Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79731 |
| ensemblid | ENSG00000137513.11 |
| hgncid | 26274 |
| symbol | NARS2 |
| name | asparaginyl-tRNA synthetase 2, mitochondrial |
| refseq_nuc | NM_024678.6 |
| refseq_prot | NP_078954.4 |
| ensembl_nuc | ENST00000281038.10 |
| ensembl_prot | ENSP00000281038.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 78435968 |
| end | 78574864 |
| strand | - |
| ver | v1.2 |
| region | chr11:78435968-78574864 |
| region5000 | chr11:78430968-78579864 |
| regionname0 | NARS2_chr11_78435968_78574864 |
| regionname5000 | NARS2_chr11_78430968_78579864 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 477 | 186 | 70 | 26 | 68 | 2 | 19 | 54 | NARS2_chr11_78430968_78579864 | NARS2 | MLGVR others(472): Show |
chr11 | 78430968 | 78579864 |
| a0002 | 1/0 | 477 | 106 | 20 | 22 | 56 | 2 | 5 | 46 | NARS2_chr11_78430968_78579864 | NARS2 | MLGVR others(472): Show |
chr11 | 78430968 | 78579864 |
| a0003 | 0/0 | 477 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | MLGVR others(472): Show |
chr11 | 78430968 | 78579864 |
| a0004 | 0/0 | 477 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | MLGVR others(472): Show |
chr11 | 78430968 | 78579864 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1431 | 144 | 32 | 26 | 65 | 2 | 18 | NARS2_chr11_78430968_78579864 | NARS2 | ATGCT others(1426): Show |
chr11 | 78430968 | 78579864 | ||
| a0001c0003 | 0/0 | 1431 | 18 | 15 | 0 | 2 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | ATGCT others(1426): Show |
chr11 | 78430968 | 78579864 | ||
| a0001c0004 | 0/0 | 1431 | 13 | 13 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | ATGCT others(1426): Show |
chr11 | 78430968 | 78579864 | ||
| a0001c0005 | 0/0 | 1431 | 5 | 5 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | ATGCT others(1426): Show |
chr11 | 78430968 | 78579864 | ||
| a0001c0006 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | ATGCT others(1426): Show |
chr11 | 78430968 | 78579864 | ||
| a0001c0007 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | ATGCT others(1426): Show |
chr11 | 78430968 | 78579864 | ||
| a0001c0010 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | ATGCT others(1426): Show |
chr11 | 78430968 | 78579864 | ||
| a0001c0011 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | ATGCT others(1426): Show |
chr11 | 78430968 | 78579864 | ||
| a0002c0002 | 1/0 | 1431 | 106 | 20 | 22 | 56 | 2 | 5 | NARS2_chr11_78430968_78579864 | NARS2 | ATGCT others(1426): Show |
chr11 | 78430968 | 78579864 | ||
| a0003c0008 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | ATGCT others(1426): Show |
chr11 | 78430968 | 78579864 | ||
| a0004c0009 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | ATGCT others(1426): Show |
chr11 | 78430968 | 78579864 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2512 | 133 | 28 | 23 | 62 | 2 | 17 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0001t0005 | 0/0 | 2512 | 6 | 2 | 1 | 3 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0001t0009 | 0/0 | 2512 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0001t0010 | 0/0 | 2512 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0001t0011 | 0/0 | 2512 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0001t0012 | 0/0 | 2512 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0001t0014 | 0/0 | 2512 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0003t0002 | 0/0 | 2512 | 2 | 0 | 0 | 2 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0003t0003 | 0/0 | 2512 | 4 | 4 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0003t0004 | 0/0 | 2512 | 3 | 3 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0003t0005 | 0/0 | 2512 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0003t0006 | 0/0 | 2513 | 7 | 7 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2508): Show |
chr11 | 78430968 | 78579864 |
| a0001c0003t0015 | 0/0 | 2512 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0004t0004 | 0/0 | 2512 | 6 | 6 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0004t0007 | 0/0 | 2512 | 6 | 6 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0004t0013 | 0/0 | 2512 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0005t0001 | 0/0 | 2512 | 5 | 5 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0006t0003 | 0/0 | 2512 | 2 | 2 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0007t0003 | 0/0 | 2512 | 2 | 2 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0010t0001 | 0/0 | 2512 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0001c0011t0003 | 0/0 | 2512 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0002c0002t0002 | 0/0 | 2512 | 86 | 9 | 20 | 51 | 2 | 4 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0002c0002t0003 | 1/0 | 2512 | 14 | 7 | 2 | 3 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0002c0002t0005 | 0/0 | 2512 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0002c0002t0008 | 0/0 | 2512 | 4 | 4 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0002c0002t0016 | 0/0 | 2512 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0003c0008t0003 | 0/0 | 2512 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| a0004c0009t0002 | 0/0 | 2512 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | GTAGC others(2507): Show |
chr11 | 78430968 | 78579864 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0009g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0010g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0012g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0001t0014g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0005g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0003t0015g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0004t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0004t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0004t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0004t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0004t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0004t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0004t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0004t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0004t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0004t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0004t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0004t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0004t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0005t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0005t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0006t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0006t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0007t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0007t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0010t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0001c0011t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0008g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0002c0002t0016g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0003c0008t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| a0004c0009t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0162 | EUR | GBR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | CHS | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | CHS | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0249 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0248 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0183 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0191 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0212 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0220 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0232 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0221 | AMR | PUR | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01255 | hp1 | a0001 | c0001 | t0009 | g0060 | AMR | CLM | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0199 | AMR | CLM | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0134 | AMR | CLM | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0250 | AMR | CLM | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0189 | EUR | IBS | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01884 | hp1 | a0001 | c0004 | t0007 | g0154 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01891 | hp1 | a0001 | c0005 | t0001 | g0074 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0178 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0181 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0179 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01978 | hp1 | a0002 | c0002 | t0003 | g0174 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01978 | hp2 | a0001 | c0001 | t0012 | g0151 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0255 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0177 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0233 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | KHV | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0256 | EAS | KHV | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0235 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02055 | hp2 | a0001 | c0003 | t0004 | g0274 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0253 | EAS | KHV | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0228 | EAS | KHV | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0180 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | CDX | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CDX | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02257 | hp2 | a0001 | c0004 | t0007 | g0155 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02258 | hp2 | a0002 | c0002 | t0003 | g0240 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0247 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0203 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0200 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02451 | hp1 | a0001 | c0003 | t0006 | g0264 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0132 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02572 | hp1 | a0002 | c0002 | t0003 | g0242 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0243 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02615 | hp1 | a0001 | c0005 | t0001 | g0146 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02615 | hp2 | a0002 | c0002 | t0003 | g0288 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02622 | hp1 | a0002 | c0002 | t0008 | g0292 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0244 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02630 | hp1 | a0001 | c0003 | t0006 | g0265 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02630 | hp2 | a0001 | c0004 | t0004 | g0282 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02647 | hp2 | a0002 | c0002 | t0008 | g0290 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02717 | hp1 | a0001 | c0003 | t0003 | g0169 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02723 | hp2 | a0001 | c0003 | t0003 | g0167 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0252 | SAS | PJL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02809 | hp1 | a0001 | c0003 | t0006 | g0261 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02809 | hp2 | a0001 | c0007 | t0003 | g0273 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02818 | hp1 | a0001 | c0011 | t0003 | g0271 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02818 | hp2 | a0002 | c0002 | t0003 | g0245 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02886 | hp2 | a0001 | c0004 | t0013 | g0153 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02895 | hp1 | a0001 | c0003 | t0003 | g0170 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02895 | hp2 | a0002 | c0002 | t0008 | g0291 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02965 | hp2 | a0001 | c0003 | t0006 | g0260 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02970 | hp1 | a0003 | c0008 | t0003 | g0159 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0287 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0236 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02976 | hp2 | a0001 | c0004 | t0004 | g0285 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03041 | hp1 | a0001 | c0004 | t0004 | g0283 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03041 | hp2 | a0002 | c0002 | t0003 | g0241 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03098 | hp1 | a0001 | c0004 | t0007 | g0157 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03098 | hp2 | a0001 | c0006 | t0003 | g0279 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03130 | hp1 | a0001 | c0003 | t0015 | g0266 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0237 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03139 | hp2 | a0001 | c0003 | t0004 | g0275 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03195 | hp1 | a0001 | c0007 | t0003 | g0272 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03195 | hp2 | a0001 | c0003 | t0006 | g0259 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03225 | hp1 | a0001 | c0003 | t0006 | g0262 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0238 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03453 | hp1 | a0001 | c0004 | t0004 | g0284 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03453 | hp2 | a0001 | c0005 | t0001 | g0145 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03486 | hp1 | a0001 | c0003 | t0003 | g0168 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0144 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03490 | hp1 | a0001 | c0003 | t0005 | g0131 | SAS | PJL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0254 | SAS | PJL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03516 | hp1 | a0002 | c0002 | t0003 | g0239 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0161 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03540 | hp2 | a0001 | c0005 | t0001 | g0049 | AFR | GWD | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03579 | hp1 | a0001 | c0004 | t0007 | g0152 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03579 | hp2 | a0001 | c0006 | t0003 | g0280 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0246 | SAS | BEB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG04184 | hp2 | a0002 | c0002 | t0003 | g0251 | SAS | BEB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0171 | SAS | STU | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | CHB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18747 | hp1 | a0002 | c0002 | t0003 | g0218 | EAS | CHB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | CHB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | YRI | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18941 | hp2 | a0002 | c0002 | t0016 | g0294 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18968 | hp2 | a0001 | c0003 | t0002 | g0258 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18971 | hp2 | a0002 | c0002 | t0003 | g0227 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18983 | hp2 | a0002 | c0002 | t0005 | g0001 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18987 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19003 | hp1 | a0001 | c0003 | t0002 | g0257 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19043 | hp1 | a0002 | c0002 | t0003 | g0289 | AFR | LWK | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19084 | hp2 | a0001 | c0010 | t0001 | g0017 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19090 | hp1 | a0002 | c0002 | t0003 | g0172 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA19240 | hp2 | a0001 | c0003 | t0004 | g0276 | AFR | YRI | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA20129 | hp1 | a0002 | c0002 | t0008 | g0293 | AFR | ASW | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ASW | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA20905 | hp1 | a0001 | c0001 | t0010 | g0120 | SAS | GIH | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | GIH | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0204 | AMR | CLM | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02109 | hp1 | a0001 | c0003 | t0006 | g0263 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0206 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02486 | hp1 | a0001 | c0004 | t0007 | g0158 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0192 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03471 | hp1 | a0001 | c0004 | t0004 | g0286 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | USA | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| HG06807 | hp2 | a0004 | c0009 | t0002 | g0160 | AFR | USA | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA20300 | hp1 | a0001 | c0004 | t0007 | g0156 | AFR | USA | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0136 | AFR | USA | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA21309 | hp1 | a0001 | c0004 | t0004 | g0281 | AFR | LWK | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0009 | REF | REF | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0003 | g0173 | REF | REF | NARS2_chr11_78430968_78579864 | NARS2 | chr11 | 78430968 | 78579864 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:78568744 | T | G | 1 | a0001 | 185 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(182): Show |
missense_variant | MODERATE | c.260A>C | p.Asn87Thr | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/14 | 636/2512 | 260/1434 | 87/477 | chr11 | 78568744 | |||
| chr11:78574368 | C | T | 1 | a0004 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.121G>A | p.Gly41Arg | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/14 | 497/2512 | 121/1434 | 41/477 | chr11 | 78574368 | |||
| chr11:78574463 | C | G | 1 | a0003 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.26G>C | p.Arg9Pro | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/14 | 402/2512 | 26/1434 | 9/477 | chr11 | 78574463 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:78465945 | G | A | 1 | a0001c0010 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.1095C>T | p.Phe365Phe | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/14 | 1471/2512 | 1095/1434 | 365/477 | chr11 | 78465945 | |||
| chr11:78493165 | C | T | 3 | a0001c0005 a0001c0007 a0001c0011 |
8 | HG01891.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
synonymous_variant | LOW | c.720G>A | p.Pro240Pro | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/14 | 1096/2512 | 720/1434 | 240/477 | chr11 | 78493165 | |||
| chr11:78566222 | T | C | 1 | a0001c0006 | 2 | HG03098.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.423A>G | p.Gln141Gln | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/14 | 799/2512 | 423/1434 | 141/477 | chr11 | 78566222 | |||
| chr11:78566231 | A | G | 5 | a0001c0001 a0001c0004 a0001c0005 others(2): Show |
164 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(161): Show |
synonymous_variant | LOW | c.414T>C | p.Tyr138Tyr | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/14 | 790/2512 | 414/1434 | 138/477 | chr11 | 78566231 | |||
| chr11:78568635 | G | A | 1 | a0001c0011 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.369C>T | p.Ala123Ala | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/14 | 745/2512 | 369/1434 | 123/477 | chr11 | 78568635 | |||
| chr11:78568698 | T | C | 1 | a0001c0004 | 13 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(10): Show |
synonymous_variant | LOW | c.306A>G | p.Pro102Pro | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/14 | 682/2512 | 306/1434 | 102/477 | chr11 | 78568698 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:78435975 | T | TA | 1 | a0001c0003t0006 | 7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*694dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 14/14 | 694 | chr11 | 78435975 | ||||||
| chr11:78436009 | A | G | 7 | a0001c0001t0005 a0001c0003t0002 a0001c0003t0005 others(4): Show |
98 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*661T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 14/14 | 661 | chr11 | 78436009 | ||||||
| chr11:78436328 | T | C | 7 | a0001c0001t0011 a0001c0003t0004 a0001c0003t0006 others(4): Show |
23 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*342A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 14/14 | 342 | chr11 | 78436328 | ||||||
| chr11:78436394 | A | G | 1 | a0001c0001t0010 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*276T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 14/14 | 276 | chr11 | 78436394 | ||||||
| chr11:78436424 | G | A | 1 | a0001c0003t0015 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*246C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 14/14 | 246 | chr11 | 78436424 | ||||||
| chr11:78436471 | G | A | 7 | a0001c0001t0011 a0001c0003t0004 a0001c0003t0006 others(4): Show |
23 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*199C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 14/14 | 199 | chr11 | 78436471 | ||||||
| chr11:78436666 | C | T | 2 | a0001c0001t0009 a0001c0001t0014 |
2 | HG01255.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 14/14 | 4 | chr11 | 78436666 | ||||||
| chr11:78574515 | G | T | 2 | a0001c0004t0007 a0001c0004t0013 |
7 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-27C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/14 | 27 | chr11 | 78574515 | ||||||
| chr11:78574623 | G | A | 1 | a0001c0001t0012 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-135C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/14 | 135 | chr11 | 78574623 | ||||||
| chr11:78574755 | G | C | 1 | a0002c0002t0008 | 4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-267C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/14 | 267 | chr11 | 78574755 | ||||||
| chr11:78574771 | G | A | 1 | a0002c0002t0016 | 1 | NA18941.hp2 | 5_prime_UTR_variant | MODIFIER | c.-283C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/14 | 283 | chr11 | 78574771 | ||||||
| chr11:78574830 | A | T | 10 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(7): Show |
150 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(147): Show |
5_prime_UTR_variant | MODIFIER | c.-342T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/14 | 342 | chr11 | 78574830 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:78437024 | T | C | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1290-210A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78437024 | |||||||
| chr11:78437154 | C | A | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1290-340G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78437154 | |||||||
| chr11:78437154 | C | T | 1 | a0001c0004t0007g0152 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1290-340G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78437154 | |||||||
| chr11:78437163 | T | C | 23 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(20): Show |
23 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1290-349A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78437163 | |||||||
| chr11:78437231 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1290-417C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78437231 | |||||||
| chr11:78437242 | G | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1290-428C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78437242 | |||||||
| chr11:78437626 | A | C | 11 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1290-812T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78437626 | |||||||
| chr11:78437639 | T | C | 2 | a0001c0001t0005g0121 a0002c0002t0002g0213 |
2 | NA18960.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1290-825A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78437639 | |||||||
| chr11:78437953 | T | A | 10 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(7): Show |
10 | HG02055.hp2 HG02630.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1290-1139A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78437953 | |||||||
| chr11:78437974 | C | CA | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
267 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.1290-1161dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78437974 | |||||||
| chr11:78437974 | C | CAA | 23 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0137 others(20): Show |
23 | HG02109.hp1 HG02135.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1290-1162_1290-116 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78437974 | |||||||
| chr11:78437993 | GA | G | 104 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1290-1180delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78437993 | |||||||
| chr11:78438138 | C | T | 10 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1290-1324G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78438138 | |||||||
| chr11:78438187 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1290-1373T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78438187 | |||||||
| chr11:78438226 | A | G | 2 | a0001c0001t0005g0124 a0002c0002t0002g0234 |
2 | NA18967.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1290-1412T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78438226 | |||||||
| chr11:78438233 | T | C | 2 | a0001c0003t0002g0257 a0001c0003t0002g0258 |
2 | NA18968.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1290-1419A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78438233 | |||||||
| chr11:78438283 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1290-1469G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78438283 | |||||||
| chr11:78438294 | T | A | 149 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(146): Show |
149 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.1290-1480A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78438294 | |||||||
| chr11:78438319 | C | T | 98 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(95): Show |
98 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1290-1505G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78438319 | |||||||
| chr11:78438469 | C | T | 2 | a0002c0002t0002g0183 a0002c0002t0002g0191 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1290-1655G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78438469 | |||||||
| chr11:78438529 | T | C | 1 | a0002c0002t0002g0267 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1290-1715A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78438529 | |||||||
| chr11:78438827 | G | T | 10 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1290-2013C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78438827 | |||||||
| chr11:78438915 | C | T | 133 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(130): Show |
133 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.1290-2101G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78438915 | |||||||
| chr11:78438980 | A | AT | 10 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0002g0176 others(7): Show |
10 | HG01123.hp1 HG01175.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1289+2110dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78438980 | |||||||
| chr11:78438988 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1289+2103A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78438988 | |||||||
| chr11:78439259 | G | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
7 | NA18946.hp2 NA18949.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.1289+1832C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78439259 | |||||||
| chr11:78439366 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1289+1725C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78439366 | |||||||
| chr11:78439395 | C | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1289+1696G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78439395 | |||||||
| chr11:78439407 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1289+1684A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78439407 | |||||||
| chr11:78439546 | G | A | 133 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(130): Show |
133 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.1289+1545C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78439546 | |||||||
| chr11:78439565 | G | C | 23 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(20): Show |
23 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1289+1526C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78439565 | |||||||
| chr11:78439614 | T | C | 1 | a0001c0004t0013g0153 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1289+1477A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78439614 | |||||||
| chr11:78439644 | T | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1289+1447A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78439644 | |||||||
| chr11:78439870 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1289+1221A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78439870 | |||||||
| chr11:78440020 | A | C | 2 | a0002c0002t0003g0288 a0002c0002t0003g0289 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1289+1071T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78440020 | |||||||
| chr11:78440212 | C | T | 5 | a0001c0004t0007g0152 a0002c0002t0003g0239 a0002c0002t0003g0240 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1289+879G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78440212 | |||||||
| chr11:78440255 | G | C | 4 | a0002c0002t0002g0165 a0002c0002t0002g0166 a0002c0002t0002g0184 others(1): Show |
4 | NA18747.hp2 NA18949.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1289+836C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78440255 | |||||||
| chr11:78440256 | G | T | 23 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(20): Show |
23 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1289+835C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78440256 | |||||||
| chr11:78440282 | T | C | 1 | a0002c0002t0003g0251 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1289+809A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78440282 | |||||||
| chr11:78440457 | T | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0067 a0001c0001t0001g0079 others(2): Show |
5 | NA18939.hp1 NA18941.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.1289+634A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78440457 | |||||||
| chr11:78440463 | G | C | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1289+628C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78440463 | |||||||
| chr11:78440536 | AT | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0088 a0001c0001t0001g0093 others(5): Show |
8 | HG00735.hp1 HG01106.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1289+554delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78440536 | |||||||
| chr11:78440585 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1289+506A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78440585 | |||||||
| chr11:78440842 | A | G | 17 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(14): Show |
17 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1289+249T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78440842 | |||||||
| chr11:78440883 | G | C | 1 | a0001c0001t0001g0002 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1289+208C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78440883 | |||||||
| chr11:78440929 | A | T | 1 | a0002c0002t0008g0291 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1289+162T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78440929 | |||||||
| chr11:78440964 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1289+127G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 13/13 | chr11 | 78440964 | |||||||
| chr11:78441264 | G | C | 1 | a0002c0002t0003g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1263-147C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78441264 | |||||||
| chr11:78441321 | G | A | 1 | a0002c0002t0002g0268 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1263-204C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78441321 | |||||||
| chr11:78441710 | C | CA | 27 | a0001c0001t0001g0073 a0001c0001t0001g0084 a0001c0001t0011g0132 others(24): Show |
27 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1263-594dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78441710 | |||||||
| chr11:78441858 | G | A | 1 | a0001c0004t0004g0286 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1263-741C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78441858 | |||||||
| chr11:78441863 | T | C | 7 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1263-746A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78441863 | |||||||
| chr11:78441892 | A | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1263-775T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78441892 | |||||||
| chr11:78442167 | A | G | 23 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(20): Show |
23 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1263-1050T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78442167 | |||||||
| chr11:78442512 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1262+1149C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78442512 | |||||||
| chr11:78442621 | TTC | T | 100 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(97): Show |
100 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1262+1038_1262+103 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78442621 | |||||||
| chr11:78442622 | TC | T | 33 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(30): Show |
33 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1262+1038delG | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78442622 | |||||||
| chr11:78442623 | C | T | 13 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1262+1038G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78442623 | |||||||
| chr11:78442725 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1262+936A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78442725 | |||||||
| chr11:78442840 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1262+821G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78442840 | |||||||
| chr11:78442873 | G | A | 59 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(56): Show |
59 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1262+788C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78442873 | |||||||
| chr11:78442933 | A | G | 1 | a0002c0002t0002g0250 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1262+728T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78442933 | |||||||
| chr11:78443088 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02129.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.1262+573C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443088 | |||||||
| chr11:78443102 | G | A | 97 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(94): Show |
97 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1262+559C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443102 | |||||||
| chr11:78443156 | T | C | 1 | a0001c0001t0001g0003 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1262+505A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443156 | |||||||
| chr11:78443187 | G | A | 5 | a0001c0003t0015g0266 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1262+474C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443187 | |||||||
| chr11:78443243 | G | A | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1262+418C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443243 | |||||||
| chr11:78443244 | T | C | 1 | a0002c0002t0002g0268 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1262+417A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443244 | |||||||
| chr11:78443252 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0037 |
2 | NA18946.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1262+409C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443252 | |||||||
| chr11:78443266 | G | A | 16 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(13): Show |
16 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1262+395C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443266 | |||||||
| chr11:78443310 | C | G | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1262+351G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443310 | |||||||
| chr11:78443321 | C | T | 6 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0005t0001g0074 others(3): Show |
6 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1262+340G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443321 | |||||||
| chr11:78443326 | C | CA | 10 | a0001c0001t0001g0072 a0001c0001t0001g0100 a0001c0005t0001g0074 others(7): Show |
10 | HG01891.hp1 HG02738.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1262+334dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443326 | |||||||
| chr11:78443326 | C | CAA | 28 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(25): Show |
28 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1262+333_1262+334d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443326 | |||||||
| chr11:78443326 | CA | C | 9 | a0001c0001t0001g0050 a0001c0001t0001g0069 a0001c0001t0001g0080 others(6): Show |
9 | HG01256.hp1 HG02055.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1262+334delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443326 | |||||||
| chr11:78443355 | T | G | 123 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0135 others(120): Show |
123 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.1262+306A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443355 | |||||||
| chr11:78443504 | G | A | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1262+157C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443504 | |||||||
| chr11:78443509 | A | G | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1262+152T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443509 | |||||||
| chr11:78443564 | G | A | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1262+97C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 12/13 | chr11 | 78443564 | |||||||
| chr11:78443846 | G | A | 10 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(7): Show |
10 | HG02055.hp2 HG02630.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1165-88C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78443846 | |||||||
| chr11:78443920 | T | C | 16 | a0001c0001t0001g0081 a0001c0001t0001g0135 a0001c0001t0001g0137 others(13): Show |
16 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1165-162A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78443920 | |||||||
| chr11:78444040 | T | C | 150 | a0001c0001t0001g0081 a0001c0001t0001g0135 a0001c0001t0001g0137 others(147): Show |
150 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.1165-282A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444040 | |||||||
| chr11:78444043 | C | T | 2 | a0002c0002t0002g0163 a0002c0002t0002g0164 |
2 | NA18947.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1165-285G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444043 | |||||||
| chr11:78444044 | A | G | 103 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(100): Show |
103 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1165-286T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444044 | |||||||
| chr11:78444055 | T | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-297A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444055 | |||||||
| chr11:78444074 | A | C | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1165-316T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444074 | |||||||
| chr11:78444233 | T | G | 16 | a0001c0001t0001g0081 a0001c0001t0001g0135 a0001c0001t0001g0137 others(13): Show |
16 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1165-475A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444233 | |||||||
| chr11:78444280 | T | C | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1165-522A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444280 | |||||||
| chr11:78444446 | T | G | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165-688A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444446 | |||||||
| chr11:78444494 | C | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1165-736G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444494 | |||||||
| chr11:78444697 | C | T | 7 | a0002c0002t0002g0165 a0002c0002t0002g0166 a0002c0002t0002g0184 others(4): Show |
7 | HG02135.hp1 NA18747.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.1165-939G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444697 | |||||||
| chr11:78444722 | C | A | 150 | a0001c0001t0001g0081 a0001c0001t0001g0135 a0001c0001t0001g0137 others(147): Show |
150 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.1165-964G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444722 | |||||||
| chr11:78444727 | C | A | 1 | a0002c0002t0002g0214 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1165-969G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444727 | |||||||
| chr11:78444727 | C | CAAAA | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-973_1165-970d others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444727 | |||||||
| chr11:78444727 | C | CAAAGAAA others(1): Show |
9 | a0001c0003t0005g0131 a0002c0002t0002g0161 a0002c0002t0002g0175 others(6): Show |
9 | HG01516.hp1 HG02040.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.1165-970_1165-969i others(10): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444727 | |||||||
| chr11:78444727 | C | CAAAGAAA others(2): Show |
84 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(81): Show |
84 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1165-970_1165-969i others(11): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444727 | |||||||
| chr11:78444727 | C | CAAAGAAA others(3): Show |
3 | a0002c0002t0002g0165 a0002c0002t0002g0184 a0002c0002t0002g0203 |
3 | HG02293.hp1 NA18747.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1165-970_1165-969i others(12): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444727 | |||||||
| chr11:78444727 | C | CAAAGAAA others(5): Show |
2 | a0001c0005t0001g0074 a0001c0005t0001g0146 |
2 | HG01891.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1165-970_1165-969i others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444727 | |||||||
| chr11:78444727 | C | CAAAGAAA others(6): Show |
2 | a0001c0005t0001g0144 a0001c0005t0001g0145 |
2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1165-970_1165-969i others(15): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444727 | |||||||
| chr11:78444727 | C | CAAAGAAA others(8): Show |
2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1165-970_1165-969i others(17): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444727 | |||||||
| chr11:78444730 | A | AC | 16 | a0001c0001t0001g0081 a0001c0001t0001g0135 a0001c0001t0001g0137 others(13): Show |
16 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1165-973_1165-972i others(3): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444730 | |||||||
| chr11:78444731 | A | AC | 6 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0003t0003g0167 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165-974_1165-973i others(3): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444731 | |||||||
| chr11:78444731 | A | C | 2 | a0001c0006t0003g0280 a0003c0008t0003g0159 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1165-973T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444731 | |||||||
| chr11:78444732 | A | C | 32 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0053 others(29): Show |
32 | HG01192.hp1 HG01255.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.1165-974T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444732 | |||||||
| chr11:78444760 | A | T | 3 | a0002c0002t0002g0166 a0002c0002t0002g0184 a0002c0002t0002g0225 |
3 | NA18949.hp1 NA19000.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1165-1002T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78444760 | |||||||
| chr11:78445211 | A | T | 15 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(12): Show |
15 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1165-1453T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78445211 | |||||||
| chr11:78445639 | A | T | 24 | a0001c0001t0001g0053 a0001c0001t0011g0132 a0001c0003t0004g0274 others(21): Show |
24 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1165-1881T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78445639 | |||||||
| chr11:78445645 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1165-1887T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78445645 | |||||||
| chr11:78445646 | T | A | 155 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0135 others(152): Show |
155 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(152): Show |
intron_variant | MODIFIER | c.1165-1888A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78445646 | |||||||
| chr11:78445779 | G | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-2021C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78445779 | |||||||
| chr11:78445817 | A | G | 3 | a0002c0002t0002g0183 a0002c0002t0002g0191 a0002c0002t0002g0221 |
3 | HG01070.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1165-2059T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78445817 | |||||||
| chr11:78445914 | T | C | 155 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0135 others(152): Show |
155 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(152): Show |
intron_variant | MODIFIER | c.1165-2156A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78445914 | |||||||
| chr11:78446263 | A | G | 149 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(146): Show |
149 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.1165-2505T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78446263 | |||||||
| chr11:78446355 | A | G | 156 | a0001c0001t0001g0081 a0001c0001t0001g0127 a0001c0001t0001g0128 others(153): Show |
156 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.1165-2597T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78446355 | |||||||
| chr11:78446431 | A | G | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-2673T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78446431 | |||||||
| chr11:78446583 | A | C | 4 | a0002c0002t0002g0177 a0002c0002t0002g0178 a0002c0002t0002g0179 others(1): Show |
4 | HG01928.hp2 HG01975.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-2825T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78446583 | |||||||
| chr11:78446594 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1165-2836G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78446594 | |||||||
| chr11:78446627 | T | C | 1 | a0001c0001t0005g0142 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1165-2869A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78446627 | |||||||
| chr11:78446788 | A | T | 1 | a0001c0001t0001g0102 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1165-3030T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78446788 | |||||||
| chr11:78446933 | C | T | 1 | a0001c0003t0003g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1165-3175G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78446933 | |||||||
| chr11:78446937 | C | A | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1165-3179G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78446937 | |||||||
| chr11:78446943 | A | T | 1 | a0002c0002t0002g0255 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1165-3185T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78446943 | |||||||
| chr11:78447005 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1165-3247G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447005 | |||||||
| chr11:78447045 | C | CA | 27 | a0001c0001t0001g0068 a0001c0001t0001g0139 a0001c0001t0001g0140 others(24): Show |
27 | HG01891.hp1 HG01975.hp1 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.1165-3288dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447045 | |||||||
| chr11:78447045 | C | CAA | 10 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(7): Show |
10 | HG02055.hp2 HG02630.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1165-3289_1165-328 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447045 | |||||||
| chr11:78447045 | CA | C | 98 | a0001c0001t0001g0094 a0001c0001t0005g0121 a0001c0001t0005g0124 others(95): Show |
98 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1165-3288delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447045 | |||||||
| chr11:78447169 | T | TG | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1165-3412_1165-341 others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447169 | |||||||
| chr11:78447269 | T | G | 23 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(20): Show |
23 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1165-3511A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447269 | |||||||
| chr11:78447369 | C | G | 1 | a0002c0002t0002g0268 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1165-3611G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447369 | |||||||
| chr11:78447412 | T | C | 1 | a0002c0002t0002g0188 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1165-3654A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447412 | |||||||
| chr11:78447475 | C | A | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1165-3717G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447475 | |||||||
| chr11:78447476 | T | C | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1165-3718A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447476 | |||||||
| chr11:78447477 | C | T | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1165-3719G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447477 | |||||||
| chr11:78447485 | C | G | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1165-3727G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447485 | |||||||
