Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 53343 |
| ensemblid | ENSG00000170502.13 |
| hgncid | 8056 |
| symbol | NUDT9 |
| name | nudix hydrolase 9 |
| refseq_nuc | NM_024047.5 |
| refseq_prot | NP_076952.1 |
| ensembl_nuc | ENST00000302174.9 |
| ensembl_prot | ENSP00000303575.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 87422573 |
| end | 87459455 |
| strand | + |
| ver | v1.2 |
| region | chr4:87422573-87459455 |
| region5000 | chr4:87417573-87464455 |
| regionname0 | NUDT9_chr4_87422573_87459455 |
| regionname5000 | NUDT9_chr4_87417573_87464455 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 350 | 388 | 89 | 54 | 196 | 16 | 31 | 150 | NUDT9_chr4_87417573_87464455 | NUDT9 | MAGRL others(345): Show |
chr4 | 87417573 | 87464455 |
| a0002 | 0/0 | 350 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | MAGRL others(345): Show |
chr4 | 87417573 | 87464455 |
| a0003 | 0/0 | 57 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | MAGRL others(52): Show |
chr4 | 87417573 | 87464455 |
| a0004 | 0/0 | 350 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | MAGRL others(345): Show |
chr4 | 87417573 | 87464455 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1050 | 354 | 56 | 53 | 196 | 16 | 31 | NUDT9_chr4_87417573_87464455 | NUDT9 | ATGGC others(1045): Show |
chr4 | 87417573 | 87464455 | ||
| a0001c0002 | 0/0 | 1050 | 34 | 33 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | ATGGC others(1045): Show |
chr4 | 87417573 | 87464455 | ||
| a0002c0003 | 0/0 | 1050 | 10 | 9 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | ATGGC others(1045): Show |
chr4 | 87417573 | 87464455 | ||
| a0002c0004 | 0/0 | 1050 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | ATGGC others(1045): Show |
chr4 | 87417573 | 87464455 | ||
| a0003c0006 | 0/0 | 368 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | ATGGC others(363): Show |
chr4 | 87417573 | 87464455 | ||
| a0004c0005 | 0/0 | 1050 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | ATGGC others(1045): Show |
chr4 | 87417573 | 87464455 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2820 | 245 | 19 | 37 | 148 | 12 | 27 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0001c0001t0002 | 0/0 | 2807 | 70 | 17 | 8 | 42 | 1 | 2 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2802): Show |
chr4 | 87417573 | 87464455 |
| a0001c0001t0003 | 0/0 | 2820 | 8 | 0 | 5 | 0 | 2 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0001c0001t0004 | 0/0 | 2807 | 16 | 15 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2802): Show |
chr4 | 87417573 | 87464455 |
| a0001c0001t0005 | 0/0 | 2820 | 5 | 0 | 0 | 5 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0001c0001t0008 | 0/0 | 2807 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2802): Show |
chr4 | 87417573 | 87464455 |
| a0001c0001t0009 | 0/0 | 2820 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0001c0001t0010 | 0/0 | 2820 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0001c0001t0012 | 0/0 | 2820 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0001c0001t0013 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0001c0001t0015 | 0/0 | 2820 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0001c0001t0017 | 0/0 | 2807 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2802): Show |
chr4 | 87417573 | 87464455 |
| a0001c0001t0018 | 0/0 | 2807 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2802): Show |
chr4 | 87417573 | 87464455 |
| a0001c0001t0019 | 0/0 | 2807 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2802): Show |
chr4 | 87417573 | 87464455 |
| a0001c0002t0001 | 0/0 | 2820 | 23 | 22 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0001c0002t0006 | 0/0 | 2820 | 4 | 4 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0001c0002t0007 | 0/0 | 2820 | 4 | 4 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0001c0002t0011 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0001c0002t0014 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0001c0002t0020 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0002c0003t0003 | 0/0 | 2820 | 10 | 9 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| a0002c0004t0002 | 0/0 | 2807 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2802): Show |
chr4 | 87417573 | 87464455 |
| a0002c0004t0016 | 0/0 | 2807 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2802): Show |
chr4 | 87417573 | 87464455 |
| a0003c0006t0001 | 0/0 | 2138 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2133): Show |
chr4 | 87417573 | 87464455 |
| a0004c0005t0001 | 0/0 | 2820 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | GCGGC others(2815): Show |
chr4 | 87417573 | 87464455 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 62 | 6 | 7 | 32 | 4 | 12 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0002 | 0/0 | 48 | 4 | 1 | 42 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0004 | 0/0 | 38 | 1 | 15 | 14 | 3 | 5 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0007 | 0/0 | 7 | 1 | 2 | 3 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0018 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0021 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0003 | 0/0 | 46 | 6 | 7 | 30 | 1 | 2 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0003g0005 | 0/0 | 8 | 0 | 5 | 0 | 2 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0004g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0004g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0005g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0010g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0015g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0017g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0018g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0001t0019g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0001g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0006g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0007g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0001c0002t0020g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0002c0003t0003g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0002c0003t0003g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0002c0004t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0002c0004t0016g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0003c0006t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| a0004c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | GBR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00639 | hp2 | a0002 | c0003 | t0003 | g0022 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01255 | hp1 | a0001 | c0001 | t0012 | g0001 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01884 | hp1 | a0002 | c0003 | t0003 | g0008 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01928 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01928 | hp2 | a0003 | c0006 | t0001 | g0073 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02145 | hp2 | a0001 | c0001 | t0018 | g0095 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CDX | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02257 | hp2 | a0002 | c0003 | t0003 | g0022 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02258 | hp2 | a0001 | c0002 | t0006 | g0014 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02717 | hp1 | a0002 | c0003 | t0003 | g0008 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02809 | hp1 | a0001 | c0002 | t0007 | g0010 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02922 | hp2 | a0001 | c0002 | t0014 | g0010 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02976 | hp1 | a0001 | c0002 | t0006 | g0014 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03041 | hp2 | a0002 | c0004 | t0002 | g0112 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0014 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03139 | hp1 | a0002 | c0003 | t0003 | g0022 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03139 | hp2 | a0002 | c0004 | t0016 | g0106 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03209 | hp1 | a0002 | c0003 | t0003 | g0008 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0072 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03486 | hp1 | a0002 | c0003 | t0003 | g0008 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03540 | hp1 | a0002 | c0003 | t0003 | g0008 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0067 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03831 | hp2 | a0004 | c0005 | t0001 | g0001 | SAS | BEB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG04228 | hp2 | a0001 | c0001 | t0017 | g0101 | SAS | STU | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | YRI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | YRI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | LWK | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0110 | AFR | LWK | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19043 | hp2 | a0001 | c0002 | t0007 | g0010 | AFR | LWK | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19078 | hp2 | a0001 | c0001 | t0015 | g0028 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | YRI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | YRI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA20129 | hp1 | a0001 | c0002 | t0006 | g0014 | AFR | ASW | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA20129 | hp2 | a0001 | c0002 | t0007 | g0010 | AFR | ASW | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0062 | EUR | TSI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02486 | hp1 | a0001 | c0002 | t0011 | g0115 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02486 | hp2 | a0001 | c0002 | t0007 | g0010 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03471 | hp1 | a0001 | c0002 | t0020 | g0041 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG03471 | hp2 | a0002 | c0003 | t0003 | g0008 | AFR | MSL | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | USA | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| HG06807 | hp2 | a0002 | c0003 | t0003 | g0008 | AFR | USA | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | USA | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| NA21309 | hp2 | a0001 | c0001 | t0019 | g0003 | AFR | LWK | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0056 | REF | REF | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | NUDT9_chr4_87417573_87464455 | NUDT9 | chr4 | 87417573 | 87464455 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:87431836 | TCACCATG others(22167): Show |
T | 1 | a0003 | 1 | HG01928.hp2 | exon_loss_variant | HIGH | c.108-3136_790-353de others(1): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 87431836 | ||||||
| chr4:87435021 | G | C | 1 | a0001 | 2 | HG00733.hp2 HG00735.hp2 |
missense_variant | MODERATE | c.148G>C | p.Val50Leu | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/8 | 481/2820 | 148/1053 | 50/350 | chr4 | 87435021 | |||
| chr4:87457911 | A | G | 1 | a0002 | 12 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
missense_variant | MODERATE | c.943A>G | p.Asn315Asp | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 1276/2820 | 943/1053 | 315/350 | chr4 | 87457911 | |||
| chr4:87457989 | G | A | 1 | a0004 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.1021G>A | p.Glu341Lys | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 1354/2820 | 1021/1053 | 341/350 | chr4 | 87457989 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:87422911 | G | C | 2 | a0001c0002 a0002c0003 |
44 | HG00639.hp2 HG01167.hp2 HG01884.hp1 others(41): Show |
synonymous_variant | LOW | c.6G>C | p.Ala2Ala | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/8 | 339/2820 | 6/1053 | 2/350 | chr4 | 87422911 | |||
| chr4:87438304 | C | T | 1 | a0001c0002 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.375C>T | p.Asn125Asn | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/8 | 708/2820 | 375/1053 | 125/350 | chr4 | 87438304 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:87422737 | A | T | 1 | a0001c0002t0020 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-169A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/8 | 169 | chr4 | 87422737 | ||||||
| chr4:87422760 | AGCTACTC others(6): Show |
A | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(5): Show |
93 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(90): Show |
5_prime_UTR_variant | MODIFIER | c.-144_-132delCTACTC others(7): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/8 | 132 | INFO_REALIGN_3_PRIME | chr4 | 87422760 | |||||
| chr4:87422845 | G | C | 1 | a0001c0001t0009 | 1 | HG01928.hp1 | 5_prime_UTR_variant | MODIFIER | c.-61G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/8 | 61 | chr4 | 87422845 | ||||||
| chr4:87458071 | A | G | 1 | a0001c0001t0005 | 5 | NA18964.hp1 NA18973.hp2 NA18980.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*50A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 50 | chr4 | 87458071 | ||||||
| chr4:87458107 | G | A | 1 | a0001c0001t0010 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*86G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 86 | chr4 | 87458107 | ||||||
| chr4:87458214 | C | T | 1 | a0001c0001t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*193C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 193 | chr4 | 87458214 | ||||||
| chr4:87458379 | G | C | 1 | a0001c0002t0006 | 4 | HG02258.hp2 HG02976.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*358G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 358 | chr4 | 87458379 | ||||||
| chr4:87458391 | G | A | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(8): Show |
97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*370G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 370 | chr4 | 87458391 | ||||||
| chr4:87458525 | A | G | 1 | a0001c0001t0015 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*504A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 504 | chr4 | 87458525 | ||||||
| chr4:87458617 | A | G | 2 | a0001c0002t0007 a0001c0002t0014 |
