0148 a0001c0001t0001g0255 a0001c0001t0001g0256 others(21): Show |
24 | HG01081.hp1 HG01243.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.180+1121C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489857 | |||||||
| chr5:168489858 | A | C | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.180+1122A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489858 | |||||||
| chr5:168489859 | G | A | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.180+1123G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489859 | |||||||
| chr5:168489898 | T | C | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.180+1162T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489898 | |||||||
| chr5:168489899 | C | T | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.180+1163C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489899 | |||||||
| chr5:168489901 | A | C | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.180+1165A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168489901 | |||||||
| chr5:168490066 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.180+1330G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490066 | |||||||
| chr5:168490094 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.180+1358G>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490094 | |||||||
| chr5:168490109 | C | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(28): Show |
34 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(31): Show |
intron_variant | MODIFIER | c.180+1373C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490109 | |||||||
| chr5:168490146 | G | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(29): Show |
35 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.180+1410G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490146 | |||||||
| chr5:168490276 | T | A | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.180+1540T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490276 | |||||||
| chr5:168490397 | G | C | 21 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0158 others(18): Show |
21 | HG01074.hp1 HG01099.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.180+1661G>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490397 | |||||||
| chr5:168490457 | T | C | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.180+1721T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490457 | |||||||
| chr5:168490499 | C | A | 256 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(253): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.180+1763C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490499 | |||||||
| chr5:168490556 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.180+1820T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490556 | |||||||
| chr5:168490635 | G | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(21): Show |
27 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.180+1899G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490635 | |||||||
| chr5:168490756 | A | G | 1 | a0001c0001t0001g0269 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.181-1903A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490756 | |||||||
| chr5:168490941 | A | G | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.181-1718A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490941 | |||||||
| chr5:168490942 | G | A | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.181-1717G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490942 | |||||||
| chr5:168490964 | C | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0357 a0001c0001t0001g0358 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.181-1695C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168490964 | |||||||
| chr5:168491079 | G | A | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG03710.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.181-1580G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491079 | |||||||
| chr5:168491084 | C | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.181-1575C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491084 | |||||||
| chr5:168491085 | C | G | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.181-1574C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491085 | |||||||
| chr5:168491131 | G | A | 1 | a0001c0001t0001g0311 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.181-1528G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491131 | |||||||
| chr5:168491132 | G | T | 1 | a0002c0002t0001g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.181-1527G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491132 | |||||||
| chr5:168491158 | T | C | 1 | a0002c0004t0001g0140 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.181-1501T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491158 | |||||||
| chr5:168491174 | A | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(30): Show |
36 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(33): Show |
intron_variant | MODIFIER | c.181-1485A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491174 | |||||||
| chr5:168491204 | C | G | 30 | a0001c0001t0002g0145 a0003c0005t0001g0002 a0003c0005t0001g0007 others(27): Show |
35 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.181-1455C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491204 | |||||||
| chr5:168491330 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG00735.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.181-1329C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491330 | |||||||
| chr5:168491337 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.181-1322G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491337 | |||||||
| chr5:168491658 | G | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(256): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.181-1001G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491658 | |||||||
| chr5:168491787 | T | C | 51 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0310 others(48): Show |
51 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.181-872T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491787 | |||||||
| chr5:168491896 | G | GATAC | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(1): Show |
4 | HG00733.hp2 HG01891.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-763_181-762ins others(4): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491896 | |||||||
| chr5:168491921 | T | C | 259 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(256): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.181-738T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491921 | |||||||
| chr5:168491931 | A | C | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG02080.hp2 HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.181-728A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168491931 | |||||||
| chr5:168491946 | C | CT | 19 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0001g0137 others(16): Show |
19 | HG00642.hp2 HG01255.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.181-690dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 168491946 | ||||||
| chr5:168491946 | CT | C | 27 | a0002c0002t0001g0072 a0002c0004t0001g0071 a0003c0005t0001g0002 others(24): Show |
31 | HG00140.hp1 HG00639.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.181-690delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 168491946 | ||||||
| chr5:168491946 | CTT | C | 25 | a0001c0001t0001g0148 a0001c0001t0001g0172 a0001c0001t0001g0173 others(22): Show |
25 | HG00544.hp1 HG00558.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.181-691_181-690del others(2): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 168491946 | ||||||
| chr5:168491946 | CTTT | C | 176 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.181-692_181-690del others(3): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 168491946 | ||||||
| chr5:168491946 | CTTTT | C | 29 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0301 others(26): Show |
32 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.181-693_181-690del others(4): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 168491946 | ||||||
| chr5:168492007 | A | C | 7 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0005t0001g0037 others(4): Show |
7 | NA18949.hp2 NA18954.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-652A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168492007 | |||||||
| chr5:168492143 | C | T | 1 | a0001c0003t0002g0297 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.181-516C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168492143 | |||||||
| chr5:168492282 | T | C | 2 | a0003c0005t0001g0020 a0003c0005t0001g0022 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.181-377T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168492282 | |||||||
| chr5:168492286 | G | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0357 a0001c0001t0001g0358 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.181-373G>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168492286 | |||||||
| chr5:168492452 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | NA18942.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.181-207T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168492452 | |||||||
| chr5:168492466 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.181-193C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168492466 | |||||||
| chr5:168492523 | G | A | 2 | a0001c0001t0002g0272 a0001c0001t0002g0273 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.181-136G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168492523 | |||||||
| chr5:168492531 | C | T | 1 | a0003c0005t0001g0039 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.181-128C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168492531 | |||||||
| chr5:168492543 | G | A | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.181-116G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168492543 | |||||||
| chr5:168492618 | T | A | 259 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(256): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.181-41T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 2/14 | chr5 | 168492618 | |||||||
| chr5:168493011 | CT | C | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.369+170delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 168493011 | ||||||
| chr5:168493064 | A | G | 38 | a0001c0001t0001g0015 a0001c0001t0001g0156 a0001c0001t0001g0174 others(35): Show |
39 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.369+217A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | chr5 | 168493064 | |||||||
| chr5:168493349 | G | A | 91 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(88): Show |
96 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.369+502G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | chr5 | 168493349 | |||||||
| chr5:168493416 | A | G | 1 | a0001c0001t0001g0309 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.370-478A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | chr5 | 168493416 | |||||||
| chr5:168493592 | C | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(58): Show |
69 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.370-302C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | chr5 | 168493592 | |||||||
| chr5:168493621 | G | A | 15 | a0003c0005t0001g0020 a0003c0005t0001g0022 a0003c0005t0001g0027 others(12): Show |
16 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.370-273G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | chr5 | 168493621 | |||||||
| chr5:168493633 | C | CA | 55 | a0001c0001t0001g0019 a0001c0001t0001g0153 a0001c0001t0001g0154 others(52): Show |
56 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.370-240dupA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 168493633 | ||||||
| chr5:168493633 | C | CAA | 72 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0051 others(69): Show |
74 | HG00323.hp2 HG00408.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.370-241_370-240dup others(2): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 168493633 | ||||||
| chr5:168493633 | C | CAAA | 17 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0053 others(14): Show |
18 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.370-242_370-240dup others(3): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 168493633 | ||||||
| chr5:168493633 | C | CAAAA | 25 | a0001c0001t0001g0147 a0003c0005t0001g0002 a0003c0005t0001g0007 others(22): Show |
30 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.370-243_370-240dup others(4): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 168493633 | ||||||
| chr5:168493633 | CA | C | 9 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0205 others(6): Show |
9 | HG01168.hp2 HG01256.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.370-240delA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 168493633 | ||||||
| chr5:168493662 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.370-232A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | chr5 | 168493662 | |||||||
| chr5:168493664 | G | A | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.370-230G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | chr5 | 168493664 | |||||||
| chr5:168493720 | G | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(59): Show |
70 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.370-174G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | chr5 | 168493720 | |||||||
| chr5:168493835 | A | G | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.370-59A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 3/14 | chr5 | 168493835 | |||||||
| chr5:168494042 | C | G | 262 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.478+40C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 4/14 | chr5 | 168494042 | |||||||
| chr5:168494349 | G | A | 6 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(3): Show |
6 | HG01243.hp2 HG02486.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-201G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 4/14 | chr5 | 168494349 | |||||||
| chr5:168494384 | A | G | 92 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(89): Show |
97 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.479-166A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 4/14 | chr5 | 168494384 | |||||||