| chr11:78447487 | A | T | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1165-3729T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447487 | |||||||
| chr11:78447488 | C | T | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1165-3730G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447488 | |||||||
| chr11:78447496 | T | C | 104 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1165-3738A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447496 | |||||||
| chr11:78447634 | G | GTA | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-3878_1165-387 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447634 | |||||||
| chr11:78447639 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0141 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1165-3881A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447639 | |||||||
| chr11:78447897 | G | A | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1165-4139C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447897 | |||||||
| chr11:78447902 | G | A | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1165-4144C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78447902 | |||||||
| chr11:78448032 | CTA | C | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1165-4276_1165-427 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448032 | |||||||
| chr11:78448074 | A | G | 1 | a0001c0001t0001g0014 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1165-4316T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448074 | |||||||
| chr11:78448178 | A | T | 1 | a0001c0007t0003g0273 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1165-4420T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448178 | |||||||
| chr11:78448185 | A | G | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1165-4427T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448185 | |||||||
| chr11:78448319 | C | CT | 32 | a0001c0001t0001g0050 a0001c0001t0011g0132 a0001c0003t0004g0274 others(29): Show |
32 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(29): Show |
intron_variant | MODIFIER | c.1165-4562dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448319 | |||||||
| chr11:78448319 | C | CTT | 97 | a0001c0001t0005g0070 a0001c0001t0005g0136 a0001c0001t0005g0142 others(94): Show |
97 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1165-4563_1165-456 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448319 | |||||||
| chr11:78448319 | C | CTTT | 6 | a0001c0001t0005g0121 a0001c0001t0005g0134 a0002c0002t0002g0175 others(3): Show |
6 | HG01261.hp1 NA18955.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-4564_1165-456 others(7): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448319 | |||||||
| chr11:78448378 | G | A | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(53): Show |
56 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1165-4620C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448378 | |||||||
| chr11:78448380 | G | A | 98 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(95): Show |
98 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1165-4622C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448380 | |||||||
| chr11:78448490 | T | C | 155 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0135 others(152): Show |
155 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(152): Show |
intron_variant | MODIFIER | c.1165-4732A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448490 | |||||||
| chr11:78448556 | C | A | 6 | a0001c0003t0006g0260 a0001c0003t0006g0261 a0001c0003t0006g0262 others(3): Show |
6 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-4798G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448556 | |||||||
| chr11:78448564 | T | C | 1 | a0002c0002t0002g0193 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1165-4806A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448564 | |||||||
| chr11:78448845 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1165-5087G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448845 | |||||||
| chr11:78448907 | C | T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1165-5149G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78448907 | |||||||
| chr11:78449074 | C | T | 146 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(143): Show |
146 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.1165-5316G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449074 | |||||||
| chr11:78449115 | T | C | 2 | a0002c0002t0002g0183 a0002c0002t0002g0191 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1165-5357A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449115 | |||||||
| chr11:78449123 | C | T | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1165-5365G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449123 | |||||||
| chr11:78449133 | G | GT | 44 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0018 others(41): Show |
44 | HG02055.hp2 HG02080.hp2 HG02083.hp1 others(41): Show |
intron_variant | MODIFIER | c.1165-5376dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449133 | |||||||
| chr11:78449133 | G | GTT | 6 | a0001c0001t0001g0016 a0001c0001t0001g0150 a0001c0003t0006g0263 others(3): Show |
6 | HG02109.hp1 HG02976.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-5377_1165-537 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449133 | |||||||
| chr11:78449133 | GT | G | 34 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0135 others(31): Show |
34 | HG00597.hp1 HG01175.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.1165-5376delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449133 | |||||||
| chr11:78449133 | GTT | G | 94 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0141 others(91): Show |
94 | HG00099.hp2 HG00408.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.1165-5377_1165-537 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449133 | |||||||
| chr11:78449140 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1165-5382A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449140 | |||||||
| chr11:78449157 | T | G | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1165-5399A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449157 | |||||||
| chr11:78449198 | C | T | 23 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(20): Show |
23 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1165-5440G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449198 | |||||||
| chr11:78449228 | C | G | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1165-5470G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449228 | |||||||
| chr11:78449293 | G | A | 2 | a0002c0002t0002g0196 a0002c0002t0002g0209 |
2 | HG02040.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1165-5535C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449293 | |||||||
| chr11:78449476 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02129.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.1165-5718G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449476 | |||||||
| chr11:78449490 | A | T | 22 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(19): Show |
22 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.1165-5732T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449490 | |||||||
| chr11:78449518 | T | C | 23 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(20): Show |
23 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1165-5760A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449518 | |||||||
| chr11:78449560 | C | T | 2 | a0001c0001t0005g0121 a0002c0002t0002g0213 |
2 | NA18960.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1165-5802G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449560 | |||||||
| chr11:78449562 | C | T | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1165-5804G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449562 | |||||||
| chr11:78449581 | G | A | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-5823C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449581 | |||||||
| chr11:78449733 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1165-5975T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449733 | |||||||
| chr11:78449764 | T | C | 16 | a0001c0001t0001g0021 a0001c0001t0001g0083 a0001c0001t0001g0085 others(13): Show |
16 | HG00621.hp2 HG01978.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1165-6006A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449764 | |||||||
| chr11:78449839 | G | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-6081C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449839 | |||||||
| chr11:78449885 | A | G | 1 | a0001c0003t0015g0266 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1165-6127T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78449885 | |||||||
| chr11:78450302 | A | G | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1165-6544T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450302 | |||||||
| chr11:78450315 | C | T | 155 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0135 others(152): Show |
155 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(152): Show |
intron_variant | MODIFIER | c.1165-6557G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450315 | |||||||
| chr11:78450326 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1165-6568A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450326 | |||||||
| chr11:78450335 | G | A | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1165-6577C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450335 | |||||||
| chr11:78450384 | T | C | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1165-6626A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450384 | |||||||
| chr11:78450406 | A | T | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1165-6648T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450406 | |||||||
| chr11:78450565 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1165-6807A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450565 | |||||||
| chr11:78450666 | C | CT | 17 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0029 others(14): Show |
17 | HG00621.hp2 HG01192.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.1165-6909dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450666 | |||||||
| chr11:78450666 | C | CTT | 9 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(6): Show |
9 | HG02055.hp2 HG02630.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1165-6910_1165-690 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450666 | |||||||
| chr11:78450666 | C | CTTT | 8 | a0001c0003t0006g0260 a0001c0003t0006g0261 a0001c0003t0006g0262 others(5): Show |
8 | HG02040.hp1 HG02109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165-6911_1165-690 others(7): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450666 | |||||||
| chr11:78450666 | CT | C | 92 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0134 others(89): Show |
92 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.1165-6909delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450666 | |||||||
| chr11:78450761 | G | A | 1 | a0001c0003t0006g0260 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1165-7003C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450761 | |||||||
| chr11:78450883 | T | C | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165-7125A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450883 | |||||||
| chr11:78450902 | T | TA | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1165-7145dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450902 | |||||||
| chr11:78450930 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1165-7172G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78450930 | |||||||
| chr11:78451194 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1165-7436C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78451194 | |||||||
| chr11:78451212 | T | A | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165-7454A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78451212 | |||||||
| chr11:78451249 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1165-7491T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78451249 | |||||||
| chr11:78451283 | T | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1165-7525A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78451283 | |||||||
| chr11:78451300 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0044 others(1): Show |
4 | HG00621.hp1 HG02080.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-7542T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78451300 | |||||||
| chr11:78451319 | C | A | 1 | a0001c0001t0001g0065 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1165-7561G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78451319 | |||||||
| chr11:78451346 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1165-7588A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78451346 | |||||||
| chr11:78451602 | A | G | 1 | a0001c0004t0004g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1165-7844T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78451602 | |||||||
| chr11:78451627 | G | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-7869C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78451627 | |||||||
| chr11:78451825 | C | G | 1 | a0001c0001t0012g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1165-8067G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78451825 | |||||||
| chr11:78451938 | C | T | 15 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(12): Show |
15 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1165-8180G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78451938 | |||||||
| chr11:78451952 | C | T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1165-8194G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78451952 | |||||||
| chr11:78452001 | C | T | 5 | a0002c0002t0002g0246 a0002c0002t0002g0247 a0002c0002t0002g0248 others(2): Show |
5 | HG00642.hp2 HG00735.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1165-8243G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452001 | |||||||
| chr11:78452023 | C | T | 3 | a0002c0002t0002g0185 a0002c0002t0002g0224 a0002c0002t0002g0228 |
3 | HG02135.hp1 NA18948.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1165-8265G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452023 | |||||||
| chr11:78452107 | A | AT | 6 | a0001c0001t0001g0084 a0001c0001t0005g0124 a0001c0005t0001g0074 others(3): Show |
6 | HG01891.hp1 HG02615.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165-8350dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452107 | |||||||
| chr11:78452117 | T | A | 1 | a0001c0001t0001g0043 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1165-8359A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452117 | |||||||
| chr11:78452117 | TA | T | 3 | a0002c0002t0002g0179 a0002c0002t0002g0215 a0002c0002t0002g0224 |
3 | HG01975.hp2 NA18939.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1165-8360delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452117 | |||||||
| chr11:78452118 | A | T | 120 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(117): Show |
120 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.1165-8360T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452118 | |||||||
| chr11:78452282 | T | C | 1 | a0001c0004t0013g0153 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1165-8524A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452282 | |||||||
| chr11:78452444 | G | A | 3 | a0002c0002t0002g0166 a0002c0002t0002g0184 a0002c0002t0002g0225 |
3 | NA18949.hp1 NA19000.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1165-8686C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452444 | |||||||
| chr11:78452496 | C | A | 1 | a0001c0001t0001g0150 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1165-8738G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452496 | |||||||
| chr11:78452563 | C | T | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-8805G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452563 | |||||||
| chr11:78452572 | T | A | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1165-8814A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452572 | |||||||
| chr11:78452590 | G | A | 98 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(95): Show |
98 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1165-8832C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452590 | |||||||
| chr11:78452647 | G | A | 4 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(1): Show |
4 | HG02055.hp2 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165-8889C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452647 | |||||||
| chr11:78452665 | T | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-8907A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452665 | |||||||
| chr11:78452835 | T | C | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1165-9077A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78452835 | |||||||
| chr11:78453105 | G | A | 1 | a0001c0001t0014g0287 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1165-9347C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78453105 | |||||||
| chr11:78453544 | C | T | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-9786G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78453544 | |||||||
| chr11:78453938 | T | G | 33 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0048 others(30): Show |
33 | HG00621.hp2 HG00735.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1165-10180A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78453938 | |||||||
| chr11:78454064 | A | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0117 |
2 | NA19087.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1165-10306T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454064 | |||||||
| chr11:78454127 | GACA | G | 17 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(14): Show |
17 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1165-10372_1165-10 others(9): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454127 | |||||||
| chr11:78454129 | C | A | 1 | a0001c0001t0005g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1165-10371G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454129 | |||||||
| chr11:78454188 | T | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0072 others(3): Show |
6 | HG01884.hp2 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-10430A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454188 | |||||||
| chr11:78454281 | T | C | 5 | a0001c0003t0015g0266 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165-10523A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454281 | |||||||
| chr11:78454297 | T | C | 147 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(144): Show |
147 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.1165-10539A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454297 | |||||||
| chr11:78454309 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1165-10551A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454309 | |||||||
| chr11:78454516 | C | T | 1 | a0002c0002t0016g0294 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1165-10758G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454516 | |||||||
| chr11:78454570 | C | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1165-10812G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454570 | |||||||
| chr11:78454579 | G | A | 1 | a0002c0002t0002g0171 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1165-10821C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454579 | |||||||
| chr11:78454624 | G | GT | 29 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(26): Show |
29 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1165-10867dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454624 | |||||||
| chr11:78454624 | GT | G | 14 | a0001c0001t0001g0021 a0001c0001t0001g0083 a0001c0001t0001g0085 others(11): Show |
14 | HG00621.hp2 HG01070.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.1165-10867delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454624 | |||||||
| chr11:78454658 | G | A | 1 | a0002c0002t0002g0161 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1165-10900C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454658 | |||||||
| chr11:78454695 | T | C | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165-10937A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454695 | |||||||
| chr11:78454702 | T | A | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165-10944A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454702 | |||||||
| chr11:78454776 | G | A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1165-11018C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454776 | |||||||
| chr11:78454894 | A | T | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+10982T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78454894 | |||||||
| chr11:78455031 | A | G | 3 | a0002c0002t0002g0185 a0002c0002t0002g0224 a0002c0002t0002g0228 |
3 | HG02135.hp1 NA18948.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1164+10845T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455031 | |||||||
| chr11:78455126 | T | TACACTAG others(3): Show |
1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1164+10749_1164+10 others(16): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455126 | |||||||
| chr11:78455127 | T | G | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1164+10749A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455127 | |||||||
| chr11:78455128 | T | C | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1164+10748A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455128 | |||||||
| chr11:78455129 | T | G | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1164+10747A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455129 | |||||||
| chr11:78455131 | C | G | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1164+10745G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455131 | |||||||
| chr11:78455132 | A | T | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1164+10744T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455132 | |||||||
| chr11:78455388 | CTT | C | 5 | a0002c0002t0002g0165 a0002c0002t0002g0166 a0002c0002t0002g0184 others(2): Show |
5 | NA18747.hp2 NA18949.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1164+10486_1164+10 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455388 | |||||||
| chr11:78455391 | A | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
5 | HG01081.hp1 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1164+10485T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455391 | |||||||
| chr11:78455407 | G | A | 13 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1164+10469C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455407 | |||||||
| chr11:78455551 | A | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1164+10325T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455551 | |||||||
| chr11:78455675 | T | C | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+10201A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455675 | |||||||
| chr11:78455815 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1164+10061A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455815 | |||||||
| chr11:78455841 | T | A | 13 | a0001c0001t0001g0021 a0001c0001t0001g0083 a0001c0001t0001g0085 others(10): Show |
13 | HG00621.hp2 HG01978.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1164+10035A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455841 | |||||||
| chr11:78455863 | A | G | 23 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(20): Show |
23 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1164+10013T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455863 | |||||||
| chr11:78455884 | C | A | 128 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(125): Show |
128 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.1164+9992G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455884 | |||||||
| chr11:78455921 | C | T | 127 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(124): Show |
127 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.1164+9955G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455921 | |||||||
| chr11:78455970 | T | C | 1 | a0002c0002t0002g0268 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1164+9906A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455970 | |||||||
| chr11:78455989 | T | TA | 4 | a0002c0002t0002g0175 a0002c0002t0002g0186 a0002c0002t0002g0198 others(1): Show |
4 | NA18955.hp1 NA18973.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+9886dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78455989 | |||||||
| chr11:78456086 | T | G | 2 | a0002c0002t0002g0162 a0002c0002t0002g0254 |
2 | HG00099.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1164+9790A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78456086 | |||||||
| chr11:78456179 | C | T | 10 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1164+9697G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78456179 | |||||||
| chr11:78456437 | T | C | 1 | a0001c0001t0001g0029 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1164+9439A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78456437 | |||||||
| chr11:78456439 | T | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1164+9437A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78456439 | |||||||
| chr11:78456501 | C | T | 1 | a0002c0002t0003g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1164+9375G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78456501 | |||||||
| chr11:78456515 | G | A | 4 | a0001c0001t0001g0068 a0002c0002t0003g0172 a0002c0002t0003g0174 others(1): Show |
4 | HG01975.hp1 HG01978.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+9361C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78456515 | |||||||
| chr11:78456518 | G | C | 2 | a0001c0001t0005g0136 a0001c0001t0005g0142 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1164+9358C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78456518 | |||||||
| chr11:78456851 | G | A | 1 | a0001c0004t0007g0154 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1164+9025C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78456851 | |||||||
| chr11:78456865 | T | C | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1164+9011A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78456865 | |||||||
| chr11:78457087 | C | T | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+8789G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78457087 | |||||||
| chr11:78457510 | A | G | 23 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(20): Show |
23 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1164+8366T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78457510 | |||||||
| chr11:78457557 | T | A | 98 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(95): Show |
98 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1164+8319A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78457557 | |||||||
| chr11:78457659 | C | T | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1164+8217G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78457659 | |||||||
| chr11:78457686 | T | C | 10 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(7): Show |
10 | HG02055.hp2 HG02630.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1164+8190A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78457686 | |||||||
| chr11:78457749 | G | A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1164+8127C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78457749 | |||||||
| chr11:78457797 | A | AAC | 3 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0100 |
3 | NA18941.hp1 NA18950.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1164+8077_1164+807 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78457797 | |||||||
| chr11:78457797 | AAC | A | 19 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(16): Show |
19 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1164+8077_1164+807 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78457797 | |||||||
| chr11:78457797 | AACAC | A | 6 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0003t0003g0167 others(3): Show |
6 | HG02615.hp2 HG02723.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164+8075_1164+807 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78457797 | |||||||
| chr11:78457797 | AACACACA others(1): Show |
A | 6 | a0002c0002t0002g0162 a0002c0002t0002g0254 a0002c0002t0002g0268 others(3): Show |
6 | HG00099.hp2 HG02970.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+8071_1164+807 others(12): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78457797 | |||||||
| chr11:78457797 | AACACACA others(3): Show |
A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
144 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(141): Show |
intron_variant | MODIFIER | c.1164+8069_1164+807 others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78457797 | |||||||
| chr11:78457797 | AACACACA others(5): Show |
A | 2 | a0001c0004t0007g0157 a0001c0004t0007g0158 |
2 | HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1164+8067_1164+807 others(16): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78457797 | |||||||
| chr11:78457970 | C | T | 1 | a0002c0002t0002g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1164+7906G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78457970 | |||||||
| chr11:78458199 | T | C | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1164+7677A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78458199 | |||||||
| chr11:78458264 | C | T | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1164+7612G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78458264 | |||||||
| chr11:78458488 | AGGTGG | A | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1164+7383_1164+738 others(9): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78458488 | |||||||
| chr11:78458515 | G | C | 1 | a0004c0009t0002g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1164+7361C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78458515 | |||||||
| chr11:78458739 | C | T | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1164+7137G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78458739 | |||||||
| chr11:78458778 | T | G | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1164+7098A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78458778 | |||||||
| chr11:78458826 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1164+7050A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78458826 | |||||||
| chr11:78458839 | C | G | 129 | a0001c0001t0001g0135 a0001c0001t0005g0070 a0001c0001t0005g0121 others(126): Show |
129 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1164+7037G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78458839 | |||||||
| chr11:78458929 | G | T | 128 | a0001c0001t0001g0135 a0001c0001t0005g0121 a0001c0001t0005g0124 others(125): Show |
128 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.1164+6947C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78458929 | |||||||
| chr11:78458996 | G | GT | 7 | a0001c0001t0001g0088 a0001c0001t0001g0093 a0001c0001t0001g0094 others(4): Show |
7 | HG00735.hp1 HG01106.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.1164+6879_1164+688 others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78458996 | |||||||
| chr11:78458997 | C | T | 7 | a0001c0001t0001g0088 a0001c0001t0001g0093 a0001c0001t0001g0094 others(4): Show |
7 | HG00735.hp1 HG01106.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.1164+6879G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78458997 | |||||||
| chr11:78459042 | C | T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1164+6834G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459042 | |||||||
| chr11:78459168 | ACCTCCCA others(348): Show |
A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+6353_1164+670 others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459168 | |||||||
| chr11:78459204 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0117 |
2 | NA19087.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1164+6672C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459204 | |||||||
| chr11:78459210 | G | A | 1 | a0002c0002t0002g0204 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1164+6666C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459210 | |||||||
| chr11:78459364 | G | A | 2 | a0002c0002t0002g0182 a0002c0002t0002g0187 |
2 | NA18982.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1164+6512C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459364 | |||||||
| chr11:78459393 | C | A | 6 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | HG01192.hp1 HG01255.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+6483G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459393 | |||||||
| chr11:78459398 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1164+6478C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459398 | |||||||
| chr11:78459516 | C | T | 23 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(20): Show |
23 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1164+6360G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459516 | |||||||
| chr11:78459524 | C | T | 1 | a0001c0003t0006g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1164+6352G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459524 | |||||||
| chr11:78459662 | T | G | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1164+6214A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459662 | |||||||
| chr11:78459765 | C | T | 147 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(144): Show |
147 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.1164+6111G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459765 | |||||||
| chr11:78459779 | CGTCTTTT others(5): Show |
C | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+6085_1164+609 others(16): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459779 | |||||||
| chr11:78459793 | G | C | 1 | a0001c0001t0001g0071 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1164+6083C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459793 | |||||||
| chr11:78459795 | G | A | 104 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1164+6081C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459795 | |||||||
| chr11:78459819 | C | T | 1 | a0001c0004t0013g0153 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1164+6057G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459819 | |||||||
| chr11:78459830 | A | C | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1164+6046T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459830 | |||||||
| chr11:78459832 | G | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+6044C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459832 | |||||||
| chr11:78459877 | T | A | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1164+5999A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459877 | |||||||
| chr11:78459955 | G | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0075 |
2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1164+5921C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459955 | |||||||
| chr11:78459971 | T | C | 1 | a0001c0003t0006g0260 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1164+5905A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78459971 | |||||||
| chr11:78460059 | G | A | 2 | a0001c0001t0005g0121 a0002c0002t0002g0213 |
2 | NA18960.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1164+5817C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78460059 | |||||||
| chr11:78460215 | A | G | 128 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(125): Show |
128 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.1164+5661T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78460215 | |||||||
| chr11:78460253 | G | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1164+5623C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78460253 | |||||||
| chr11:78460263 | T | C | 1 | a0001c0004t0007g0154 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1164+5613A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78460263 | |||||||
| chr11:78460271 | A | AT | 44 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0001c0001t0001g0135 others(41): Show |
44 | HG01071.hp2 HG01884.hp1 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.1164+5604dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78460271 | |||||||
| chr11:78460271 | A | ATTTT | 102 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(99): Show |
102 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.1164+5601_1164+560 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78460271 | |||||||
| chr11:78460289 | T | A | 13 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1164+5587A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78460289 | |||||||
| chr11:78460292 | G | A | 147 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(144): Show |
147 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.1164+5584C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78460292 | |||||||
| chr11:78460396 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1164+5480A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78460396 | |||||||
| chr11:78460409 | G | A | 1 | a0002c0002t0003g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1164+5467C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78460409 | |||||||
| chr11:78460772 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1164+5104G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78460772 | |||||||
| chr11:78460967 | T | C | 5 | a0001c0003t0015g0266 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1164+4909A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78460967 | |||||||
| chr11:78460989 | C | T | 1 | a0002c0002t0002g0211 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1164+4887G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78460989 | |||||||
| chr11:78461069 | G | A | 12 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(9): Show |
12 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1164+4807C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461069 | |||||||
| chr11:78461307 | T | C | 128 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(125): Show |
128 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.1164+4569A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461307 | |||||||
| chr11:78461360 | G | C | 1 | a0002c0002t0003g0288 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1164+4516C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461360 | |||||||
| chr11:78461381 | A | T | 16 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1164+4495T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461381 | |||||||
| chr11:78461387 | C | A | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+4489G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461387 | |||||||
| chr11:78461387 | C | G | 1 | a0001c0006t0003g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1164+4489G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461387 | |||||||
| chr11:78461602 | T | TA | 52 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(49): Show |
52 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1164+4273dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461602 | |||||||
| chr11:78461602 | T | TAAAAAA | 6 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(3): Show |
6 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+4268_1164+427 others(10): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461602 | |||||||
| chr11:78461602 | T | TAAAAAAA others(3): Show |
3 | a0001c0005t0001g0144 a0001c0005t0001g0145 a0001c0006t0003g0280 |
3 | HG03453.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1164+4264_1164+427 others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461602 | |||||||
| chr11:78461602 | T | TAAAAAAA others(5): Show |
1 | a0001c0005t0001g0074 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1164+4262_1164+427 others(16): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461602 | |||||||
| chr11:78461602 | T | TAAAAAAA others(17): Show |
1 | a0001c0001t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1164+4250_1164+427 others(28): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461602 | |||||||
| chr11:78461602 | TA | T | 12 | a0001c0001t0001g0065 a0001c0001t0001g0071 a0001c0001t0001g0077 others(9): Show |
12 | HG01256.hp2 HG01975.hp1 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.1164+4273delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461602 | |||||||
| chr11:78461602 | TAAAAAAA others(2): Show |
T | 12 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(9): Show |
12 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1164+4265_1164+427 others(13): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461602 | |||||||
| chr11:78461602 | TAAAAAAA others(4): Show |
T | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+4263_1164+427 others(15): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461602 | |||||||
| chr11:78461649 | A | G | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1164+4227T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461649 | |||||||
| chr11:78461751 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1164+4125G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461751 | |||||||
| chr11:78461783 | C | CA | 43 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0027 others(40): Show |
43 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(40): Show |
intron_variant | MODIFIER | c.1164+4092dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461783 | |||||||
| chr11:78461783 | C | CAA | 13 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG02257.hp2 HG02258.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1164+4091_1164+409 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461783 | |||||||
| chr11:78461783 | CAAAAAA | C | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1164+4087_1164+409 others(10): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461783 | |||||||
| chr11:78461810 | G | A | 104 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1164+4066C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461810 | |||||||
| chr11:78461826 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1164+4050C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461826 | |||||||
| chr11:78461860 | G | A | 2 | a0002c0002t0002g0178 a0002c0002t0002g0180 |
2 | HG01928.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1164+4016C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461860 | |||||||
| chr11:78461870 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1164+4006A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461870 | |||||||
| chr11:78461940 | A | G | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1164+3936T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461940 | |||||||
| chr11:78461973 | A | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1164+3903T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461973 | |||||||
| chr11:78461996 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0082 others(1): Show |
4 | HG01256.hp1 HG01928.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+3880T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78461996 | |||||||
| chr11:78462012 | A | G | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0003t0003g0167 others(2): Show |
5 | HG02723.hp2 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1164+3864T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462012 | |||||||
| chr11:78462114 | A | G | 149 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(146): Show |
149 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.1164+3762T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462114 | |||||||
| chr11:78462251 | C | T | 103 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(100): Show |
103 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1164+3625G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462251 | |||||||
| chr11:78462257 | T | C | 6 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0005t0001g0074 others(3): Show |
6 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+3619A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462257 | |||||||
| chr11:78462343 | G | A | 12 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(9): Show |
12 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1164+3533C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462343 | |||||||
| chr11:78462377 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0098 others(1): Show |
4 | HG00099.hp1 HG01175.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+3499C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462377 | |||||||
| chr11:78462393 | C | A | 147 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(144): Show |
147 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.1164+3483G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462393 | |||||||
| chr11:78462538 | G | A | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1164+3338C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462538 | |||||||
| chr11:78462560 | C | T | 149 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(146): Show |
149 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.1164+3316G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462560 | |||||||
| chr11:78462646 | A | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1164+3230T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462646 | |||||||
| chr11:78462777 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1164+3099G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462777 | |||||||
| chr11:78462789 | A | T | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1164+3087T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462789 | |||||||
| chr11:78462856 | C | T | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+3020G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462856 | |||||||
| chr11:78462869 | A | ATCTAC | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+3002_1164+300 others(9): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462869 | |||||||
| chr11:78462986 | A | T | 1 | a0001c0001t0005g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1164+2890T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78462986 | |||||||
| chr11:78463150 | G | C | 105 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(102): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1164+2726C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463150 | |||||||
| chr11:78463219 | A | C | 1 | a0001c0003t0006g0264 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1164+2657T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463219 | |||||||
| chr11:78463328 | A | C | 1 | a0001c0006t0003g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1164+2548T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463328 | |||||||
| chr11:78463339 | C | T | 1 | a0002c0002t0003g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1164+2537G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463339 | |||||||
| chr11:78463468 | C | T | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+2408G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463468 | |||||||
| chr11:78463665 | G | A | 5 | a0001c0003t0015g0266 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1164+2211C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463665 | |||||||
| chr11:78463705 | G | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1164+2171C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463705 | |||||||
| chr11:78463713 | C | CA | 47 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0022 others(44): Show |
47 | HG00099.hp1 HG00741.hp1 HG01934.hp2 others(44): Show |
intron_variant | MODIFIER | c.1164+2162dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463713 | |||||||
| chr11:78463713 | C | CAA | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(134): Show |
intron_variant | MODIFIER | c.1164+2161_1164+216 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463713 | |||||||
| chr11:78463713 | C | CAAA | 49 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0029 others(46): Show |
49 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1164+2160_1164+216 others(7): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463713 | |||||||
| chr11:78463713 | C | CAAAA | 10 | a0001c0001t0001g0097 a0001c0003t0003g0167 a0001c0003t0003g0168 others(7): Show |
10 | HG01175.hp1 HG01192.hp1 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1164+2159_1164+216 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463713 | |||||||
| chr11:78463713 | C | CAAAAAA | 9 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164+2157_1164+216 others(10): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463713 | |||||||
| chr11:78463713 | CA | C | 13 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1164+2162delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463713 | |||||||
| chr11:78463713 | CAA | C | 9 | a0001c0003t0006g0259 a0001c0004t0004g0281 a0001c0004t0004g0282 others(6): Show |
9 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164+2161_1164+216 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463713 | |||||||
| chr11:78463725 | A | C | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1164+2151T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463725 | |||||||
| chr11:78463736 | A | C | 1 | a0001c0004t0013g0153 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1164+2140T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463736 | |||||||
| chr11:78463738 | C | A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1164+2138G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463738 | |||||||