5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*596A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 596 | chr4 | 87458617 | ||||||
| chr4:87458640 | A | G | 1 | a0001c0001t0018 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*619A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 619 | chr4 | 87458640 | ||||||
| chr4:87458849 | G | T | 1 | a0001c0001t0013 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*828G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 828 | chr4 | 87458849 | ||||||
| chr4:87458855 | G | A | 1 | a0002c0004t0016 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*834G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 834 | chr4 | 87458855 | ||||||
| chr4:87458951 | G | A | 2 | a0001c0001t0008 a0001c0002t0011 |
3 | HG02280.hp1 HG02486.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*930G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 930 | chr4 | 87458951 | ||||||
| chr4:87459053 | A | G | 1 | a0001c0001t0012 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1032A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 1032 | chr4 | 87459053 | ||||||
| chr4:87459230 | G | A | 1 | a0001c0002t0014 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1209G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 1209 | chr4 | 87459230 | ||||||
| chr4:87459231 | C | A | 1 | a0001c0002t0014 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1210C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 1210 | chr4 | 87459231 | ||||||
| chr4:87459255 | T | C | 1 | a0001c0001t0017 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1234T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 8/8 | 1234 | chr4 | 87459255 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:87423162 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0042 |
3 | HG03486.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.107+150T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423162 | |||||||
| chr4:87423349 | A | G | 14 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0024 others(11): Show |
32 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.107+337A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423349 | |||||||
| chr4:87423463 | T | A | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.107+451T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423463 | |||||||
| chr4:87423499 | A | T | 28 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(25): Show |
78 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.107+487A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423499 | |||||||
| chr4:87423518 | CCTT | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+509_107+511del others(3): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87423518 | ||||||
| chr4:87423647 | C | A | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.107+635C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423647 | |||||||
| chr4:87423664 | T | G | 1 | a0001c0001t0001g0044 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.107+652T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423664 | |||||||
| chr4:87423855 | G | A | 1 | a0001c0002t0006g0014 | 4 | HG02258.hp2 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+843G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423855 | |||||||
| chr4:87423921 | A | G | 8 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0040 others(5): Show |
20 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.107+909A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87423921 | |||||||
| chr4:87424096 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.107+1084A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424096 | |||||||
| chr4:87424110 | G | T | 4 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0002c0003t0003g0008 others(1): Show |
12 | HG00639.hp2 HG01167.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+1098G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424110 | |||||||
| chr4:87424147 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.107+1135C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424147 | |||||||
| chr4:87424160 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.107+1148C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424160 | |||||||
| chr4:87424245 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.107+1233C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424245 | |||||||
| chr4:87424253 | CGTTTT | C | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+1242_107+1246d others(7): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424253 | |||||||
| chr4:87424254 | G | GT | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(29): Show |
85 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.107+1265dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | ||||||
| chr4:87424254 | G | GTT | 25 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(22): Show |
67 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.107+1264_107+1265d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | ||||||
| chr4:87424254 | G | GTTT | 9 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(6): Show |
22 | HG01168.hp2 HG01243.hp1 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.107+1263_107+1265d others(5): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | ||||||
| chr4:87424254 | G | GTTTT | 7 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(4): Show |
10 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+1262_107+1265d others(6): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | ||||||
| chr4:87424254 | G | GTTTTTTT others(7): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0055 |
4 | HG02132.hp1 NA18965.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+1253_107+1254i others(16): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | ||||||
| chr4:87424254 | G | GTTTTTTT others(8): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0044 |
3 | NA18979.hp2 NA19066.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.107+1253_107+1254i others(17): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | ||||||
| chr4:87424254 | G | T | 2 | a0002c0004t0002g0112 a0002c0004t0016g0106 |
2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.107+1242G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424254 | |||||||
| chr4:87424254 | GT | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0078 others(8): Show |
21 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.107+1265delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | ||||||
| chr4:87424254 | GTT | G | 5 | a0001c0002t0001g0015 a0001c0002t0001g0041 a0001c0002t0007g0010 others(2): Show |
11 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+1264_107+1265d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | ||||||
| chr4:87424254 | GTTTT | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0059 others(3): Show |
10 | HG01123.hp2 HG01192.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+1262_107+1265d others(6): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | ||||||
| chr4:87424254 | GTTTTT | G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0057 others(17): Show |
70 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.107+1261_107+1265d others(7): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87424254 | ||||||
| chr4:87424258 | T | A | 2 | a0001c0002t0001g0092 a0001c0002t0001g0093 |
2 | HG01167.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.107+1246T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424258 | |||||||
| chr4:87424259 | T | A | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+1247T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424259 | |||||||
| chr4:87424296 | G | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0029 others(21): Show |
80 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+1284G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424296 | |||||||
| chr4:87424367 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.107+1355C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424367 | |||||||
| chr4:87424395 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.107+1383G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424395 | |||||||
| chr4:87424416 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.107+1404C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424416 | |||||||
| chr4:87424474 | A | G | 1 | a0001c0001t0004g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107+1462A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424474 | |||||||
| chr4:87424475 | T | C | 13 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0024 others(10): Show |
31 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(28): Show |
intron_variant | MODIFIER | c.107+1463T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424475 | |||||||
| chr4:87424607 | T | G | 9 | a0001c0001t0002g0036 a0001c0001t0002g0097 a0001c0001t0002g0098 others(6): Show |
10 | HG01884.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+1595T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424607 | |||||||
| chr4:87424711 | A | G | 2 | a0001c0001t0004g0013 a0001c0001t0004g0070 |
5 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+1699A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424711 | |||||||
| chr4:87424719 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+1707C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424719 | |||||||
| chr4:87424727 | A | C | 1 | a0001c0001t0001g0035 | 2 | HG01934.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.107+1715A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424727 | |||||||
| chr4:87424755 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.107+1743C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424755 | |||||||
| chr4:87424825 | A | G | 17 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0024 others(14): Show |
43 | HG00639.hp2 HG01167.hp2 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.107+1813A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87424825 | |||||||
| chr4:87425358 | G | A | 39 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0029 others(36): Show |
107 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.107+2346G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425358 | |||||||
| chr4:87425380 | G | C | 1 | a0001c0002t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.107+2368G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425380 | |||||||
| chr4:87425391 | C | CT | 24 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(21): Show |
85 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.107+2399dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425391 | ||||||
| chr4:87425391 | C | CTT | 10 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0053 others(7): Show |
22 | HG00099.hp2 HG01257.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.107+2398_107+2399d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425391 | ||||||
| chr4:87425391 | CT | C | 10 | a0001c0001t0002g0036 a0001c0001t0002g0097 a0001c0001t0002g0098 others(7): Show |
11 | HG01884.hp2 HG02630.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+2399delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425391 | ||||||
| chr4:87425391 | CTT | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0029 others(21): Show |
80 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+2398_107+2399d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425391 | ||||||
| chr4:87425445 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.107+2433A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425445 | |||||||
| chr4:87425455 | C | T | 9 | a0001c0001t0002g0036 a0001c0001t0002g0097 a0001c0001t0002g0098 others(6): Show |
10 | HG01884.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+2443C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425455 | |||||||
| chr4:87425517 | C | T | 1 | a0001c0001t0002g0038 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.107+2505C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425517 | |||||||
| chr4:87425544 | A | G | 1 | a0001c0002t0001g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.107+2532A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425544 | |||||||
| chr4:87425546 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.107+2534C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425546 | |||||||
| chr4:87425632 | C | A | 2 | a0001c0001t0002g0097 a0001c0001t0002g0098 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+2620C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425632 | |||||||
| chr4:87425673 | G | A | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.107+2661G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425673 | |||||||
| chr4:87425712 | G | GA | 6 | a0001c0001t0001g0031 a0001c0001t0002g0099 a0001c0001t0002g0105 others(3): Show |
7 | HG00642.hp2 HG01109.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+2719dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425712 | ||||||
| chr4:87425712 | G | GAAA | 13 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(10): Show |
70 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.107+2717_107+2719d others(5): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425712 | ||||||
| chr4:87425712 | G | GAAAA | 6 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0045 others(3): Show |
9 | HG01168.hp2 HG04115.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.107+2716_107+2719d others(6): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425712 | ||||||
| chr4:87425712 | GA | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0057 a0001c0001t0001g0058 others(13): Show |
63 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.107+2719delA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87425712 | ||||||
| chr4:87425713 | A | G | 5 | a0001c0001t0001g0085 a0001c0002t0001g0015 a0001c0002t0001g0039 others(2): Show |
9 | HG02055.hp2 HG02148.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.107+2701A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425713 | |||||||