| chr5:168494420 | A | G | 1 | a0001c0001t0001g0349 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.479-130A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 4/14 | chr5 | 168494420 | |||||||
| chr5:168494494 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.479-56C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 4/14 | chr5 | 168494494 | |||||||
| chr5:168494658 | T | G | 1 | a0001c0001t0001g0180 | 1 | NA18952.hp2 | splice_region_variant&intron_variant | LOW | c.579+8T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 5/14 | chr5 | 168494658 | |||||||
| chr5:168494749 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
7 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+99A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 5/14 | chr5 | 168494749 | |||||||
| chr5:168494796 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(58): Show |
69 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.579+146G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 5/14 | chr5 | 168494796 | |||||||
| chr5:168495002 | A | AT | 34 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(31): Show |
37 | HG00673.hp1 HG01993.hp2 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.580-299dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr5 | 168495002 | ||||||
| chr5:168495002 | AT | A | 92 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(89): Show |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.580-299delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr5 | 168495002 | ||||||
| chr5:168495068 | T | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(21): Show |
27 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.580-247T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 5/14 | chr5 | 168495068 | |||||||
| chr5:168495090 | A | G | 15 | a0003c0005t0001g0020 a0003c0005t0001g0022 a0003c0005t0001g0027 others(12): Show |
16 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.580-225A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 5/14 | chr5 | 168495090 | |||||||
| chr5:168495126 | C | T | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.580-189C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 5/14 | chr5 | 168495126 | |||||||
| chr5:168495239 | T | C | 2 | a0002c0004t0001g0075 a0002c0004t0001g0076 |
2 | NA18941.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.580-76T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 5/14 | chr5 | 168495239 | |||||||
| chr5:168495272 | T | C | 2 | a0002c0002t0001g0077 a0002c0002t0001g0078 |
2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.580-43T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 5/14 | chr5 | 168495272 | |||||||
| chr5:168495456 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0151 a0001c0001t0001g0152 |
4 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.701+20G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168495456 | |||||||
| chr5:168495458 | A | G | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.701+22A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168495458 | |||||||
| chr5:168495473 | T | C | 5 | a0001c0001t0001g0133 a0001c0007t0001g0047 a0001c0007t0001g0048 others(2): Show |
5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.701+37T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168495473 | |||||||
| chr5:168495514 | C | T | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | NA18964.hp1 NA18981.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.701+78C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168495514 | |||||||
| chr5:168495573 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(92): Show |
108 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.701+137C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168495573 | |||||||
| chr5:168495628 | T | G | 33 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(30): Show |
36 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(33): Show |
intron_variant | MODIFIER | c.701+192T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168495628 | |||||||
| chr5:168495712 | A | G | 1 | a0003c0006t0001g0029 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.701+276A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168495712 | |||||||
| chr5:168495891 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.701+455A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168495891 | |||||||
| chr5:168496075 | G | A | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.701+639G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168496075 | |||||||
| chr5:168496120 | T | TG | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02818.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.701+684_701+685ins others(1): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168496120 | |||||||
| chr5:168496152 | A | G | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.701+716A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168496152 | |||||||
| chr5:168496195 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.701+759A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168496195 | |||||||
| chr5:168496361 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0051 others(15): Show |
20 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.702-867A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168496361 | |||||||
| chr5:168496371 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.702-857T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168496371 | |||||||
| chr5:168496378 | CA | C | 248 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(245): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.702-834delA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 168496378 | ||||||
| chr5:168496386 | A | G | 1 | a0001c0001t0001g0355 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.702-842A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168496386 | |||||||
| chr5:168496504 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.702-724A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168496504 | |||||||
| chr5:168496524 | C | T | 2 | a0002c0004t0001g0075 a0002c0004t0001g0076 |
2 | NA18941.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.702-704C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168496524 | |||||||
| chr5:168496672 | C | T | 2 | a0001c0003t0002g0289 a0001c0003t0002g0290 |
2 | NA18952.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.702-556C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168496672 | |||||||
| chr5:168496704 | G | A | 6 | a0002c0002t0001g0073 a0002c0002t0001g0079 a0002c0002t0001g0080 others(3): Show |
6 | HG00642.hp1 HG02683.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.702-524G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168496704 | |||||||
| chr5:168496726 | C | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(30): Show |
36 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(33): Show |
intron_variant | MODIFIER | c.702-502C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168496726 | |||||||
| chr5:168496763 | C | T | 2 | a0002c0004t0001g0120 a0002c0004t0001g0121 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.702-465C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168496763 | |||||||
| chr5:168497105 | T | G | 1 | a0001c0001t0001g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.702-123T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168497105 | |||||||
| chr5:168497118 | T | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(58): Show |
69 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.702-110T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168497118 | |||||||
| chr5:168497169 | T | G | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.702-59T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 6/14 | chr5 | 168497169 | |||||||
| chr5:168497400 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.822+52T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168497400 | |||||||
| chr5:168497487 | C | T | 2 | a0003c0005t0001g0020 a0003c0005t0001g0022 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.822+139C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168497487 | |||||||
| chr5:168497522 | CT | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(58): Show |
69 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.822+184delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 168497522 | ||||||
| chr5:168497569 | G | T | 2 | a0001c0001t0001g0347 a0001c0001t0001g0348 |
2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.822+221G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168497569 | |||||||
| chr5:168497612 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.822+264G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168497612 | |||||||
| chr5:168497688 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.822+340C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168497688 | |||||||
| chr5:168497736 | G | A | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.822+388G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168497736 | |||||||
| chr5:168497923 | C | T | 291 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(288): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.822+575C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168497923 | |||||||
| chr5:168498004 | G | A | 2 | a0001c0001t0002g0272 a0001c0001t0002g0273 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.822+656G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168498004 | |||||||
| chr5:168498025 | G | T | 291 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(288): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.822+677G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168498025 | |||||||
| chr5:168498122 | C | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.822+774C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168498122 | |||||||
| chr5:168498135 | G | A | 1 | a0002c0002t0001g0082 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.822+787G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168498135 | |||||||
| chr5:168498202 | G | T | 7 | a0002c0002t0001g0072 a0002c0002t0001g0114 a0002c0002t0001g0115 others(4): Show |
7 | HG01123.hp1 HG01256.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+854G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168498202 | |||||||
| chr5:168498249 | A | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
15 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.822+901A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168498249 | |||||||
| chr5:168498263 | A | C | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02818.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.822+915A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168498263 | |||||||
| chr5:168498398 | C | A | 91 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(88): Show |
96 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.822+1050C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168498398 | |||||||
| chr5:168498546 | G | A | 59 | a0001c0001t0001g0019 a0001c0001t0001g0307 a0001c0001t0001g0308 others(56): Show |
60 | HG00323.hp2 HG00408.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.822+1198G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168498546 | |||||||
| chr5:168498677 | T | G | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0349 |
3 | HG00735.hp2 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.822+1329T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168498677 | |||||||
| chr5:168498753 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | NA18950.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.822+1405G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168498753 | |||||||
| chr5:168499172 | A | G | 14 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(11): Show |
18 | HG00423.hp2 HG02155.hp2 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-1419A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168499172 | |||||||
| chr5:168499324 | A | T | 92 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(89): Show |
97 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.823-1267A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168499324 | |||||||
| chr5:168499460 | A | G | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.823-1131A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168499460 | |||||||
| chr5:168499553 | T | G | 20 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(17): Show |
20 | HG01081.hp1 HG01243.hp2 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.823-1038T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168499553 | |||||||
| chr5:168499708 | T | TA | 39 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(36): Show |
45 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.823-873dupA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 168499708 | ||||||
| chr5:168499708 | TA | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.823-873delA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 168499708 | ||||||
| chr5:168499747 | A | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.823-844A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168499747 | |||||||
| chr5:168499768 | T | C | 33 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(30): Show |
38 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.823-823T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168499768 | |||||||
| chr5:168500043 | G | C | 77 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(74): Show |
88 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.823-548G>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168500043 | |||||||
| chr5:168500079 | T | G | 1 | a0003c0005t0001g0038 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.823-512T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168500079 | |||||||
| chr5:168500136 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0230 |
2 | HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.823-455G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168500136 | |||||||
| chr5:168500143 | TGCCACTC others(2): Show |
T | 77 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(74): Show |
88 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.823-437_823-429del others(9): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 168500143 | ||||||