| chr11:78463890 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1164+1986G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463890 | |||||||
| chr11:78463929 | C | T | 13 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1164+1947G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78463929 | |||||||
| chr11:78464092 | C | G | 1 | a0002c0002t0003g0242 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1164+1784G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464092 | |||||||
| chr11:78464127 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1164+1749A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464127 | |||||||
| chr11:78464196 | C | T | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1164+1680G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464196 | |||||||
| chr11:78464212 | G | T | 125 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(122): Show |
125 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.1164+1664C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464212 | |||||||
| chr11:78464320 | C | T | 1 | a0001c0004t0007g0156 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1164+1556G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464320 | |||||||
| chr11:78464360 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1164+1516G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464360 | |||||||
| chr11:78464467 | T | C | 1 | a0002c0002t0002g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1164+1409A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464467 | |||||||
| chr11:78464602 | A | G | 1 | a0001c0005t0001g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1164+1274T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464602 | |||||||
| chr11:78464811 | G | C | 1 | a0001c0005t0001g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1164+1065C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464811 | |||||||
| chr11:78464909 | C | T | 1 | a0002c0002t0003g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1164+967G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464909 | |||||||
| chr11:78464941 | C | G | 154 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0135 others(151): Show |
154 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.1164+935G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464941 | |||||||
| chr11:78464956 | C | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1164+920G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464956 | |||||||
| chr11:78464958 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1164+918G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464958 | |||||||
| chr11:78464964 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1164+912C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464964 | |||||||
| chr11:78464970 | G | A | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+906C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78464970 | |||||||
| chr11:78465026 | C | T | 112 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(109): Show |
112 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.1164+850G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465026 | |||||||
| chr11:78465028 | C | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+848G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465028 | |||||||
| chr11:78465030 | C | T | 1 | a0001c0004t0007g0154 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1164+846G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465030 | |||||||
| chr11:78465090 | G | T | 1 | a0001c0006t0003g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1164+786C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465090 | |||||||
| chr11:78465104 | G | A | 2 | a0002c0002t0002g0248 a0002c0002t0002g0249 |
2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1164+772C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465104 | |||||||
| chr11:78465117 | C | T | 4 | a0002c0002t0003g0239 a0002c0002t0003g0240 a0002c0002t0003g0241 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+759G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465117 | |||||||
| chr11:78465196 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1164+680G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465196 | |||||||
| chr11:78465211 | G | A | 1 | a0001c0004t0004g0281 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1164+665C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465211 | |||||||
| chr11:78465223 | A | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1164+653T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465223 | |||||||
| chr11:78465233 | C | T | 1 | a0002c0002t0005g0001 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1164+643G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465233 | |||||||
| chr11:78465241 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1164+635G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465241 | |||||||
| chr11:78465243 | C | T | 10 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1164+633G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465243 | |||||||
| chr11:78465353 | A | G | 2 | a0002c0002t0002g0197 a0002c0002t0002g0201 |
2 | NA18945.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1164+523T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465353 | |||||||
| chr11:78465403 | A | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1164+473T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465403 | |||||||
| chr11:78465450 | G | C | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+426C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465450 | |||||||
| chr11:78465453 | C | T | 1 | a0001c0006t0003g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1164+423G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465453 | |||||||
| chr11:78465454 | G | A | 1 | a0002c0002t0002g0233 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1164+422C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465454 | |||||||
| chr11:78465492 | C | T | 2 | a0002c0002t0002g0215 a0002c0002t0002g0216 |
2 | NA18939.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1164+384G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465492 | |||||||
| chr11:78465671 | A | T | 1 | a0001c0001t0001g0011 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1164+205T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465671 | |||||||
| chr11:78465762 | A | G | 18 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0011g0132 others(15): Show |
18 | HG02055.hp2 HG02451.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.1164+114T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 11/13 | chr11 | 78465762 | |||||||
| chr11:78466017 | T | A | 1 | a0002c0002t0003g0245 | 1 | HG02818.hp2 | splice_region_variant&intron_variant | LOW | c.1027-4A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466017 | |||||||
| chr11:78466025 | A | C | 1 | a0001c0001t0001g0069 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1027-12T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466025 | |||||||
| chr11:78466054 | G | A | 1 | a0001c0004t0004g0286 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1027-41C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466054 | |||||||
| chr11:78466095 | A | G | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027-82T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466095 | |||||||
| chr11:78466108 | C | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1027-95G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466108 | |||||||
| chr11:78466266 | C | G | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1027-253G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466266 | |||||||
| chr11:78466278 | C | A | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
54 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1027-265G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466278 | |||||||
| chr11:78466401 | T | C | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1027-388A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466401 | |||||||
| chr11:78466490 | G | GT | 5 | a0001c0003t0015g0266 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027-478dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466490 | |||||||
| chr11:78466499 | G | C | 5 | a0001c0003t0015g0266 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027-486C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466499 | |||||||
| chr11:78466549 | C | T | 12 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(9): Show |
12 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1027-536G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466549 | |||||||
| chr11:78466573 | C | T | 107 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(104): Show |
107 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1027-560G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466573 | |||||||
| chr11:78466643 | G | T | 2 | a0001c0004t0007g0157 a0001c0004t0007g0158 |
2 | HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1027-630C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466643 | |||||||
| chr11:78466730 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1027-717G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466730 | |||||||
| chr11:78466777 | G | A | 1 | a0002c0002t0002g0219 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1027-764C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466777 | |||||||
| chr11:78466968 | GT | G | 146 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(143): Show |
146 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.1027-956delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466968 | |||||||
| chr11:78466985 | T | C | 1 | a0001c0001t0005g0136 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1027-972A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466985 | |||||||
| chr11:78466998 | A | G | 1 | a0001c0005t0001g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1027-985T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78466998 | |||||||
| chr11:78467121 | T | C | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1027-1108A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467121 | |||||||
| chr11:78467380 | T | TA | 6 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0005t0001g0074 others(3): Show |
6 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027-1368dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467380 | |||||||
| chr11:78467408 | G | A | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1027-1395C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467408 | |||||||
| chr11:78467542 | A | AAAAT | 8 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0003t0015g0266 others(5): Show |
8 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1027-1533_1027-153 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467542 | |||||||
| chr11:78467542 | AAAAT | A | 82 | a0001c0001t0001g0088 a0001c0001t0005g0070 a0001c0001t0005g0121 others(79): Show |
82 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1027-1533_1027-153 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467542 | |||||||
| chr11:78467555 | A | T | 1 | a0002c0002t0002g0277 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1027-1542T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467555 | |||||||
| chr11:78467559 | A | T | 8 | a0001c0001t0005g0136 a0001c0001t0005g0142 a0002c0002t0002g0161 others(5): Show |
8 | HG00099.hp2 HG02083.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.1027-1546T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467559 | |||||||
| chr11:78467563 | A | T | 33 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(30): Show |
33 | HG00099.hp2 HG00735.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1027-1550T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467563 | |||||||
| chr11:78467563 | AAATAAAT others(1): Show |
A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0044 others(1): Show |
4 | HG00621.hp1 HG02080.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-1558_1027-155 others(12): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467563 | |||||||
| chr11:78467567 | A | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
185 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1027-1554T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467567 | |||||||
| chr11:78467571 | T | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0057 others(32): Show |
35 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.1027-1558A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467571 | |||||||
| chr11:78467575 | T | A | 7 | a0001c0003t0004g0275 a0001c0004t0013g0153 a0001c0005t0001g0074 others(4): Show |
7 | HG01891.hp1 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1027-1562A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467575 | |||||||
| chr11:78467579 | T | A | 1 | a0001c0005t0001g0144 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1027-1566A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467579 | |||||||
| chr11:78467599 | TAAAC | T | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1027-1590_1027-158 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467599 | |||||||
| chr11:78467823 | G | A | 11 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1026+1424C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467823 | |||||||
| chr11:78467939 | T | C | 16 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1026+1308A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78467939 | |||||||
| chr11:78468030 | G | A | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026+1217C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468030 | |||||||
| chr11:78468039 | G | GA | 22 | a0001c0001t0001g0047 a0001c0001t0001g0056 a0001c0001t0001g0087 others(19): Show |
22 | HG01346.hp2 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1026+1207dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468039 | |||||||
| chr11:78468039 | GA | G | 17 | a0001c0001t0001g0147 a0001c0001t0005g0070 a0001c0001t0011g0132 others(14): Show |
17 | HG02055.hp2 HG02451.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1026+1207delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468039 | |||||||
| chr11:78468190 | A | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1026+1057T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468190 | |||||||
| chr11:78468214 | C | CA | 13 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1026+1032dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468214 | |||||||
| chr11:78468222 | C | A | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+1025G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468222 | |||||||
| chr11:78468247 | T | C | 128 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(125): Show |
128 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.1026+1000A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468247 | |||||||
| chr11:78468290 | C | T | 128 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(125): Show |
128 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.1026+957G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468290 | |||||||
| chr11:78468310 | G | GA | 19 | a0001c0001t0001g0020 a0001c0001t0001g0044 a0001c0001t0001g0050 others(16): Show |
19 | HG02080.hp1 HG02145.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.1026+936dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468310 | |||||||
| chr11:78468310 | G | GAAAAAAA | 6 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0005t0001g0074 others(3): Show |
6 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026+930_1026+936d others(9): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468310 | |||||||
| chr11:78468310 | G | GAAAAAAA others(4): Show |
1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1026+926_1026+936d others(13): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468310 | |||||||
| chr11:78468310 | G | GAAAAAAA others(5): Show |
4 | a0001c0003t0006g0261 a0001c0003t0006g0262 a0001c0003t0006g0263 others(1): Show |
4 | HG02109.hp1 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+925_1026+936d others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468310 | |||||||
| chr11:78468310 | G | GAAAAAAA others(6): Show |
2 | a0001c0003t0006g0260 a0001c0003t0006g0265 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1026+924_1026+936d others(15): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468310 | |||||||
| chr11:78468310 | G | GAAAAAAA others(7): Show |
1 | a0001c0003t0006g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1026+923_1026+936d others(16): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468310 | |||||||
| chr11:78468310 | G | GAAAAAAA others(10): Show |
4 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0285 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+920_1026+936d others(19): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468310 | |||||||
| chr11:78468310 | G | GAAAAAAA others(11): Show |
1 | a0001c0004t0004g0283 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1026+919_1026+936d others(20): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468310 | |||||||
| chr11:78468310 | G | GAAAAAAA others(14): Show |
1 | a0001c0004t0004g0284 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1026+936_1026+937i others(23): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468310 | |||||||
| chr11:78468310 | G | GAAAAAAA others(18): Show |
1 | a0001c0004t0004g0286 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1026+936_1026+937i others(27): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468310 | |||||||
| chr11:78468310 | G | GGAAAAAA others(1): Show |
82 | a0001c0001t0005g0070 a0001c0001t0005g0134 a0001c0001t0005g0136 others(79): Show |
82 | HG00099.hp2 HG00408.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1026+936_1026+937i others(10): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468310 | |||||||
| chr11:78468310 | G | GGAAAAAA others(2): Show |
11 | a0001c0001t0005g0121 a0001c0001t0005g0124 a0002c0002t0002g0176 others(8): Show |
11 | HG00735.hp2 HG01192.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1026+936_1026+937i others(11): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468310 | |||||||
| chr11:78468310 | G | GGAAAAAA others(3): Show |
1 | a0002c0002t0002g0225 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1026+936_1026+937i others(12): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468310 | |||||||
| chr11:78468329 | G | A | 8 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(5): Show |
8 | HG02630.hp2 HG02886.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026+918C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468329 | |||||||
| chr11:78468330 | A | G | 1 | a0002c0002t0002g0234 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1026+917T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468330 | |||||||
| chr11:78468411 | C | CT | 6 | a0001c0003t0002g0257 a0001c0003t0015g0266 a0002c0002t0008g0290 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026+835dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468411 | |||||||
| chr11:78468452 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1026+795C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468452 | |||||||
| chr11:78468693 | C | T | 5 | a0001c0003t0015g0266 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026+554G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468693 | |||||||
| chr11:78468789 | T | G | 16 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1026+458A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468789 | |||||||
| chr11:78468792 | C | CT | 23 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0059 others(20): Show |
23 | HG01175.hp1 HG01934.hp2 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.1026+454dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468792 | |||||||
| chr11:78468792 | CT | C | 9 | a0001c0001t0009g0060 a0001c0004t0007g0152 a0001c0004t0007g0154 others(6): Show |
9 | HG01255.hp1 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1026+454delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468792 | |||||||
| chr11:78468987 | C | T | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026+260G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78468987 | |||||||
| chr11:78469038 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1026+209T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78469038 | |||||||
| chr11:78469052 | T | C | 6 | a0001c0003t0006g0260 a0001c0003t0006g0261 a0001c0003t0006g0262 others(3): Show |
6 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026+195A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78469052 | |||||||
| chr11:78469064 | G | A | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026+183C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78469064 | |||||||
| chr11:78469133 | A | G | 98 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(95): Show |
98 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1026+114T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 10/13 | chr11 | 78469133 | |||||||
| chr11:78469349 | A | G | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.960-36T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469349 | |||||||
| chr11:78469393 | C | T | 1 | a0001c0003t0002g0257 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.960-80G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469393 | |||||||
| chr11:78469461 | A | T | 112 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(109): Show |
112 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.960-148T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469461 | |||||||
| chr11:78469462 | A | C | 112 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(109): Show |
112 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.960-149T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469462 | |||||||
| chr11:78469733 | G | A | 1 | a0001c0003t0006g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.960-420C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469733 | |||||||
| chr11:78469750 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.960-437C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469750 | |||||||
| chr11:78469759 | T | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.960-446A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469759 | |||||||
| chr11:78469764 | C | CAG | 24 | a0001c0001t0005g0136 a0001c0001t0005g0142 a0001c0003t0003g0169 others(21): Show |
24 | HG00099.hp2 HG01891.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.960-453_960-452dup others(2): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469764 | |||||||
| chr11:78469775 | A | AGC | 81 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(78): Show |
81 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.960-463_960-462ins others(2): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469775 | |||||||
| chr11:78469803 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.960-490A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469803 | |||||||
| chr11:78469832 | G | A | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.960-519C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469832 | |||||||
| chr11:78469874 | G | A | 16 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.960-561C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469874 | |||||||
| chr11:78469940 | G | A | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.960-627C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469940 | |||||||
| chr11:78469940 | G | T | 2 | a0002c0002t0003g0288 a0002c0002t0003g0289 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.960-627C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78469940 | |||||||
| chr11:78470050 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.960-737C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78470050 | |||||||
| chr11:78470053 | C | A | 1 | a0001c0001t0005g0142 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.960-740G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78470053 | |||||||
| chr11:78470156 | C | T | 1 | a0001c0006t0003g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.960-843G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78470156 | |||||||
| chr11:78470281 | A | G | 1 | a0002c0002t0002g0250 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.960-968T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78470281 | |||||||
| chr11:78470284 | A | C | 3 | a0002c0002t0002g0176 a0002c0002t0002g0196 a0002c0002t0002g0209 |
3 | HG02040.hp1 NA18998.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.960-971T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78470284 | |||||||
| chr11:78470314 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.960-1001A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78470314 | |||||||
| chr11:78470560 | C | T | 1 | a0002c0002t0002g0161 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.960-1247G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78470560 | |||||||
| chr11:78470787 | T | C | 4 | a0002c0002t0002g0175 a0002c0002t0002g0186 a0002c0002t0002g0198 others(1): Show |
4 | NA18955.hp1 NA18973.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-1474A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78470787 | |||||||
| chr11:78470882 | A | AT | 131 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(128): Show |
131 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.960-1570dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78470882 | |||||||
| chr11:78470882 | A | ATT | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
123 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.960-1571_960-1570d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78470882 | |||||||
| chr11:78470882 | A | ATTT | 18 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0029 others(15): Show |
18 | HG00735.hp1 HG01106.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.960-1572_960-1570d others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78470882 | |||||||
| chr11:78470882 | A | ATTTTT | 9 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.960-1574_960-1570d others(7): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78470882 | |||||||
| chr11:78471314 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.960-2001T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471314 | |||||||
| chr11:78471520 | C | CT | 98 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(95): Show |
98 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.960-2208dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471520 | |||||||
| chr11:78471609 | G | A | 13 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.960-2296C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471609 | |||||||
| chr11:78471614 | A | C | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.960-2301T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471614 | |||||||
| chr11:78471640 | C | T | 1 | a0002c0002t0002g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.960-2327G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471640 | |||||||
| chr11:78471668 | A | G | 7 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.960-2355T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471668 | |||||||
| chr11:78471683 | C | G | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.960-2370G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471683 | |||||||
| chr11:78471699 | C | A | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.960-2386G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471699 | |||||||
| chr11:78471738 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.960-2425A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471738 | |||||||
| chr11:78471747 | A | T | 1 | a0002c0002t0002g0209 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.960-2434T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471747 | |||||||
| chr11:78471748 | T | C | 1 | a0002c0002t0002g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.960-2435A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471748 | |||||||
| chr11:78471881 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.960-2568A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471881 | |||||||
| chr11:78471967 | A | G | 1 | a0001c0006t0003g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.960-2654T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471967 | |||||||
| chr11:78471969 | C | G | 128 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(125): Show |
128 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.960-2656G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78471969 | |||||||
| chr11:78472031 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.960-2718G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78472031 | |||||||
| chr11:78472076 | C | T | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-2763G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78472076 | |||||||
| chr11:78472324 | C | T | 112 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(109): Show |
112 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.960-3011G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78472324 | |||||||
| chr11:78472401 | C | T | 2 | a0001c0001t0005g0121 a0002c0002t0002g0213 |
2 | NA18960.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.960-3088G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78472401 | |||||||
| chr11:78472405 | A | G | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.960-3092T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78472405 | |||||||
| chr11:78472411 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.960-3098T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78472411 | |||||||
| chr11:78472427 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.960-3114G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78472427 | |||||||
| chr11:78472487 | T | C | 112 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(109): Show |
112 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.960-3174A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78472487 | |||||||
| chr11:78472589 | T | A | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.960-3276A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78472589 | |||||||
| chr11:78472836 | T | A | 118 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(115): Show |
118 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.960-3523A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78472836 | |||||||
| chr11:78473275 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.960-3962A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78473275 | |||||||
| chr11:78473403 | T | C | 1 | a0002c0002t0003g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.960-4090A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78473403 | |||||||
| chr11:78473421 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.960-4108C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78473421 | |||||||
| chr11:78473464 | GT | G | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-4152delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78473464 | |||||||
| chr11:78473514 | T | A | 134 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(131): Show |
134 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.960-4201A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78473514 | |||||||
| chr11:78473627 | C | G | 1 | a0001c0001t0001g0051 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.960-4314G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78473627 | |||||||
| chr11:78473921 | T | C | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.959+4517A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78473921 | |||||||
| chr11:78473943 | C | G | 10 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.959+4495G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78473943 | |||||||
| chr11:78474151 | T | G | 16 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+4287A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78474151 | |||||||
| chr11:78474523 | T | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0077 others(5): Show |
8 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.959+3915A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78474523 | |||||||
| chr11:78474537 | T | C | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+3901A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78474537 | |||||||
| chr11:78474590 | G | C | 104 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.959+3848C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78474590 | |||||||
| chr11:78474616 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.959+3822C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78474616 | |||||||
| chr11:78474823 | T | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.959+3615A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78474823 | |||||||
| chr11:78474896 | G | A | 16 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+3542C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78474896 | |||||||
| chr11:78474911 | C | CT | 22 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(19): Show |
22 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.959+3526dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78474911 | |||||||
| chr11:78474923 | C | T | 128 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(125): Show |
128 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.959+3515G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78474923 | |||||||
| chr11:78474974 | C | T | 11 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.959+3464G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78474974 | |||||||
| chr11:78475006 | A | C | 1 | a0002c0002t0002g0270 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.959+3432T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475006 | |||||||
| chr11:78475091 | G | A | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.959+3347C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475091 | |||||||
| chr11:78475127 | T | TA | 146 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(143): Show |
146 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.959+3310dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475127 | |||||||
| chr11:78475156 | A | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.959+3282T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475156 | |||||||
| chr11:78475192 | C | T | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.959+3246G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475192 | |||||||
| chr11:78475275 | T | C | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.959+3163A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475275 | |||||||
| chr11:78475379 | A | G | 12 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(9): Show |
12 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.959+3059T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475379 | |||||||
| chr11:78475463 | T | A | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.959+2975A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475463 | |||||||
| chr11:78475540 | C | A | 1 | a0001c0001t0005g0070 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.959+2898G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475540 | |||||||
| chr11:78475547 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.959+2891C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475547 | |||||||
| chr11:78475580 | CT | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
91 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.959+2857delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475580 | |||||||
| chr11:78475580 | CTT | C | 9 | a0001c0001t0001g0100 a0001c0001t0001g0141 a0001c0001t0001g0143 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.959+2856_959+2857d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475580 | |||||||
| chr11:78475580 | CTTT | C | 7 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | HG02258.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.959+2855_959+2857d others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475580 | |||||||
| chr11:78475580 | CTTTTTTT others(3): Show |
C | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.959+2848_959+2857d others(12): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475580 | |||||||
| chr11:78475580 | CTTTTTTT others(4): Show |
C | 9 | a0001c0003t0002g0258 a0001c0003t0003g0169 a0001c0003t0003g0170 others(6): Show |
9 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.959+2847_959+2857d others(13): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475580 | |||||||
| chr11:78475580 | CTTTTTTT others(5): Show |
C | 109 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(106): Show |
109 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.959+2846_959+2857d others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475580 | |||||||
| chr11:78475580 | CTTTTTTT others(6): Show |
C | 3 | a0001c0004t0004g0285 a0002c0002t0002g0163 a0002c0002t0002g0224 |
3 | HG02976.hp2 NA18959.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.959+2845_959+2857d others(15): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475580 | |||||||
| chr11:78475580 | CTTTTTTT others(8): Show |
C | 4 | a0001c0001t0001g0053 a0001c0001t0001g0062 a0001c0001t0010g0120 others(1): Show |
4 | HG01071.hp2 HG03927.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+2843_959+2857d others(17): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475580 | |||||||
| chr11:78475641 | G | A | 112 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(109): Show |
112 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.959+2797C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475641 | |||||||
| chr11:78475762 | A | T | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.959+2676T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78475762 | |||||||
| chr11:78476043 | G | A | 1 | a0002c0002t0002g0246 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.959+2395C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78476043 | |||||||
| chr11:78476050 | C | G | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.959+2388G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78476050 | |||||||
| chr11:78476112 | G | C | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.959+2326C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78476112 | |||||||
| chr11:78476130 | C | T | 10 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.959+2308G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78476130 | |||||||
| chr11:78476378 | C | T | 10 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(7): Show |
10 | HG02055.hp2 HG02630.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.959+2060G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78476378 | |||||||
| chr11:78476385 | G | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.959+2053C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78476385 | |||||||
| chr11:78476497 | C | A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.959+1941G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78476497 | |||||||
| chr11:78476501 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.959+1937G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78476501 | |||||||
| chr11:78476532 | C | A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.959+1906G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78476532 | |||||||
| chr11:78476849 | A | C | 12 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(9): Show |
12 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.959+1589T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78476849 | |||||||
| chr11:78476854 | T | G | 1 | a0001c0001t0001g0045 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.959+1584A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78476854 | |||||||
| chr11:78476873 | A | G | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.959+1565T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78476873 | |||||||
| chr11:78477250 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0098 a0001c0001t0001g0115 |
3 | HG01175.hp2 HG01261.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.959+1188T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78477250 | |||||||
| chr11:78477341 | C | T | 7 | a0001c0001t0005g0121 a0002c0002t0002g0182 a0002c0002t0002g0187 others(4): Show |
7 | NA18941.hp2 NA18957.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.959+1097G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78477341 | |||||||
| chr11:78477421 | T | C | 1 | a0002c0002t0002g0176 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.959+1017A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78477421 | |||||||
| chr11:78477581 | C | G | 128 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(125): Show |
128 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.959+857G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78477581 | |||||||
| chr11:78477601 | T | G | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.959+837A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78477601 | |||||||
| chr11:78477749 | G | A | 146 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(143): Show |
146 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.959+689C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78477749 | |||||||
| chr11:78477782 | T | C | 2 | a0001c0001t0005g0124 a0002c0002t0002g0234 |
2 | NA18967.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.959+656A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78477782 | |||||||
| chr11:78477849 | C | T | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.959+589G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78477849 | |||||||
| chr11:78477903 | A | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0001g0062 others(2): Show |
5 | HG01071.hp2 HG02293.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.959+535T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78477903 | |||||||
| chr11:78478066 | T | C | 16 | a0001c0001t0011g0132 a0001c0003t0004g0274 a0001c0003t0004g0275 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+372A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78478066 | |||||||
| chr11:78478087 | G | T | 149 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(146): Show |
149 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.959+351C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78478087 | |||||||
| chr11:78478163 | AAT | A | 10 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(7): Show |
10 | HG02055.hp2 HG02630.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.959+273_959+274del others(2): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78478163 | |||||||
| chr11:78478290 | G | A | 1 | a0001c0004t0013g0153 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.959+148C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 9/13 | chr11 | 78478290 | |||||||
| chr11:78478512 | T | C | 111 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(108): Show |
111 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.922-37A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 8/13 | chr11 | 78478512 | |||||||
| chr11:78478558 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.921+27A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 8/13 | chr11 | 78478558 | |||||||
| chr11:78478770 | G | A | 1 | a0001c0007t0003g0273 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.823-87C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78478770 | |||||||
| chr11:78478792 | C | G | 1 | a0002c0002t0002g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.823-109G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78478792 | |||||||
| chr11:78478993 | G | C | 13 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(10): Show |
13 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.823-310C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78478993 | |||||||
| chr11:78478993 | G | T | 1 | a0001c0004t0013g0153 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.823-310C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78478993 | |||||||
| chr11:78479002 | A | C | 7 | a0001c0004t0004g0283 a0001c0005t0001g0049 a0001c0005t0001g0074 others(4): Show |
7 | HG01891.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-319T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479002 | |||||||
| chr11:78479152 | C | T | 2 | a0001c0001t0005g0121 a0002c0002t0002g0213 |
2 | NA18960.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.823-469G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479152 | |||||||
| chr11:78479294 | T | A | 119 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(116): Show |
119 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.823-611A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479294 | |||||||
| chr11:78479413 | T | G | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.823-730A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479413 | |||||||
| chr11:78479436 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.823-753C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479436 | |||||||
| chr11:78479444 | G | C | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-761C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479444 | |||||||
| chr11:78479602 | A | T | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.823-919T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479602 | |||||||
| chr11:78479665 | T | C | 1 | a0002c0002t0002g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.823-982A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479665 | |||||||
| chr11:78479670 | C | G | 127 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(124): Show |
127 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.823-987G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479670 | |||||||
| chr11:78479671 | G | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-988C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479671 | |||||||
| chr11:78479703 | A | C | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-1020T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479703 | |||||||
| chr11:78479717 | G | C | 126 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(123): Show |
126 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.823-1034C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479717 | |||||||
| chr11:78479762 | C | T | 152 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(149): Show |
152 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.823-1079G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479762 | |||||||
| chr11:78479793 | G | A | 1 | a0001c0006t0003g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.823-1110C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479793 | |||||||
| chr11:78479799 | G | A | 1 | a0001c0003t0006g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.823-1116C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78479799 | |||||||
| chr11:78480138 | G | A | 15 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(12): Show |
15 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.823-1455C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78480138 | |||||||
| chr11:78480288 | C | T | 10 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0001g0111 others(7): Show |
10 | HG01081.hp2 HG01123.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.823-1605G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78480288 | |||||||
| chr11:78480305 | ACGCAGGC others(13): Show |
A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.823-1642_823-1623d others(22): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78480305 | |||||||
| chr11:78480307 | G | A | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-1624C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78480307 | |||||||
| chr11:78480465 | G | T | 2 | a0002c0002t0003g0288 a0002c0002t0003g0289 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.823-1782C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78480465 | |||||||
| chr11:78480508 | G | T | 1 | a0001c0001t0001g0029 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.823-1825C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78480508 | |||||||
| chr11:78480524 | G | C | 7 | a0001c0005t0001g0049 a0001c0005t0001g0074 a0001c0005t0001g0144 others(4): Show |
7 | HG01891.hp1 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-1841C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78480524 | |||||||
| chr11:78480592 | T | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.823-1909A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78480592 | |||||||
| chr11:78480619 | T | TA | 23 | a0001c0001t0001g0073 a0001c0003t0003g0167 a0001c0003t0003g0168 others(20): Show |
23 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.823-1937dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78480619 | |||||||
| chr11:78480619 | T | TAA | 118 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(115): Show |
118 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.823-1938_823-1937d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78480619 | |||||||
| chr11:78480619 | T | TAAAA | 15 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(12): Show |
15 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.823-1940_823-1937d others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78480619 | |||||||
| chr11:78480694 | TG | T | 157 | a0001c0001t0001g0079 a0001c0001t0001g0135 a0001c0001t0001g0137 others(154): Show |
157 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.823-2012delC | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78480694 | |||||||