| chr4:87425803 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.107+2791C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425803 | |||||||
| chr4:87425835 | A | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
167 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.107+2823A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425835 | |||||||
| chr4:87425836 | A | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
167 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.107+2824A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87425836 | |||||||
| chr4:87426124 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.107+3112A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426124 | |||||||
| chr4:87426216 | T | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(87): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.107+3204T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426216 | |||||||
| chr4:87426255 | AC | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+3244delC | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426255 | |||||||
| chr4:87426360 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0029 others(21): Show |
80 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+3348A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426360 | |||||||
| chr4:87426396 | GTCTTAAT others(2): Show |
G | 2 | a0001c0001t0004g0012 a0001c0001t0004g0066 |
5 | HG01109.hp1 HG02258.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+3390_107+3398d others(11): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87426396 | ||||||
| chr4:87426415 | C | CT | 7 | a0001c0001t0001g0064 a0001c0001t0004g0012 a0001c0001t0004g0030 others(4): Show |
11 | HG01109.hp1 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.107+3415dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87426415 | ||||||
| chr4:87426500 | C | G | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+3488C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426500 | |||||||
| chr4:87426651 | C | T | 5 | a0001c0002t0001g0024 a0001c0002t0001g0039 a0001c0002t0001g0116 others(2): Show |
11 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+3639C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426651 | |||||||
| chr4:87426661 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.107+3649G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426661 | |||||||
| chr4:87426935 | CA | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(15): Show |
78 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.107+3934delA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87426935 | ||||||
| chr4:87426945 | A | C | 1 | a0001c0001t0004g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.107+3933A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426945 | |||||||
| chr4:87426960 | C | A | 2 | a0001c0001t0004g0068 a0001c0001t0004g0071 |
2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.107+3948C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426960 | |||||||
| chr4:87426997 | A | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(73): Show |
250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.107+3985A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87426997 | |||||||
| chr4:87427119 | C | CA | 7 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0052 others(4): Show |
10 | HG00735.hp1 HG00735.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+4123dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87427119 | ||||||
| chr4:87427119 | CA | C | 7 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0002g0036 others(4): Show |
8 | HG02630.hp1 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+4123delA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87427119 | ||||||
| chr4:87427122 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0058 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.107+4126_107+4141d others(18): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87427122 | ||||||
| chr4:87427138 | T | TA | 28 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(25): Show |
99 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.107+4139dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87427138 | ||||||
| chr4:87427172 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+4160G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427172 | |||||||
| chr4:87427183 | G | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+4171G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427183 | |||||||
| chr4:87427187 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.107+4175A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427187 | |||||||
| chr4:87427284 | C | T | 1 | a0002c0004t0016g0106 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.107+4272C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427284 | |||||||
| chr4:87427559 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+4547C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427559 | |||||||
| chr4:87427644 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.107+4632T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427644 | |||||||
| chr4:87427723 | C | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(87): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.107+4711C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427723 | |||||||
| chr4:87427870 | G | T | 27 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(24): Show |
77 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.107+4858G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427870 | |||||||
| chr4:87427956 | T | G | 1 | a0001c0001t0002g0038 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.107+4944T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87427956 | |||||||
| chr4:87428014 | A | G | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+5002A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428014 | |||||||
| chr4:87428048 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+5036C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428048 | |||||||
| chr4:87428086 | C | T | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.107+5074C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428086 | |||||||
| chr4:87428219 | CAG | C | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+5210_107+5211d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87428219 | ||||||
| chr4:87428233 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.107+5221G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428233 | |||||||
| chr4:87428533 | GATATT | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(87): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.107+5529_107+5533d others(7): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87428533 | ||||||
| chr4:87428669 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(86): Show |
281 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.107+5657A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428669 | |||||||
| chr4:87428698 | A | T | 1 | a0001c0001t0001g0082 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.107+5686A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428698 | |||||||
| chr4:87428704 | T | TG | 3 | a0001c0001t0001g0089 a0002c0003t0003g0008 a0002c0003t0003g0022 |
11 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.107+5696dupG | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87428704 | ||||||
| chr4:87428858 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0065 |
2 | HG02135.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.107+5846G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428858 | |||||||
| chr4:87428905 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0052 |
3 | HG01168.hp2 HG01981.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.107+5893C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87428905 | |||||||
| chr4:87429035 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.108-5946A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429035 | |||||||
| chr4:87429040 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.108-5941C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429040 | |||||||
| chr4:87429151 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.108-5830G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429151 | |||||||
| chr4:87429193 | C | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.108-5788C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429193 | |||||||
| chr4:87429314 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(86): Show |
281 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.108-5667A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429314 | |||||||
| chr4:87429395 | C | G | 1 | a0001c0001t0002g0037 | 2 | HG02165.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.108-5586C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429395 | |||||||
| chr4:87429438 | GC | G | 15 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0037 others(12): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.108-5541delC | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87429438 | ||||||
| chr4:87429473 | A | G | 1 | a0001c0002t0001g0116 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.108-5508A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429473 | |||||||
| chr4:87429687 | CG | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(22): Show |
87 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.108-5293delG | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429687 | |||||||
| chr4:87429743 | C | T | 5 | a0001c0002t0001g0009 a0001c0002t0001g0040 a0001c0002t0001g0041 others(2): Show |
11 | HG01891.hp2 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.108-5238C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429743 | |||||||
| chr4:87429807 | T | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(86): Show |
281 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.108-5174T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429807 | |||||||
| chr4:87429886 | A | G | 5 | a0001c0002t0001g0009 a0001c0002t0001g0040 a0001c0002t0001g0041 others(2): Show |
11 | HG01891.hp2 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.108-5095A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429886 | |||||||
| chr4:87429894 | T | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.108-5087T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429894 | |||||||
| chr4:87429908 | G | A | 1 | a0002c0003t0003g0022 | 3 | HG00639.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.108-5073G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87429908 | |||||||
| chr4:87430047 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.108-4934A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430047 | |||||||
| chr4:87430066 | C | T | 2 | a0001c0001t0004g0013 a0001c0001t0004g0070 |
5 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-4915C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430066 | |||||||
| chr4:87430129 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0042 |
3 | HG03486.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.108-4852A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430129 | |||||||
| chr4:87430228 | G | C | 27 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(24): Show |
77 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.108-4753G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430228 | |||||||
| chr4:87430452 | T | C | 27 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(24): Show |
77 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.108-4529T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430452 | |||||||
| chr4:87430630 | A | C | 3 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0118 |
3 | HG01167.hp2 HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.108-4351A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430630 | |||||||
| chr4:87430726 | A | G | 15 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0037 others(12): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.108-4255A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87430726 | |||||||
| chr4:87430895 | CTTGA | C | 1 | a0001c0001t0001g0017 | 3 | HG01192.hp1 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.108-4082_108-4079d others(6): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87430895 | ||||||
| chr4:87431178 | G | T | 1 | a0001c0001t0004g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.108-3803G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431178 | |||||||
| chr4:87431206 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.108-3775C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431206 | |||||||
| chr4:87431273 | C | G | 1 | a0001c0001t0002g0111 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.108-3708C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431273 | |||||||
| chr4:87431333 | G | T | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.108-3648G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431333 | |||||||
| chr4:87431334 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.108-3647C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431334 | |||||||
| chr4:87431587 | A | G | 15 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0037 others(12): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.108-3394A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431587 | |||||||
| chr4:87431709 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.108-3272T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431709 | |||||||
| chr4:87431858 | G | T | 1 | a0001c0001t0001g0002 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.108-3123G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431858 | |||||||
| chr4:87431860 | A | T | 1 | a0001c0001t0001g0002 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.108-3121A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431860 | |||||||
| chr4:87431865 | T | TTTTTTTT others(613): Show |
1 | a0001c0001t0001g0002 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.108-3116_108-3115i others(622): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431865 | |||||||