| chr5:168500200 | C | CA | 126 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(123): Show |
136 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.823-369dupA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 168500200 | ||||||
| chr5:168500200 | C | CAA | 44 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(41): Show |
44 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.823-370_823-369dup others(2): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 168500200 | ||||||
| chr5:168500200 | CA | C | 49 | a0001c0001t0001g0019 a0001c0001t0001g0133 a0001c0001t0001g0153 others(46): Show |
50 | HG00323.hp2 HG00639.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.823-369delA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 168500200 | ||||||
| chr5:168500338 | T | A | 1 | a0002c0004t0001g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.823-253T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168500338 | |||||||
| chr5:168500511 | A | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0051 others(14): Show |
19 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.823-80A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168500511 | |||||||
| chr5:168500536 | A | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.823-55A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168500536 | |||||||
| chr5:168500545 | T | A | 1 | a0002c0004t0001g0084 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.823-46T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168500545 | |||||||
| chr5:168500571 | T | A | 6 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(3): Show |
6 | HG01243.hp2 HG02486.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-20T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 7/14 | chr5 | 168500571 | |||||||
| chr5:168500938 | A | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02818.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.952+218A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168500938 | |||||||
| chr5:168500974 | T | C | 2 | a0004c0008t0001g0149 a0004c0008t0001g0150 |
2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.952+254T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168500974 | |||||||
| chr5:168501008 | G | A | 1 | a0002c0004t0001g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.952+288G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168501008 | |||||||
| chr5:168501162 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.952+442A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168501162 | |||||||
| chr5:168501367 | A | AT | 44 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(41): Show |
50 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.953-632dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 168501367 | ||||||
| chr5:168501425 | AT | A | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.953-569delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 168501425 | ||||||
| chr5:168501433 | A | T | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.953-568A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168501433 | |||||||
| chr5:168501500 | A | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(12): Show |
16 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(13): Show |
intron_variant | MODIFIER | c.953-501A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168501500 | |||||||
| chr5:168501520 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.953-481C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168501520 | |||||||
| chr5:168501552 | A | G | 1 | a0002c0004t0001g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.953-449A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168501552 | |||||||
| chr5:168501580 | G | A | 5 | a0001c0001t0001g0154 a0001c0001t0001g0159 a0001c0001t0001g0164 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.953-421G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168501580 | |||||||
| chr5:168501637 | C | G | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.953-364C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168501637 | |||||||
| chr5:168501648 | G | A | 2 | a0003c0005t0001g0035 a0003c0005t0001g0038 |
2 | NA18949.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.953-353G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168501648 | |||||||
| chr5:168501727 | A | AATT | 91 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(88): Show |
96 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.953-272_953-271ins others(3): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 168501727 | ||||||
| chr5:168501741 | G | A | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.953-260G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168501741 | |||||||
| chr5:168501824 | C | A | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.953-177C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168501824 | |||||||
| chr5:168501960 | C | A | 1 | a0003c0005t0001g0036 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.953-41C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 8/14 | chr5 | 168501960 | |||||||
| chr5:168502118 | C | G | 1 | a0001c0001t0001g0014 | 2 | NA18939.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1057+13C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502118 | |||||||
| chr5:168502151 | T | G | 1 | a0002c0002t0001g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1057+46T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502151 | |||||||
| chr5:168502300 | A | G | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02818.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1057+195A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502300 | |||||||
| chr5:168502340 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1057+235C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502340 | |||||||
| chr5:168502341 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | NA18942.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1057+236G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502341 | |||||||
| chr5:168502361 | A | AAT | 27 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0051 others(24): Show |
29 | HG00099.hp1 HG01884.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.1057+279_1057+280d others(4): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502361 | ||||||
| chr5:168502369 | T | C | 1 | a0001c0003t0002g0282 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1057+264T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502369 | |||||||
| chr5:168502380 | A | AT | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0260 others(4): Show |
7 | HG00735.hp2 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057+276dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502380 | ||||||
| chr5:168502380 | A | ATT | 11 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(8): Show |
15 | HG00423.hp2 HG00639.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1057+276_1057+277i others(4): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502380 | ||||||
| chr5:168502380 | A | ATTT | 5 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0269 others(2): Show |
5 | HG01943.hp1 HG02451.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1057+276_1057+277i others(5): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502380 | ||||||
| chr5:168502380 | A | T | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1057+275A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502380 | |||||||
| chr5:168502381 | TA | T | 4 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0346 others(1): Show |
4 | HG00639.hp1 HG01167.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057+277delA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502381 | |||||||
| chr5:168502382 | A | AT | 57 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0247 others(54): Show |
58 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.1057+278dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502382 | ||||||
| chr5:168502382 | A | ATT | 6 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0003c0005t0001g0033 others(3): Show |
6 | HG02145.hp1 NA18949.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057+278_1057+279i others(4): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502382 | ||||||
| chr5:168502382 | A | ATTT | 10 | a0003c0006t0001g0006 a0003c0006t0001g0023 a0003c0006t0001g0024 others(7): Show |
11 | HG00140.hp1 HG00741.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1057+278_1057+279i others(5): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502382 | ||||||
| chr5:168502382 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057+278_1057+279i others(14): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502382 | ||||||
| chr5:168502382 | A | T | 26 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0260 others(23): Show |
30 | HG00423.hp2 HG00639.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1057+277A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502382 | |||||||
| chr5:168502384 | A | AT | 15 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0174 others(12): Show |
15 | HG00673.hp1 HG01109.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1057+291dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502384 | ||||||
| chr5:168502384 | A | ATAT | 11 | a0001c0001t0001g0210 a0001c0001t0001g0220 a0001c0001t0001g0227 others(8): Show |
11 | HG01243.hp2 HG02976.hp1 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.1057+280_1057+281i others(5): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502384 | ||||||
| chr5:168502384 | A | ATATATAT others(38): Show |
1 | a0001c0001t0001g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1057+280_1057+281i others(47): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502384 | ||||||
| chr5:168502384 | A | ATATATAT others(13): Show |
1 | a0001c0007t0001g0047 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1057+280_1057+281i others(22): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502384 | ||||||
| chr5:168502384 | A | ATATATTT others(9): Show |
1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1057+280_1057+281i others(18): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502384 | ||||||
| chr5:168502384 | A | ATATATTT others(11): Show |
1 | a0001c0001t0001g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1057+280_1057+281i others(20): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502384 | ||||||
| chr5:168502384 | A | ATATTTTT others(8): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0069 a0001c0001t0001g0136 |
3 | HG02895.hp1 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1057+280_1057+281i others(17): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502384 | ||||||
| chr5:168502384 | A | ATATTTTT others(9): Show |
1 | a0001c0001t0001g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1057+280_1057+281i others(18): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502384 | ||||||
| chr5:168502384 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1057+291_1057+292i others(15): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502384 | ||||||
| chr5:168502384 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0009 a0001c0001t0001g0068 |
2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1057+291_1057+292i others(18): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502384 | ||||||
| chr5:168502384 | A | T | 121 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0133 others(118): Show |
128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1057+279A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502384 | |||||||
| chr5:168502384 | ATT | A | 12 | a0001c0001t0002g0299 a0001c0003t0002g0276 a0001c0003t0002g0280 others(9): Show |
12 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1057+290_1057+291d others(4): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502384 | ||||||
| chr5:168502385 | T | TA | 60 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0015 others(57): Show |
63 | HG00423.hp1 HG00438.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.1057+280_1057+281i others(3): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502385 | |||||||
| chr5:168502385 | T | TATA | 28 | a0001c0001t0001g0012 a0001c0001t0001g0159 a0001c0001t0001g0171 others(25): Show |
29 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.1057+280_1057+281i others(5): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502385 | |||||||
| chr5:168502386 | T | A | 20 | a0001c0001t0001g0064 a0001c0003t0002g0005 a0001c0003t0002g0016 others(17): Show |
25 | HG00609.hp1 HG00673.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.1057+281T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502386 | |||||||
| chr5:168502387 | T | A | 10 | a0001c0001t0001g0167 a0001c0001t0001g0178 a0001c0001t0001g0181 others(7): Show |
10 | HG00558.hp1 HG00558.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1057+282T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502387 | |||||||
| chr5:168502388 | T | A | 4 | a0001c0003t0002g0282 a0001c0003t0002g0283 a0001c0003t0002g0287 others(1): Show |
4 | HG00438.hp1 HG00621.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057+283T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502388 | |||||||
| chr5:168502397 | A | T | 37 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(34): Show |
42 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1057+292A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502397 | |||||||
| chr5:168502462 | C | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
15 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.1057+357C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502462 | |||||||
| chr5:168502512 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
7 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057+407A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502512 | |||||||
| chr5:168502568 | A | AT | 104 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0058 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1057+483dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502568 | ||||||
| chr5:168502568 | AT | A | 6 | a0001c0001t0001g0164 a0001c0001t0002g0272 a0001c0001t0002g0273 others(3): Show |