| chr11:78480765 | TTAAAG | T | 5 | a0001c0003t0015g0266 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-2087_823-2083d others(7): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78480765 | |||||||
| chr11:78481102 | T | G | 99 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(96): Show |
99 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.823-2419A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78481102 | |||||||
| chr11:78481119 | CCTAA | C | 15 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(12): Show |
15 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.823-2440_823-2437d others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78481119 | |||||||
| chr11:78481136 | T | C | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-2453A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78481136 | |||||||
| chr11:78481268 | A | G | 2 | a0001c0001t0001g0061 a0001c0003t0005g0131 |
2 | HG03017.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.823-2585T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78481268 | |||||||
| chr11:78481473 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.823-2790C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78481473 | |||||||
| chr11:78481492 | C | T | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-2809G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78481492 | |||||||
| chr11:78481661 | G | A | 151 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(148): Show |
151 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.823-2978C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78481661 | |||||||
| chr11:78481794 | A | G | 15 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(12): Show |
15 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.823-3111T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78481794 | |||||||
| chr11:78481922 | G | A | 142 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(139): Show |
142 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.823-3239C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78481922 | |||||||
| chr11:78482196 | A | G | 135 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(132): Show |
135 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.823-3513T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78482196 | |||||||
| chr11:78482250 | T | C | 1 | a0002c0002t0002g0252 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.823-3567A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78482250 | |||||||
| chr11:78482253 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.823-3570T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78482253 | |||||||
| chr11:78482482 | A | G | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.823-3799T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78482482 | |||||||
| chr11:78482485 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.823-3802A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78482485 | |||||||
| chr11:78482498 | A | G | 135 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(132): Show |
135 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.823-3815T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78482498 | |||||||
| chr11:78482604 | G | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
7 | NA18946.hp2 NA18949.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-3921C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78482604 | |||||||
| chr11:78482619 | C | T | 1 | a0002c0002t0002g0214 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.823-3936G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78482619 | |||||||
| chr11:78482875 | T | C | 135 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(132): Show |
135 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.823-4192A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78482875 | |||||||
| chr11:78482911 | C | G | 1 | a0001c0001t0005g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.823-4228G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78482911 | |||||||
| chr11:78483074 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.823-4391C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483074 | |||||||
| chr11:78483155 | C | T | 156 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(153): Show |
156 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.823-4472G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483155 | |||||||
| chr11:78483208 | C | G | 1 | a0002c0002t0002g0187 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.823-4525G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483208 | |||||||
| chr11:78483235 | T | C | 10 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(7): Show |
10 | HG02055.hp2 HG02630.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.823-4552A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483235 | |||||||
| chr11:78483384 | G | A | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-4701C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483384 | |||||||
| chr11:78483519 | C | T | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.823-4836G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483519 | |||||||
| chr11:78483587 | C | T | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.823-4904G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483587 | |||||||
| chr11:78483626 | A | G | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-4943T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483626 | |||||||
| chr11:78483627 | C | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0046 others(3): Show |
6 | HG01981.hp2 HG02135.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-4944G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483627 | |||||||
| chr11:78483643 | C | T | 1 | a0001c0001t0010g0120 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.823-4960G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483643 | |||||||
| chr11:78483829 | T | C | 1 | a0002c0002t0002g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.823-5146A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483829 | |||||||
| chr11:78483879 | G | GA | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-5197dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483879 | |||||||
| chr11:78483890 | A | T | 120 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(117): Show |
120 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.823-5207T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483890 | |||||||
| chr11:78483903 | T | G | 1 | a0001c0004t0007g0154 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.823-5220A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78483903 | |||||||
| chr11:78484003 | C | G | 1 | a0001c0010t0001g0017 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.823-5320G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484003 | |||||||
| chr11:78484031 | C | A | 2 | a0002c0002t0003g0288 a0002c0002t0003g0289 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.823-5348G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484031 | |||||||
| chr11:78484166 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0044 others(3): Show |
6 | HG00621.hp1 HG02080.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-5483G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484166 | |||||||
| chr11:78484174 | A | G | 25 | a0002c0002t0002g0163 a0002c0002t0002g0164 a0002c0002t0002g0176 others(22): Show |
25 | HG00597.hp1 HG01081.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.823-5491T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484174 | |||||||
| chr11:78484220 | A | T | 9 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.823-5537T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484220 | |||||||
| chr11:78484284 | A | G | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-5601T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484284 | |||||||
| chr11:78484349 | A | G | 3 | a0002c0002t0002g0161 a0002c0002t0002g0246 a0002c0002t0002g0256 |
3 | HG02040.hp2 HG03540.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.823-5666T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484349 | |||||||
| chr11:78484381 | T | C | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.823-5698A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484381 | |||||||
| chr11:78484384 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.823-5701T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484384 | |||||||
| chr11:78484638 | C | A | 15 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(12): Show |
15 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.823-5955G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484638 | |||||||
| chr11:78484664 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.823-5981G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484664 | |||||||
| chr11:78484732 | C | T | 1 | a0002c0002t0002g0202 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.823-6049G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484732 | |||||||
| chr11:78484812 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.823-6129C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484812 | |||||||
| chr11:78484878 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.823-6195G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78484878 | |||||||
| chr11:78485046 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.823-6363G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78485046 | |||||||
| chr11:78485051 | C | G | 1 | a0002c0002t0002g0161 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.823-6368G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78485051 | |||||||
| chr11:78485073 | G | A | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.823-6390C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78485073 | |||||||
| chr11:78485365 | G | C | 141 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(138): Show |
141 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.823-6682C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78485365 | |||||||
| chr11:78485403 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.823-6720T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78485403 | |||||||
| chr11:78485407 | C | A | 10 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(7): Show |
10 | HG02055.hp2 HG02630.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.823-6724G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78485407 | |||||||
| chr11:78485532 | C | A | 5 | a0002c0002t0002g0247 a0002c0002t0002g0248 a0002c0002t0002g0249 others(2): Show |
5 | HG00642.hp2 HG00735.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-6849G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78485532 | |||||||
| chr11:78485554 | TG | T | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-6872delC | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78485554 | |||||||
| chr11:78485667 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.823-6984A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78485667 | |||||||
| chr11:78485779 | C | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | NA19002.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.823-7096G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78485779 | |||||||
| chr11:78485906 | C | T | 7 | a0001c0001t0005g0121 a0002c0002t0002g0182 a0002c0002t0002g0187 others(4): Show |
7 | NA18941.hp2 NA18957.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+7157G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78485906 | |||||||
| chr11:78486154 | A | C | 149 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(146): Show |
149 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.822+6909T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78486154 | |||||||
| chr11:78486179 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.822+6884T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78486179 | |||||||
| chr11:78486204 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.822+6859A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78486204 | |||||||
| chr11:78486237 | G | C | 99 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(96): Show |
99 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.822+6826C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78486237 | |||||||
| chr11:78486407 | A | T | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+6656T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78486407 | |||||||
| chr11:78486873 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02145.hp1 HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.822+6190C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78486873 | |||||||
| chr11:78486984 | T | C | 156 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(153): Show |
156 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.822+6079A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78486984 | |||||||
| chr11:78487098 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.822+5965C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78487098 | |||||||
| chr11:78487104 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.822+5959G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78487104 | |||||||
| chr11:78487131 | G | T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.822+5932C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78487131 | |||||||
| chr11:78487354 | T | TA | 21 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0052 others(18): Show |
21 | HG01255.hp1 HG01255.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.822+5708dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78487354 | |||||||
| chr11:78487354 | TAAAA | T | 8 | a0001c0005t0001g0049 a0001c0005t0001g0074 a0001c0005t0001g0144 others(5): Show |
8 | HG01891.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+5705_822+5708d others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78487354 | |||||||
| chr11:78487355 | A | T | 1 | a0002c0002t0003g0227 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.822+5708T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78487355 | |||||||
| chr11:78487460 | T | C | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.822+5603A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78487460 | |||||||
| chr11:78487627 | G | A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.822+5436C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78487627 | |||||||
| chr11:78487745 | T | G | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.822+5318A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78487745 | |||||||
| chr11:78487821 | A | T | 1 | a0001c0001t0001g0053 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.822+5242T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78487821 | |||||||
| chr11:78487836 | T | C | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.822+5227A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78487836 | |||||||
| chr11:78488135 | C | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+4928G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78488135 | |||||||
| chr11:78488234 | T | TA | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0019 others(19): Show |
22 | HG00621.hp1 HG01884.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.822+4828dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78488234 | |||||||
| chr11:78488234 | TA | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0003t0003g0167 others(6): Show |
9 | HG02486.hp1 HG02615.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.822+4828delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78488234 | |||||||
| chr11:78488234 | TAA | T | 13 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(10): Show |
13 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.822+4827_822+4828d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78488234 | |||||||
| chr11:78488234 | TAAA | T | 27 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(24): Show |
27 | HG00735.hp2 HG01981.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.822+4826_822+4828d others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78488234 | |||||||
| chr11:78488234 | TAAAA | T | 109 | a0001c0001t0005g0070 a0001c0001t0005g0121 a0001c0001t0005g0124 others(106): Show |
109 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.822+4825_822+4828d others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78488234 | |||||||
| chr11:78488262 | G | C | 1 | a0001c0003t0005g0131 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.822+4801C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78488262 | |||||||
| chr11:78488333 | T | C | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.822+4730A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78488333 | |||||||
| chr11:78488355 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.822+4708G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78488355 | |||||||
| chr11:78488566 | C | T | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.822+4497G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78488566 | |||||||
| chr11:78488589 | C | T | 8 | a0001c0005t0001g0049 a0001c0005t0001g0074 a0001c0005t0001g0144 others(5): Show |
8 | HG01891.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+4474G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78488589 | |||||||
| chr11:78488842 | C | G | 120 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(117): Show |
120 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.822+4221G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78488842 | |||||||
| chr11:78489049 | G | A | 1 | a0002c0002t0002g0202 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.822+4014C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78489049 | |||||||
| chr11:78489175 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.822+3888G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78489175 | |||||||
| chr11:78489381 | A | T | 120 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(117): Show |
120 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.822+3682T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78489381 | |||||||
| chr11:78489537 | T | C | 8 | a0001c0005t0001g0049 a0001c0005t0001g0074 a0001c0005t0001g0144 others(5): Show |
8 | HG01891.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+3526A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78489537 | |||||||
| chr11:78489607 | G | A | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.822+3456C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78489607 | |||||||
| chr11:78489775 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.822+3288C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78489775 | |||||||
| chr11:78489872 | C | G | 1 | a0001c0004t0013g0153 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.822+3191G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78489872 | |||||||
| chr11:78489973 | T | C | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.822+3090A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78489973 | |||||||
| chr11:78490052 | C | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+3011G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78490052 | |||||||
| chr11:78490101 | G | A | 15 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(12): Show |
15 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.822+2962C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78490101 | |||||||
| chr11:78490103 | C | T | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.822+2960G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78490103 | |||||||
| chr11:78490115 | T | C | 1 | a0002c0002t0002g0250 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.822+2948A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78490115 | |||||||
| chr11:78490155 | G | C | 117 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(114): Show |
117 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.822+2908C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78490155 | |||||||
| chr11:78490264 | C | T | 1 | a0002c0002t0002g0195 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.822+2799G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78490264 | |||||||
| chr11:78490288 | C | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.822+2775G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78490288 | |||||||
| chr11:78490408 | T | G | 120 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(117): Show |
120 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.822+2655A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78490408 | |||||||
| chr11:78490431 | T | C | 1 | a0002c0002t0002g0176 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.822+2632A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78490431 | |||||||
| chr11:78490591 | C | T | 15 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(12): Show |
15 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.822+2472G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78490591 | |||||||
| chr11:78490784 | G | T | 8 | a0001c0005t0001g0049 a0001c0005t0001g0074 a0001c0005t0001g0144 others(5): Show |
8 | HG01891.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+2279C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78490784 | |||||||
| chr11:78490831 | G | A | 1 | a0004c0009t0002g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+2232C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78490831 | |||||||
| chr11:78491030 | T | C | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+2033A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78491030 | |||||||
| chr11:78491315 | C | T | 10 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(7): Show |
10 | HG02055.hp2 HG02630.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.822+1748G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78491315 | |||||||
| chr11:78491342 | C | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.822+1721G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78491342 | |||||||
| chr11:78491389 | C | CA | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.822+1673_822+1674i others(3): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78491389 | |||||||
| chr11:78491503 | T | C | 11 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0006g0259 others(8): Show |
11 | HG02109.hp1 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.822+1560A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78491503 | |||||||
| chr11:78491512 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.822+1551C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78491512 | |||||||
| chr11:78491594 | T | C | 1 | a0002c0002t0003g0251 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.822+1469A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78491594 | |||||||
| chr11:78491653 | A | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
133 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.822+1410T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78491653 | |||||||
| chr11:78491662 | C | A | 1 | a0002c0002t0002g0206 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.822+1401G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78491662 | |||||||
| chr11:78491761 | C | T | 5 | a0001c0004t0007g0152 a0002c0002t0003g0239 a0002c0002t0003g0240 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+1302G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78491761 | |||||||
| chr11:78491779 | T | G | 7 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(4): Show |
7 | HG02630.hp2 HG02886.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+1284A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78491779 | |||||||
| chr11:78491865 | G | A | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
57 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.822+1198C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78491865 | |||||||
| chr11:78491897 | T | C | 2 | a0001c0001t0005g0121 a0002c0002t0002g0213 |
2 | NA18960.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.822+1166A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78491897 | |||||||
| chr11:78492088 | C | CAT | 7 | a0001c0001t0005g0136 a0001c0001t0005g0142 a0001c0004t0013g0153 others(4): Show |
7 | HG01081.hp2 HG02886.hp2 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+973_822+974dup others(2): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492088 | |||||||
| chr11:78492106 | T | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
143 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(140): Show |
intron_variant | MODIFIER | c.822+957A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492106 | |||||||
| chr11:78492106 | T | G | 1 | a0001c0001t0001g0018 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.822+957A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492106 | |||||||
| chr11:78492106 | T | TAC | 3 | a0001c0001t0001g0109 a0001c0001t0009g0060 a0001c0001t0014g0287 |
3 | HG01255.hp1 HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.822+956_822+957ins others(2): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492106 | |||||||
| chr11:78492106 | T | TACAG | 8 | a0001c0001t0001g0102 a0001c0003t0006g0259 a0001c0003t0006g0260 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.822+956_822+957ins others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492106 | |||||||
| chr11:78492108 | T | C | 21 | a0001c0001t0001g0018 a0001c0001t0001g0084 a0001c0001t0001g0102 others(18): Show |
21 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.822+955A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492108 | |||||||
| chr11:78492108 | T | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.822+955A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492108 | |||||||
| chr11:78492110 | C | G | 11 | a0001c0001t0001g0084 a0001c0001t0001g0135 a0001c0001t0001g0137 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.822+953G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492110 | |||||||
| chr11:78492110 | C | T | 1 | a0001c0003t0003g0169 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.822+953G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492110 | |||||||
| chr11:78492110 | CAG | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
76 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.822+951_822+952del others(2): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492110 | |||||||
| chr11:78492112 | G | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): Show |
90 | HG00099.hp1 HG00621.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.822+951C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492112 | |||||||
| chr11:78492112 | G | GAC | 8 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(5): Show |
8 | HG00597.hp1 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+949_822+950dup others(2): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492112 | |||||||
| chr11:78492112 | G | T | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.822+951C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492112 | |||||||
| chr11:78492116 | C | G | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.822+947G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492116 | |||||||
| chr11:78492136 | T | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.822+927A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492136 | |||||||
| chr11:78492396 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.822+667G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492396 | |||||||
| chr11:78492587 | T | G | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.822+476A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492587 | |||||||
| chr11:78492619 | T | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.822+444A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492619 | |||||||
| chr11:78492686 | C | G | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+377G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492686 | |||||||
| chr11:78492981 | C | G | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.822+82G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78492981 | |||||||
| chr11:78493027 | CACAGAT | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.822+30_822+35delAT others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 7/13 | chr11 | 78493027 | |||||||
| chr11:78493253 | T | TA | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
161 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.690-59dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78493253 | |||||||
| chr11:78493274 | C | T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.690-79G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78493274 | |||||||
| chr11:78493334 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
161 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.690-139G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78493334 | |||||||
| chr11:78493360 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
161 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.690-165G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78493360 | |||||||
| chr11:78493392 | G | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.690-197C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78493392 | |||||||
| chr11:78493403 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0065 |
2 | NA18968.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.690-208G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78493403 | |||||||
| chr11:78493420 | C | T | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.690-225G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78493420 | |||||||
| chr11:78493687 | GA | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0135 a0001c0001t0001g0137 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.690-493delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78493687 | |||||||
| chr11:78493993 | G | T | 1 | a0002c0002t0002g0222 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.690-798C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78493993 | |||||||
| chr11:78494026 | T | C | 4 | a0002c0002t0002g0217 a0002c0002t0002g0229 a0002c0002t0002g0230 others(1): Show |
4 | NA18969.hp2 NA19056.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-831A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494026 | |||||||
| chr11:78494030 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.690-835G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494030 | |||||||
| chr11:78494452 | A | G | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.690-1257T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494452 | |||||||
| chr11:78494459 | TTTTC | T | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-1268_690-1265d others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494459 | |||||||
| chr11:78494469 | C | CT | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
144 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(141): Show |
intron_variant | MODIFIER | c.690-1275dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494469 | |||||||
| chr11:78494469 | C | CTT | 13 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0066 others(10): Show |
13 | HG01192.hp1 HG01255.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.690-1276_690-1275d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494469 | |||||||
| chr11:78494473 | T | TC | 4 | a0001c0001t0001g0045 a0001c0001t0001g0050 a0001c0001t0001g0054 others(1): Show |
4 | NA18968.hp1 NA19065.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-1279_690-1278i others(3): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494473 | |||||||
| chr11:78494598 | G | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.690-1403C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494598 | |||||||
| chr11:78494602 | T | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.690-1407A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494602 | |||||||
| chr11:78494647 | C | G | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.690-1452G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494647 | |||||||
| chr11:78494657 | T | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
140 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.690-1462A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494657 | |||||||
| chr11:78494666 | T | C | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-1471A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494666 | |||||||
| chr11:78494679 | C | A | 4 | a0001c0005t0001g0074 a0001c0005t0001g0144 a0001c0005t0001g0145 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.690-1484G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494679 | |||||||
| chr11:78494829 | G | C | 2 | a0002c0002t0002g0183 a0002c0002t0002g0191 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.690-1634C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494829 | |||||||
| chr11:78494928 | C | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.690-1733G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78494928 | |||||||
| chr11:78495034 | T | C | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.690-1839A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495034 | |||||||
| chr11:78495111 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
142 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.690-1916A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495111 | |||||||
| chr11:78495288 | T | C | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.690-2093A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495288 | |||||||
| chr11:78495372 | T | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.690-2177A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495372 | |||||||
| chr11:78495447 | T | C | 1 | a0002c0002t0003g0227 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.690-2252A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495447 | |||||||
| chr11:78495518 | C | T | 1 | a0002c0002t0002g0195 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.690-2323G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495518 | |||||||
| chr11:78495560 | C | T | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.690-2365G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495560 | |||||||
| chr11:78495653 | C | T | 8 | a0001c0005t0001g0049 a0001c0005t0001g0074 a0001c0005t0001g0144 others(5): Show |
8 | HG01891.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.690-2458G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495653 | |||||||
| chr11:78495654 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.690-2459T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495654 | |||||||
| chr11:78495684 | T | C | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.690-2489A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495684 | |||||||
| chr11:78495698 | G | A | 4 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0002c0002t0003g0288 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-2503C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495698 | |||||||
| chr11:78495714 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.690-2519C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495714 | |||||||
| chr11:78495750 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.690-2555G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495750 | |||||||
| chr11:78495823 | G | A | 2 | a0002c0002t0002g0177 a0002c0002t0002g0179 |
2 | HG01975.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.690-2628C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495823 | |||||||
| chr11:78495841 | C | T | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.690-2646G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78495841 | |||||||
| chr11:78496045 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.690-2850C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78496045 | |||||||
| chr11:78496052 | G | T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.690-2857C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78496052 | |||||||
| chr11:78496130 | AAC | A | 4 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0002c0002t0003g0288 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-2937_690-2936d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78496130 | |||||||
| chr11:78496172 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.690-2977G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78496172 | |||||||
| chr11:78496249 | G | T | 2 | a0001c0001t0001g0053 a0001c0001t0010g0120 |
2 | HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.690-3054C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78496249 | |||||||
| chr11:78496285 | T | A | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.690-3090A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78496285 | |||||||
| chr11:78496347 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0133 |
2 | HG00741.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.690-3152G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78496347 | |||||||
| chr11:78496348 | A | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.690-3153T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78496348 | |||||||
| chr11:78496401 | G | A | 5 | a0001c0003t0015g0266 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.690-3206C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78496401 | |||||||
| chr11:78496484 | G | A | 15 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(12): Show |
15 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.690-3289C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78496484 | |||||||
| chr11:78496640 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
151 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.690-3445A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78496640 | |||||||
| chr11:78496735 | T | TGATA | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.690-3544_690-3541d others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78496735 | |||||||
| chr11:78496802 | T | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.690-3607A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78496802 | |||||||
| chr11:78497062 | G | A | 1 | a0002c0002t0002g0202 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.690-3867C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497062 | |||||||
| chr11:78497065 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.690-3870T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497065 | |||||||
| chr11:78497207 | A | G | 2 | a0002c0002t0003g0288 a0002c0002t0003g0289 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.690-4012T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497207 | |||||||
| chr11:78497241 | G | GA | 20 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(17): Show |
20 | HG00642.hp2 HG00735.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.690-4047dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497241 | |||||||
| chr11:78497241 | G | GAA | 7 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0005t0001g0074 others(4): Show |
7 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-4048_690-4047d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497241 | |||||||
| chr11:78497241 | G | GC | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
123 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.690-4047_690-4046i others(3): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497241 | |||||||
| chr11:78497241 | G | GCA | 7 | a0001c0001t0001g0027 a0001c0001t0001g0051 a0001c0001t0001g0085 others(4): Show |
7 | HG01175.hp2 HG01192.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.690-4047_690-4046i others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497241 | |||||||
| chr11:78497241 | GA | G | 7 | a0001c0001t0001g0016 a0001c0001t0005g0070 a0001c0001t0005g0136 others(4): Show |
7 | HG01256.hp2 HG01346.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.690-4047delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497241 | |||||||
| chr11:78497242 | A | C | 40 | a0001c0001t0001g0052 a0001c0001t0001g0066 a0001c0001t0001g0067 others(37): Show |
40 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(37): Show |
intron_variant | MODIFIER | c.690-4047T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497242 | |||||||
| chr11:78497243 | A | C | 2 | a0001c0001t0001g0016 a0001c0006t0003g0280 |
2 | HG03579.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.690-4048T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497243 | |||||||
| chr11:78497261 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.690-4066T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497261 | |||||||
| chr11:78497424 | T | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.690-4229A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497424 | |||||||
| chr11:78497434 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
150 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.690-4239A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497434 | |||||||
| chr11:78497437 | G | A | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.690-4242C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497437 | |||||||
| chr11:78497588 | A | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.690-4393T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78497588 | |||||||
| chr11:78498178 | AATG | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0077 others(4): Show |
7 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-4986_690-4984d others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498178 | |||||||
| chr11:78498224 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.690-5029A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498224 | |||||||
| chr11:78498258 | G | GA | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.690-5064dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498258 | |||||||
| chr11:78498320 | C | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.690-5125G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498320 | |||||||
| chr11:78498671 | CT | C | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
188 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(185): Show |
intron_variant | MODIFIER | c.690-5477delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498671 | |||||||
| chr11:78498699 | G | A | 1 | a0002c0002t0003g0218 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.690-5504C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498699 | |||||||
| chr11:78498833 | G | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
140 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.690-5638C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498833 | |||||||
| chr11:78498890 | CT | C | 90 | a0001c0001t0005g0121 a0001c0001t0005g0134 a0001c0001t0005g0136 others(87): Show |
90 | HG00099.hp2 HG00408.hp2 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.690-5696delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498890 | |||||||
| chr11:78498890 | CTT | C | 33 | a0001c0001t0001g0051 a0001c0001t0001g0086 a0001c0001t0001g0087 others(30): Show |
33 | HG00741.hp2 HG01175.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.690-5697_690-5696d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498890 | |||||||
| chr11:78498890 | CTTT | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
135 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.690-5698_690-5696d others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498890 | |||||||
| chr11:78498890 | CTTTT | C | 9 | a0001c0001t0001g0050 a0001c0001t0001g0148 a0001c0003t0006g0259 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.690-5699_690-5696d others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498890 | |||||||
| chr11:78498890 | CTTTTT | C | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.690-5700_690-5696d others(7): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498890 | |||||||
| chr11:78498890 | CTTTTTTT others(6): Show |
C | 8 | a0001c0005t0001g0049 a0001c0005t0001g0074 a0001c0005t0001g0144 others(5): Show |
8 | HG01891.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.690-5708_690-5696d others(15): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498890 | |||||||
| chr11:78498930 | G | A | 1 | a0001c0004t0013g0153 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.690-5735C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498930 | |||||||
| chr11:78498948 | GATGACAC others(11): Show |
G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
174 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(171): Show |
intron_variant | MODIFIER | c.690-5771_690-5754d others(20): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498948 | |||||||
| chr11:78498968 | C | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
174 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(171): Show |
intron_variant | MODIFIER | c.690-5773G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78498968 | |||||||
| chr11:78499011 | G | C | 1 | a0001c0003t0006g0261 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.690-5816C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499011 | |||||||
| chr11:78499030 | C | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
150 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.690-5835G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499030 | |||||||
| chr11:78499065 | C | T | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-5870G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499065 | |||||||
| chr11:78499077 | C | T | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.690-5882G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499077 | |||||||
| chr11:78499116 | C | T | 5 | a0001c0004t0007g0152 a0002c0002t0003g0239 a0002c0002t0003g0240 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.690-5921G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499116 | |||||||
| chr11:78499215 | C | T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.690-6020G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499215 | |||||||
| chr11:78499256 | A | G | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.690-6061T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499256 | |||||||
| chr11:78499285 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.690-6090T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499285 | |||||||
| chr11:78499296 | T | G | 7 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-6101A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499296 | |||||||
| chr11:78499380 | C | T | 1 | a0001c0010t0001g0017 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.690-6185G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499380 | |||||||
| chr11:78499456 | G | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.690-6261C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499456 | |||||||
| chr11:78499495 | A | G | 1 | a0001c0001t0001g0006 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.690-6300T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499495 | |||||||
| chr11:78499847 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
193 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(190): Show |
intron_variant | MODIFIER | c.690-6652A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499847 | |||||||
| chr11:78499935 | G | A | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.690-6740C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78499935 | |||||||
| chr11:78500045 | G | C | 5 | a0001c0003t0015g0266 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.690-6850C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78500045 | |||||||
| chr11:78500127 | T | C | 15 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(12): Show |
15 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.690-6932A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78500127 | |||||||
| chr11:78500137 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.690-6942G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78500137 | |||||||
| chr11:78500392 | T | C | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.690-7197A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78500392 | |||||||
| chr11:78500562 | C | T | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.690-7367G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78500562 | |||||||
| chr11:78500762 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.690-7567T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78500762 | |||||||
| chr11:78500839 | T | C | 2 | a0002c0002t0002g0161 a0002c0002t0002g0256 |
2 | HG02040.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.690-7644A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78500839 | |||||||
| chr11:78500864 | G | A | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.690-7669C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78500864 | |||||||
| chr11:78500882 | C | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.690-7687G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78500882 | |||||||
| chr11:78500937 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0078 others(1): Show |
4 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-7742G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78500937 | |||||||
| chr11:78500965 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.690-7770C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78500965 | |||||||
| chr11:78501076 | A | G | 2 | a0001c0001t0009g0060 a0001c0001t0014g0287 |
2 | HG01255.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.690-7881T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78501076 | |||||||
| chr11:78501113 | A | G | 2 | a0002c0002t0002g0248 a0002c0002t0002g0249 |