| chr4:87431882 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0044 others(2): Show |
7 | HG02132.hp1 NA18965.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-3099C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431882 | |||||||
| chr4:87431891 | G | A | 1 | a0001c0002t0001g0024 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.108-3090G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431891 | |||||||
| chr4:87431916 | C | G | 1 | a0001c0001t0002g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.108-3065C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431916 | |||||||
| chr4:87431932 | A | G | 1 | a0001c0001t0001g0002 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.108-3049A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87431932 | |||||||
| chr4:87432108 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.108-2873C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432108 | |||||||
| chr4:87432113 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.108-2868G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432113 | |||||||
| chr4:87432186 | G | T | 9 | a0001c0001t0002g0036 a0001c0001t0002g0097 a0001c0001t0002g0098 others(6): Show |
10 | HG01884.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.108-2795G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432186 | |||||||
| chr4:87432303 | A | G | 2 | a0001c0002t0007g0010 a0001c0002t0014g0010 |
5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-2678A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432303 | |||||||
| chr4:87432330 | T | C | 1 | a0002c0004t0016g0106 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.108-2651T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432330 | |||||||
| chr4:87432768 | G | GT | 23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(20): Show |
83 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.108-2201dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87432768 | ||||||
| chr4:87432770 | T | G | 2 | a0001c0002t0007g0010 a0001c0002t0014g0010 |
5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-2211T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432770 | |||||||
| chr4:87432780 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.108-2201T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432780 | |||||||
| chr4:87432868 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.108-2113A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432868 | |||||||
| chr4:87432987 | T | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.108-1994T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87432987 | |||||||
| chr4:87433044 | C | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
167 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.108-1937C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433044 | |||||||
| chr4:87433063 | G | A | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.108-1918G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433063 | |||||||
| chr4:87433117 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.108-1864C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433117 | |||||||
| chr4:87433231 | A | T | 9 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0030 others(6): Show |
16 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.108-1750A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433231 | |||||||
| chr4:87433251 | C | T | 9 | a0001c0001t0002g0036 a0001c0001t0002g0097 a0001c0001t0002g0098 others(6): Show |
10 | HG01884.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.108-1730C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433251 | |||||||
| chr4:87433450 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0021 |
3 | HG02572.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.108-1531G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433450 | |||||||
| chr4:87433520 | G | T | 1 | a0001c0002t0001g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.108-1461G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433520 | |||||||
| chr4:87433552 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.108-1429C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433552 | |||||||
| chr4:87433660 | T | C | 1 | a0001c0002t0001g0093 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.108-1321T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433660 | |||||||
| chr4:87433777 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.108-1204G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87433777 | |||||||
| chr4:87434030 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(21): Show |
78 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.108-951G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434030 | |||||||
| chr4:87434271 | T | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0029 others(21): Show |
80 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.108-710T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434271 | |||||||
| chr4:87434394 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.108-587A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434394 | |||||||
| chr4:87434407 | A | T | 1 | a0001c0001t0001g0002 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.108-574A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434407 | |||||||
| chr4:87434422 | C | CT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(106): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.108-543dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87434422 | ||||||
| chr4:87434626 | C | CT | 4 | a0001c0001t0001g0063 a0001c0002t0001g0015 a0001c0002t0001g0092 others(1): Show |
7 | HG01167.hp2 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-344dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87434626 | ||||||
| chr4:87434626 | CT | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(19): Show |
82 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.108-344delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 87434626 | ||||||
| chr4:87434825 | G | A | 2 | a0001c0002t0007g0010 a0001c0002t0014g0010 |
5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-156G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434825 | |||||||
| chr4:87434849 | C | T | 1 | a0001c0002t0006g0014 | 4 | HG02258.hp2 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-132C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434849 | |||||||
| chr4:87434899 | G | A | 1 | a0001c0001t0004g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.108-82G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434899 | |||||||
| chr4:87434959 | T | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0029 others(21): Show |
80 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.108-22T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 1/7 | chr4 | 87434959 | |||||||
| chr4:87435239 | G | A | 2 | a0001c0001t0001g0004 a0001c0002t0020g0041 |
2 | HG00741.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.347+19G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435239 | |||||||
| chr4:87435487 | T | G | 1 | a0001c0001t0001g0001 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.347+267T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435487 | |||||||
| chr4:87435594 | C | T | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.347+374C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435594 | |||||||
| chr4:87435647 | C | T | 29 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(26): Show |
87 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.347+427C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435647 | |||||||
| chr4:87435662 | C | A | 1 | a0001c0001t0002g0003 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.347+442C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435662 | |||||||
| chr4:87435740 | T | C | 1 | a0001c0001t0002g0003 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.347+520T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435740 | |||||||
| chr4:87435777 | A | T | 1 | a0001c0001t0002g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.347+557A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435777 | |||||||
| chr4:87435778 | T | G | 1 | a0001c0001t0002g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.347+558T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435778 | |||||||
| chr4:87435779 | G | T | 1 | a0001c0001t0002g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.347+559G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435779 | |||||||
| chr4:87435863 | A | G | 15 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0037 others(12): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.347+643A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435863 | |||||||
| chr4:87435993 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG00609.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.347+773A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87435993 | |||||||
| chr4:87436002 | A | G | 1 | a0001c0002t0006g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.347+782A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436002 | |||||||
| chr4:87436017 | G | GCT | 24 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0029 others(21): Show |
80 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.347+808_347+809dup others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87436017 | ||||||
| chr4:87436049 | A | T | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.347+829A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436049 | |||||||
| chr4:87436168 | T | C | 1 | a0001c0001t0001g0004 | 2 | HG01975.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.347+948T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436168 | |||||||
| chr4:87436239 | C | T | 1 | a0001c0001t0004g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.347+1019C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436239 | |||||||
| chr4:87436299 | C | A | 1 | a0002c0004t0002g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.347+1079C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436299 | |||||||
| chr4:87436324 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.347+1104T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436324 | |||||||
| chr4:87436668 | A | G | 9 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0030 others(6): Show |
16 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.347+1448A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436668 | |||||||
| chr4:87436690 | A | C | 29 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(26): Show |
87 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.347+1470A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436690 | |||||||
| chr4:87436706 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.347+1486A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436706 | |||||||
| chr4:87436731 | G | A | 1 | a0001c0001t0002g0003 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.347+1511G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436731 | |||||||
| chr4:87436750 | A | C | 1 | a0001c0002t0007g0010 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.348-1527A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436750 | |||||||
| chr4:87436843 | A | G | 1 | a0001c0001t0001g0002 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.348-1434A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436843 | |||||||
| chr4:87436853 | A | G | 1 | a0001c0001t0013g0072 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.348-1424A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436853 | |||||||
| chr4:87436981 | G | T | 1 | a0001c0002t0001g0015 | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-1296G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87436981 | |||||||
| chr4:87437024 | G | A | 4 | a0001c0002t0001g0024 a0001c0002t0001g0039 a0001c0002t0001g0116 others(1): Show |
7 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.348-1253G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437024 | |||||||
| chr4:87437249 | C | CA | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(18): Show |
68 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.348-1009dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437249 | ||||||
| chr4:87437249 | C | CAA | 19 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(16): Show |
75 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.348-1010_348-1009d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437249 | ||||||
| chr4:87437249 | CA | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0059 others(3): Show |
8 | HG01257.hp1 HG01261.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.348-1009delA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437249 | ||||||
| chr4:87437275 | AAG | A | 6 | a0001c0001t0004g0012 a0001c0001t0004g0030 a0001c0001t0004g0066 others(3): Show |
10 | HG01109.hp1 HG02258.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-1000_348-999de others(3): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437275 | ||||||
| chr4:87437286 | A | AT | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(17): Show |
79 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.348-983dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437286 | ||||||
| chr4:87437286 | AT | A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0029 others(22): Show |
80 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.348-983delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437286 | ||||||
| chr4:87437318 | A | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0049 |
7 | HG00408.hp2 HG02083.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.348-959A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437318 | |||||||
| chr4:87437379 | C | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0031 |
2 | NA18965.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.348-898C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437379 | |||||||