6 | HG01074.hp1 HG01099.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1057+483delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168502568 | ||||||
| chr5:168502569 | T | A | 2 | a0001c0001t0001g0147 a0001c0007t0001g0047 |
2 | HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1057+464T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502569 | |||||||
| chr5:168502632 | C | A | 76 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(73): Show |
87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057+527C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502632 | |||||||
| chr5:168502722 | C | T | 1 | a0002c0002t0001g0112 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1057+617C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502722 | |||||||
| chr5:168502836 | T | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0051 others(15): Show |
20 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.1057+731T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502836 | |||||||
| chr5:168502871 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1057+766A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502871 | |||||||
| chr5:168502995 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
7 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057+890T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168502995 | |||||||
| chr5:168503124 | G | C | 34 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(31): Show |
39 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.1057+1019G>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503124 | |||||||
| chr5:168503145 | A | G | 4 | a0001c0007t0001g0047 a0001c0007t0001g0048 a0001c0007t0001g0049 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057+1040A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503145 | |||||||
| chr5:168503218 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | NA18948.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1057+1113A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503218 | |||||||
| chr5:168503264 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1057+1159C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503264 | |||||||
| chr5:168503291 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1057+1186C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503291 | |||||||
| chr5:168503320 | G | T | 1 | a0002c0002t0001g0111 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1057+1215G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503320 | |||||||
| chr5:168503349 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1057+1244T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503349 | |||||||
| chr5:168503365 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1057+1260C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503365 | |||||||
| chr5:168503487 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1057+1382G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503487 | |||||||
| chr5:168503491 | G | A | 1 | a0002c0002t0001g0113 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1057+1386G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503491 | |||||||
| chr5:168503616 | G | GTAGT | 292 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(289): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1057+1518_1057+152 others(8): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168503616 | ||||||
| chr5:168503652 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1057+1547A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503652 | |||||||
| chr5:168503727 | G | A | 35 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(32): Show |
41 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1057+1622G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503727 | |||||||
| chr5:168503784 | A | G | 3 | a0001c0007t0001g0048 a0001c0007t0001g0049 a0001c0007t0001g0050 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1057+1679A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503784 | |||||||
| chr5:168503858 | G | A | 1 | a0002c0004t0001g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1057+1753G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503858 | |||||||
| chr5:168503872 | G | A | 291 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(288): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1057+1767G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503872 | |||||||
| chr5:168503881 | C | G | 43 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(40): Show |
49 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1057+1776C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503881 | |||||||
| chr5:168503971 | G | A | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1057+1866G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168503971 | |||||||
| chr5:168504014 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1057+1909T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504014 | |||||||
| chr5:168504062 | GA | G | 278 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(275): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1058-1943delA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168504062 | ||||||
| chr5:168504067 | A | G | 1 | a0002c0004t0001g0110 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1058-1954A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504067 | |||||||
| chr5:168504169 | T | C | 76 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(73): Show |
87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1058-1852T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504169 | |||||||
| chr5:168504199 | A | G | 2 | a0002c0002t0001g0109 a0002c0002t0001g0123 |
2 | HG00323.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1058-1822A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504199 | |||||||
| chr5:168504448 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1058-1573G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504448 | |||||||
| chr5:168504472 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1058-1549G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504472 | |||||||
| chr5:168504500 | C | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1058-1521C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504500 | |||||||
| chr5:168504521 | CA | C | 28 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(25): Show |
33 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1058-1487delA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168504521 | ||||||
| chr5:168504533 | A | G | 4 | a0001c0007t0001g0047 a0001c0007t0001g0048 a0001c0007t0001g0049 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058-1488A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504533 | |||||||
| chr5:168504535 | G | A | 30 | a0001c0001t0002g0299 a0001c0003t0002g0005 a0001c0003t0002g0016 others(27): Show |
35 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1058-1486G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504535 | |||||||
| chr5:168504536 | A | G | 30 | a0001c0001t0002g0299 a0001c0003t0002g0005 a0001c0003t0002g0016 others(27): Show |
35 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1058-1485A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504536 | |||||||
| chr5:168504558 | G | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
15 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.1058-1463G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504558 | |||||||
| chr5:168504602 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1058-1419G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504602 | |||||||
| chr5:168504616 | T | G | 43 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(40): Show |
49 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1058-1405T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504616 | |||||||
| chr5:168504668 | A | C | 92 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(89): Show |
97 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1058-1353A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504668 | |||||||
| chr5:168504743 | TG | T | 4 | a0001c0007t0001g0047 a0001c0007t0001g0048 a0001c0007t0001g0049 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058-1277delG | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504743 | |||||||
| chr5:168504847 | C | T | 21 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0158 others(18): Show |
21 | HG01074.hp1 HG01099.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1058-1174C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504847 | |||||||
| chr5:168504879 | C | T | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1058-1142C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504879 | |||||||
| chr5:168504896 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1058-1125A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168504896 | |||||||
| chr5:168505012 | A | AT | 7 | a0001c0001t0001g0153 a0001c0001t0001g0301 a0001c0001t0001g0302 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058-1003dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168505012 | ||||||
| chr5:168505104 | C | A | 197 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(194): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1058-917C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505104 | |||||||
| chr5:168505197 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
7 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1058-824G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505197 | |||||||
| chr5:168505221 | T | C | 46 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(43): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1058-800T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505221 | |||||||
| chr5:168505386 | T | A | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1058-635T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505386 | |||||||
| chr5:168505512 | A | C | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1058-509A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505512 | |||||||
| chr5:168505530 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1058-491C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505530 | |||||||
| chr5:168505535 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1058-486C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505535 | |||||||
| chr5:168505554 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1058-467C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505554 | |||||||
| chr5:168505559 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1058-462C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505559 | |||||||
| chr5:168505559 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1058-462C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505559 | |||||||
| chr5:168505577 | C | G | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0266 others(3): Show |
6 | HG01943.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1058-444C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505577 | |||||||
| chr5:168505594 | C | G | 1 | a0002c0002t0001g0078 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1058-427C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505594 | |||||||
| chr5:168505705 | A | G | 1 | a0002c0004t0001g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1058-316A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505705 | |||||||
| chr5:168505714 | GA | G | 13 | a0001c0001t0001g0059 a0001c0001t0001g0133 a0001c0001t0001g0147 others(10): Show |
13 | HG01081.hp1 HG01109.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1058-286delA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168505714 | ||||||
| chr5:168505714 | GAA | G | 224 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.1058-287_1058-286d others(4): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168505714 | ||||||
| chr5:168505714 | GAAA | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0151 a0001c0001t0001g0152 others(11): Show |
14 | HG00438.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1058-288_1058-286d others(5): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168505714 | ||||||
| chr5:168505714 | GAAAAA | G | 28 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(25): Show |
32 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1058-290_1058-286d others(7): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 168505714 | ||||||
| chr5:168505831 | T | C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(8): Show |
12 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1058-190T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505831 | |||||||
| chr5:168505881 | T | C | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1058-140T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505881 | |||||||
| chr5:168505887 | T | C | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1058-134T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 9/14 | chr5 | 168505887 | |||||||
| chr5:168506210 | A | G | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1236+11A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 10/14 | chr5 | 168506210 | |||||||
| chr5:168506219 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1236+20T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 10/14 | chr5 | 168506219 | |||||||
| chr5:168506377 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1236+178C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 10/14 | chr5 | 168506377 | |||||||
| chr5:168506425 | A | G | 76 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(73): Show |
87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1236+226A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 10/14 | chr5 | 168506425 | |||||||
| chr5:168506542 | G | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
15 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.1237-180G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 10/14 | chr5 | 168506542 | |||||||
| chr5:168506668 | C | CT | 53 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0310 others(50): Show |
53 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1237-43dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 168506668 | ||||||
| chr5:168506668 | CT | C | 7 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(4): Show |