2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.690-7918T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78501113 | |||||||
| chr11:78501317 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.690-8122C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78501317 | |||||||
| chr11:78501427 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.690-8232A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78501427 | |||||||
| chr11:78501697 | T | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
156 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.690-8502A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78501697 | |||||||
| chr11:78501838 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.690-8643T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78501838 | |||||||
| chr11:78501873 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.690-8678G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78501873 | |||||||
| chr11:78502146 | G | C | 1 | a0001c0003t0003g0169 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.690-8951C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502146 | |||||||
| chr11:78502254 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0062 |
2 | HG01071.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.690-9059A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502254 | |||||||
| chr11:78502310 | T | G | 2 | a0001c0004t0004g0283 a0001c0004t0004g0285 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.690-9115A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502310 | |||||||
| chr11:78502369 | A | T | 6 | a0002c0002t0002g0235 a0002c0002t0002g0236 a0002c0002t0002g0237 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.690-9174T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502369 | |||||||
| chr11:78502554 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.690-9359A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502554 | |||||||
| chr11:78502717 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.690-9522C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502717 | |||||||
| chr11:78502729 | G | A | 1 | a0001c0004t0007g0158 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.690-9534C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502729 | |||||||
| chr11:78502855 | G | T | 1 | a0001c0006t0003g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.690-9660C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502855 | |||||||
| chr11:78502868 | A | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
173 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.690-9673T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502868 | |||||||
| chr11:78502931 | T | C | 36 | a0001c0001t0005g0070 a0001c0001t0005g0134 a0002c0002t0002g0163 others(33): Show |
36 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.690-9736A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502931 | |||||||
| chr11:78502973 | A | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
172 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.690-9778T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502973 | |||||||
| chr11:78502984 | A | ACT | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
175 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(172): Show |
intron_variant | MODIFIER | c.690-9791_690-9790d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502984 | |||||||
| chr11:78502991 | C | CA | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
121 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.690-9797dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502991 | |||||||
| chr11:78502991 | C | CAA | 7 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0047 others(4): Show |
7 | HG01928.hp1 HG02257.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.690-9798_690-9797d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502991 | |||||||
| chr11:78502991 | C | CAAAAAAA others(2): Show |
11 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0004g0275 others(8): Show |
11 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.690-9805_690-9797d others(11): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502991 | |||||||
| chr11:78502991 | C | CAAAAAAA others(3): Show |
16 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0081 others(13): Show |
16 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.690-9806_690-9797d others(12): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502991 | |||||||
| chr11:78502991 | C | CAAAAAAA others(4): Show |
9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0072 others(6): Show |
9 | HG01884.hp2 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.690-9807_690-9797d others(13): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502991 | |||||||
| chr11:78502991 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0128 a0001c0004t0007g0152 a0002c0002t0003g0240 others(1): Show |
4 | HG02258.hp2 HG03041.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.690-9808_690-9797d others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502991 | |||||||
| chr11:78502991 | C | CAAAAAAA others(6): Show |
2 | a0001c0006t0003g0280 a0002c0002t0003g0239 |
2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.690-9809_690-9797d others(15): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502991 | |||||||
| chr11:78502991 | C | CAAAAAAA others(7): Show |
1 | a0002c0002t0003g0242 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.690-9810_690-9797d others(16): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78502991 | |||||||
| chr11:78503120 | C | T | 1 | a0001c0004t0007g0158 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.690-9925G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503120 | |||||||
| chr11:78503128 | A | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.690-9933T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503128 | |||||||
| chr11:78503315 | G | GCACACCC others(3): Show |
1 | a0001c0001t0001g0042 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.690-10121_690-1012 others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503315 | |||||||
| chr11:78503318 | A | C | 1 | a0001c0001t0001g0042 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.690-10123T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503318 | |||||||
| chr11:78503327 | T | G | 4 | a0001c0005t0001g0049 a0001c0007t0003g0272 a0001c0007t0003g0273 others(1): Show |
4 | HG02809.hp2 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-10132A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503327 | |||||||
| chr11:78503382 | C | T | 1 | a0002c0002t0003g0172 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.690-10187G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503382 | |||||||
| chr11:78503401 | C | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.690-10206G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503401 | |||||||
| chr11:78503501 | G | A | 10 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(7): Show |
10 | HG02055.hp2 HG02630.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.690-10306C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503501 | |||||||
| chr11:78503503 | G | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
140 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.690-10308C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503503 | |||||||
| chr11:78503546 | C | A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.690-10351G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503546 | |||||||
| chr11:78503552 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.690-10357A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503552 | |||||||
| chr11:78503620 | G | T | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.690-10425C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503620 | |||||||
| chr11:78503623 | T | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.690-10428A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503623 | |||||||
| chr11:78503627 | C | T | 123 | a0001c0001t0001g0081 a0001c0001t0001g0135 a0001c0001t0001g0137 others(120): Show |
123 | HG00099.hp2 HG00597.hp1 HG00642.hp2 others(120): Show |
intron_variant | MODIFIER | c.690-10432G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503627 | |||||||
| chr11:78503743 | T | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0046 others(3): Show |
6 | HG01981.hp2 HG02135.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.690-10548A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503743 | |||||||
| chr11:78503832 | G | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
140 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.690-10637C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78503832 | |||||||
| chr11:78504036 | A | C | 1 | a0001c0003t0003g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.690-10841T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504036 | |||||||
| chr11:78504036 | A | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
148 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.690-10841T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504036 | |||||||
| chr11:78504150 | T | A | 1 | a0001c0001t0001g0079 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.690-10955A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504150 | |||||||
| chr11:78504152 | T | C | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.690-10957A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504152 | |||||||
| chr11:78504434 | GT | G | 85 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(82): Show |
85 | HG00099.hp2 HG00408.hp2 HG01081.hp2 others(82): Show |
intron_variant | MODIFIER | c.690-11240delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504434 | |||||||
| chr11:78504434 | GTT | G | 20 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0003t0004g0274 others(17): Show |
20 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.690-11241_690-1124 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504434 | |||||||
| chr11:78504435 | T | TTTGG | 8 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0053 others(5): Show |
8 | HG01934.hp1 HG02257.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.690-11241_690-1124 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504435 | |||||||
| chr11:78504436 | T | TTGG | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
128 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.690-11242_690-1124 others(7): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504436 | |||||||
| chr11:78504437 | T | TGG | 11 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(8): Show |
11 | HG01081.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.690-11243_690-1124 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504437 | |||||||
| chr11:78504438 | T | G | 7 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0006t0003g0279 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.690-11243A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504438 | |||||||
| chr11:78504439 | T | G | 24 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(21): Show |
24 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.690-11244A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504439 | |||||||
| chr11:78504440 | T | G | 18 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0003t0004g0274 others(15): Show |
18 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.690-11245A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504440 | |||||||
| chr11:78504459 | G | T | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.690-11264C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504459 | |||||||
| chr11:78504852 | A | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
154 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.690-11657T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78504852 | |||||||
| chr11:78505060 | TA | T | 6 | a0001c0001t0001g0073 a0001c0003t0003g0170 a0002c0002t0008g0290 others(3): Show |
6 | HG02145.hp2 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.690-11866delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505060 | |||||||
| chr11:78505191 | G | A | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
150 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.690-11996C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505191 | |||||||
| chr11:78505269 | TAC | T | 24 | a0001c0003t0002g0258 a0001c0003t0004g0276 a0002c0002t0002g0164 others(21): Show |
24 | HG00408.hp2 HG00735.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.690-12076_690-1207 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505269 | |||||||
| chr11:78505269 | TACAC | T | 36 | a0001c0001t0005g0121 a0001c0001t0005g0124 a0001c0001t0005g0136 others(33): Show |
36 | HG01123.hp1 HG01346.hp2 HG01516.hp1 others(33): Show |
intron_variant | MODIFIER | c.690-12078_690-1207 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505269 | |||||||
| chr11:78505269 | TACACAC | T | 29 | a0001c0001t0001g0103 a0001c0001t0001g0117 a0001c0001t0001g0135 others(26): Show |
29 | HG01106.hp2 HG01261.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.690-12080_690-1207 others(10): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505269 | |||||||
| chr11:78505269 | TACACACA others(1): Show |
T | 18 | a0001c0001t0001g0114 a0001c0001t0001g0123 a0001c0001t0005g0142 others(15): Show |
18 | HG01346.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.690-12082_690-1207 others(12): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505269 | |||||||
| chr11:78505269 | TACACACA others(3): Show |
T | 30 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0082 others(27): Show |
30 | HG00099.hp2 HG01255.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.690-12084_690-1207 others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505269 | |||||||
| chr11:78505269 | TACACACA others(5): Show |
T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(31): Show |
34 | HG00621.hp2 HG00741.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.690-12086_690-1207 others(16): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505269 | |||||||
| chr11:78505269 | TACACACA others(7): Show |
T | 33 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(30): Show |
33 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.690-12088_690-1207 others(18): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505269 | |||||||
| chr11:78505269 | TACACACA others(9): Show |
T | 43 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(40): Show |
43 | HG00408.hp1 HG00597.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.690-12090_690-1207 others(20): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505269 | |||||||
| chr11:78505269 | TACACACA others(11): Show |
T | 6 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0001t0001g0084 others(3): Show |
6 | HG03130.hp2 HG03209.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.690-12092_690-1207 others(22): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505269 | |||||||
| chr11:78505269 | TACACACA others(13): Show |
T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0033 |
2 | NA18973.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.690-12094_690-1207 others(24): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505269 | |||||||
| chr11:78505269 | TACACACA others(19): Show |
T | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.690-12100_690-1207 others(30): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505269 | |||||||
| chr11:78505269 | TACACACA others(21): Show |
T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | HG01081.hp1 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-12102_690-1207 others(32): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505269 | |||||||
| chr11:78505293 | CACACACA others(25): Show |
C | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.690-12130_690-1209 others(36): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505293 | |||||||
| chr11:78505305 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.690-12110G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505305 | |||||||
| chr11:78505315 | CACACACA others(3): Show |
C | 1 | a0002c0002t0002g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.690-12130_690-1212 others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505315 | |||||||
| chr11:78505317 | CACACACA others(1): Show |
C | 3 | a0001c0001t0005g0070 a0001c0003t0003g0170 a0001c0004t0004g0286 |
3 | HG02895.hp1 HG03471.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.690-12130_690-1212 others(12): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505317 | |||||||
| chr11:78505321 | CACAT | C | 3 | a0001c0004t0004g0282 a0001c0004t0004g0283 a0001c0004t0004g0285 |
3 | HG02630.hp2 HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.690-12130_690-1212 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505321 | |||||||
| chr11:78505331 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.690-12136A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505331 | |||||||
| chr11:78505478 | C | G | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.690-12283G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505478 | |||||||
| chr11:78505485 | A | G | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.690-12290T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505485 | |||||||
| chr11:78505649 | T | C | 11 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.690-12454A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505649 | |||||||
| chr11:78505688 | T | A | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.690-12493A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505688 | |||||||
| chr11:78505766 | T | A | 2 | a0002c0002t0002g0178 a0002c0002t0002g0180 |
2 | HG01928.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.690-12571A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505766 | |||||||
| chr11:78505777 | T | C | 8 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.690-12582A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505777 | |||||||
| chr11:78505946 | C | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
154 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.690-12751G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78505946 | |||||||
| chr11:78506181 | T | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.690-12986A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78506181 | |||||||
| chr11:78506191 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
162 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.690-12996C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78506191 | |||||||
| chr11:78506408 | C | A | 2 | a0002c0002t0002g0190 a0002c0002t0002g0222 |
2 | NA18984.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.690-13213G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78506408 | |||||||
| chr11:78506414 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.690-13219C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78506414 | |||||||
| chr11:78506468 | T | C | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.690-13273A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78506468 | |||||||
| chr11:78506641 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
126 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.690-13446A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78506641 | |||||||
| chr11:78507048 | A | C | 6 | a0001c0005t0001g0049 a0001c0007t0003g0272 a0001c0007t0003g0273 others(3): Show |
6 | HG02615.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.690-13853T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78507048 | |||||||
| chr11:78507085 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.690-13890A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78507085 | |||||||
| chr11:78507159 | A | AC | 102 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
102 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.690-13965dupG | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78507159 | |||||||
| chr11:78507159 | A | C | 2 | a0001c0001t0001g0035 a0002c0002t0002g0267 |
2 | NA18963.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.690-13964T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78507159 | |||||||
| chr11:78507364 | C | T | 3 | a0001c0003t0006g0261 a0001c0003t0006g0263 a0001c0003t0006g0265 |
3 | HG02109.hp1 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.690-14169G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78507364 | |||||||
| chr11:78507510 | A | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
139 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.690-14315T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78507510 | |||||||
| chr11:78507522 | C | CT | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
144 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(141): Show |
intron_variant | MODIFIER | c.690-14328dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78507522 | |||||||
| chr11:78507875 | C | CCATT | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
154 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.690-14681_690-1468 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78507875 | |||||||
| chr11:78507897 | C | T | 4 | a0001c0005t0001g0049 a0001c0007t0003g0272 a0001c0007t0003g0273 others(1): Show |
4 | HG02809.hp2 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-14702G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78507897 | |||||||
| chr11:78507899 | G | T | 1 | a0001c0005t0001g0145 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.690-14704C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78507899 | |||||||
| chr11:78508333 | A | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.690-15138T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78508333 | |||||||
| chr11:78508354 | C | T | 5 | a0001c0001t0001g0147 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.690-15159G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78508354 | |||||||
| chr11:78508587 | C | CA | 19 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0006g0259 others(16): Show |
19 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.690-15393dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78508587 | |||||||
| chr11:78508593 | A | AC | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.690-15399_690-1539 others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78508593 | |||||||
| chr11:78508593 | A | C | 2 | a0001c0001t0005g0142 a0002c0002t0002g0268 |
2 | NA18906.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.690-15398T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78508593 | |||||||
| chr11:78508607 | C | CA | 9 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(6): Show |
9 | HG02109.hp1 HG02300.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.690-15413dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78508607 | |||||||
| chr11:78508618 | C | A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
153 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(150): Show |
intron_variant | MODIFIER | c.690-15423G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78508618 | |||||||
| chr11:78508678 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.690-15483G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78508678 | |||||||
| chr11:78508680 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
154 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.690-15485G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78508680 | |||||||
| chr11:78508796 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.690-15601C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78508796 | |||||||
| chr11:78508834 | A | T | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.690-15639T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78508834 | |||||||
| chr11:78508929 | A | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
154 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.690-15734T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78508929 | |||||||
| chr11:78509143 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.690-15948A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509143 | |||||||
| chr11:78509305 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.690-16110G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509305 | |||||||
| chr11:78509384 | T | C | 2 | a0002c0002t0003g0288 a0002c0002t0003g0289 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.690-16189A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509384 | |||||||
| chr11:78509390 | G | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
155 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.690-16195C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509390 | |||||||
| chr11:78509509 | TCTAA | T | 7 | a0002c0002t0002g0199 a0002c0002t0002g0200 a0002c0002t0002g0203 others(4): Show |
7 | HG01081.hp2 HG01123.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-16318_690-1631 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509509 | |||||||
| chr11:78509564 | T | C | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.690-16369A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509564 | |||||||
| chr11:78509583 | A | C | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
155 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.690-16388T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509583 | |||||||
| chr11:78509588 | C | T | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.690-16393G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509588 | |||||||
| chr11:78509663 | C | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0111 |
2 | HG01516.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.690-16468G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509663 | |||||||
| chr11:78509754 | G | A | 1 | a0002c0002t0002g0225 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.690-16559C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509754 | |||||||
| chr11:78509781 | C | T | 1 | a0001c0003t0006g0262 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.690-16586G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509781 | |||||||
| chr11:78509826 | C | CA | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
134 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.690-16632dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509826 | |||||||
| chr11:78509826 | C | CAA | 7 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(4): Show |
7 | HG01081.hp1 HG02647.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.690-16633_690-1663 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509826 | |||||||
| chr11:78509919 | T | G | 2 | a0002c0002t0003g0288 a0002c0002t0003g0289 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.690-16724A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509919 | |||||||
| chr11:78509946 | A | G | 2 | a0002c0002t0003g0288 a0002c0002t0003g0289 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.690-16751T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78509946 | |||||||
| chr11:78510094 | G | C | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.690-16899C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78510094 | |||||||
| chr11:78510100 | A | G | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.690-16905T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78510100 | |||||||
| chr11:78510461 | T | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.690-17266A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78510461 | |||||||
| chr11:78510513 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.690-17318A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78510513 | |||||||
| chr11:78510615 | C | T | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.690-17420G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78510615 | |||||||
| chr11:78510652 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
154 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.690-17457G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78510652 | |||||||
| chr11:78510967 | G | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
155 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.690-17772C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78510967 | |||||||
| chr11:78510978 | C | T | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.690-17783G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78510978 | |||||||
| chr11:78511017 | A | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.690-17822T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511017 | |||||||
| chr11:78511129 | G | T | 4 | a0002c0002t0002g0185 a0002c0002t0002g0224 a0002c0002t0002g0228 others(1): Show |
4 | HG02135.hp1 NA18747.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+17713C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511129 | |||||||
| chr11:78511340 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.689+17502T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511340 | |||||||
| chr11:78511378 | C | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
155 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.689+17464G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511378 | |||||||
| chr11:78511384 | C | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.689+17458G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511384 | |||||||
| chr11:78511486 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.689+17356C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511486 | |||||||
| chr11:78511573 | C | T | 8 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.689+17269G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511573 | |||||||
| chr11:78511642 | C | T | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.689+17200G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511642 | |||||||
| chr11:78511672 | G | A | 1 | a0002c0002t0002g0161 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.689+17170C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511672 | |||||||
| chr11:78511679 | T | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.689+17163A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511679 | |||||||
| chr11:78511689 | C | T | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+17153G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511689 | |||||||
| chr11:78511721 | GA | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
153 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(150): Show |
intron_variant | MODIFIER | c.689+17120delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511721 | |||||||
| chr11:78511767 | T | G | 1 | a0001c0001t0001g0036 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.689+17075A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511767 | |||||||
| chr11:78511780 | T | C | 3 | a0002c0002t0002g0185 a0002c0002t0002g0224 a0002c0002t0002g0228 |
3 | HG02135.hp1 NA18948.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.689+17062A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511780 | |||||||
| chr11:78511840 | T | C | 1 | a0001c0006t0003g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.689+17002A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511840 | |||||||
| chr11:78511982 | C | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
155 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.689+16860G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78511982 | |||||||
| chr11:78512312 | T | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.689+16530A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78512312 | |||||||
| chr11:78512441 | T | C | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.689+16401A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78512441 | |||||||
| chr11:78512685 | C | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
188 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(185): Show |
intron_variant | MODIFIER | c.689+16157G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78512685 | |||||||
| chr11:78512756 | T | C | 20 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(17): Show |
20 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.689+16086A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78512756 | |||||||
| chr11:78512777 | T | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.689+16065A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78512777 | |||||||
| chr11:78512950 | T | C | 2 | a0002c0002t0003g0288 a0002c0002t0003g0289 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.689+15892A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78512950 | |||||||
| chr11:78512980 | T | G | 9 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.689+15862A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78512980 | |||||||
| chr11:78513039 | C | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
3 | HG02559.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.689+15803G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78513039 | |||||||
| chr11:78513175 | G | A | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.689+15667C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78513175 | |||||||
| chr11:78513253 | T | C | 1 | a0002c0002t0002g0246 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.689+15589A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78513253 | |||||||
| chr11:78513346 | C | CT | 30 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0004g0274 others(27): Show |
30 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.689+15495dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78513346 | |||||||
| chr11:78513346 | CT | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.689+15495delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78513346 | |||||||
| chr11:78513390 | A | G | 1 | a0001c0004t0007g0154 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.689+15452T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78513390 | |||||||
| chr11:78513439 | T | C | 1 | a0002c0002t0002g0189 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.689+15403A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78513439 | |||||||
| chr11:78513552 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.689+15290G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78513552 | |||||||
| chr11:78513638 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.689+15204G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78513638 | |||||||
| chr11:78513862 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
188 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(185): Show |
intron_variant | MODIFIER | c.689+14980T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78513862 | |||||||
| chr11:78513937 | G | A | 10 | a0002c0002t0002g0183 a0002c0002t0002g0190 a0002c0002t0002g0191 others(7): Show |
10 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.689+14905C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78513937 | |||||||
| chr11:78514112 | A | T | 23 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(20): Show |
23 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.689+14730T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78514112 | |||||||
| chr11:78514177 | C | T | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.689+14665G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78514177 | |||||||
| chr11:78514185 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.689+14657G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78514185 | |||||||
| chr11:78514215 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
166 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.689+14627A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78514215 | |||||||
| chr11:78514495 | A | C | 1 | a0001c0001t0014g0287 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.689+14347T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78514495 | |||||||
| chr11:78514709 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.689+14133C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78514709 | |||||||
| chr11:78514908 | T | C | 9 | a0001c0001t0001g0023 a0001c0003t0006g0259 a0001c0003t0006g0260 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.689+13934A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78514908 | |||||||
| chr11:78515025 | C | T | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.689+13817G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78515025 | |||||||
| chr11:78515214 | C | T | 1 | a0001c0003t0002g0257 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.689+13628G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78515214 | |||||||
| chr11:78515318 | T | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
187 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(184): Show |
intron_variant | MODIFIER | c.689+13524A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78515318 | |||||||
| chr11:78515467 | A | C | 9 | a0001c0001t0001g0003 a0001c0004t0007g0156 a0001c0004t0007g0157 others(6): Show |
9 | HG02486.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.689+13375T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78515467 | |||||||
| chr11:78515475 | C | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
155 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.689+13367G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78515475 | |||||||
| chr11:78515544 | G | A | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.689+13298C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78515544 | |||||||
| chr11:78515686 | T | TA | 6 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(3): Show |
6 | HG00621.hp1 HG00621.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.689+13155dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78515686 | |||||||
| chr11:78515687 | A | G | 41 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0004g0274 others(38): Show |
41 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.689+13155T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78515687 | |||||||
| chr11:78515699 | A | C | 50 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(47): Show |
50 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(47): Show |
intron_variant | MODIFIER | c.689+13143T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78515699 | |||||||
| chr11:78515703 | A | T | 1 | a0001c0001t0001g0020 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.689+13139T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78515703 | |||||||
| chr11:78515713 | G | A | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.689+13129C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78515713 | |||||||
| chr11:78515724 | G | C | 1 | a0001c0010t0001g0017 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.689+13118C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78515724 | |||||||
| chr11:78515831 | T | G | 1 | a0002c0002t0005g0001 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.689+13011A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78515831 | |||||||
| chr11:78516005 | T | A | 1 | a0002c0002t0003g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.689+12837A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516005 | |||||||
| chr11:78516094 | G | T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.689+12748C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516094 | |||||||
| chr11:78516122 | G | A | 5 | a0001c0011t0003g0271 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.689+12720C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516122 | |||||||
| chr11:78516209 | T | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+12633A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516209 | |||||||
| chr11:78516214 | G | T | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.689+12628C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516214 | |||||||
| chr11:78516215 | A | G | 6 | a0001c0003t0006g0260 a0001c0003t0006g0261 a0001c0003t0006g0262 others(3): Show |
6 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.689+12627T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516215 | |||||||
| chr11:78516350 | C | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.689+12492G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516350 | |||||||
| chr11:78516366 | T | C | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.689+12476A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516366 | |||||||
| chr11:78516432 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.689+12410A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516432 | |||||||
| chr11:78516450 | G | T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.689+12392C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516450 | |||||||
| chr11:78516452 | A | G | 1 | a0002c0002t0003g0218 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.689+12390T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516452 | |||||||
| chr11:78516514 | A | G | 18 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0004t0004g0281 others(15): Show |
18 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.689+12328T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516514 | |||||||
| chr11:78516522 | G | A | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.689+12320C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516522 | |||||||
| chr11:78516744 | T | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.689+12098A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516744 | |||||||
| chr11:78516770 | T | C | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.689+12072A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516770 | |||||||
| chr11:78516988 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.689+11854C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78516988 | |||||||
| chr11:78517020 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0062 |
2 | HG01071.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.689+11822A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78517020 | |||||||
| chr11:78517076 | A | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.689+11766T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78517076 | |||||||
| chr11:78517192 | GATTCAAA others(4): Show |
G | 5 | a0001c0005t0001g0049 a0001c0005t0001g0074 a0001c0005t0001g0144 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.689+11639_689+1164 others(15): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78517192 | |||||||
| chr11:78517410 | C | G | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.689+11432G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78517410 | |||||||
| chr11:78517666 | A | G | 1 | a0001c0001t0001g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.689+11176T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78517666 | |||||||
| chr11:78518061 | T | C | 1 | a0001c0001t0012g0151 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.689+10781A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78518061 | |||||||
| chr11:78518121 | C | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
133 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.689+10721G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78518121 | |||||||
| chr11:78518130 | A | C | 1 | a0001c0001t0001g0007 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.689+10712T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78518130 | |||||||
| chr11:78518328 | G | C | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+10514C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78518328 | |||||||
| chr11:78518496 | T | C | 1 | a0001c0005t0001g0145 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.689+10346A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78518496 | |||||||
| chr11:78518566 | A | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
187 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(184): Show |
intron_variant | MODIFIER | c.689+10276T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78518566 | |||||||
| chr11:78518568 | A | T | 2 | a0001c0005t0001g0049 a0001c0005t0001g0146 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.689+10274T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78518568 | |||||||
| chr11:78518674 | C | T | 4 | a0001c0001t0005g0121 a0002c0002t0002g0182 a0002c0002t0002g0187 others(1): Show |
4 | NA18960.hp2 NA18982.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+10168G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78518674 | |||||||
| chr11:78518682 | C | T | 36 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0004g0274 others(33): Show |
36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.689+10160G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78518682 | |||||||
| chr11:78518835 | G | A | 36 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0004g0274 others(33): Show |
36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.689+10007C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78518835 | |||||||
| chr11:78518878 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0010g0120 |
2 | HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.689+9964A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78518878 | |||||||
| chr11:78518997 | C | T | 19 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0028 others(16): Show |
19 | HG00099.hp1 HG00642.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.689+9845G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78518997 | |||||||
| chr11:78519089 | T | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+9753A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519089 | |||||||
| chr11:78519102 | T | C | 1 | a0002c0002t0002g0175 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.689+9740A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519102 | |||||||
| chr11:78519210 | G | A | 1 | a0002c0002t0002g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.689+9632C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519210 | |||||||
| chr11:78519257 | C | T | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.689+9585G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519257 | |||||||
| chr11:78519514 | A | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+9328T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519514 | |||||||
| chr11:78519537 | G | C | 3 | a0002c0002t0002g0161 a0002c0002t0002g0246 a0002c0002t0002g0256 |
3 | HG02040.hp2 HG03540.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.689+9305C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519537 | |||||||
| chr11:78519568 | C | G | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.689+9274G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519568 | |||||||
| chr11:78519610 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.689+9232A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519610 | |||||||
| chr11:78519703 | G | GT | 40 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0059 others(37): Show |
40 | HG01884.hp1 HG01891.hp1 HG01978.hp2 others(37): Show |
intron_variant | MODIFIER | c.689+9138dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519703 | |||||||
| chr11:78519703 | GT | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+9138delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519703 | |||||||
| chr11:78519723 | G | A | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.689+9119C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519723 | |||||||
| chr11:78519764 | G | T | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.689+9078C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519764 | |||||||
| chr11:78519785 | C | T | 1 | a0002c0002t0002g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.689+9057G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519785 | |||||||
| chr11:78519826 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.689+9016C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519826 | |||||||
| chr11:78519894 | C | T | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.689+8948G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519894 | |||||||
| chr11:78519934 | C | G | 1 | a0002c0002t0002g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.689+8908G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78519934 | |||||||
| chr11:78520028 | T | C | 6 | a0002c0002t0002g0246 a0002c0002t0002g0247 a0002c0002t0002g0248 others(3): Show |
6 | HG00642.hp2 HG00735.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.689+8814A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78520028 | |||||||
| chr11:78520159 | A | G | 16 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(13): Show |
16 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.689+8683T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78520159 | |||||||
| chr11:78520459 | C | T | 1 | a0001c0005t0001g0144 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.689+8383G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78520459 | |||||||
| chr11:78520726 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.689+8116G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78520726 | |||||||
| chr11:78520749 | G | A | 49 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(46): Show |
49 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(46): Show |
intron_variant | MODIFIER | c.689+8093C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78520749 | |||||||
| chr11:78520877 | G | A | 1 | a0002c0002t0002g0250 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.689+7965C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78520877 | |||||||
| chr11:78520972 | C | T | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.689+7870G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78520972 | |||||||
| chr11:78521001 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.689+7841A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521001 | |||||||