| chr4:87437419 | G | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(26): Show |
88 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.348-858G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437419 | |||||||
| chr4:87437449 | T | A | 10 | a0001c0001t0002g0003 a0001c0001t0002g0036 a0001c0001t0002g0097 others(7): Show |
11 | HG01884.hp2 HG02630.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.348-828T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437449 | |||||||
| chr4:87437465 | C | G | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-812C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437465 | |||||||
| chr4:87437465 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.348-812C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437465 | |||||||
| chr4:87437477 | G | A | 3 | a0002c0003t0003g0008 a0002c0003t0003g0022 a0002c0004t0016g0106 |
11 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.348-800G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437477 | |||||||
| chr4:87437485 | T | C | 4 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0002c0003t0003g0008 others(1): Show |
12 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.348-792T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437485 | |||||||
| chr4:87437490 | A | G | 6 | a0001c0001t0002g0036 a0001c0001t0002g0104 a0001c0002t0001g0041 others(3): Show |
15 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.348-787A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437490 | |||||||
| chr4:87437497 | T | C | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-780T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437497 | |||||||
| chr4:87437498 | G | A | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-779G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437498 | |||||||
| chr4:87437502 | A | G | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-775A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437502 | |||||||
| chr4:87437515 | T | A | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-762T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437515 | |||||||
| chr4:87437516 | ATT | A | 4 | a0001c0002t0001g0024 a0001c0002t0001g0116 a0001c0002t0001g0117 others(1): Show |
5 | HG02109.hp2 HG02723.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.348-755_348-754del others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437516 | ||||||
| chr4:87437531 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0054 |
2 | HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.348-746A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437531 | |||||||
| chr4:87437532 | T | C | 5 | a0001c0002t0001g0024 a0001c0002t0001g0039 a0001c0002t0011g0115 others(2): Show |
16 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.348-745T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437532 | |||||||
| chr4:87437539 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0002g0036 a0001c0002t0001g0040 others(3): Show |
14 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.348-738C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437539 | |||||||
| chr4:87437544 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0002c0003t0003g0008 others(1): Show |
12 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.348-733A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437544 | |||||||
| chr4:87437549 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0075 others(8): Show |
21 | HG01109.hp1 HG02165.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.348-728A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437549 | |||||||
| chr4:87437555 | G | A | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-722G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437555 | |||||||
| chr4:87437559 | G | C | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-718G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437559 | |||||||
| chr4:87437563 | T | C | 4 | a0001c0001t0001g0090 a0001c0001t0002g0003 a0002c0003t0003g0008 others(1): Show |
16 | HG00639.hp2 HG01884.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.348-714T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437563 | |||||||
| chr4:87437577 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0002c0003t0003g0008 others(1): Show |
12 | HG00639.hp2 HG01884.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.348-700T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437577 | |||||||
| chr4:87437584 | T | C | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-693T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437584 | |||||||
| chr4:87437622 | G | A | 2 | a0001c0001t0002g0003 a0001c0002t0001g0092 |
3 | HG02451.hp2 NA18962.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.348-655G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437622 | |||||||
| chr4:87437637 | T | A | 1 | a0001c0001t0002g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.348-640T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437637 | |||||||
| chr4:87437686 | A | C | 1 | a0001c0002t0001g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.348-591A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437686 | |||||||
| chr4:87437801 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.348-476A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437801 | |||||||
| chr4:87437822 | A | G | 1 | a0001c0002t0001g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.348-455A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87437822 | |||||||
| chr4:87437976 | CCTT | C | 3 | a0001c0001t0004g0013 a0001c0001t0004g0070 a0001c0002t0001g0093 |
6 | HG01167.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.348-297_348-295del others(3): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87437976 | ||||||
| chr4:87438039 | G | A | 2 | a0001c0002t0007g0010 a0001c0002t0014g0010 |
5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-238G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87438039 | |||||||
| chr4:87438049 | TA | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0053 |
6 | HG00673.hp1 NA18953.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.348-226delA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87438049 | ||||||
| chr4:87438138 | G | GA | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(29): Show |
97 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.348-124dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87438138 | ||||||
| chr4:87438138 | GA | G | 20 | a0001c0001t0001g0017 a0001c0001t0002g0003 a0001c0001t0002g0023 others(17): Show |
70 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.348-124delA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 87438138 | ||||||
| chr4:87438140 | A | G | 1 | a0001c0001t0002g0003 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.348-137A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87438140 | |||||||
| chr4:87438213 | A | T | 1 | a0001c0002t0001g0015 | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-64A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87438213 | |||||||
| chr4:87438262 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.348-15G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 2/7 | chr4 | 87438262 | |||||||
| chr4:87438584 | T | TA | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
166 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.443+213dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 87438584 | ||||||
| chr4:87438634 | T | C | 3 | a0001c0001t0001g0001 a0001c0001t0009g0001 a0001c0001t0012g0001 |
3 | HG01255.hp1 HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.443+262T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438634 | |||||||
| chr4:87438733 | T | C | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.443+361T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438733 | |||||||
| chr4:87438740 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.443+368G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438740 | |||||||
| chr4:87438766 | C | T | 1 | a0001c0002t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.443+394C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438766 | |||||||
| chr4:87438791 | A | G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0105 |
8 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.443+419A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438791 | |||||||
| chr4:87438799 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(90): Show |
293 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.443+427C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438799 | |||||||
| chr4:87438856 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
166 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.443+484T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438856 | |||||||
| chr4:87438904 | C | T | 4 | a0001c0002t0001g0024 a0001c0002t0001g0039 a0001c0002t0001g0116 others(1): Show |
7 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.443+532C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87438904 | |||||||
| chr4:87439077 | G | A | 27 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(24): Show |
84 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.443+705G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439077 | |||||||
| chr4:87439090 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0076 |
3 | NA18997.hp1 NA19081.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.443+718C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439090 | |||||||
| chr4:87439097 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.443+725C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439097 | |||||||
| chr4:87439109 | T | C | 5 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0040 others(2): Show |
14 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.443+737T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439109 | |||||||
| chr4:87439131 | A | G | 4 | a0001c0002t0001g0024 a0001c0002t0001g0039 a0001c0002t0001g0116 others(1): Show |
7 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.443+759A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439131 | |||||||
| chr4:87439140 | T | C | 1 | a0001c0001t0001g0004 | 2 | NA18952.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.443+768T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439140 | |||||||
| chr4:87439145 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0105 |
3 | HG00639.hp1 HG00642.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.443+773G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439145 | |||||||
| chr4:87439153 | G | A | 1 | a0001c0002t0011g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.443+781G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439153 | |||||||
| chr4:87439165 | C | CA | 31 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(28): Show |
105 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.443+804dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 87439165 | ||||||
| chr4:87439165 | C | CAA | 25 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(22): Show |
82 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.443+803_443+804dup others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 87439165 | ||||||
| chr4:87439313 | C | T | 2 | a0002c0004t0002g0112 a0002c0004t0016g0106 |
2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.443+941C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439313 | |||||||
| chr4:87439450 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.443+1078G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439450 | |||||||
| chr4:87439517 | T | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(91): Show |
294 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.443+1145T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439517 | |||||||
| chr4:87439679 | C | T | 1 | a0001c0001t0001g0017 | 3 | HG01192.hp1 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.443+1307C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439679 | |||||||
| chr4:87439873 | A | G | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.443+1501A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87439873 | |||||||
| chr4:87440204 | T | C | 1 | a0001c0001t0013g0072 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444-1625T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440204 | |||||||
| chr4:87440281 | C | A | 31 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(28): Show |
96 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.444-1548C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440281 | |||||||
| chr4:87440412 | T | G | 1 | a0001c0001t0001g0004 | 4 | NA18961.hp1 NA18962.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-1417T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440412 | |||||||
| chr4:87440512 | C | T | 1 | a0001c0001t0001g0017 | 3 | HG01192.hp1 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.444-1317C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440512 | |||||||
| chr4:87440564 | C | T | 15 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0037 others(12): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.444-1265C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440564 | |||||||
| chr4:87440569 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.444-1260C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440569 | |||||||
| chr4:87440586 | G | A | 31 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(28): Show |
96 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.444-1243G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440586 | |||||||
| chr4:87440845 | C | CA | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
165 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.444-974dupA | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 87440845 | ||||||
| chr4:87440856 | T | A | 1 | a0001c0001t0001g0004 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.444-973T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87440856 | |||||||
| chr4:87441104 | A | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0031 |