8 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1237-43delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 168506668 | ||||||
| chr5:168506948 | A | G | 14 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
15 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.1346+117A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168506948 | |||||||
| chr5:168506992 | A | C | 4 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
4 | HG00099.hp1 HG03710.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346+161A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168506992 | |||||||
| chr5:168507005 | G | A | 30 | a0001c0001t0002g0299 a0001c0003t0002g0005 a0001c0003t0002g0016 others(27): Show |
35 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1346+174G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507005 | |||||||
| chr5:168507066 | G | T | 21 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0158 others(18): Show |
21 | HG01074.hp1 HG01099.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1346+235G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507066 | |||||||
| chr5:168507178 | T | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0357 a0001c0001t0001g0358 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1346+347T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507178 | |||||||
| chr5:168507217 | T | C | 93 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(90): Show |
98 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1346+386T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507217 | |||||||
| chr5:168507237 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0265 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1346+406A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507237 | |||||||
| chr5:168507388 | C | T | 51 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0310 others(48): Show |
51 | HG00323.hp2 HG00408.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1346+557C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507388 | |||||||
| chr5:168507389 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1346+558G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507389 | |||||||
| chr5:168507448 | T | C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
15 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.1346+617T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507448 | |||||||
| chr5:168507559 | A | G | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02818.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1346+728A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507559 | |||||||
| chr5:168507571 | T | C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(8): Show |
12 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1346+740T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507571 | |||||||
| chr5:168507592 | T | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0357 a0001c0001t0001g0358 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1346+761T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507592 | |||||||
| chr5:168507656 | A | G | 14 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
15 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.1346+825A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507656 | |||||||
| chr5:168507856 | A | G | 99 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(96): Show |
104 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1346+1025A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507856 | |||||||
| chr5:168507877 | C | CA | 33 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(30): Show |
33 | HG00735.hp1 HG01081.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1346+1063dupA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168507877 | ||||||
| chr5:168507877 | CA | C | 18 | a0001c0001t0001g0152 a0001c0001t0001g0327 a0001c0003t0002g0291 others(15): Show |
19 | HG00140.hp1 HG00408.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.1346+1063delA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168507877 | ||||||
| chr5:168507954 | C | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
15 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.1346+1123C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168507954 | |||||||
| chr5:168508011 | T | C | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1346+1180T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508011 | |||||||
| chr5:168508024 | C | G | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1346+1193C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508024 | |||||||
| chr5:168508041 | A | T | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1346+1210A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508041 | |||||||
| chr5:168508048 | A | G | 6 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(3): Show |
6 | HG01243.hp2 HG02486.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346+1217A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508048 | |||||||
| chr5:168508291 | T | G | 3 | a0001c0001t0001g0301 a0001c0001t0001g0303 a0001c0001t0001g0306 |
3 | HG01243.hp2 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1346+1460T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508291 | |||||||
| chr5:168508309 | C | T | 1 | a0001c0007t0001g0047 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1346+1478C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508309 | |||||||
| chr5:168508326 | A | T | 1 | a0001c0001t0001g0249 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1346+1495A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508326 | |||||||
| chr5:168508545 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
5 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346+1714G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508545 | |||||||
| chr5:168508593 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1346+1762G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508593 | |||||||
| chr5:168508599 | G | A | 3 | a0002c0004t0001g0110 a0002c0004t0001g0134 a0002c0004t0001g0135 |
3 | HG02698.hp2 HG03927.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1346+1768G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508599 | |||||||
| chr5:168508619 | C | CA | 80 | a0001c0001t0001g0019 a0001c0001t0001g0151 a0001c0001t0001g0167 others(77): Show |
82 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1346+1813dupA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168508619 | ||||||
| chr5:168508619 | C | CAA | 29 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0261 others(26): Show |
33 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.1346+1812_1346+181 others(6): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168508619 | ||||||
| chr5:168508619 | C | CAAA | 10 | a0001c0001t0001g0137 a0001c0001t0002g0272 a0001c0003t0002g0016 others(7): Show |
11 | HG00408.hp2 HG00609.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.1346+1811_1346+181 others(7): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168508619 | ||||||
| chr5:168508619 | CA | C | 50 | a0001c0001t0001g0133 a0001c0001t0001g0166 a0001c0001t0001g0173 others(47): Show |
50 | HG00408.hp1 HG00639.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1346+1813delA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168508619 | ||||||
| chr5:168508619 | CAAA | C | 7 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(4): Show |
8 | HG02145.hp2 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1346+1811_1346+181 others(7): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168508619 | ||||||
| chr5:168508619 | CAAAA | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0051 others(18): Show |
23 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.1346+1810_1346+181 others(8): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168508619 | ||||||
| chr5:168508745 | A | G | 3 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0353 |
3 | HG00408.hp1 HG02523.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1347-1836A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508745 | |||||||
| chr5:168508773 | C | G | 1 | a0001c0007t0001g0047 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1347-1808C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508773 | |||||||
| chr5:168508781 | C | T | 1 | a0001c0007t0001g0047 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1347-1800C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508781 | |||||||
| chr5:168508782 | C | G | 1 | a0001c0007t0001g0047 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1347-1799C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508782 | |||||||
| chr5:168508793 | G | A | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1347-1788G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508793 | |||||||
| chr5:168508823 | G | A | 1 | a0002c0004t0001g0134 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1347-1758G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508823 | |||||||
| chr5:168508833 | T | C | 1 | a0001c0010t0001g0062 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1347-1748T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508833 | |||||||
| chr5:168508852 | G | A | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0269 others(1): Show |
4 | HG01943.hp1 HG02451.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1347-1729G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508852 | |||||||
| chr5:168508871 | CCT | C | 4 | a0002c0002t0001g0090 a0002c0002t0001g0091 a0002c0002t0001g0093 others(1): Show |
4 | HG01175.hp2 HG01517.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1347-1705_1347-170 others(6): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168508871 | ||||||
| chr5:168508978 | G | C | 1 | a0002c0004t0001g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1347-1603G>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508978 | |||||||
| chr5:168508995 | T | G | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1347-1586T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168508995 | |||||||
| chr5:168509007 | A | G | 1 | a0001c0003t0002g0279 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1347-1574A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509007 | |||||||
| chr5:168509014 | G | A | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1347-1567G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509014 | |||||||
| chr5:168509125 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1347-1456G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509125 | |||||||
| chr5:168509155 | C | T | 4 | a0001c0007t0001g0047 a0001c0007t0001g0048 a0001c0007t0001g0049 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-1426C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509155 | |||||||
| chr5:168509316 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1347-1265A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509316 | |||||||
| chr5:168509327 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1347-1254G>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509327 | |||||||
| chr5:168509417 | T | C | 2 | a0002c0004t0001g0075 a0002c0004t0001g0076 |
2 | NA18941.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1347-1164T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509417 | |||||||
| chr5:168509418 | A | G | 292 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(289): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1347-1163A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509418 | |||||||
| chr5:168509438 | A | AC | 31 | a0001c0001t0001g0148 a0001c0001t0001g0193 a0001c0001t0001g0196 others(28): Show |
36 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1347-1130dupC | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168509438 | ||||||
| chr5:168509438 | AC | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(114): Show |
125 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.1347-1130delC | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168509438 | ||||||
| chr5:168509438 | ACC | A | 103 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0065 others(100): Show |
110 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1347-1131_1347-113 others(6): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168509438 | ||||||
| chr5:168509438 | ACCC | A | 22 | a0001c0001t0001g0133 a0001c0001t0001g0147 a0001c0001t0001g0154 others(19): Show |
22 | HG00408.hp2 HG01884.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.1347-1132_1347-113 others(7): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168509438 | ||||||
| chr5:168509438 | ACCCC | A | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1347-1133_1347-113 others(8): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168509438 | ||||||
| chr5:168509441 | C | G | 2 | a0002c0004t0001g0075 a0002c0004t0001g0076 |
2 | NA18941.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1347-1140C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509441 | |||||||
| chr5:168509451 | C | G | 1 | a0001c0001t0001g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1347-1130C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509451 | |||||||
| chr5:168509588 | C | T | 3 | a0001c0001t0001g0322 a0001c0001t0001g0341 a0001c0001t0001g0342 |
3 | NA18747.hp2 NA18987.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1347-993C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509588 | |||||||
| chr5:168509663 | CT | C | 292 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(289): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1347-904delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 168509663 | ||||||
| chr5:168509720 | A | T | 1 | a0001c0001t0001g0189 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1347-861A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509720 | |||||||
| chr5:168509878 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02818.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1347-703G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509878 | |||||||
| chr5:168509901 | T | A | 52 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0310 others(49): Show |
52 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1347-680T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168509901 | |||||||