| chr11:78521037 | C | T | 14 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.689+7805G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521037 | |||||||
| chr11:78521038 | G | A | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.689+7804C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521038 | |||||||
| chr11:78521057 | TC | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | HG01070.hp1 NA18946.hp2 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+7784delG | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521057 | |||||||
| chr11:78521058 | C | CA | 15 | a0001c0001t0001g0011 a0001c0001t0001g0054 a0001c0001t0001g0083 others(12): Show |
15 | HG02055.hp2 HG02300.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.689+7783_689+7784i others(3): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521058 | |||||||
| chr11:78521059 | C | A | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
179 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(176): Show |
intron_variant | MODIFIER | c.689+7783G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521059 | |||||||
| chr11:78521078 | T | TAAA | 36 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0004g0274 others(33): Show |
36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.689+7763_689+7764i others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521078 | |||||||
| chr11:78521124 | T | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG02145.hp1 HG02258.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.689+7718A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521124 | |||||||
| chr11:78521136 | T | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0002c0002t0003g0251 |
3 | HG01071.hp2 HG02293.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.689+7706A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521136 | |||||||
| chr11:78521154 | TTCTC | T | 14 | a0001c0001t0001g0029 a0001c0003t0006g0259 a0001c0003t0006g0260 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.689+7684_689+7687d others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521154 | |||||||
| chr11:78521160 | C | T | 1 | a0001c0003t0015g0266 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.689+7682G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521160 | |||||||
| chr11:78521168 | T | A | 1 | a0001c0001t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.689+7674A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521168 | |||||||
| chr11:78521299 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.689+7543C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521299 | |||||||
| chr11:78521399 | G | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
187 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(184): Show |
intron_variant | MODIFIER | c.689+7443C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521399 | |||||||
| chr11:78521517 | G | A | 36 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0004g0274 others(33): Show |
36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.689+7325C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521517 | |||||||
| chr11:78521530 | C | T | 36 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0004g0274 others(33): Show |
36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.689+7312G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521530 | |||||||
| chr11:78521586 | C | T | 16 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(13): Show |
16 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.689+7256G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521586 | |||||||
| chr11:78521597 | C | T | 3 | a0001c0001t0001g0126 a0001c0003t0003g0167 a0001c0003t0003g0168 |
3 | HG02723.hp2 HG03486.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.689+7245G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521597 | |||||||
| chr11:78521606 | T | C | 35 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0004g0274 others(32): Show |
35 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.689+7236A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521606 | |||||||
| chr11:78521661 | G | A | 5 | a0002c0002t0002g0197 a0002c0002t0002g0201 a0002c0002t0002g0215 others(2): Show |
5 | NA18939.hp2 NA18945.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.689+7181C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521661 | |||||||
| chr11:78521707 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.689+7135C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521707 | |||||||
| chr11:78521739 | G | A | 2 | a0001c0004t0007g0155 a0001c0004t0013g0153 |
2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.689+7103C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521739 | |||||||
| chr11:78521769 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0072 others(6): Show |
9 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.689+7073C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521769 | |||||||
| chr11:78521789 | C | CA | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.689+7052dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521789 | |||||||
| chr11:78521789 | C | CAA | 6 | a0001c0001t0001g0031 a0001c0001t0001g0061 a0001c0001t0001g0079 others(3): Show |
6 | HG02738.hp2 HG03017.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.689+7051_689+7052d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521789 | |||||||
| chr11:78521789 | C | CAAA | 12 | a0001c0001t0001g0067 a0001c0004t0004g0281 a0001c0004t0004g0282 others(9): Show |
12 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.689+7050_689+7052d others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521789 | |||||||
| chr11:78521789 | C | CAAAA | 18 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(15): Show |
18 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.689+7049_689+7052d others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521789 | |||||||
| chr11:78521789 | C | CAAAAAAA others(5): Show |
2 | a0001c0003t0004g0275 a0001c0003t0004g0276 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.689+7041_689+7052d others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521789 | |||||||
| chr11:78521789 | C | CAAAAAAA others(6): Show |
1 | a0001c0003t0004g0274 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.689+7040_689+7052d others(15): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521789 | |||||||
| chr11:78521809 | A | G | 1 | a0002c0002t0002g0203 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.689+7033T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521809 | |||||||
| chr11:78521810 | G | A | 8 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(5): Show |
8 | HG02257.hp2 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+7032C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521810 | |||||||
| chr11:78521819 | G | A | 1 | a0002c0002t0002g0254 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.689+7023C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521819 | |||||||
| chr11:78521922 | T | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.689+6920A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521922 | |||||||
| chr11:78521990 | G | A | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.689+6852C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521990 | |||||||
| chr11:78521998 | T | G | 36 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0004g0274 others(33): Show |
36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.689+6844A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78521998 | |||||||
| chr11:78522036 | C | T | 5 | a0001c0005t0001g0049 a0001c0005t0001g0074 a0001c0005t0001g0144 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.689+6806G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78522036 | |||||||
| chr11:78522119 | A | AT | 14 | a0001c0001t0001g0029 a0001c0001t0001g0063 a0001c0001t0001g0064 others(11): Show |
14 | HG01106.hp1 HG01891.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.689+6722dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78522119 | |||||||
| chr11:78522119 | A | ATT | 13 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(10): Show |
13 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.689+6721_689+6722d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78522119 | |||||||
| chr11:78522119 | A | ATTT | 14 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.689+6720_689+6722d others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78522119 | |||||||
| chr11:78522119 | A | ATTTT | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.689+6719_689+6722d others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78522119 | |||||||
| chr11:78522119 | AT | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0072 others(10): Show |
13 | HG01884.hp2 HG02486.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.689+6722delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78522119 | |||||||
| chr11:78522130 | T | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.689+6712A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78522130 | |||||||
| chr11:78522395 | T | A | 49 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(46): Show |
49 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(46): Show |
intron_variant | MODIFIER | c.689+6447A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78522395 | |||||||
| chr11:78522430 | C | T | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+6412G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78522430 | |||||||
| chr11:78523060 | A | C | 1 | a0001c0010t0001g0017 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.689+5782T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78523060 | |||||||
| chr11:78523174 | T | C | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.689+5668A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78523174 | |||||||
| chr11:78523202 | G | A | 1 | a0002c0002t0002g0253 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.689+5640C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78523202 | |||||||
| chr11:78523303 | T | TA | 49 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(46): Show |
49 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(46): Show |
intron_variant | MODIFIER | c.689+5538dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78523303 | |||||||
| chr11:78523334 | G | A | 2 | a0001c0001t0005g0121 a0002c0002t0002g0213 |
2 | NA18960.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.689+5508C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78523334 | |||||||
| chr11:78523744 | C | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
186 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(183): Show |
intron_variant | MODIFIER | c.689+5098G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78523744 | |||||||
| chr11:78523777 | G | A | 3 | a0001c0004t0004g0283 a0001c0004t0004g0284 a0001c0004t0004g0285 |
3 | HG02976.hp2 HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.689+5065C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78523777 | |||||||
| chr11:78523898 | G | A | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.689+4944C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78523898 | |||||||
| chr11:78523931 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.689+4911A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78523931 | |||||||
| chr11:78523935 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.689+4907G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78523935 | |||||||
| chr11:78523944 | C | T | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.689+4898G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78523944 | |||||||
| chr11:78524049 | C | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
173 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.689+4793G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78524049 | |||||||
| chr11:78524154 | G | A | 5 | a0001c0011t0003g0271 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.689+4688C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78524154 | |||||||
| chr11:78524157 | C | T | 41 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0004g0274 others(38): Show |
41 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.689+4685G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78524157 | |||||||
| chr11:78524301 | G | A | 1 | a0001c0003t0015g0266 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.689+4541C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78524301 | |||||||
| chr11:78524386 | CCAA | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
135 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.689+4453_689+4455d others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78524386 | |||||||
| chr11:78524421 | A | C | 8 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(5): Show |
8 | HG02257.hp2 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+4421T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78524421 | |||||||
| chr11:78524459 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.689+4383T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78524459 | |||||||
| chr11:78524891 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.689+3951G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78524891 | |||||||
| chr11:78524978 | T | A | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.689+3864A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78524978 | |||||||
| chr11:78525031 | A | C | 5 | a0001c0005t0001g0049 a0001c0005t0001g0074 a0001c0005t0001g0144 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.689+3811T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78525031 | |||||||
| chr11:78525072 | C | T | 4 | a0002c0002t0002g0175 a0002c0002t0002g0186 a0002c0002t0002g0198 others(1): Show |
4 | NA18955.hp1 NA18973.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+3770G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78525072 | |||||||
| chr11:78525106 | G | A | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.689+3736C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78525106 | |||||||
| chr11:78525114 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0141 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.689+3728C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78525114 | |||||||
| chr11:78525218 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.689+3624T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78525218 | |||||||
| chr11:78525219 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.689+3623A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78525219 | |||||||
| chr11:78525312 | C | G | 49 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(46): Show |
49 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(46): Show |
intron_variant | MODIFIER | c.689+3530G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78525312 | |||||||
| chr11:78525443 | C | T | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.689+3399G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78525443 | |||||||
| chr11:78525634 | T | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+3208A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78525634 | |||||||
| chr11:78525902 | A | G | 41 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0004g0274 others(38): Show |
41 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.689+2940T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78525902 | |||||||
| chr11:78525987 | T | C | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.689+2855A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78525987 | |||||||
| chr11:78526047 | T | C | 1 | a0002c0002t0002g0234 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.689+2795A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78526047 | |||||||
| chr11:78526156 | C | A | 5 | a0001c0011t0003g0271 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.689+2686G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78526156 | |||||||
| chr11:78526224 | C | T | 2 | a0002c0002t0002g0277 a0002c0002t0002g0278 |
2 | NA18963.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.689+2618G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78526224 | |||||||
| chr11:78526289 | G | T | 1 | a0002c0002t0002g0212 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.689+2553C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78526289 | |||||||
| chr11:78526520 | A | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
192 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(189): Show |
intron_variant | MODIFIER | c.689+2322T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78526520 | |||||||
| chr11:78526703 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.689+2139G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78526703 | |||||||
| chr11:78526787 | A | G | 1 | a0002c0002t0008g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.689+2055T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78526787 | |||||||
| chr11:78526924 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.689+1918G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78526924 | |||||||
| chr11:78527080 | A | C | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.689+1762T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78527080 | |||||||
| chr11:78527087 | T | C | 2 | a0001c0007t0003g0272 a0001c0007t0003g0273 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.689+1755A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78527087 | |||||||
| chr11:78527423 | A | G | 11 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.689+1419T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78527423 | |||||||
| chr11:78527449 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.689+1393A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78527449 | |||||||
| chr11:78527467 | C | G | 1 | a0004c0009t0002g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.689+1375G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78527467 | |||||||
| chr11:78528360 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.689+482T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78528360 | |||||||
| chr11:78528580 | T | A | 25 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0006g0259 others(22): Show |
25 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.689+262A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78528580 | |||||||
| chr11:78528590 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0092 others(1): Show |
4 | NA18939.hp1 NA18941.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.689+252G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78528590 | |||||||
| chr11:78528716 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.689+126A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78528716 | |||||||
| chr11:78528741 | G | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0075 |
2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.689+101C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 6/13 | chr11 | 78528741 | |||||||
| chr11:78529173 | A | T | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-237T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78529173 | |||||||
| chr11:78529190 | A | G | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.595-254T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78529190 | |||||||
| chr11:78529248 | G | T | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.595-312C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78529248 | |||||||
| chr11:78529492 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.595-556A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78529492 | |||||||
| chr11:78529675 | T | C | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.595-739A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78529675 | |||||||
| chr11:78529690 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.595-754G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78529690 | |||||||
| chr11:78529727 | T | C | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.595-791A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78529727 | |||||||
| chr11:78529815 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.595-879G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78529815 | |||||||
| chr11:78529839 | A | G | 1 | a0001c0006t0003g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.595-903T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78529839 | |||||||
| chr11:78529896 | T | C | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.595-960A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78529896 | |||||||
| chr11:78529978 | G | T | 35 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(32): Show |
35 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.595-1042C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78529978 | |||||||
| chr11:78530098 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.595-1162T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78530098 | |||||||
| chr11:78530153 | C | T | 2 | a0001c0001t0005g0136 a0001c0001t0005g0142 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.595-1217G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78530153 | |||||||
| chr11:78530334 | C | A | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.595-1398G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78530334 | |||||||
| chr11:78530384 | T | C | 4 | a0002c0002t0002g0217 a0002c0002t0002g0229 a0002c0002t0002g0230 others(1): Show |
4 | NA18969.hp2 NA19056.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.595-1448A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78530384 | |||||||
| chr11:78530447 | A | T | 4 | a0002c0002t0002g0185 a0002c0002t0002g0224 a0002c0002t0002g0228 others(1): Show |
4 | HG02135.hp1 NA18747.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-1511T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78530447 | |||||||
| chr11:78530477 | T | G | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.595-1541A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78530477 | |||||||
| chr11:78530489 | T | G | 5 | a0001c0005t0001g0049 a0001c0005t0001g0074 a0001c0005t0001g0144 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-1553A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78530489 | |||||||
| chr11:78530535 | G | A | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.595-1599C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78530535 | |||||||
| chr11:78530536 | C | T | 4 | a0002c0002t0002g0235 a0002c0002t0002g0236 a0002c0002t0002g0237 others(1): Show |
4 | HG02055.hp1 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.595-1600G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78530536 | |||||||
| chr11:78530595 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.595-1659A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78530595 | |||||||
| chr11:78530712 | C | T | 5 | a0001c0011t0003g0271 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.595-1776G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78530712 | |||||||
| chr11:78530950 | A | G | 32 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0006g0259 others(29): Show |
32 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.595-2014T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78530950 | |||||||
| chr11:78530976 | T | A | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.595-2040A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78530976 | |||||||
| chr11:78531011 | T | C | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.595-2075A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78531011 | |||||||
| chr11:78531078 | C | A | 1 | a0002c0002t0002g0202 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.595-2142G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78531078 | |||||||
| chr11:78531105 | A | C | 1 | a0001c0001t0001g0046 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.595-2169T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78531105 | |||||||
| chr11:78531155 | C | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.595-2219G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78531155 | |||||||
| chr11:78531178 | G | A | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.595-2242C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78531178 | |||||||
| chr11:78531344 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.595-2408T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78531344 | |||||||
| chr11:78531396 | C | T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.595-2460G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78531396 | |||||||
| chr11:78531432 | T | C | 12 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(9): Show |
12 | HG02055.hp2 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.595-2496A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78531432 | |||||||
| chr11:78531437 | A | G | 11 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.595-2501T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78531437 | |||||||
| chr11:78531528 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0002c0002t0003g0251 |
3 | HG01071.hp2 HG02293.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.595-2592T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78531528 | |||||||
| chr11:78531536 | C | T | 8 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(5): Show |
8 | HG02257.hp2 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-2600G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78531536 | |||||||
| chr11:78531569 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
166 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.595-2633A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78531569 | |||||||
| chr11:78531827 | A | G | 1 | a0002c0002t0002g0229 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.595-2891T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78531827 | |||||||
| chr11:78532052 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.595-3116A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78532052 | |||||||
| chr11:78532088 | C | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.595-3152G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78532088 | |||||||
| chr11:78532240 | A | C | 18 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0004t0004g0281 others(15): Show |
18 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.595-3304T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78532240 | |||||||
| chr11:78532250 | C | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595-3314G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78532250 | |||||||
| chr11:78532665 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02717.hp2 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.595-3729A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78532665 | |||||||
| chr11:78532697 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.595-3761A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78532697 | |||||||
| chr11:78532756 | C | A | 1 | a0001c0001t0001g0043 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.595-3820G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78532756 | |||||||
| chr11:78532921 | A | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595-3985T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78532921 | |||||||
| chr11:78532963 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.595-4027T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78532963 | |||||||
| chr11:78532978 | T | G | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.595-4042A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78532978 | |||||||
| chr11:78533101 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.595-4165G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78533101 | |||||||
| chr11:78533124 | C | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
140 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.595-4188G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78533124 | |||||||
| chr11:78533246 | G | T | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-4310C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78533246 | |||||||
| chr11:78533398 | A | G | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.595-4462T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78533398 | |||||||
| chr11:78533465 | A | G | 1 | a0001c0004t0007g0154 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.595-4529T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78533465 | |||||||
| chr11:78533764 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.595-4828T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78533764 | |||||||
| chr11:78533777 | C | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
138 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.595-4841G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78533777 | |||||||
| chr11:78533790 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.595-4854A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78533790 | |||||||
| chr11:78533839 | T | C | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.595-4903A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78533839 | |||||||
| chr11:78534052 | C | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595-5116G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78534052 | |||||||
| chr11:78534288 | G | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
135 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.595-5352C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78534288 | |||||||
| chr11:78534291 | T | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-5355A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78534291 | |||||||
| chr11:78534315 | G | A | 1 | a0002c0002t0002g0209 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.595-5379C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78534315 | |||||||
| chr11:78534329 | T | C | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-5393A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78534329 | |||||||
| chr11:78534343 | G | A | 1 | a0002c0002t0003g0288 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.595-5407C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78534343 | |||||||
| chr11:78534467 | A | G | 1 | a0001c0003t0003g0169 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.595-5531T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78534467 | |||||||
| chr11:78534503 | T | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.595-5567A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78534503 | |||||||
| chr11:78534527 | C | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.595-5591G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78534527 | |||||||
| chr11:78534542 | T | C | 16 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0003t0006g0259 others(13): Show |
16 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.595-5606A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78534542 | |||||||
| chr11:78534655 | T | A | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-5719A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78534655 | |||||||
| chr11:78534803 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.595-5867A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78534803 | |||||||
| chr11:78535030 | C | T | 1 | a0002c0002t0002g0250 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.595-6094G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535030 | |||||||
| chr11:78535051 | A | G | 1 | a0002c0002t0003g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.595-6115T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535051 | |||||||
| chr11:78535126 | A | G | 10 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(7): Show |
10 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.595-6190T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535126 | |||||||
| chr11:78535203 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.595-6267C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535203 | |||||||
| chr11:78535492 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.595-6556A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535492 | |||||||
| chr11:78535508 | A | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02145.hp1 HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.595-6572T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535508 | |||||||
| chr11:78535526 | T | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
147 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.595-6590A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535526 | |||||||
| chr11:78535586 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.595-6650G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535586 | |||||||
| chr11:78535590 | T | A | 6 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0002c0002t0003g0239 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.595-6654A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535590 | |||||||
| chr11:78535595 | T | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595-6659A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535595 | |||||||
| chr11:78535682 | T | C | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.595-6746A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535682 | |||||||
| chr11:78535721 | G | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
190 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(187): Show |
intron_variant | MODIFIER | c.595-6785C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535721 | |||||||
| chr11:78535722 | C | T | 7 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.595-6786G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535722 | |||||||
| chr11:78535730 | A | C | 1 | a0001c0001t0001g0055 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.595-6794T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535730 | |||||||
| chr11:78535774 | C | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595-6838G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535774 | |||||||
| chr11:78535981 | A | G | 7 | a0001c0001t0001g0048 a0001c0001t0001g0076 a0001c0001t0001g0096 others(4): Show |
7 | HG01192.hp1 HG01255.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.595-7045T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78535981 | |||||||
| chr11:78536196 | C | A | 8 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.595-7260G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78536196 | |||||||
| chr11:78536295 | T | C | 2 | a0002c0002t0002g0194 a0002c0002t0002g0207 |
2 | HG02155.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.595-7359A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78536295 | |||||||
| chr11:78536314 | T | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595-7378A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78536314 | |||||||
| chr11:78536378 | T | C | 16 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0003t0006g0259 others(13): Show |
16 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.595-7442A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78536378 | |||||||
| chr11:78536403 | T | C | 1 | a0002c0002t0002g0270 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.595-7467A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78536403 | |||||||
| chr11:78536408 | C | T | 8 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(5): Show |
8 | HG02257.hp2 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-7472G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78536408 | |||||||
| chr11:78536564 | T | C | 3 | a0002c0002t0002g0235 a0002c0002t0002g0236 a0002c0002t0002g0237 |
3 | HG02055.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.595-7628A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78536564 | |||||||
| chr11:78536688 | G | A | 1 | a0004c0009t0002g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.595-7752C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78536688 | |||||||
| chr11:78537089 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.595-8153G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78537089 | |||||||
| chr11:78537163 | C | G | 7 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0011t0003g0271 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.595-8227G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78537163 | |||||||
| chr11:78537351 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
164 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.595-8415T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78537351 | |||||||
| chr11:78537615 | T | C | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.595-8679A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78537615 | |||||||
| chr11:78537642 | A | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-8706T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78537642 | |||||||
| chr11:78537821 | T | A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595-8885A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78537821 | |||||||
| chr11:78537982 | A | C | 8 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.595-9046T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78537982 | |||||||
| chr11:78538109 | G | A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595-9173C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538109 | |||||||
| chr11:78538168 | C | T | 2 | a0001c0001t0005g0136 a0001c0001t0005g0142 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.595-9232G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538168 | |||||||
| chr11:78538291 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.595-9355T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538291 | |||||||
| chr11:78538421 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.595-9485C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538421 | |||||||
| chr11:78538432 | A | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
63 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.595-9496T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538432 | |||||||
| chr11:78538507 | G | C | 2 | a0001c0007t0003g0272 a0001c0007t0003g0273 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.595-9571C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538507 | |||||||
| chr11:78538724 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.595-9788C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538724 | |||||||
| chr11:78538778 | G | A | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-9842C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538778 | |||||||
| chr11:78538823 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.595-9887C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538823 | |||||||
| chr11:78538866 | G | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.595-9930C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538866 | |||||||
| chr11:78538882 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.595-9946G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538882 | |||||||
| chr11:78538912 | G | A | 1 | a0002c0002t0002g0165 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.595-9976C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538912 | |||||||
| chr11:78538973 | C | T | 1 | a0001c0005t0001g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.595-10037G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538973 | |||||||
| chr11:78538974 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.595-10038C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538974 | |||||||
| chr11:78538982 | G | A | 1 | a0002c0002t0002g0194 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.595-10046C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538982 | |||||||
| chr11:78538989 | C | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595-10053G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538989 | |||||||
| chr11:78538994 | C | CA | 18 | a0001c0001t0005g0124 a0001c0003t0005g0131 a0002c0002t0002g0195 others(15): Show |
18 | HG00735.hp2 HG01981.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.595-10059dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAA | 19 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0068 others(16): Show |
19 | HG00597.hp1 HG01081.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.595-10060_595-1005 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAAA | 17 | a0001c0001t0001g0084 a0001c0004t0004g0281 a0001c0004t0004g0282 others(14): Show |
17 | HG01123.hp1 HG01175.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.595-10061_595-1005 others(7): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAAAA | 6 | a0001c0001t0001g0069 a0001c0004t0004g0284 a0001c0004t0004g0285 others(3): Show |
6 | HG02257.hp2 HG02976.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.595-10062_595-1005 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0026 a0001c0001t0001g0047 |
2 | HG01081.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.595-10070_595-1005 others(16): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAAAAAAA others(6): Show |
6 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0055 others(3): Show |
6 | HG01975.hp1 NA18612.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.595-10071_595-1005 others(17): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAAAAAAA others(7): Show |
6 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0038 others(3): Show |
6 | HG01978.hp1 HG01981.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.595-10072_595-1005 others(18): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0046 a0001c0001t0001g0059 a0001c0001t0001g0061 others(1): Show |
4 | HG02135.hp2 HG03017.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.595-10073_595-1005 others(19): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0066 |
2 | HG02886.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.595-10074_595-1005 others(20): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAAAAAAA others(10): Show |
1 | a0002c0002t0003g0227 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.595-10075_595-1005 others(21): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.595-10078_595-1005 others(24): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAAAAAAA others(16): Show |
3 | a0001c0001t0001g0012 a0001c0001t0001g0130 a0001c0001t0001g0147 |
3 | HG01934.hp2 NA18987.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.595-10081_595-1005 others(27): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAAAAAAA others(19): Show |
1 | a0001c0001t0001g0150 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.595-10084_595-1005 others(30): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0027 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.595-10085_595-1005 others(31): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.595-10089_595-1005 others(35): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | CAAA | C | 12 | a0001c0001t0001g0042 a0001c0001t0001g0123 a0001c0001t0011g0132 others(9): Show |
12 | HG02109.hp1 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.595-10061_595-1005 others(7): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | CAAAA | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(26): Show |
29 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.595-10062_595-1005 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | CAAAAAA | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0032 others(11): Show |
14 | HG00621.hp1 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.595-10064_595-1005 others(10): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | CAAAAAAA | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
60 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.595-10065_595-1005 others(11): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | CAAAAAAA others(2): Show |
C | 8 | a0001c0001t0001g0067 a0001c0001t0001g0135 a0001c0001t0001g0137 others(5): Show |
8 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-10067_595-1005 others(13): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78538994 | CAAAAAAA others(4): Show |
C | 3 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0003c0008t0003g0159 |
3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.595-10069_595-1005 others(15): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78538994 | |||||||
| chr11:78539208 | G | A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595-10272C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78539208 | |||||||
| chr11:78539325 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.595-10389G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78539325 | |||||||
| chr11:78539412 | G | A | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.595-10476C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78539412 | |||||||
| chr11:78539703 | T | C | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.595-10767A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78539703 | |||||||
| chr11:78539766 | G | A | 1 | a0001c0003t0003g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.595-10830C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78539766 | |||||||
| chr11:78539790 | C | G | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-10854G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78539790 | |||||||
| chr11:78539799 | G | A | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-10863C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78539799 | |||||||
| chr11:78539910 | A | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.595-10974T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78539910 | |||||||
| chr11:78540068 | G | A | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.595-11132C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78540068 | |||||||
| chr11:78540178 | A | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-11242T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78540178 | |||||||
| chr11:78540198 | T | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
185 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(182): Show |
intron_variant | MODIFIER | c.595-11262A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78540198 | |||||||
| chr11:78540439 | T | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.595-11503A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78540439 | |||||||
| chr11:78540486 | CT | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
138 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.595-11551delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78540486 | |||||||
| chr11:78540916 | TGGGAGGC others(3): Show |
T | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-11990_595-1198 others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78540916 | |||||||
| chr11:78541019 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.595-12083G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541019 | |||||||
| chr11:78541031 | C | T | 1 | a0002c0002t0002g0214 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.595-12095G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541031 | |||||||
| chr11:78541032 | G | A | 26 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0003g0169 others(23): Show |
26 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.595-12096C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541032 | |||||||
| chr11:78541044 | A | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-12108T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541044 | |||||||
| chr11:78541078 | G | C | 1 | a0004c0009t0002g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.595-12142C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541078 | |||||||
| chr11:78541097 | T | G | 1 | a0001c0006t0003g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.595-12161A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541097 | |||||||
| chr11:78541123 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.595-12187C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541123 | |||||||
| chr11:78541160 | C | CA | 7 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.595-12225dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541160 | |||||||
| chr11:78541203 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.595-12267G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541203 | |||||||
| chr11:78541333 | C | CT | 8 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-12398dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541333 | |||||||
| chr11:78541441 | T | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595-12505A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541441 | |||||||
| chr11:78541529 | T | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.595-12593A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541529 | |||||||
| chr11:78541736 | A | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595-12800T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541736 | |||||||
| chr11:78541768 | A | G | 5 | a0001c0011t0003g0271 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.595-12832T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541768 | |||||||
| chr11:78541784 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.595-12848C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78541784 | |||||||
| chr11:78542004 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.595-13068T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78542004 | |||||||
| chr11:78542104 | G | T | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.595-13168C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78542104 | |||||||
| chr11:78542257 | T | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.595-13321A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78542257 | |||||||