2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.444-725A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441104 | |||||||
| chr4:87441143 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.444-686A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441143 | |||||||
| chr4:87441215 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.444-614T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441215 | |||||||
| chr4:87441548 | A | G | 1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.444-281A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441548 | |||||||
| chr4:87441563 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.444-266T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441563 | |||||||
| chr4:87441696 | A | G | 1 | a0001c0001t0002g0003 | 6 | HG02055.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.444-133A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441696 | |||||||
| chr4:87441752 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
166 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.444-77C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 3/7 | chr4 | 87441752 | |||||||
| chr4:87441935 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
19 | HG00544.hp2 HG00673.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.530+20A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87441935 | |||||||
| chr4:87441955 | A | C | 3 | a0001c0001t0001g0004 a0001c0001t0005g0004 a0001c0001t0005g0029 |
8 | HG02080.hp1 NA18952.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.530+40A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87441955 | |||||||
| chr4:87442033 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.530+118G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442033 | |||||||
| chr4:87442065 | C | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(15): Show |
68 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.530+150C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442065 | |||||||
| chr4:87442279 | G | A | 6 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0040 others(3): Show |
15 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.530+364G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442279 | |||||||
| chr4:87442323 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.530+408C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442323 | |||||||
| chr4:87442330 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.530+415A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442330 | |||||||
| chr4:87442613 | AAC | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0011 |
6 | NA18949.hp1 NA18964.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.530+702_530+703del others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87442613 | ||||||
| chr4:87442720 | T | C | 2 | a0002c0004t0002g0112 a0002c0004t0016g0106 |
2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.530+805T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442720 | |||||||
| chr4:87442828 | CAG | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0027 |
3 | HG03490.hp2 HG03492.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.530+914_530+915del others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442828 | |||||||
| chr4:87442983 | A | G | 2 | a0001c0002t0007g0010 a0001c0002t0014g0010 |
5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+1068A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87442983 | |||||||
| chr4:87443054 | T | A | 4 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0109 others(1): Show |
7 | HG00408.hp1 HG00423.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.530+1139T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443054 | |||||||
| chr4:87443116 | G | A | 4 | a0002c0003t0003g0008 a0002c0003t0003g0022 a0002c0004t0002g0112 others(1): Show |
12 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.530+1201G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443116 | |||||||
| chr4:87443179 | T | C | 15 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0037 others(12): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.530+1264T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443179 | |||||||
| chr4:87443243 | G | A | 1 | a0001c0001t0004g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.530+1328G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443243 | |||||||
| chr4:87443260 | CAT | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(20): Show |
86 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.530+1346_530+1347d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443260 | |||||||
| chr4:87443352 | A | G | 1 | a0001c0001t0001g0017 | 3 | HG01192.hp1 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.530+1437A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443352 | |||||||
| chr4:87443473 | A | G | 1 | a0001c0002t0001g0015 | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+1558A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443473 | |||||||
| chr4:87443605 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG00642.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.530+1690C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443605 | |||||||
| chr4:87443664 | A | G | 2 | a0002c0004t0002g0112 a0002c0004t0016g0106 |
2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.530+1749A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443664 | |||||||
| chr4:87443682 | G | A | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.530+1767G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443682 | |||||||
| chr4:87443722 | C | A | 1 | a0002c0003t0003g0022 | 3 | HG00639.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.530+1807C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443722 | |||||||
| chr4:87443761 | A | G | 3 | a0001c0001t0004g0013 a0001c0001t0004g0070 a0001c0002t0001g0093 |
6 | HG01167.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.530+1846A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443761 | |||||||
| chr4:87443895 | T | C | 1 | a0001c0001t0001g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.530+1980T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443895 | |||||||
| chr4:87443913 | G | A | 11 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0024 others(8): Show |
29 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.530+1998G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443913 | |||||||
| chr4:87443920 | G | A | 1 | a0001c0001t0004g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.530+2005G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443920 | |||||||
| chr4:87443931 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
166 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530+2016C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87443931 | |||||||
| chr4:87444092 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.530+2177T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444092 | |||||||
| chr4:87444176 | A | C | 1 | a0001c0002t0020g0041 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.530+2261A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444176 | |||||||
| chr4:87444296 | A | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(6): Show |
32 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.530+2381A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444296 | |||||||
| chr4:87444335 | T | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(79): Show |
264 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.530+2420T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444335 | |||||||
| chr4:87444475 | T | C | 1 | a0002c0004t0016g0106 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.530+2560T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444475 | |||||||
| chr4:87444607 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.530+2692T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444607 | |||||||
| chr4:87444678 | G | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(119): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.530+2763G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444678 | |||||||
| chr4:87444790 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.530+2875C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444790 | |||||||
| chr4:87444987 | C | T | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.530+3072C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87444987 | |||||||
| chr4:87445093 | C | G | 1 | a0001c0001t0001g0004 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.530+3178C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445093 | |||||||
| chr4:87445180 | G | C | 1 | a0001c0002t0014g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.530+3265G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445180 | |||||||
| chr4:87445335 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.530+3420T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445335 | |||||||
| chr4:87445349 | C | T | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.530+3434C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445349 | |||||||
| chr4:87445474 | G | A | 1 | a0001c0002t0001g0015 | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+3559G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445474 | |||||||
| chr4:87445567 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.531-3575A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445567 | |||||||
| chr4:87445765 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.531-3377A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445765 | |||||||
| chr4:87445853 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.531-3289C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445853 | |||||||
| chr4:87445879 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.531-3263T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445879 | |||||||
| chr4:87445896 | C | T | 1 | a0001c0002t0001g0024 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.531-3246C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445896 | |||||||
| chr4:87445933 | CT | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0032 others(3): Show |
8 | HG01167.hp1 HG01256.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.531-3194delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87445933 | ||||||
| chr4:87445994 | T | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(79): Show |
264 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.531-3148T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87445994 | |||||||
| chr4:87446015 | C | T | 32 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(29): Show |
97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.531-3127C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446015 | |||||||
| chr4:87446079 | A | G | 1 | a0001c0001t0001g0004 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.531-3063A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446079 | |||||||
| chr4:87446087 | C | T | 3 | a0001c0001t0003g0005 a0001c0001t0010g0062 a0001c0001t0017g0101 |
10 | HG00140.hp2 HG01123.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.531-3055C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446087 | |||||||
| chr4:87446091 | T | G | 1 | a0001c0001t0001g0002 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.531-3051T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446091 | |||||||
| chr4:87446247 | C | CT | 27 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(24): Show |
98 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.531-2876dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87446247 | ||||||
| chr4:87446247 | C | CTT | 29 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(26): Show |
67 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.531-2877_531-2876d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87446247 | ||||||
| chr4:87446247 | C | CTTT | 35 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(32): Show |
87 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.531-2878_531-2876d others(5): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87446247 | ||||||
| chr4:87446247 | C | CTTTT | 4 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0002g0036 others(1): Show |
6 | HG01884.hp1 HG02155.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-2879_531-2876d others(6): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87446247 | ||||||
| chr4:87446247 | C | CTTTTT | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
9 | HG00639.hp2 HG02257.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.531-2880_531-2876d others(7): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87446247 | ||||||
| chr4:87446317 | C | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(15): Show |
68 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.531-2825C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446317 | |||||||
| chr4:87446355 | C | T | 1 | a0001c0001t0004g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.531-2787C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446355 | |||||||
| chr4:87446373 | C | G | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.531-2769C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446373 | |||||||
| chr4:87446411 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0011 |
6 | NA18949.hp1 NA18964.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.531-2731A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446411 | |||||||
| chr4:87446435 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.531-2707A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446435 | |||||||
| chr4:87446589 | G | A | 2 | a0001c0002t0001g0024 a0001c0002t0001g0039 |
3 | HG02572.hp1 HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.531-2553G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446589 | |||||||
| chr4:87446638 | A | G | 1 | a0001c0002t0001g0015 | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.531-2504A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446638 | |||||||