| chr5:168510001 | G | A | 4 | a0001c0007t0001g0047 a0001c0007t0001g0048 a0001c0007t0001g0049 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-580G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168510001 | |||||||
| chr5:168510050 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0168 |
2 | HG01981.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1347-531C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168510050 | |||||||
| chr5:168510134 | A | G | 62 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(59): Show |
72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1347-447A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168510134 | |||||||
| chr5:168510182 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1347-399T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168510182 | |||||||
| chr5:168510248 | C | G | 15 | a0003c0005t0001g0020 a0003c0005t0001g0022 a0003c0005t0001g0027 others(12): Show |
16 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1347-333C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168510248 | |||||||
| chr5:168510327 | G | A | 3 | a0001c0007t0001g0048 a0001c0007t0001g0049 a0001c0007t0001g0050 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1347-254G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168510327 | |||||||
| chr5:168510410 | G | A | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1347-171G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168510410 | |||||||
| chr5:168510417 | T | C | 1 | a0002c0002t0001g0105 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1347-164T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168510417 | |||||||
| chr5:168510451 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1347-130C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 11/14 | chr5 | 168510451 | |||||||
| chr5:168510796 | A | C | 29 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(26): Show |
29 | HG00408.hp1 HG00733.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.1452+110A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168510796 | |||||||
| chr5:168510818 | T | C | 2 | a0001c0007t0001g0048 a0001c0007t0001g0049 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1452+132T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168510818 | |||||||
| chr5:168510899 | C | A | 14 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(11): Show |
18 | HG00423.hp2 HG02155.hp2 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.1452+213C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168510899 | |||||||
| chr5:168510919 | G | A | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1452+233G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168510919 | |||||||
| chr5:168510957 | A | T | 62 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(59): Show |
72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1452+271A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168510957 | |||||||
| chr5:168510968 | T | C | 2 | a0001c0001t0001g0241 a0001c0001t0001g0243 |
2 | NA18964.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1452+282T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168510968 | |||||||
| chr5:168511056 | A | G | 2 | a0001c0003t0002g0284 a0001c0003t0002g0286 |
2 | HG00408.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1452+370A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511056 | |||||||
| chr5:168511076 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1452+390C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511076 | |||||||
| chr5:168511112 | T | C | 14 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(11): Show |
18 | HG00423.hp2 HG02155.hp2 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.1452+426T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511112 | |||||||
| chr5:168511188 | A | C | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1452+502A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511188 | |||||||
| chr5:168511195 | A | AT | 52 | a0001c0001t0001g0148 a0001c0001t0001g0219 a0001c0001t0001g0255 others(49): Show |
57 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1452+527dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 168511195 | ||||||
| chr5:168511195 | AT | A | 30 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0065 others(27): Show |
31 | HG00323.hp2 HG01167.hp1 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.1452+527delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 168511195 | ||||||
| chr5:168511195 | ATT | A | 32 | a0001c0001t0001g0069 a0001c0001t0002g0272 a0001c0001t0002g0273 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1452+526_1452+527d others(4): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 168511195 | ||||||
| chr5:168511196 | T | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0155 a0001c0001t0001g0180 others(6): Show |
10 | HG00558.hp1 HG02015.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.1452+510T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511196 | |||||||
| chr5:168511366 | G | A | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1452+680G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511366 | |||||||
| chr5:168511377 | G | C | 1 | a0001c0003t0002g0279 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1452+691G>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511377 | |||||||
| chr5:168511447 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1452+761C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511447 | |||||||
| chr5:168511528 | G | A | 62 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(59): Show |
72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1452+842G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511528 | |||||||
| chr5:168511534 | C | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+848C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511534 | |||||||
| chr5:168511535 | T | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+849T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511535 | |||||||
| chr5:168511536 | G | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+850G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511536 | |||||||
| chr5:168511537 | G | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+851G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511537 | |||||||
| chr5:168511538 | T | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+852T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511538 | |||||||
| chr5:168511539 | C | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+853C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511539 | |||||||
| chr5:168511541 | A | G | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1452+855A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511541 | |||||||
| chr5:168511542 | G | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+856G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511542 | |||||||
| chr5:168511543 | G | T | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+857G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511543 | |||||||
| chr5:168511544 | C | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+858C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511544 | |||||||
| chr5:168511546 | C | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+860C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511546 | |||||||
| chr5:168511549 | C | T | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+863C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511549 | |||||||
| chr5:168511551 | G | T | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+865G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511551 | |||||||
| chr5:168511552 | G | T | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+866G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511552 | |||||||
| chr5:168511553 | C | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+867C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511553 | |||||||
| chr5:168511555 | C | T | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+869C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511555 | |||||||
| chr5:168511557 | G | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+871G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511557 | |||||||
| chr5:168511559 | C | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+873C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511559 | |||||||
| chr5:168511561 | G | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+875G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511561 | |||||||
| chr5:168511564 | G | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+878G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511564 | |||||||
| chr5:168511568 | A | T | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+882A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511568 | |||||||
| chr5:168511569 | G | T | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+883G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511569 | |||||||
| chr5:168511571 | G | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+885G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511571 | |||||||
| chr5:168511572 | G | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+886G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511572 | |||||||
| chr5:168511576 | G | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+890G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511576 | |||||||
| chr5:168511579 | C | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+893C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511579 | |||||||
| chr5:168511580 | A | T | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+894A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511580 | |||||||
| chr5:168511581 | G | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+895G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511581 | |||||||
| chr5:168511583 | C | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+897C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511583 | |||||||
| chr5:168511585 | T | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+899T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511585 | |||||||
| chr5:168511586 | C | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+900C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511586 | |||||||
| chr5:168511592 | G | T | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+906G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511592 | |||||||
| chr5:168511596 | G | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+910G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511596 | |||||||
| chr5:168511597 | T | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+911T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511597 | |||||||
| chr5:168511598 | T | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+912T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511598 | |||||||
| chr5:168511600 | G | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+914G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511600 | |||||||
| chr5:168511602 | C | T | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+916C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511602 | |||||||
| chr5:168511604 | G | T | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+918G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511604 | |||||||
| chr5:168511605 | C | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+919C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511605 | |||||||
| chr5:168511606 | C | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+920C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511606 | |||||||
| chr5:168511607 | T | A | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+921T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511607 | |||||||
| chr5:168511615 | A | T | 1 | a0003c0006t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452+929A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168511615 | |||||||
| chr5:168512089 | G | A | 14 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(11): Show |
14 | HG01081.hp1 HG01943.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1452+1403G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168512089 | |||||||
| chr5:168512105 | C | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0365 |
2 | HG01981.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1452+1419C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168512105 | |||||||
| chr5:168512123 | TTACAGGC others(1): Show |
T | 21 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0158 others(18): Show |
21 | HG01074.hp1 HG01099.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1452+1440_1452+144 others(12): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 168512123 | ||||||
| chr5:168512142 | C | T | 1 | a0001c0001t0001g0340 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1452+1456C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168512142 | |||||||
| chr5:168512260 | T | C | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02818.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1452+1574T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168512260 | |||||||
| chr5:168512331 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02818.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1452+1645G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168512331 | |||||||
| chr5:168512360 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1452+1674G>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168512360 | |||||||
| chr5:168512369 | C | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1452+1683C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168512369 | |||||||
| chr5:168512372 | A | G | 62 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(59): Show |
72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1452+1686A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168512372 | |||||||
| chr5:168512377 | C | T | 63 | a0001c0001t0001g0156 a0001c0001t0002g0145 a0001c0001t0002g0272 others(60): Show |
73 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1452+1691C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168512377 | |||||||
| chr5:168512478 | T | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1452+1792T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168512478 | |||||||