| chr11:78542459 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.595-13523A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78542459 | |||||||
| chr11:78542486 | T | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-13550A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78542486 | |||||||
| chr11:78542530 | T | C | 31 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0031 others(28): Show |
31 | HG01934.hp2 HG01975.hp1 HG01978.hp1 others(28): Show |
intron_variant | MODIFIER | c.595-13594A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78542530 | |||||||
| chr11:78542548 | G | A | 1 | a0002c0002t0002g0223 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.595-13612C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78542548 | |||||||
| chr11:78542662 | G | A | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.595-13726C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78542662 | |||||||
| chr11:78542711 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.595-13775G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78542711 | |||||||
| chr11:78542744 | T | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-13808A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78542744 | |||||||
| chr11:78542849 | T | A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595-13913A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78542849 | |||||||
| chr11:78542954 | G | A | 24 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0003t0004g0274 others(21): Show |
24 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.595-14018C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78542954 | |||||||
| chr11:78542965 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.595-14029T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78542965 | |||||||
| chr11:78543102 | C | T | 8 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(5): Show |
8 | HG02257.hp2 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-14166G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543102 | |||||||
| chr11:78543213 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.595-14277A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543213 | |||||||
| chr11:78543224 | C | A | 1 | a0001c0001t0001g0029 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.595-14288G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543224 | |||||||
| chr11:78543367 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
138 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.595-14431G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543367 | |||||||
| chr11:78543378 | T | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.595-14442A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543378 | |||||||
| chr11:78543431 | T | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.595-14495A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543431 | |||||||
| chr11:78543508 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.595-14572A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543508 | |||||||
| chr11:78543567 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0082 others(1): Show |
4 | HG01256.hp1 HG01928.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-14631A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543567 | |||||||
| chr11:78543601 | A | C | 2 | a0001c0007t0003g0272 a0001c0007t0003g0273 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.595-14665T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543601 | |||||||
| chr11:78543660 | A | G | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.595-14724T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543660 | |||||||
| chr11:78543674 | C | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.595-14738G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543674 | |||||||
| chr11:78543701 | G | C | 1 | a0004c0009t0002g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.595-14765C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543701 | |||||||
| chr11:78543902 | G | A | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.595-14966C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543902 | |||||||
| chr11:78543908 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.595-14972C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543908 | |||||||
| chr11:78543913 | C | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
138 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.595-14977G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78543913 | |||||||
| chr11:78544011 | T | A | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.595-15075A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544011 | |||||||
| chr11:78544018 | C | CA | 12 | a0001c0001t0005g0142 a0001c0003t0002g0257 a0002c0002t0002g0205 others(9): Show |
12 | HG01175.hp1 HG02083.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.595-15083dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544018 | |||||||
| chr11:78544018 | C | CAA | 25 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0003t0004g0274 others(22): Show |
25 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.595-15084_595-1508 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544018 | |||||||
| chr11:78544018 | C | CAAA | 21 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(18): Show |
21 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.595-15085_595-1508 others(7): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544018 | |||||||
| chr11:78544018 | C | CAAAA | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(96): Show |
99 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.595-15086_595-1508 others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544018 | |||||||
| chr11:78544018 | C | CAAAAA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(38): Show |
41 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.595-15087_595-1508 others(9): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544018 | |||||||
| chr11:78544244 | A | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+15295T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544244 | |||||||
| chr11:78544249 | C | A | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.594+15290G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544249 | |||||||
| chr11:78544251 | A | G | 1 | a0002c0002t0002g0165 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.594+15288T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544251 | |||||||
| chr11:78544338 | T | C | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.594+15201A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544338 | |||||||
| chr11:78544343 | T | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
138 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.594+15196A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544343 | |||||||
| chr11:78544376 | A | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
185 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(182): Show |
intron_variant | MODIFIER | c.594+15163T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544376 | |||||||
| chr11:78544424 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.594+15115A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544424 | |||||||
| chr11:78544511 | C | T | 9 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.594+15028G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544511 | |||||||
| chr11:78544590 | C | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+14949G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544590 | |||||||
| chr11:78544648 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.594+14891C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544648 | |||||||
| chr11:78544724 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.594+14815T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544724 | |||||||
| chr11:78544726 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.594+14813C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544726 | |||||||
| chr11:78544788 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0117 |
2 | NA19087.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.594+14751G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544788 | |||||||
| chr11:78544795 | C | CA | 43 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(40): Show |
43 | HG00642.hp2 HG01106.hp2 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.594+14743dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544795 | |||||||
| chr11:78544795 | CA | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
120 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.594+14743delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544795 | |||||||
| chr11:78544795 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0122 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.594+14732_594+1474 others(16): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544795 | |||||||
| chr11:78544839 | G | A | 1 | a0001c0003t0006g0265 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.594+14700C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544839 | |||||||
| chr11:78544840 | C | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+14699G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544840 | |||||||
| chr11:78544841 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0086 |
2 | HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.594+14698C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544841 | |||||||
| chr11:78544848 | T | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+14691A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544848 | |||||||
| chr11:78544936 | C | T | 2 | a0001c0007t0003g0272 a0001c0007t0003g0273 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.594+14603G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78544936 | |||||||
| chr11:78545032 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.594+14507C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545032 | |||||||
| chr11:78545300 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.594+14239G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545300 | |||||||
| chr11:78545311 | T | C | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.594+14228A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545311 | |||||||
| chr11:78545320 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.594+14219T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545320 | |||||||
| chr11:78545495 | T | G | 6 | a0001c0003t0015g0266 a0001c0011t0003g0271 a0002c0002t0008g0290 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+14044A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545495 | |||||||
| chr11:78545511 | G | A | 8 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(5): Show |
8 | HG02257.hp2 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+14028C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545511 | |||||||
| chr11:78545514 | A | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+14025T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545514 | |||||||
| chr11:78545524 | C | CT | 23 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0027 others(20): Show |
23 | HG01106.hp1 HG01106.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.594+14014dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545524 | |||||||
| chr11:78545524 | C | CTT | 15 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(12): Show |
15 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.594+14013_594+1401 others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545524 | |||||||
| chr11:78545524 | CT | C | 9 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(6): Show |
9 | HG01081.hp2 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.594+14014delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545524 | |||||||
| chr11:78545594 | G | A | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+13945C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545594 | |||||||
| chr11:78545674 | A | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+13865T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545674 | |||||||
| chr11:78545734 | G | A | 2 | a0001c0001t0005g0121 a0002c0002t0002g0213 |
2 | NA18960.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.594+13805C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545734 | |||||||
| chr11:78545740 | G | C | 1 | a0002c0002t0002g0219 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.594+13799C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545740 | |||||||
| chr11:78545764 | C | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+13775G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545764 | |||||||
| chr11:78545776 | T | C | 2 | a0001c0007t0003g0272 a0001c0007t0003g0273 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.594+13763A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545776 | |||||||
| chr11:78545795 | A | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.594+13744T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545795 | |||||||
| chr11:78545818 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.594+13721C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545818 | |||||||
| chr11:78545822 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
188 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(185): Show |
intron_variant | MODIFIER | c.594+13717T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545822 | |||||||
| chr11:78545884 | T | C | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.594+13655A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545884 | |||||||
| chr11:78545950 | A | G | 2 | a0002c0002t0003g0288 a0002c0002t0003g0289 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.594+13589T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545950 | |||||||
| chr11:78545952 | C | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.594+13587G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78545952 | |||||||
| chr11:78546017 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.594+13522T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546017 | |||||||
| chr11:78546093 | A | G | 1 | a0001c0003t0015g0266 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.594+13446T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546093 | |||||||
| chr11:78546186 | G | A | 39 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0003g0169 others(36): Show |
39 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.594+13353C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546186 | |||||||
| chr11:78546226 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.594+13313C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546226 | |||||||
| chr11:78546242 | A | G | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.594+13297T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546242 | |||||||
| chr11:78546256 | C | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.594+13283G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546256 | |||||||
| chr11:78546462 | T | C | 19 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0004t0004g0281 others(16): Show |
19 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.594+13077A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546462 | |||||||
| chr11:78546480 | A | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+13059T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546480 | |||||||
| chr11:78546616 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.594+12923A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546616 | |||||||
| chr11:78546798 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.594+12741G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546798 | |||||||
| chr11:78546843 | A | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+12696T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546843 | |||||||
| chr11:78546844 | T | A | 1 | a0002c0002t0002g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.594+12695A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546844 | |||||||
| chr11:78546902 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.594+12637A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546902 | |||||||
| chr11:78546904 | A | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+12635T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546904 | |||||||
| chr11:78546931 | A | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+12608T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78546931 | |||||||
| chr11:78547000 | C | G | 5 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0004t0007g0156 others(2): Show |
5 | HG02486.hp1 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+12539G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547000 | |||||||
| chr11:78547021 | T | A | 1 | a0001c0001t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.594+12518A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547021 | |||||||
| chr11:78547101 | G | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
192 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(189): Show |
intron_variant | MODIFIER | c.594+12438C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547101 | |||||||
| chr11:78547109 | C | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+12430G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547109 | |||||||
| chr11:78547266 | G | T | 2 | a0001c0007t0003g0272 a0001c0007t0003g0273 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.594+12273C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547266 | |||||||
| chr11:78547506 | GA | G | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+12032delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547506 | |||||||
| chr11:78547523 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0150 |
2 | HG02129.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.594+12016A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547523 | |||||||
| chr11:78547605 | C | G | 5 | a0001c0005t0001g0049 a0001c0005t0001g0074 a0001c0005t0001g0144 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.594+11934G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547605 | |||||||
| chr11:78547654 | A | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+11885T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547654 | |||||||
| chr11:78547736 | C | A | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.594+11803G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547736 | |||||||
| chr11:78547740 | T | C | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.594+11799A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547740 | |||||||
| chr11:78547902 | T | C | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+11637A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547902 | |||||||
| chr11:78547931 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.594+11608A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547931 | |||||||
| chr11:78547999 | C | T | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.594+11540G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78547999 | |||||||
| chr11:78548011 | A | G | 2 | a0002c0002t0003g0288 a0002c0002t0003g0289 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.594+11528T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548011 | |||||||
| chr11:78548150 | C | T | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.594+11389G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548150 | |||||||
| chr11:78548151 | G | A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+11388C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548151 | |||||||
| chr11:78548196 | G | A | 1 | a0002c0002t0002g0214 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.594+11343C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548196 | |||||||
| chr11:78548259 | T | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.594+11280A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548259 | |||||||
| chr11:78548286 | T | C | 1 | a0002c0002t0005g0001 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.594+11253A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548286 | |||||||
| chr11:78548351 | TAAAAACG others(22): Show |
T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.594+11159_594+1118 others(33): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548351 | |||||||
| chr11:78548356 | ACGTTTAA others(3): Show |
A | 1 | a0001c0001t0001g0042 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.594+11173_594+1118 others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548356 | |||||||
| chr11:78548683 | G | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+10856C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548683 | |||||||
| chr11:78548740 | G | A | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.594+10799C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548740 | |||||||
| chr11:78548770 | G | A | 3 | a0002c0002t0002g0215 a0002c0002t0002g0216 a0002c0002t0002g0269 |
3 | NA18939.hp2 NA18970.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.594+10769C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548770 | |||||||
| chr11:78548800 | A | T | 1 | a0001c0001t0009g0060 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.594+10739T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548800 | |||||||
| chr11:78548886 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.594+10653A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548886 | |||||||
| chr11:78548964 | G | C | 1 | a0002c0002t0002g0161 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.594+10575C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548964 | |||||||
| chr11:78548988 | A | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+10551T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78548988 | |||||||
| chr11:78549005 | A | G | 1 | a0002c0002t0003g0251 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.594+10534T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78549005 | |||||||
| chr11:78549024 | C | A | 1 | a0001c0001t0001g0092 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.594+10515G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78549024 | |||||||
| chr11:78549034 | G | A | 1 | a0002c0002t0002g0234 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.594+10505C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78549034 | |||||||
| chr11:78549099 | G | T | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.594+10440C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78549099 | |||||||
| chr11:78549115 | C | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.594+10424G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78549115 | |||||||
| chr11:78549297 | A | G | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.594+10242T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78549297 | |||||||
| chr11:78549420 | T | C | 1 | a0001c0003t0003g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.594+10119A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78549420 | |||||||
| chr11:78549474 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.594+10065A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78549474 | |||||||
| chr11:78549653 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.594+9886T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78549653 | |||||||
| chr11:78549723 | A | C | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.594+9816T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78549723 | |||||||
| chr11:78549893 | T | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+9646A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78549893 | |||||||
| chr11:78550226 | G | C | 1 | a0001c0001t0001g0038 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.594+9313C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78550226 | |||||||
| chr11:78550267 | A | T | 1 | a0002c0002t0002g0219 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.594+9272T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78550267 | |||||||
| chr11:78550408 | C | T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.594+9131G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78550408 | |||||||
| chr11:78550432 | T | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0002c0002t0003g0227 |
3 | NA18971.hp2 NA19002.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.594+9107A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78550432 | |||||||
| chr11:78550657 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
147 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.594+8882A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78550657 | |||||||
| chr11:78550879 | G | A | 1 | a0002c0002t0002g0268 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.594+8660C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78550879 | |||||||
| chr11:78550915 | G | A | 1 | a0002c0002t0003g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.594+8624C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78550915 | |||||||
| chr11:78550976 | CCATA | C | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.594+8559_594+8562d others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78550976 | |||||||
| chr11:78550983 | T | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+8556A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78550983 | |||||||
| chr11:78551135 | G | A | 2 | a0001c0007t0003g0272 a0001c0007t0003g0273 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.594+8404C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551135 | |||||||
| chr11:78551157 | T | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+8382A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551157 | |||||||
| chr11:78551198 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.594+8341T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551198 | |||||||
| chr11:78551216 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
128 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.594+8323C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551216 | |||||||
| chr11:78551278 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
147 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.594+8261T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551278 | |||||||
| chr11:78551360 | A | C | 16 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0003t0006g0259 others(13): Show |
16 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.594+8179T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551360 | |||||||
| chr11:78551365 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.594+8174T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551365 | |||||||
| chr11:78551375 | G | A | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+8164C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551375 | |||||||
| chr11:78551511 | T | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+8028A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551511 | |||||||
| chr11:78551518 | T | C | 5 | a0001c0011t0003g0271 a0002c0002t0008g0290 a0002c0002t0008g0291 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+8021A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551518 | |||||||
| chr11:78551572 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
147 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.594+7967A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551572 | |||||||
| chr11:78551622 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.594+7917C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551622 | |||||||
| chr11:78551710 | G | C | 2 | a0001c0007t0003g0272 a0001c0007t0003g0273 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.594+7829C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551710 | |||||||
| chr11:78551832 | C | A | 1 | a0002c0002t0002g0254 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.594+7707G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551832 | |||||||
| chr11:78551903 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0126 |
3 | HG01192.hp1 HG01255.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.594+7636G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551903 | |||||||
| chr11:78551996 | C | G | 1 | a0002c0002t0002g0246 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.594+7543G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78551996 | |||||||
| chr11:78552048 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.594+7491T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78552048 | |||||||
| chr11:78552081 | T | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.594+7458A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78552081 | |||||||
| chr11:78552155 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
5 | HG01081.hp1 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+7384G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78552155 | |||||||
| chr11:78552218 | T | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
5 | HG01081.hp1 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+7321A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78552218 | |||||||
| chr11:78552285 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
147 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.594+7254T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78552285 | |||||||
| chr11:78552345 | A | G | 1 | a0002c0002t0002g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.594+7194T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78552345 | |||||||
| chr11:78552351 | C | T | 1 | a0002c0002t0002g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.594+7188G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78552351 | |||||||
| chr11:78552490 | G | A | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+7049C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78552490 | |||||||
| chr11:78552699 | C | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+6840G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78552699 | |||||||
| chr11:78552801 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.594+6738G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78552801 | |||||||
| chr11:78553156 | G | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
138 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.594+6383C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553156 | |||||||
| chr11:78553185 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
147 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.594+6354T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553185 | |||||||
| chr11:78553375 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
151 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.594+6164T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553375 | |||||||
| chr11:78553435 | T | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+6104A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553435 | |||||||
| chr11:78553445 | T | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+6094A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553445 | |||||||
| chr11:78553450 | G | A | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+6089C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553450 | |||||||
| chr11:78553456 | T | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.594+6083A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553456 | |||||||
| chr11:78553537 | A | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
147 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.594+6002T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553537 | |||||||
| chr11:78553566 | G | T | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.594+5973C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553566 | |||||||
| chr11:78553604 | A | T | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.594+5935T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553604 | |||||||
| chr11:78553701 | T | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+5838A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553701 | |||||||
| chr11:78553760 | G | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+5779C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553760 | |||||||
| chr11:78553789 | G | T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.594+5750C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553789 | |||||||
| chr11:78553801 | G | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
5 | HG01081.hp1 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+5738C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553801 | |||||||
| chr11:78553824 | C | A | 2 | a0001c0007t0003g0272 a0001c0007t0003g0273 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.594+5715G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553824 | |||||||
| chr11:78553924 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.594+5615A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78553924 | |||||||
| chr11:78554098 | T | C | 1 | a0001c0006t0003g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.594+5441A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554098 | |||||||
| chr11:78554164 | A | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
148 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.594+5375T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554164 | |||||||
| chr11:78554327 | T | C | 2 | a0001c0007t0003g0272 a0001c0007t0003g0273 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.594+5212A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554327 | |||||||
| chr11:78554357 | G | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
146 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.594+5182C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554357 | |||||||
| chr11:78554449 | A | T | 1 | a0001c0004t0013g0153 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.594+5090T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554449 | |||||||
| chr11:78554500 | C | CGTGTGTG others(17): Show |
2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.594+5038_594+5039i others(26): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554500 | |||||||
| chr11:78554500 | C | CGTGTGTG others(5): Show |
1 | a0001c0005t0001g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.594+5038_594+5039i others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554500 | |||||||
| chr11:78554500 | C | CGTGTGTG others(9): Show |
7 | a0001c0004t0004g0285 a0001c0004t0007g0155 a0001c0004t0013g0153 others(4): Show |
7 | HG01891.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.594+5038_594+5039i others(18): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554500 | |||||||
| chr11:78554500 | C | CGTGTGTG others(11): Show |
4 | a0001c0004t0004g0282 a0001c0004t0004g0283 a0001c0004t0004g0284 others(1): Show |
4 | HG02630.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.594+5038_594+5039i others(20): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554500 | |||||||
| chr11:78554500 | C | CGTGTGTG others(15): Show |
1 | a0001c0004t0004g0281 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.594+5038_594+5039i others(24): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554500 | |||||||
| chr11:78554500 | CGTGTGTG others(7): Show |
C | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.594+5025_594+5038d others(16): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554500 | |||||||
| chr11:78554508 | C | CGT | 6 | a0001c0011t0003g0271 a0002c0002t0002g0268 a0002c0002t0008g0290 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+5029_594+5030d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554508 | |||||||
| chr11:78554508 | C | CGTGCGTG others(11): Show |
2 | a0001c0001t0001g0089 a0001c0001t0001g0111 |
2 | HG01516.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.594+5030_594+5031i others(20): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554508 | |||||||
| chr11:78554508 | C | CGTGTGTG others(3): Show |
22 | a0001c0001t0001g0135 a0001c0001t0001g0138 a0001c0001t0001g0139 others(19): Show |
22 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.594+5021_594+5030d others(12): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554508 | |||||||
| chr11:78554508 | C | CGTGTGTG others(5): Show |
17 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(14): Show |
17 | HG01071.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.594+5019_594+5030d others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554508 | |||||||
| chr11:78554508 | C | CGTGTGTG others(7): Show |
42 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(39): Show |
42 | HG00408.hp1 HG00735.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.594+5017_594+5030d others(16): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554508 | |||||||
| chr11:78554508 | C | CGTGTGTG others(9): Show |
58 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0016 others(55): Show |
58 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.594+5015_594+5030d others(18): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554508 | |||||||
| chr11:78554508 | C | CGTGTGTG others(11): Show |
17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0024 others(14): Show |
17 | HG00099.hp1 HG00642.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.594+5013_594+5030d others(20): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554508 | |||||||
| chr11:78554508 | C | CGTGTGTG others(13): Show |
4 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0076 others(1): Show |
4 | HG02273.hp2 HG03927.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.594+5011_594+5030d others(22): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554508 | |||||||
| chr11:78554508 | C | T | 16 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0004t0004g0281 others(13): Show |
16 | HG01891.hp1 HG01993.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.594+5031G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554508 | |||||||
| chr11:78554508 | CGTGTGT | C | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.594+5025_594+5030d others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554508 | |||||||
| chr11:78554510 | T | C | 1 | a0002c0002t0002g0233 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.594+5029A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554510 | |||||||
| chr11:78554609 | G | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
139 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.594+4930C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554609 | |||||||
| chr11:78554621 | T | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
148 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.594+4918A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554621 | |||||||
| chr11:78554699 | G | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.594+4840C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554699 | |||||||
| chr11:78554746 | A | G | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.594+4793T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554746 | |||||||
| chr11:78554843 | T | G | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.594+4696A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78554843 | |||||||
| chr11:78555001 | T | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.594+4538A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78555001 | |||||||
| chr11:78555070 | C | T | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.594+4469G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78555070 | |||||||
| chr11:78555082 | C | T | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.594+4457G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78555082 | |||||||
| chr11:78555166 | A | G | 2 | a0001c0007t0003g0272 a0001c0007t0003g0273 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.594+4373T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78555166 | |||||||
| chr11:78555181 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
190 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(187): Show |
intron_variant | MODIFIER | c.594+4358A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78555181 | |||||||
| chr11:78555329 | T | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+4210A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78555329 | |||||||
| chr11:78555353 | G | A | 1 | a0002c0002t0002g0217 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.594+4186C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78555353 | |||||||
| chr11:78555370 | G | A | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.594+4169C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78555370 | |||||||
| chr11:78555491 | G | C | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.594+4048C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78555491 | |||||||
| chr11:78555550 | T | C | 5 | a0001c0004t0007g0152 a0002c0002t0003g0239 a0002c0002t0003g0240 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.594+3989A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78555550 | |||||||
| chr11:78555556 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
149 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.594+3983T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78555556 | |||||||
| chr11:78555878 | T | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
138 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.594+3661A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78555878 | |||||||
| chr11:78555954 | G | C | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+3585C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78555954 | |||||||
| chr11:78556147 | T | C | 16 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0003t0006g0259 others(13): Show |
16 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.594+3392A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78556147 | |||||||
| chr11:78556404 | T | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+3135A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78556404 | |||||||
| chr11:78556420 | G | A | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+3119C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78556420 | |||||||
| chr11:78556579 | T | C | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.594+2960A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78556579 | |||||||
| chr11:78556587 | G | C | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+2952C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78556587 | |||||||
| chr11:78556649 | A | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+2890T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78556649 | |||||||
| chr11:78556752 | T | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+2787A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78556752 | |||||||
| chr11:78556875 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0065 |
2 | NA18968.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.594+2664A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78556875 | |||||||
| chr11:78557089 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.594+2450T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78557089 | |||||||
| chr11:78557479 | A | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
163 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.594+2060T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78557479 | |||||||
| chr11:78557577 | T | C | 1 | a0002c0002t0003g0218 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.594+1962A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78557577 | |||||||
| chr11:78557610 | A | G | 9 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.594+1929T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78557610 | |||||||
| chr11:78557830 | A | C | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+1709T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78557830 | |||||||
| chr11:78557832 | C | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
180 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(177): Show |
intron_variant | MODIFIER | c.594+1707G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78557832 | |||||||
| chr11:78557836 | CTT | C | 11 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0004t0007g0156 others(8): Show |
11 | HG01891.hp1 HG02486.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.594+1701_594+1702d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78557836 | |||||||
| chr11:78557903 | T | A | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.594+1636A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78557903 | |||||||
| chr11:78557943 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.594+1596A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78557943 | |||||||
| chr11:78557995 | C | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(5): Show |
8 | HG00408.hp1 HG00597.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+1544G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78557995 | |||||||
| chr11:78558173 | C | T | 6 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | HG01192.hp1 HG01255.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+1366G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78558173 | |||||||
| chr11:78558228 | T | G | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+1311A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78558228 | |||||||
| chr11:78558323 | T | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.594+1216A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78558323 | |||||||
| chr11:78558343 | C | T | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+1196G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78558343 | |||||||
| chr11:78558535 | A | T | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+1004T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78558535 | |||||||
| chr11:78558549 | C | A | 3 | a0002c0002t0002g0219 a0002c0002t0002g0226 a0002c0002t0002g0270 |
3 | NA18980.hp1 NA18993.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.594+990G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78558549 | |||||||
| chr11:78558650 | A | G | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG01106.hp1 HG01891.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+889T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78558650 | |||||||
| chr11:78558906 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.594+633A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78558906 | |||||||
| chr11:78558915 | G | A | 170 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
170 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.594+624C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78558915 | |||||||
| chr11:78558939 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
134 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.594+600A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78558939 | |||||||
| chr11:78558954 | C | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
144 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(141): Show |
intron_variant | MODIFIER | c.594+585G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78558954 | |||||||
| chr11:78558974 | C | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
134 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.594+565G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78558974 | |||||||
| chr11:78559074 | G | A | 1 | a0002c0002t0002g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.594+465C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78559074 | |||||||
| chr11:78559119 | C | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
145 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.594+420G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78559119 | |||||||
| chr11:78559128 | C | A | 2 | a0001c0007t0003g0272 a0001c0007t0003g0273 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.594+411G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78559128 | |||||||
| chr11:78559240 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.594+299A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78559240 | |||||||
| chr11:78559258 | A | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.594+281T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78559258 | |||||||
| chr11:78559301 | C | CA | 101 | a0001c0001t0001g0072 a0001c0001t0001g0135 a0001c0001t0001g0137 others(98): Show |
101 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.594+237dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78559301 | |||||||
| chr11:78559301 | C | CAA | 37 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0050 others(34): Show |
37 | HG00099.hp1 HG01106.hp2 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.594+236_594+237dup others(2): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78559301 | |||||||
| chr11:78559301 | C | CAAA | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(107): Show |
110 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.594+235_594+237dup others(3): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78559301 | |||||||
| chr11:78559301 | C | CAAAA | 25 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(22): Show |
25 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.594+234_594+237dup others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 5/13 | chr11 | 78559301 | |||||||
| chr11:78559808 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.514-189A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78559808 | |||||||
| chr11:78559906 | A | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.514-287T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78559906 | |||||||
| chr11:78560010 | A | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-391T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78560010 | |||||||