| chr4:87446724 | A | G | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.531-2418A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446724 | |||||||
| chr4:87446750 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.531-2392G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446750 | |||||||
| chr4:87446978 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.531-2164A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446978 | |||||||
| chr4:87446988 | C | G | 2 | a0001c0002t0007g0010 a0001c0002t0014g0010 |
5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.531-2154C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87446988 | |||||||
| chr4:87447003 | G | A | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.531-2139G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447003 | |||||||
| chr4:87447080 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.531-2062T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447080 | |||||||
| chr4:87447167 | A | G | 1 | a0001c0001t0002g0003 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.531-1975A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447167 | |||||||
| chr4:87447198 | G | A | 3 | a0001c0002t0001g0024 a0001c0002t0001g0039 a0001c0002t0001g0116 |
6 | HG02572.hp1 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.531-1944G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447198 | |||||||
| chr4:87447476 | GT | G | 33 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(30): Show |
98 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.531-1652delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87447476 | ||||||
| chr4:87447486 | T | G | 14 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0079 others(11): Show |
27 | HG00408.hp1 HG00423.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.531-1656T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447486 | |||||||
| chr4:87447487 | T | G | 6 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0040 others(3): Show |
15 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.531-1655T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447487 | |||||||
| chr4:87447501 | G | T | 32 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(29): Show |
97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.531-1641G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447501 | |||||||
| chr4:87447579 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.531-1563G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447579 | |||||||
| chr4:87447591 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0033 |
2 | HG00558.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.531-1551T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447591 | |||||||
| chr4:87447678 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
166 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.531-1464A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447678 | |||||||
| chr4:87447760 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.531-1382C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447760 | |||||||
| chr4:87447833 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.531-1309A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447833 | |||||||
| chr4:87447935 | G | A | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.531-1207G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87447935 | |||||||
| chr4:87448034 | T | A | 2 | a0001c0001t0001g0044 a0001c0001t0013g0072 |
2 | HG03225.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.531-1108T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448034 | |||||||
| chr4:87448035 | A | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0028 others(8): Show |
19 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.531-1107A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448035 | |||||||
| chr4:87448036 | A | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0076 others(1): Show |
10 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.531-1106A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448036 | |||||||
| chr4:87448040 | A | C | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.531-1102A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448040 | |||||||
| chr4:87448055 | T | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0088 |
7 | HG00438.hp2 HG02040.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.531-1087T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448055 | |||||||
| chr4:87448138 | A | AT | 17 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0031 others(14): Show |
33 | HG00423.hp1 HG01952.hp2 HG02027.hp2 others(30): Show |
intron_variant | MODIFIER | c.531-980dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87448138 | ||||||
| chr4:87448138 | AT | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(59): Show |
190 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.531-980delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87448138 | ||||||
| chr4:87448138 | ATT | A | 9 | a0001c0001t0001g0046 a0001c0001t0002g0097 a0001c0001t0002g0098 others(6): Show |
16 | HG00140.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.531-981_531-980del others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 87448138 | ||||||
| chr4:87448207 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0061 |
5 | NA18961.hp1 NA18962.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-935C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448207 | |||||||
| chr4:87448223 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
166 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.531-919C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448223 | |||||||
| chr4:87448411 | T | G | 1 | a0001c0001t0001g0001 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.531-731T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448411 | |||||||
| chr4:87448442 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.531-700C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448442 | |||||||
| chr4:87448446 | A | G | 18 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0029 others(15): Show |
66 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.531-696A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448446 | |||||||
| chr4:87448521 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.531-621G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448521 | |||||||
| chr4:87448634 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0029 others(14): Show |
65 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.531-508C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448634 | |||||||
| chr4:87448657 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.531-485T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448657 | |||||||
| chr4:87448723 | T | A | 4 | a0001c0002t0001g0024 a0001c0002t0001g0039 a0001c0002t0001g0116 others(1): Show |
10 | HG02258.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.531-419T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448723 | |||||||
| chr4:87448744 | A | C | 1 | a0001c0001t0019g0003 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.531-398A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448744 | |||||||
| chr4:87448746 | T | C | 1 | a0002c0004t0016g0106 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.531-396T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 4/7 | chr4 | 87448746 | |||||||
| chr4:87449453 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.642+200G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87449453 | |||||||
| chr4:87449530 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.642+277C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87449530 | |||||||
| chr4:87449590 | A | G | 1 | a0001c0001t0009g0001 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.642+337A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87449590 | |||||||
| chr4:87449737 | T | A | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.642+484T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87449737 | |||||||
| chr4:87449867 | T | C | 3 | a0001c0001t0004g0013 a0001c0001t0004g0070 a0001c0002t0001g0093 |
6 | HG01167.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.642+614T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87449867 | |||||||
| chr4:87450038 | A | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
166 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.642+785A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450038 | |||||||
| chr4:87450174 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.642+921C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450174 | |||||||
| chr4:87450259 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.642+1006C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450259 | |||||||
| chr4:87450339 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0029 others(15): Show |
66 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.642+1086G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450339 | |||||||
| chr4:87450372 | CTTTTTCT others(5): Show |
C | 1 | a0001c0002t0020g0041 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.642+1125_642+1136d others(14): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 87450372 | ||||||
| chr4:87450378 | C | CT | 5 | a0001c0001t0001g0001 a0001c0001t0002g0003 a0001c0001t0008g0110 others(2): Show |
9 | HG03225.hp1 HG03491.hp2 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.642+1145dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 87450378 | ||||||
| chr4:87450378 | CT | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(56): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.642+1145delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 87450378 | ||||||
| chr4:87450378 | CTT | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0003g0005 others(3): Show |
16 | HG00639.hp2 HG01256.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.642+1144_642+1145d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 87450378 | ||||||
| chr4:87450383 | T | C | 1 | a0001c0001t0002g0003 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.642+1130T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450383 | |||||||
| chr4:87450384 | T | C | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.642+1131T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450384 | |||||||
| chr4:87450412 | A | T | 1 | a0001c0001t0001g0001 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.642+1159A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450412 | |||||||
| chr4:87450464 | C | T | 1 | a0001c0002t0001g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.643-1125C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450464 | |||||||
| chr4:87450487 | C | G | 2 | a0001c0002t0007g0010 a0001c0002t0014g0010 |
5 | HG02486.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-1102C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450487 | |||||||
| chr4:87450523 | C | T | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.643-1066C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450523 | |||||||
| chr4:87450666 | T | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(79): Show |
263 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.643-923T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450666 | |||||||
| chr4:87450765 | G | A | 1 | a0001c0002t0001g0116 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.643-824G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450765 | |||||||
| chr4:87450789 | C | A | 16 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0037 others(13): Show |
65 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.643-800C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450789 | |||||||
| chr4:87450804 | C | T | 1 | a0001c0001t0013g0072 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.643-785C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450804 | |||||||
| chr4:87450887 | C | G | 1 | a0001c0002t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-702C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450887 | |||||||
| chr4:87450990 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.643-599G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87450990 | |||||||
| chr4:87451257 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.643-332G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87451257 | |||||||
| chr4:87451356 | G | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0075 |
4 | HG02165.hp1 NA18946.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-233G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87451356 | |||||||
| chr4:87451520 | ACTC | A | 4 | a0001c0002t0001g0009 a0001c0002t0001g0040 a0001c0002t0001g0117 others(1): Show |
10 | HG01891.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.643-68_643-66delCT others(1): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 5/7 | chr4 | 87451520 | |||||||
| chr4:87451797 | T | C | 3 | a0001c0001t0002g0003 a0001c0001t0002g0111 a0001c0001t0002g0114 |
4 | HG02071.hp1 HG02074.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+62T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87451797 | |||||||
| chr4:87451855 | A | C | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.789+120A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87451855 | |||||||
| chr4:87451926 | T | G | 1 | a0001c0002t0001g0116 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.789+191T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87451926 | |||||||
| chr4:87451960 | TTC | T | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+226_789+227del others(2): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87451960 | |||||||
| chr4:87451973 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.789+238T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87451973 | |||||||
| chr4:87451979 | A | G | 16 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0037 others(13): Show |