| chr5:168512657 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1452+1971G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168512657 | |||||||
| chr5:168512734 | C | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1452+2048C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168512734 | |||||||
| chr5:168513016 | T | C | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1452+2330T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513016 | |||||||
| chr5:168513052 | C | CTT | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1452+2376_1452+237 others(6): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 168513052 | ||||||
| chr5:168513076 | C | T | 57 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(54): Show |
62 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1452+2390C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513076 | |||||||
| chr5:168513107 | A | G | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1452+2421A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513107 | |||||||
| chr5:168513203 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1452+2517G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513203 | |||||||
| chr5:168513211 | A | C | 1 | a0001c0001t0001g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1452+2525A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513211 | |||||||
| chr5:168513221 | A | AT | 21 | a0001c0001t0001g0011 a0001c0001t0001g0148 a0001c0001t0001g0151 others(18): Show |
22 | HG00733.hp1 HG00735.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1452+2553dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 168513221 | ||||||
| chr5:168513221 | A | T | 7 | a0001c0001t0001g0308 a0001c0001t0001g0329 a0001c0001t0001g0334 others(4): Show |
7 | HG00099.hp2 HG01123.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.1452+2535A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513221 | |||||||
| chr5:168513221 | AT | A | 11 | a0001c0001t0001g0061 a0001c0001t0001g0203 a0001c0001t0001g0240 others(8): Show |
11 | HG00639.hp2 HG01167.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.1452+2553delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 168513221 | ||||||
| chr5:168513277 | C | G | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1452+2591C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513277 | |||||||
| chr5:168513312 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1452+2626G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513312 | |||||||
| chr5:168513317 | C | T | 1 | a0002c0004t0001g0096 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1452+2631C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513317 | |||||||
| chr5:168513386 | C | G | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1452+2700C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513386 | |||||||
| chr5:168513467 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1452+2781A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513467 | |||||||
| chr5:168513643 | G | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1452+2957G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513643 | |||||||
| chr5:168513669 | A | AAGAGTCT others(339): Show |
1 | a0001c0001t0001g0250 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1452+3002_1452+300 others(350): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 168513669 | ||||||
| chr5:168513669 | A | AAGAGTCT others(340): Show |
1 | a0001c0001t0001g0251 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1452+3002_1452+300 others(351): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 168513669 | ||||||
| chr5:168513721 | C | A | 32 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0299 others(29): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1452+3035C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513721 | |||||||
| chr5:168513890 | G | A | 62 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(59): Show |
72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1453-2888G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513890 | |||||||
| chr5:168513905 | T | G | 4 | a0001c0007t0001g0047 a0001c0007t0001g0048 a0001c0007t0001g0049 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1453-2873T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513905 | |||||||
| chr5:168513914 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1453-2864G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513914 | |||||||
| chr5:168513995 | G | T | 1 | a0001c0001t0001g0314 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1453-2783G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168513995 | |||||||
| chr5:168514007 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1453-2771C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514007 | |||||||
| chr5:168514067 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1453-2711T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514067 | |||||||
| chr5:168514115 | T | G | 33 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(30): Show |
38 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1453-2663T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514115 | |||||||
| chr5:168514228 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1453-2550C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514228 | |||||||
| chr5:168514231 | A | G | 33 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(30): Show |
38 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1453-2547A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514231 | |||||||
| chr5:168514257 | C | T | 4 | a0001c0007t0001g0047 a0001c0007t0001g0048 a0001c0007t0001g0049 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1453-2521C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514257 | |||||||
| chr5:168514279 | C | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
15 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.1453-2499C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514279 | |||||||
| chr5:168514307 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0170 |
2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1453-2471C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514307 | |||||||
| chr5:168514334 | C | T | 1 | a0002c0002t0001g0085 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1453-2444C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514334 | |||||||
| chr5:168514354 | A | C | 1 | a0001c0001t0001g0316 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1453-2424A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514354 | |||||||
| chr5:168514360 | T | C | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02818.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1453-2418T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514360 | |||||||
| chr5:168514449 | G | A | 62 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(59): Show |
72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1453-2329G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514449 | |||||||
| chr5:168514527 | T | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0051 others(39): Show |
44 | HG00673.hp1 HG01081.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.1453-2251T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514527 | |||||||
| chr5:168514569 | A | C | 89 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(86): Show |
94 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1453-2209A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514569 | |||||||
| chr5:168514763 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1453-2015A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514763 | |||||||
| chr5:168514829 | T | C | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02818.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1453-1949T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514829 | |||||||
| chr5:168514853 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1453-1925A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514853 | |||||||
| chr5:168514860 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1453-1918C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514860 | |||||||
| chr5:168514911 | T | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(21): Show |
27 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.1453-1867T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514911 | |||||||
| chr5:168514985 | C | T | 62 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(59): Show |
72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1453-1793C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168514985 | |||||||
| chr5:168515084 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1453-1694A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168515084 | |||||||
| chr5:168515208 | G | A | 91 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(88): Show |
96 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1453-1570G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168515208 | |||||||
| chr5:168515413 | A | G | 4 | a0001c0007t0001g0047 a0001c0007t0001g0048 a0001c0007t0001g0049 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1453-1365A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168515413 | |||||||
| chr5:168515431 | A | G | 1 | a0002c0002t0001g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1453-1347A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168515431 | |||||||
| chr5:168515540 | A | C | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1453-1238A>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168515540 | |||||||
| chr5:168515593 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(91): Show |
107 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1453-1185G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168515593 | |||||||
| chr5:168515621 | T | C | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1453-1157T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168515621 | |||||||
| chr5:168515626 | G | A | 6 | a0002c0002t0001g0073 a0002c0002t0001g0079 a0002c0002t0001g0080 others(3): Show |
6 | HG00642.hp1 HG02683.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453-1152G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168515626 | |||||||
| chr5:168515732 | C | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1453-1046C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168515732 | |||||||
| chr5:168515760 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1453-1018C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168515760 | |||||||
| chr5:168515857 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1453-921C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168515857 | |||||||
| chr5:168516020 | G | T | 1 | a0001c0001t0001g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1453-758G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168516020 | |||||||
| chr5:168516085 | G | T | 76 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(73): Show |
87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1453-693G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168516085 | |||||||
| chr5:168516189 | T | TA | 6 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
7 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1453-587dupA | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 168516189 | ||||||
| chr5:168516192 | C | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
7 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1453-586C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168516192 | |||||||
| chr5:168516193 | C | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
7 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1453-585C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168516193 | |||||||
| chr5:168516355 | C | G | 1 | a0002c0002t0001g0077 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1453-423C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168516355 | |||||||
| chr5:168516413 | TG | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(21): Show |
27 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.1453-363delG | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 168516413 | ||||||
| chr5:168516533 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(21): Show |
27 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.1453-245C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168516533 | |||||||
| chr5:168516588 | C | T | 1 | a0003c0005t0001g0038 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1453-190C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168516588 | |||||||
| chr5:168516627 | C | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1453-151C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168516627 | |||||||
| chr5:168516714 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1453-64A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168516714 | |||||||
| chr5:168516723 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1453-55C>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168516723 | |||||||
| chr5:168516761 | T | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0064 |
2 | HG02135.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1453-17T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 12/14 | chr5 | 168516761 | |||||||
| chr5:168516999 | T | G | 1 | a0001c0001t0001g0219 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1625+49T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168516999 | |||||||
| chr5:168517020 | C | CT | 39 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0066 others(36): Show |
45 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1625+83dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 168517020 | ||||||
| chr5:168517028 | T | G | 1 | a0002c0002t0001g0098 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1625+78T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517028 | |||||||
| chr5:168517043 | C | T | 4 | a0001c0007t0001g0047 a0001c0007t0001g0048 a0001c0007t0001g0049 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1625+93C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517043 | |||||||
| chr5:168517139 | T | G | 1 | a0001c0001t0001g0070 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1625+189T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517139 | |||||||