| chr11:78560092 | C | CT | 8 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-474dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78560092 | |||||||
| chr11:78560454 | A | G | 16 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0003t0006g0259 others(13): Show |
16 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.514-835T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78560454 | |||||||
| chr11:78560568 | A | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
201 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(198): Show |
intron_variant | MODIFIER | c.514-949T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78560568 | |||||||
| chr11:78560874 | A | C | 2 | a0002c0002t0002g0247 a0002c0002t0002g0255 |
2 | HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.514-1255T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78560874 | |||||||
| chr11:78560910 | C | T | 27 | a0001c0003t0003g0169 a0001c0003t0003g0170 a0001c0003t0006g0259 others(24): Show |
27 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.514-1291G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78560910 | |||||||
| chr11:78561095 | A | AT | 11 | a0001c0003t0015g0266 a0001c0004t0004g0281 a0001c0004t0004g0282 others(8): Show |
11 | HG02622.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.514-1477dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78561095 | |||||||
| chr11:78561180 | G | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
127 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.514-1561C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78561180 | |||||||
| chr11:78561192 | C | G | 1 | a0001c0004t0004g0281 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.514-1573G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78561192 | |||||||
| chr11:78561242 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.514-1623C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78561242 | |||||||
| chr11:78561343 | G | A | 1 | a0001c0001t0010g0120 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.514-1724C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78561343 | |||||||
| chr11:78561352 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.514-1733T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78561352 | |||||||
| chr11:78561471 | C | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
137 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.514-1852G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78561471 | |||||||
| chr11:78562031 | T | TCAAAAAA | 6 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0004g0274 others(3): Show |
6 | HG02055.hp2 HG02723.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-2419_514-2413d others(9): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78562031 | |||||||
| chr11:78562031 | TCAAAAAA | T | 26 | a0001c0001t0001g0045 a0001c0001t0001g0088 a0001c0001t0001g0127 others(23): Show |
26 | HG00099.hp2 HG01884.hp1 HG02148.hp2 others(23): Show |
intron_variant | MODIFIER | c.514-2419_514-2413d others(9): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78562031 | |||||||
| chr11:78562173 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.514-2554G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78562173 | |||||||
| chr11:78562203 | T | A | 1 | a0002c0002t0003g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.514-2584A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78562203 | |||||||
| chr11:78562224 | G | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.514-2605C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78562224 | |||||||
| chr11:78562463 | A | C | 1 | a0002c0002t0002g0176 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.514-2844T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78562463 | |||||||
| chr11:78562485 | G | C | 2 | a0001c0006t0003g0279 a0001c0006t0003g0280 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.514-2866C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78562485 | |||||||
| chr11:78562818 | A | C | 8 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.514-3199T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78562818 | |||||||
| chr11:78562821 | G | C | 1 | a0001c0001t0001g0018 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.514-3202C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78562821 | |||||||
| chr11:78562825 | C | T | 13 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(10): Show |
13 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.514-3206G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78562825 | |||||||
| chr11:78562867 | T | C | 1 | a0001c0001t0005g0070 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.514-3248A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78562867 | |||||||
| chr11:78562902 | T | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
147 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.513+3230A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78562902 | |||||||
| chr11:78563032 | C | T | 3 | a0002c0002t0003g0288 a0002c0002t0003g0289 a0003c0008t0003g0159 |
3 | HG02615.hp2 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513+3100G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563032 | |||||||
| chr11:78563045 | GTATCACA others(16): Show |
G | 1 | a0001c0001t0005g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.513+3064_513+3086d others(25): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563045 | |||||||
| chr11:78563123 | T | G | 8 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+3009A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563123 | |||||||
| chr11:78563215 | A | AT | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
143 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(140): Show |
intron_variant | MODIFIER | c.513+2916dupA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563215 | |||||||
| chr11:78563215 | A | ATT | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(7): Show |
10 | HG00621.hp2 HG02080.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.513+2915_513+2916d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563215 | |||||||
| chr11:78563215 | A | ATTT | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+2914_513+2916d others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563215 | |||||||
| chr11:78563215 | A | ATTTT | 6 | a0001c0004t0007g0152 a0001c0004t0007g0156 a0001c0004t0007g0157 others(3): Show |
6 | HG02486.hp1 HG02886.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+2913_513+2916d others(6): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563215 | |||||||
| chr11:78563279 | G | T | 5 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(2): Show |
5 | HG02055.hp2 HG02809.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+2853C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563279 | |||||||
| chr11:78563286 | C | T | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.513+2846G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563286 | |||||||
| chr11:78563368 | A | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
164 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.513+2764T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563368 | |||||||
| chr11:78563369 | C | T | 7 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0001c0004t0007g0155 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.513+2763G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563369 | |||||||
| chr11:78563456 | T | G | 1 | a0001c0001t0005g0121 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.513+2676A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563456 | |||||||
| chr11:78563591 | G | A | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.513+2541C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563591 | |||||||
| chr11:78563606 | T | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
186 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(183): Show |
intron_variant | MODIFIER | c.513+2526A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563606 | |||||||
| chr11:78563660 | G | A | 15 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(12): Show |
15 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.513+2472C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563660 | |||||||
| chr11:78563762 | C | T | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+2370G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563762 | |||||||
| chr11:78563808 | G | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
149 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.513+2324C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563808 | |||||||
| chr11:78563812 | C | T | 2 | a0001c0003t0003g0167 a0001c0003t0003g0168 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.513+2320G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563812 | |||||||
| chr11:78563829 | C | CA | 83 | a0001c0003t0002g0257 a0001c0003t0002g0258 a0001c0003t0005g0131 others(80): Show |
83 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.513+2302dupT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563829 | |||||||
| chr11:78563829 | C | CAA | 10 | a0002c0002t0002g0164 a0002c0002t0002g0228 a0002c0002t0002g0229 others(7): Show |
10 | HG01175.hp1 HG01993.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+2301_513+2302d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563829 | |||||||
| chr11:78563829 | CA | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0082 others(3): Show |
6 | HG00741.hp2 HG01256.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+2302delT | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563829 | |||||||
| chr11:78563829 | CAA | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(22): Show |
25 | HG00621.hp2 HG00642.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.513+2301_513+2302d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563829 | |||||||
| chr11:78563837 | A | AAAC | 7 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0001c0004t0007g0155 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.513+2294_513+2295i others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563837 | |||||||
| chr11:78563842 | A | C | 7 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0001c0004t0007g0155 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.513+2290T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563842 | |||||||
| chr11:78563843 | A | ATAT | 4 | a0001c0003t0006g0260 a0001c0003t0006g0261 a0001c0003t0006g0262 others(1): Show |
4 | HG02630.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+2288_513+2289i others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563843 | |||||||
| chr11:78563845 | A | T | 5 | a0001c0003t0006g0260 a0001c0003t0006g0261 a0001c0003t0006g0262 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+2287T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563845 | |||||||
| chr11:78563847 | A | C | 7 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0001c0004t0007g0155 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.513+2285T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563847 | |||||||
| chr11:78563847 | A | T | 7 | a0001c0003t0006g0260 a0001c0003t0006g0261 a0001c0003t0006g0262 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.513+2285T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563847 | |||||||
| chr11:78563849 | A | T | 9 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.513+2283T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563849 | |||||||
| chr11:78563850 | AAAT | A | 9 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(6): Show |
9 | HG03831.hp2 NA18949.hp2 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.513+2279_513+2281d others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563850 | |||||||
| chr11:78563851 | A | AT | 6 | a0002c0002t0002g0171 a0002c0002t0002g0235 a0002c0002t0002g0236 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+2280_513+2281i others(3): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563851 | |||||||
| chr11:78563851 | A | T | 19 | a0001c0001t0001g0021 a0001c0001t0001g0081 a0001c0001t0001g0133 others(16): Show |
19 | HG00621.hp2 HG00741.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.513+2281T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563851 | |||||||
| chr11:78563852 | AT | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(11): Show |
14 | HG00408.hp1 HG00597.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.513+2279delA | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563852 | |||||||
| chr11:78563853 | T | A | 54 | a0001c0001t0001g0041 a0001c0001t0001g0058 a0001c0001t0001g0067 others(51): Show |
54 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.513+2279A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563853 | |||||||
| chr11:78563855 | T | A | 3 | a0001c0001t0001g0043 a0001c0005t0001g0145 a0001c0005t0001g0146 |
3 | HG02615.hp1 HG03453.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.513+2277A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563855 | |||||||
| chr11:78563864 | A | G | 89 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(86): Show |
89 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.513+2268T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563864 | |||||||
| chr11:78563866 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
60 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.513+2266T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563866 | |||||||
| chr11:78563868 | ATG | A | 89 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(86): Show |
89 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.513+2262_513+2263d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563868 | |||||||
| chr11:78563870 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
60 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.513+2262C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563870 | |||||||
| chr11:78563871 | T | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
149 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.513+2261A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563871 | |||||||
| chr11:78563873 | T | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
149 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.513+2259A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563873 | |||||||
| chr11:78563873 | T | TAC | 15 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(12): Show |
15 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.513+2257_513+2258d others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563873 | |||||||
| chr11:78563875 | C | G | 8 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+2257G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563875 | |||||||
| chr11:78563883 | C | CAAT | 4 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0003g0169 others(1): Show |
4 | HG02717.hp1 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+2248_513+2249i others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563883 | |||||||
| chr11:78563883 | C | CAATATT | 6 | a0001c0003t0006g0260 a0001c0003t0006g0261 a0001c0003t0006g0262 others(3): Show |
6 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+2248_513+2249i others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563883 | |||||||
| chr11:78563883 | C | CAATATTA others(5): Show |
2 | a0001c0003t0006g0259 a0001c0003t0015g0266 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.513+2248_513+2249i others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563883 | |||||||
| chr11:78563885 | G | GTATTAT | 17 | a0001c0003t0005g0131 a0002c0002t0002g0161 a0002c0002t0002g0162 others(14): Show |
17 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.513+2241_513+2246d others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563885 | |||||||
| chr11:78563885 | G | GTATTATT others(2): Show |
4 | a0001c0011t0003g0271 a0002c0002t0002g0246 a0002c0002t0003g0288 others(1): Show |
4 | HG02615.hp2 HG02818.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+2238_513+2246d others(11): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563885 | |||||||
| chr11:78563885 | G | GTATTATT others(5): Show |
13 | a0001c0003t0004g0276 a0001c0007t0003g0272 a0001c0007t0003g0273 others(10): Show |
13 | HG02258.hp2 HG02572.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.513+2235_513+2246d others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563885 | |||||||
| chr11:78563885 | G | GTATTATT others(8): Show |
5 | a0002c0002t0002g0235 a0002c0002t0002g0236 a0002c0002t0002g0237 others(2): Show |
5 | HG02055.hp1 HG02647.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+2232_513+2246d others(17): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563885 | |||||||
| chr11:78563885 | G | GTATTATT others(11): Show |
1 | a0001c0003t0004g0275 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.513+2229_513+2246d others(20): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563885 | |||||||
| chr11:78563885 | G | GTATTATT others(14): Show |
1 | a0001c0003t0004g0274 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.513+2226_513+2246d others(23): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563885 | |||||||
| chr11:78563885 | G | T | 12 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0003g0169 others(9): Show |
12 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.513+2247C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563885 | |||||||
| chr11:78563885 | GTAT | G | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+2244_513+2246d others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563885 | |||||||
| chr11:78563885 | GTATTAT | G | 4 | a0001c0005t0001g0144 a0001c0005t0001g0145 a0001c0005t0001g0146 others(1): Show |
4 | HG02615.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+2241_513+2246d others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563885 | |||||||
| chr11:78563918 | T | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
75 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.513+2214A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563918 | |||||||
| chr11:78563918 | T | TTAC | 65 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(62): Show |
65 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.513+2213_513+2214i others(5): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563918 | |||||||
| chr11:78563918 | T | TTATTAC | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(2): Show |
5 | HG01934.hp1 HG04228.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+2213_513+2214i others(8): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563918 | |||||||
| chr11:78563918 | T | TTATTATT others(5): Show |
1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.513+2213_513+2214i others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563918 | |||||||
| chr11:78563995 | G | A | 6 | a0001c0003t0006g0260 a0001c0003t0006g0261 a0001c0003t0006g0262 others(3): Show |
6 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+2137C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78563995 | |||||||
| chr11:78564066 | T | A | 10 | a0002c0002t0002g0161 a0002c0002t0002g0246 a0002c0002t0002g0247 others(7): Show |
10 | HG00642.hp2 HG00735.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.513+2066A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564066 | |||||||
| chr11:78564099 | C | T | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.513+2033G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564099 | |||||||
| chr11:78564105 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.513+2027C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564105 | |||||||
| chr11:78564143 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.513+1989C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564143 | |||||||
| chr11:78564160 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
149 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.513+1972T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564160 | |||||||
| chr11:78564208 | A | G | 1 | a0002c0002t0002g0171 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.513+1924T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564208 | |||||||
| chr11:78564326 | G | C | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+1806C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564326 | |||||||
| chr11:78564330 | G | A | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+1802C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564330 | |||||||
| chr11:78564557 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.513+1575T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564557 | |||||||
| chr11:78564630 | A | G | 15 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(12): Show |
15 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.513+1502T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564630 | |||||||
| chr11:78564673 | T | C | 6 | a0001c0003t0005g0131 a0002c0002t0002g0162 a0002c0002t0002g0253 others(3): Show |
6 | HG00099.hp2 HG02083.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+1459A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564673 | |||||||
| chr11:78564678 | A | C | 2 | a0001c0001t0001g0011 a0001c0011t0003g0271 |
2 | HG02300.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.513+1454T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564678 | |||||||
| chr11:78564697 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
182 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.513+1435T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564697 | |||||||
| chr11:78564715 | G | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.513+1417C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564715 | |||||||
| chr11:78564885 | G | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
162 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.513+1247C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564885 | |||||||
| chr11:78564910 | G | T | 5 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(2): Show |
5 | HG02055.hp2 HG02809.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+1222C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564910 | |||||||
| chr11:78564967 | G | A | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.513+1165C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78564967 | |||||||
| chr11:78565005 | G | A | 1 | a0002c0002t0002g0255 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.513+1127C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78565005 | |||||||
| chr11:78565207 | A | C | 3 | a0001c0005t0001g0144 a0001c0005t0001g0145 a0001c0005t0001g0146 |
3 | HG02615.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.513+925T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78565207 | |||||||
| chr11:78565249 | G | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02129.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.513+883C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78565249 | |||||||
| chr11:78565278 | C | T | 15 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(12): Show |
15 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.513+854G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78565278 | |||||||
| chr11:78565370 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
164 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.513+762A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78565370 | |||||||
| chr11:78565607 | G | C | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.513+525C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78565607 | |||||||
| chr11:78565628 | C | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
186 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(183): Show |
intron_variant | MODIFIER | c.513+504G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78565628 | |||||||
| chr11:78565638 | T | C | 7 | a0001c0004t0007g0152 a0001c0004t0007g0154 a0001c0004t0007g0155 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.513+494A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78565638 | |||||||
| chr11:78565656 | T | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.513+476A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78565656 | |||||||
| chr11:78565657 | G | A | 8 | a0001c0003t0006g0259 a0001c0003t0006g0260 a0001c0003t0006g0261 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+475C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78565657 | |||||||
| chr11:78565953 | T | C | 2 | a0001c0006t0003g0279 a0001c0006t0003g0280 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.513+179A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78565953 | |||||||
| chr11:78566036 | A | T | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+96T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78566036 | |||||||
| chr11:78566111 | A | G | 1 | a0002c0002t0002g0162 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.513+21T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 4/13 | chr11 | 78566111 | |||||||
| chr11:78566597 | T | C | 1 | a0002c0002t0002g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.373-325A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78566597 | |||||||
| chr11:78566608 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.373-336A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78566608 | |||||||
| chr11:78566662 | A | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
164 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.373-390T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78566662 | |||||||
| chr11:78566679 | T | C | 2 | a0001c0006t0003g0279 a0001c0006t0003g0280 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.373-407A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78566679 | |||||||
| chr11:78566682 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.373-410A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78566682 | |||||||
| chr11:78566693 | A | G | 5 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0003g0169 others(2): Show |
5 | HG02717.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-421T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78566693 | |||||||
| chr11:78566970 | C | CTTTT | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
164 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.373-699_373-698ins others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78566970 | |||||||
| chr11:78567080 | T | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
149 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.373-808A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567080 | |||||||
| chr11:78567085 | A | C | 2 | a0001c0006t0003g0279 a0001c0006t0003g0280 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.373-813T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567085 | |||||||
| chr11:78567375 | G | T | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.373-1103C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567375 | |||||||
| chr11:78567379 | C | G | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.373-1107G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567379 | |||||||
| chr11:78567384 | A | T | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.373-1112T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567384 | |||||||
| chr11:78567387 | A | T | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.373-1115T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567387 | |||||||
| chr11:78567389 | G | T | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.373-1117C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567389 | |||||||
| chr11:78567390 | G | C | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.373-1118C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567390 | |||||||
| chr11:78567391 | C | T | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.373-1119G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567391 | |||||||
| chr11:78567407 | T | G | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.373-1135A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567407 | |||||||
| chr11:78567408 | A | T | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.373-1136T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567408 | |||||||
| chr11:78567411 | A | T | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.373-1139T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567411 | |||||||
| chr11:78567415 | A | T | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.373-1143T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567415 | |||||||
| chr11:78567417 | T | G | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.373-1145A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567417 | |||||||
| chr11:78567418 | T | A | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.373-1146A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567418 | |||||||
| chr11:78567459 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | NA18999.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.372+1173C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567459 | |||||||
| chr11:78567463 | G | A | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.372+1169C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567463 | |||||||
| chr11:78567466 | A | C | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.372+1166T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567466 | |||||||
| chr11:78567473 | G | A | 1 | a0001c0003t0006g0265 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.372+1159C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567473 | |||||||
| chr11:78567498 | T | C | 2 | a0001c0006t0003g0279 a0001c0006t0003g0280 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.372+1134A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567498 | |||||||
| chr11:78567521 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
164 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.372+1111G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567521 | |||||||
| chr11:78567743 | T | C | 1 | a0001c0006t0003g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.372+889A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567743 | |||||||
| chr11:78567746 | T | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
149 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.372+886A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567746 | |||||||
| chr11:78567855 | T | C | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.372+777A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567855 | |||||||
| chr11:78567940 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
164 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.372+692G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567940 | |||||||
| chr11:78567959 | C | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
164 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.372+673G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78567959 | |||||||
| chr11:78568105 | C | T | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+527G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78568105 | |||||||
| chr11:78568170 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.372+462T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78568170 | |||||||
| chr11:78568269 | A | G | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+363T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78568269 | |||||||
| chr11:78568293 | T | C | 1 | a0001c0003t0015g0266 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.372+339A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 3/13 | chr11 | 78568293 | |||||||
| chr11:78568755 | A | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | splice_region_variant&intron_variant | LOW | c.252-3T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78568755 | |||||||
| chr11:78568757 | A | G | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | splice_region_variant&intron_variant | LOW | c.252-5T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78568757 | |||||||
| chr11:78568791 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.252-39A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78568791 | |||||||
| chr11:78568917 | C | T | 2 | a0001c0003t0003g0169 a0001c0003t0003g0170 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.252-165G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78568917 | |||||||
| chr11:78568923 | G | A | 15 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(12): Show |
15 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.252-171C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78568923 | |||||||
| chr11:78568990 | A | T | 4 | a0001c0001t0001g0011 a0001c0003t0003g0167 a0001c0003t0003g0168 others(1): Show |
4 | HG02300.hp2 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-238T>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78568990 | |||||||
| chr11:78569143 | C | A | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.252-391G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78569143 | |||||||
| chr11:78569148 | TTGAC | T | 13 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(10): Show |
13 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.252-400_252-397del others(4): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78569148 | |||||||
| chr11:78569277 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
150 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.252-525T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78569277 | |||||||
| chr11:78569408 | G | A | 3 | a0001c0005t0001g0144 a0001c0005t0001g0145 a0001c0005t0001g0146 |
3 | HG02615.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.252-656C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78569408 | |||||||
| chr11:78569450 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.252-698G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78569450 | |||||||
| chr11:78569464 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
150 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.252-712A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78569464 | |||||||
| chr11:78569533 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
176 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(173): Show |
intron_variant | MODIFIER | c.252-781C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78569533 | |||||||
| chr11:78569561 | G | A | 38 | a0001c0003t0003g0167 a0001c0003t0003g0168 a0001c0003t0003g0169 others(35): Show |
38 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.252-809C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78569561 | |||||||
| chr11:78569561 | G | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
150 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.252-809C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78569561 | |||||||
| chr11:78569656 | T | C | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-904A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78569656 | |||||||
| chr11:78569766 | C | T | 1 | a0003c0008t0003g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.252-1014G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78569766 | |||||||
| chr11:78569777 | T | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
150 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.252-1025A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78569777 | |||||||
| chr11:78570080 | C | T | 2 | a0001c0006t0003g0279 a0001c0006t0003g0280 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.251+1255G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570080 | |||||||
| chr11:78570081 | T | C | 13 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(10): Show |
13 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.251+1254A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570081 | |||||||
| chr11:78570144 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(1): Show |
4 | HG00408.hp1 HG00597.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+1191G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570144 | |||||||
| chr11:78570396 | T | G | 1 | a0002c0002t0002g0267 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.251+939A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570396 | |||||||
| chr11:78570446 | G | A | 1 | a0002c0002t0002g0268 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.251+889C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570446 | |||||||
| chr11:78570672 | C | T | 13 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(10): Show |
13 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.251+663G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570672 | |||||||
| chr11:78570673 | G | A | 2 | a0001c0006t0003g0279 a0001c0006t0003g0280 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.251+662C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570673 | |||||||
| chr11:78570705 | A | G | 1 | a0001c0006t0003g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.251+630T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570705 | |||||||
| chr11:78570751 | G | T | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+584C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570751 | |||||||
| chr11:78570780 | A | G | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.251+555T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570780 | |||||||
| chr11:78570785 | T | TAAAAAAA others(27): Show |
1 | a0002c0002t0002g0269 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.251+549_251+550ins others(34): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570785 | |||||||
| chr11:78570787 | C | A | 1 | a0002c0002t0002g0269 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.251+548G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570787 | |||||||
| chr11:78570821 | A | AAAT | 3 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 |
3 | HG02055.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.251+511_251+513dup others(3): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570821 | |||||||
| chr11:78570822 | A | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
166 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.251+513T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570822 | |||||||
| chr11:78570869 | C | T | 4 | a0002c0002t0008g0290 a0002c0002t0008g0291 a0002c0002t0008g0292 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+466G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570869 | |||||||
| chr11:78570993 | A | C | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.251+342T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78570993 | |||||||
| chr11:78571028 | G | A | 2 | a0001c0006t0003g0279 a0001c0006t0003g0280 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.251+307C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78571028 | |||||||
| chr11:78571045 | TGCTATTA others(35): Show |
T | 1 | a0002c0002t0002g0166 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.251+248_251+289del others(42): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78571045 | |||||||
| chr11:78571052 | A | G | 1 | a0002c0002t0003g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.251+283T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78571052 | |||||||
| chr11:78571081 | G | A | 13 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(10): Show |
13 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.251+254C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78571081 | |||||||
| chr11:78571103 | A | G | 13 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(10): Show |
13 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.251+232T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78571103 | |||||||
| chr11:78571142 | C | T | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.251+193G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78571142 | |||||||
| chr11:78571192 | C | CGGAGTTG others(21): Show |
1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.251+115_251+142dup others(28): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 2/13 | chr11 | 78571192 | |||||||
| chr11:78571464 | C | G | 1 | a0002c0002t0002g0165 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.142-20G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78571464 | |||||||
| chr11:78571468 | T | C | 1 | a0001c0001t0011g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.142-24A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78571468 | |||||||
| chr11:78571587 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
147 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.142-143A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78571587 | |||||||
| chr11:78571652 | T | C | 1 | a0002c0002t0002g0270 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.142-208A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78571652 | |||||||
| chr11:78571671 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0005g0134 |
2 | HG00741.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.142-227C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78571671 | |||||||
| chr11:78571798 | C | G | 2 | a0001c0007t0003g0272 a0001c0007t0003g0273 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.142-354G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78571798 | |||||||
| chr11:78571833 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
163 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.142-389G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78571833 | |||||||
| chr11:78571861 | C | T | 2 | a0002c0002t0002g0163 a0002c0002t0002g0164 |
2 | NA18947.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.142-417G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78571861 | |||||||
| chr11:78571872 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.142-428C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78571872 | |||||||
| chr11:78572025 | T | C | 3 | a0001c0005t0001g0144 a0001c0005t0001g0145 a0001c0005t0001g0146 |
3 | HG02615.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.142-581A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78572025 | |||||||
| chr11:78572055 | G | A | 1 | a0001c0011t0003g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142-611C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78572055 | |||||||
| chr11:78572307 | C | T | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-863G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78572307 | |||||||
| chr11:78572316 | C | A | 3 | a0001c0004t0007g0156 a0001c0004t0007g0157 a0001c0004t0007g0158 |
3 | HG02486.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.142-872G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78572316 | |||||||
| chr11:78572317 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
165 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.142-873T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78572317 | |||||||
| chr11:78572409 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
166 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.142-965A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78572409 | |||||||
| chr11:78572477 | G | A | 5 | a0001c0003t0004g0274 a0001c0003t0004g0275 a0001c0003t0004g0276 others(2): Show |
5 | HG02055.hp2 HG02809.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-1033C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78572477 | |||||||
| chr11:78572512 | T | C | 9 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-1068A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78572512 | |||||||
| chr11:78572514 | C | A | 2 | a0001c0006t0003g0279 a0001c0006t0003g0280 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.142-1070G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78572514 | |||||||
| chr11:78572553 | G | A | 3 | a0001c0005t0001g0144 a0001c0005t0001g0145 a0001c0005t0001g0146 |
3 | HG02615.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.142-1109C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78572553 | |||||||
| chr11:78572758 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
147 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.142-1314T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78572758 | |||||||
| chr11:78572893 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | NA19002.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.142-1449A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78572893 | |||||||
| chr11:78573286 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+1062G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573286 | |||||||
| chr11:78573291 | T | G | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+1057A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573291 | |||||||
| chr11:78573292 | T | A | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+1056A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573292 | |||||||
| chr11:78573299 | T | A | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+1049A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573299 | |||||||
| chr11:78573347 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+1001C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573347 | |||||||
| chr11:78573355 | A | AGGGGAAG others(7): Show |
1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+992_141+993ins others(14): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573355 | |||||||
| chr11:78573368 | T | G | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+980A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573368 | |||||||
| chr11:78573369 | TCACAAAA others(3): Show |
T | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+969_141+978del others(10): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573369 | |||||||
| chr11:78573408 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
151 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.141+940A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573408 | |||||||
| chr11:78573425 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
156 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.141+923T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573425 | |||||||
| chr11:78573500 | C | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
163 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.141+848G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573500 | |||||||
| chr11:78573526 | ACCCTGTC others(17): Show |
A | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+798_141+821del others(24): Show |
NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573526 | |||||||
| chr11:78573537 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.141+811T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573537 | |||||||
| chr11:78573553 | A | C | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+795T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573553 | |||||||
| chr11:78573554 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+794A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573554 | |||||||
| chr11:78573562 | C | A | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+786G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573562 | |||||||
| chr11:78573607 | C | T | 6 | a0001c0004t0004g0281 a0001c0004t0004g0282 a0001c0004t0004g0283 others(3): Show |
6 | HG02630.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+741G>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573607 | |||||||
| chr11:78573612 | C | G | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+736G>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573612 | |||||||
| chr11:78573616 | T | A | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+732A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573616 | |||||||
| chr11:78573619 | G | C | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141+729C>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573619 | |||||||
| chr11:78573688 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
165 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.141+660T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573688 | |||||||
| chr11:78573777 | T | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
165 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.141+571A>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573777 | |||||||
| chr11:78573789 | A | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
3 | HG02559.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.141+559T>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573789 | |||||||
| chr11:78573904 | T | C | 1 | a0002c0002t0008g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.141+444A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78573904 | |||||||
| chr11:78574012 | G | A | 2 | a0002c0002t0002g0277 a0002c0002t0002g0278 |
2 | NA18963.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.141+336C>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78574012 | |||||||
| chr11:78574051 | T | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
165 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.141+297A>C | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78574051 | |||||||
| chr11:78574059 | G | T | 1 | a0002c0002t0002g0162 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.141+289C>A | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78574059 | |||||||
| chr11:78574067 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.141+281A>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78574067 | |||||||
| chr11:78574212 | A | C | 1 | a0002c0002t0002g0161 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.141+136T>G | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78574212 | |||||||
| chr11:78574214 | C | A | 3 | a0002c0002t0003g0288 a0002c0002t0003g0289 a0003c0008t0003g0159 |
3 | HG02615.hp2 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.141+134G>T | NARS2 | ENSG00000137513.11 | transcript | ENST00000281038.10 | protein_coding | 1/13 | chr11 | 78574214 |