65 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.789+244A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87451979 | |||||||
| chr4:87452163 | C | T | 1 | a0002c0004t0016g0106 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.789+428C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452163 | |||||||
| chr4:87452300 | G | T | 1 | a0002c0003t0003g0022 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.789+565G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452300 | |||||||
| chr4:87452311 | A | G | 32 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(29): Show |
97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.789+576A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452311 | |||||||
| chr4:87452516 | T | G | 1 | a0001c0001t0013g0072 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789+781T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452516 | |||||||
| chr4:87452606 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.789+871G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452606 | |||||||
| chr4:87452618 | T | C | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
9 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.789+883T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452618 | |||||||
| chr4:87452624 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.789+889G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452624 | |||||||
| chr4:87452663 | C | T | 1 | a0001c0001t0004g0012 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.789+928C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452663 | |||||||
| chr4:87452700 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(22): Show |
88 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.789+965C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452700 | |||||||
| chr4:87452809 | G | GT | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(48): Show |
166 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.789+1094dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 87452809 | ||||||
| chr4:87452809 | G | GTT | 7 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0045 others(4): Show |
9 | HG01167.hp2 HG01981.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.789+1093_789+1094d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 87452809 | ||||||
| chr4:87452809 | GT | G | 5 | a0001c0001t0001g0001 a0001c0001t0002g0003 a0001c0001t0002g0108 others(2): Show |
10 | HG02055.hp1 HG02071.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.789+1094delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 87452809 | ||||||
| chr4:87452809 | GTT | G | 14 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0037 others(11): Show |
56 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.789+1093_789+1094d others(4): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 87452809 | ||||||
| chr4:87452993 | G | A | 6 | a0001c0001t0004g0012 a0001c0001t0004g0030 a0001c0001t0004g0066 others(3): Show |
10 | HG01109.hp1 HG02258.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+1258G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87452993 | |||||||
| chr4:87453084 | T | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0002t0001g0041 |
4 | HG03195.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.790-1287T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453084 | |||||||
| chr4:87453107 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.790-1264C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453107 | |||||||
| chr4:87453223 | C | T | 1 | a0001c0002t0006g0014 | 4 | HG02258.hp2 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-1148C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453223 | |||||||
| chr4:87453371 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.790-1000T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453371 | |||||||
| chr4:87453498 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.790-873C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453498 | |||||||
| chr4:87453611 | G | T | 11 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0024 others(8): Show |
29 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.790-760G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453611 | |||||||
| chr4:87453780 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.790-591G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453780 | |||||||
| chr4:87453813 | A | G | 2 | a0001c0001t0004g0012 a0001c0001t0004g0066 |
3 | HG01109.hp1 HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.790-558A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453813 | |||||||
| chr4:87453861 | C | CT | 12 | a0001c0001t0001g0077 a0001c0001t0002g0036 a0001c0001t0002g0097 others(9): Show |
20 | HG00140.hp2 HG01123.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.790-495dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 87453861 | ||||||
| chr4:87453861 | CT | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0002g0003 others(2): Show |
6 | HG01070.hp1 HG02071.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.790-495delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 87453861 | ||||||
| chr4:87453928 | G | T | 2 | a0002c0003t0003g0008 a0002c0003t0003g0022 |
10 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.790-443G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453928 | |||||||
| chr4:87453985 | G | C | 1 | a0001c0002t0001g0015 | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-386G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453985 | |||||||
| chr4:87453992 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.790-379C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87453992 | |||||||
| chr4:87454059 | C | T | 1 | a0002c0004t0016g0106 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.790-312C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87454059 | |||||||
| chr4:87454181 | A | C | 2 | a0001c0001t0002g0099 a0001c0001t0002g0102 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.790-190A>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 6/7 | chr4 | 87454181 | |||||||
| chr4:87454778 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.874+323G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87454778 | |||||||
| chr4:87455464 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.874+1009C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455464 | |||||||
| chr4:87455611 | A | G | 32 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0036 others(29): Show |
97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.874+1156A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455611 | |||||||
| chr4:87455629 | CG | C | 1 | a0001c0002t0006g0014 | 4 | HG02258.hp2 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.874+1175delG | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455629 | |||||||
| chr4:87455630 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(90): Show |
290 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.874+1175G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455630 | |||||||
| chr4:87455651 | CTTTTTTC others(9): Show |
C | 1 | a0001c0001t0002g0003 | 2 | NA18948.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.874+1203_874+1218d others(18): Show |
NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 87455651 | ||||||
| chr4:87455658 | CT | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0001c0001t0001g0076 others(4): Show |
9 | HG01516.hp1 HG02897.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.874+1218delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 87455658 | ||||||
| chr4:87455812 | C | T | 1 | a0001c0001t0010g0062 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.874+1357C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455812 | |||||||
| chr4:87455822 | T | A | 4 | a0002c0003t0003g0008 a0002c0003t0003g0022 a0002c0004t0002g0112 others(1): Show |
12 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.874+1367T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455822 | |||||||
| chr4:87455852 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.874+1397G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455852 | |||||||
| chr4:87455853 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0029 others(14): Show |
65 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.874+1398G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455853 | |||||||
| chr4:87455858 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.874+1403C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455858 | |||||||
| chr4:87455894 | T | G | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.874+1439T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455894 | |||||||
| chr4:87455906 | C | T | 1 | a0001c0001t0018g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.874+1451C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87455906 | |||||||
| chr4:87456018 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.874+1563A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456018 | |||||||
| chr4:87456042 | T | A | 8 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0040 others(5): Show |
20 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.874+1587T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456042 | |||||||
| chr4:87456172 | G | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0029 others(14): Show |
65 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.875-1671G>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456172 | |||||||
| chr4:87456430 | T | C | 1 | a0001c0002t0001g0015 | 4 | HG02055.hp2 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.875-1413T>C | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456430 | |||||||
| chr4:87456501 | G | A | 1 | a0001c0001t0002g0109 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.875-1342G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456501 | |||||||
| chr4:87456582 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.875-1261A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456582 | |||||||
| chr4:87456820 | A | T | 1 | a0001c0001t0002g0111 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.875-1023A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456820 | |||||||
| chr4:87456824 | G | A | 3 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0103 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.875-1019G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87456824 | |||||||
| chr4:87457060 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.875-783C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457060 | |||||||
| chr4:87457236 | A | AT | 29 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(26): Show |
85 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.875-589dupT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 87457236 | ||||||
| chr4:87457236 | AT | A | 30 | a0001c0001t0001g0049 a0001c0001t0001g0078 a0001c0001t0002g0003 others(27): Show |
95 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.875-589delT | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 87457236 | ||||||
| chr4:87457437 | A | G | 1 | a0001c0001t0001g0019 | 3 | HG00099.hp1 HG02602.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.875-406A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457437 | |||||||
| chr4:87457455 | T | A | 1 | a0001c0001t0001g0050 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-388T>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457455 | |||||||
| chr4:87457456 | C | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(19): Show |
85 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.875-387C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457456 | |||||||
| chr4:87457461 | T | G | 1 | a0001c0001t0001g0050 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-382T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457461 | |||||||
| chr4:87457462 | C | A | 1 | a0001c0001t0001g0050 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-381C>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457462 | |||||||
| chr4:87457464 | T | G | 1 | a0001c0001t0001g0050 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-379T>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457464 | |||||||
| chr4:87457465 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-378G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457465 | |||||||
| chr4:87457466 | A | T | 1 | a0001c0001t0001g0050 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-377A>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457466 | |||||||
| chr4:87457467 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-376C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457467 | |||||||
| chr4:87457468 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.875-375C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457468 | |||||||
| chr4:87457478 | C | G | 3 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0103 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.875-365C>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457478 | |||||||
| chr4:87457484 | G | T | 4 | a0002c0003t0003g0008 a0002c0003t0003g0022 a0002c0004t0002g0112 others(1): Show |
12 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.875-359G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457484 | |||||||
| chr4:87457563 | G | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): Show |
295 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.875-280G>A | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457563 | |||||||
| chr4:87457666 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
166 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.875-177A>G | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457666 | |||||||
| chr4:87457667 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.875-176G>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457667 | |||||||
| chr4:87457780 | C | T | 1 | a0002c0004t0002g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.875-63C>T | NUDT9 | ENSG00000170502.13 | transcript | ENST00000302174.9 | protein_coding | 7/7 | chr4 | 87457780 |