| chr5:168517170 | T | C | 4 | a0003c0006t0001g0023 a0003c0006t0001g0026 a0003c0006t0001g0031 others(1): Show |
4 | HG00140.hp1 HG01070.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1625+220T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517170 | |||||||
| chr5:168517199 | G | A | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1625+249G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517199 | |||||||
| chr5:168517331 | C | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1625+381C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517331 | |||||||
| chr5:168517412 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1626-403G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517412 | |||||||
| chr5:168517430 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1626-385A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517430 | |||||||
| chr5:168517477 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1626-338C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517477 | |||||||
| chr5:168517489 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1626-326G>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517489 | |||||||
| chr5:168517536 | C | T | 21 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0158 others(18): Show |
21 | HG01074.hp1 HG01099.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1626-279C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517536 | |||||||
| chr5:168517537 | C | T | 35 | a0001c0001t0001g0307 a0001c0001t0001g0333 a0001c0001t0001g0344 others(32): Show |
40 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1626-278C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517537 | |||||||
| chr5:168517556 | C | A | 7 | a0001c0001t0001g0153 a0001c0001t0001g0301 a0001c0001t0001g0302 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1626-259C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517556 | |||||||
| chr5:168517558 | G | A | 2 | a0001c0003t0002g0289 a0001c0003t0002g0290 |
2 | NA18952.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1626-257G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517558 | |||||||
| chr5:168517560 | T | C | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1626-255T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517560 | |||||||
| chr5:168517688 | C | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1626-127C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | chr5 | 168517688 | |||||||
| chr5:168517738 | A | ATTTCTGA others(25): Show |
62 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(59): Show |
72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1626-73_1626-72ins others(32): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 168517738 | ||||||
| chr5:168517803 | G | GT | 15 | a0001c0001t0001g0229 a0001c0001t0001g0255 a0001c0001t0001g0256 others(12): Show |
15 | HG01943.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
splice_region_variant&intron_variant | LOW | c.1626-4dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 168517803 | ||||||
| chr5:168518071 | C | CT | 14 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(11): Show |
14 | HG01106.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1873+33dupT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTT | 25 | a0001c0001t0001g0341 a0001c0001t0002g0299 a0001c0003t0002g0005 others(22): Show |
30 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1873+30_1873+33dup others(4): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTT | 6 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0003t0002g0276 others(3): Show |
6 | HG00673.hp2 HG02572.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.1873+29_1873+33dup others(5): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTT | 6 | a0001c0001t0001g0147 a0001c0001t0001g0302 a0001c0001t0001g0308 others(3): Show |
6 | HG02735.hp1 HG02897.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1873+28_1873+33dup others(6): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0216 a0001c0001t0001g0260 a0001c0001t0001g0267 others(5): Show |
8 | HG00735.hp2 HG01081.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1873+26_1873+33dup others(8): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0303 a0001c0001t0001g0306 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1873+24_1873+33dup others(10): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0301 a0001c0001t0001g0305 |
2 | HG01243.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1873+23_1873+33dup others(11): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(5): Show |
4 | a0001c0001t0001g0358 a0001c0001t0001g0360 a0001c0001t0001g0361 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1873+22_1873+33dup others(12): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0318 a0001c0001t0001g0357 a0001c0001t0001g0359 |
3 | HG01192.hp2 HG02559.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1873+21_1873+33dup others(13): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0019 a0001c0001t0001g0257 a0001c0001t0001g0332 |
4 | HG01243.hp1 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1873+20_1873+33dup others(14): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(8): Show |
4 | a0001c0001t0001g0177 a0001c0001t0001g0236 a0001c0001t0001g0256 others(1): Show |
4 | HG02055.hp1 HG06807.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1873+19_1873+33dup others(15): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(9): Show |
36 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(33): Show |
39 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1873+18_1873+33dup others(16): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(10): Show |
32 | a0001c0001t0001g0014 a0001c0001t0001g0155 a0001c0001t0001g0180 others(29): Show |
33 | HG00544.hp2 HG00558.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1873+17_1873+33dup others(17): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(11): Show |
9 | a0001c0001t0001g0174 a0001c0001t0001g0182 a0001c0001t0001g0186 others(6): Show |
9 | HG02015.hp2 HG02040.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1873+16_1873+33dup others(18): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(12): Show |
4 | a0001c0001t0001g0194 a0001c0001t0001g0324 a0001c0001t0001g0352 others(1): Show |
4 | HG01123.hp2 HG02074.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1873+15_1873+33dup others(19): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(13): Show |
4 | a0001c0001t0001g0225 a0001c0001t0001g0309 a0001c0001t0001g0340 others(1): Show |
4 | HG02257.hp2 HG03130.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1873+14_1873+33dup others(20): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(14): Show |
3 | a0001c0001t0001g0200 a0001c0001t0001g0224 a0001c0001t0001g0249 |
3 | HG02083.hp2 HG04184.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1873+13_1873+33dup others(21): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(15): Show |
4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0215 others(1): Show |
4 | HG00423.hp1 HG02027.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1873+12_1873+33dup others(22): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(17): Show |
2 | a0001c0001t0001g0158 a0001c0001t0001g0164 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1873+10_1873+33dup others(24): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(18): Show |
4 | a0001c0001t0001g0159 a0001c0001t0001g0166 a0001c0001t0001g0170 others(1): Show |
4 | HG01884.hp1 HG01993.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1873+33_1873+34ins others(25): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(19): Show |
4 | a0001c0001t0001g0154 a0001c0001t0001g0165 a0001c0001t0001g0167 others(1): Show |
4 | HG02486.hp2 HG02647.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1873+33_1873+34ins others(26): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(20): Show |
7 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1873+33_1873+34ins others(27): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(21): Show |
5 | a0001c0001t0001g0161 a0001c0001t0001g0173 a0001c0001t0001g0271 others(2): Show |
5 | HG01074.hp1 HG01099.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1873+33_1873+34ins others(28): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0001g0312 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1873+33_1873+34ins others(29): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0337 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1873+33_1873+34ins others(31): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(25): Show |
6 | a0001c0001t0001g0310 a0001c0001t0001g0326 a0001c0001t0001g0335 others(3): Show |
6 | HG02523.hp2 HG02970.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1873+33_1873+34ins others(32): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(26): Show |
10 | a0001c0001t0001g0311 a0001c0001t0001g0321 a0001c0001t0001g0322 others(7): Show |
10 | HG00099.hp2 HG00323.hp2 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.1873+33_1873+34ins others(33): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(27): Show |
4 | a0001c0001t0001g0317 a0001c0001t0001g0331 a0001c0001t0001g0336 others(1): Show |
4 | NA18971.hp2 NA19003.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1873+33_1873+34ins others(34): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(28): Show |
1 | a0001c0001t0001g0347 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1873+33_1873+34ins others(35): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(29): Show |
1 | a0001c0001t0001g0348 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1873+33_1873+34ins others(36): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(30): Show |
2 | a0001c0001t0001g0345 a0001c0001t0001g0350 |
2 | HG00639.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1873+33_1873+34ins others(37): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(32): Show |
3 | a0001c0001t0001g0307 a0001c0001t0001g0351 a0001c0001t0001g0354 |
3 | HG01167.hp1 HG01346.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1873+33_1873+34ins others(39): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(33): Show |
1 | a0001c0001t0001g0316 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1873+33_1873+34ins others(40): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(34): Show |
2 | a0001c0001t0001g0327 a0001c0001t0001g0365 |
2 | HG00408.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1873+33_1873+34ins others(41): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(35): Show |
1 | a0001c0001t0001g0334 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1873+33_1873+34ins others(42): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(36): Show |
1 | a0001c0001t0001g0333 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1873+33_1873+34ins others(43): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | C | CTTTTTTT others(45): Show |
1 | a0001c0001t0001g0353 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1873+33_1873+34ins others(52): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518071 | CT | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(55): Show |
66 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.1873+33delT | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 168518071 | ||||||
| chr5:168518082 | TTTTTTTT others(7): Show |
T | 1 | a0001c0001t0001g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1873+21_1873+34del others(14): Show |
RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518082 | |||||||
| chr5:168518096 | A | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1873+34A>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518096 | |||||||
| chr5:168518097 | G | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1873+35G>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518097 | |||||||
| chr5:168518108 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1873+46G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518108 | |||||||
| chr5:168518139 | G | A | 62 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(59): Show |
72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1873+77G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518139 | |||||||
| chr5:168518164 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1873+102G>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518164 | |||||||
| chr5:168518224 | C | T | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1873+162C>T | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518224 | |||||||
| chr5:168518301 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1873+239T>C | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518301 | |||||||
| chr5:168518310 | T | A | 1 | a0001c0001t0001g0237 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1873+248T>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518310 | |||||||
| chr5:168518464 | A | G | 1 | a0003c0005t0001g0146 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1873+402A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518464 | |||||||
| chr5:168518517 | A | G | 2 | a0002c0004t0001g0045 a0002c0004t0001g0088 |
2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1873+455A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518517 | |||||||
| chr5:168518590 | A | G | 4 | a0001c0007t0001g0047 a0001c0007t0001g0048 a0001c0007t0001g0049 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1874-491A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518590 | |||||||
| chr5:168518612 | C | A | 29 | a0003c0005t0001g0002 a0003c0005t0001g0007 a0003c0005t0001g0008 others(26): Show |
34 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1874-469C>A | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518612 | |||||||
| chr5:168518642 | T | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0046 others(91): Show |
107 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1874-439T>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168518642 | |||||||
| chr5:168519071 | A | G | 62 | a0001c0001t0002g0145 a0001c0001t0002g0272 a0001c0001t0002g0273 others(59): Show |
72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1874-10A>G | RARS1 | ENSG00000113643.9 | transcript | ENST00000231572.8 | protein_coding | 14/14 | chr5 | 168519071 |