Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 221294 |
| ensemblid | ENSG00000178425.14 |
| hgncid | 21556 |
| symbol | NT5DC1 |
| name | 5'-nucleotidase domain containing 1 |
| refseq_nuc | NM_152729.3 |
| refseq_prot | NP_689942.2 |
| ensembl_nuc | ENST00000319550.9 |
| ensembl_prot | ENSP00000326858.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 116100853 |
| end | 116249497 |
| strand | + |
| ver | v1.2 |
| region | chr6:116100853-116249497 |
| region5000 | chr6:116095853-116254497 |
| regionname0 | NT5DC1_chr6_116100853_116249497 |
| regionname5000 | NT5DC1_chr6_116095853_116254497 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 455 | 297 | 92 | 55 | 104 | 12 | 32 | 92 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | MAQHF others(450): Show |
chr6 | 116095853 | 116254497 |
| a0002 | 0/0 | 455 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | MAQHF others(450): Show |
chr6 | 116095853 | 116254497 |
| a0003 | 0/0 | 455 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | MAQHF others(450): Show |
chr6 | 116095853 | 116254497 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1365 | 296 | 91 | 55 | 104 | 12 | 32 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | ATGGC others(1360): Show |
chr6 | 116095853 | 116254497 | ||
| a0001c0003 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | ATGGC others(1360): Show |
chr6 | 116095853 | 116254497 | ||
| a0002c0002 | 0/0 | 1365 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | ATGGC others(1360): Show |
chr6 | 116095853 | 116254497 | ||
| a0003c0004 | 0/0 | 1365 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | ATGGC others(1360): Show |
chr6 | 116095853 | 116254497 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6912 | 87 | 12 | 11 | 46 | 3 | 15 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6907): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0002 | 1/0 | 6919 | 55 | 19 | 17 | 9 | 4 | 5 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6914): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0003 | 0/0 | 6927 | 40 | 6 | 7 | 27 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6922): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0004 | 0/0 | 6929 | 16 | 1 | 3 | 7 | 2 | 3 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6924): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0005 | 0/0 | 6925 | 10 | 4 | 2 | 0 | 1 | 3 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6920): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0006 | 0/0 | 6931 | 10 | 4 | 1 | 4 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6926): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0007 | 0/0 | 6929 | 10 | 8 | 2 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6924): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0008 | 0/0 | 6931 | 9 | 1 | 3 | 5 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6926): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0009 | 0/0 | 6933 | 7 | 7 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6928): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0010 | 0/0 | 6931 | 7 | 7 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6926): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0011 | 0/0 | 6913 | 4 | 1 | 2 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6908): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0012 | 0/0 | 6908 | 4 | 0 | 0 | 4 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6903): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0013 | 0/0 | 6921 | 4 | 3 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6916): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0014 | 0/0 | 6925 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6920): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0015 | 0/0 | 6914 | 2 | 0 | 1 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6909): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0016 | 0/0 | 6939 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6934): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0017 | 0/0 | 6917 | 2 | 1 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6912): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0018 | 0/0 | 6927 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6922): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0019 | 0/0 | 6919 | 2 | 0 | 1 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6914): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0020 | 0/0 | 6929 | 2 | 0 | 0 | 0 | 0 | 2 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6924): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0021 | 0/0 | 6913 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6908): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0022 | 0/0 | 6912 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6907): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0023 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6905): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0024 | 0/0 | 6908 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6903): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0025 | 0/0 | 6941 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6936): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0026 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6930): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0027 | 0/0 | 6927 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6922): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0028 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6914): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0029 | 0/0 | 6929 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6924): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0030 | 0/0 | 6933 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6928): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0031 | 0/1 | 6927 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6922): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0032 | 0/0 | 6929 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6924): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0033 | 0/0 | 6937 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6932): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0034 | 0/0 | 6918 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6913): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0035 | 0/0 | 6933 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6928): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0036 | 0/0 | 6931 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6926): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0037 | 0/0 | 6919 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6914): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0038 | 0/0 | 6917 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6912): Show |
chr6 | 116095853 | 116254497 |
| a0001c0001t0039 | 0/0 | 6919 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6914): Show |
chr6 | 116095853 | 116254497 |
| a0001c0003t0014 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6920): Show |
chr6 | 116095853 | 116254497 |
| a0002c0002t0002 | 0/0 | 6919 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6914): Show |
chr6 | 116095853 | 116254497 |
| a0003c0004t0002 | 0/0 | 6919 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | CCTGT others(6914): Show |
chr6 | 116095853 | 116254497 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0011g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0011g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0011g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0012g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0012g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0012g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0012g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0013g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0013g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0013g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0013g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0014g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0014g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0015g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0015g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0016g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0016g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0017g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0017g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0018g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0018g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0019g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0019g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0020g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0020g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0021g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0022g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0023g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0024g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0025g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0026g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0027g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0028g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0029g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0030g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0031g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0032g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0033g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0034g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0035g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0036g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0037g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0038g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0039g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0003t0014g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0003c0004t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0120 | EUR | GBR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0214 | EUR | GBR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0088 | EUR | FIN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0181 | EUR | FIN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | FIN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0164 | EUR | FIN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | CHS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | CHS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0247 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0138 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00738 | hp1 | a0001 | c0001 | t0015 | g0282 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0254 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01074 | hp1 | a0001 | c0001 | t0033 | g0241 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0286 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0269 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01106 | hp2 | a0001 | c0001 | t0029 | g0050 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0081 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01168 | hp2 | a0001 | c0001 | t0011 | g0091 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01169 | hp2 | a0001 | c0001 | t0011 | g0090 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01175 | hp1 | a0001 | c0001 | t0032 | g0234 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01243 | hp2 | a0001 | c0001 | t0013 | g0096 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0248 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01361 | hp1 | a0003 | c0004 | t0002 | g0076 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0252 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0250 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01515 | hp1 | a0001 | c0001 | t0019 | g0149 | EUR | IBS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01884 | hp1 | a0001 | c0001 | t0010 | g0103 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01891 | hp1 | a0001 | c0001 | t0016 | g0116 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01891 | hp2 | a0001 | c0001 | t0023 | g0123 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01934 | hp1 | a0001 | c0001 | t0019 | g0150 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01934 | hp2 | a0001 | c0001 | t0008 | g0194 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01993 | hp2 | a0001 | c0001 | t0039 | g0075 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02055 | hp2 | a0001 | c0001 | t0027 | g0008 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02145 | hp1 | a0001 | c0001 | t0018 | g0274 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0203 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02280 | hp1 | a0001 | c0001 | t0017 | g0062 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0101 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02300 | hp1 | a0001 | c0001 | t0008 | g0249 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0102 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02451 | hp2 | a0001 | c0001 | t0018 | g0127 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0097 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0071 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0095 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02630 | hp2 | a0001 | c0001 | t0026 | g0114 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02683 | hp1 | a0001 | c0001 | t0015 | g0287 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0112 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0060 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0129 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02723 | hp2 | a0001 | c0001 | t0024 | g0122 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02735 | hp1 | a0001 | c0001 | t0011 | g0211 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02735 | hp2 | a0001 | c0001 | t0020 | g0236 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0245 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0107 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0244 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02886 | hp1 | a0001 | c0001 | t0030 | g0113 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02886 | hp2 | a0001 | c0001 | t0014 | g0143 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0288 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02896 | hp1 | a0001 | c0001 | t0038 | g0141 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0276 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0099 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02922 | hp2 | a0001 | c0001 | t0036 | g0136 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0070 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0100 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03041 | hp2 | a0001 | c0001 | t0025 | g0115 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0140 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03130 | hp1 | a0001 | c0001 | t0034 | g0279 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0144 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0242 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0131 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0104 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03225 | hp2 | a0001 | c0001 | t0035 | g0290 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0134 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0128 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0110 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0069 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03579 | hp1 | a0001 | c0001 | t0016 | g0117 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03654 | hp2 | a0001 | c0001 | t0020 | g0230 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03704 | hp2 | a0001 | c0001 | t0021 | g0221 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0212 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0251 | SAS | BEB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | BEB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0260 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0135 | SAS | BEB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0158 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | YRI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | YRI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | YRI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | YRI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18941 | hp1 | a0001 | c0001 | t0012 | g0173 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18941 | hp2 | a0001 | c0001 | t0008 | g0256 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18948 | hp2 | a0001 | c0001 | t0008 | g0032 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18968 | hp2 | a0001 | c0001 | t0012 | g0171 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18969 | hp2 | a0001 | c0001 | t0028 | g0028 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0010 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19004 | hp1 | a0001 | c0001 | t0022 | g0180 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19007 | hp1 | a0001 | c0001 | t0012 | g0170 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19010 | hp2 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0118 | AFR | LWK | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | LWK | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0132 | AFR | LWK | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19068 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19081 | hp1 | a0001 | c0001 | t0008 | g0040 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19083 | hp2 | a0001 | c0001 | t0012 | g0168 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | ASW | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0182 | AFR | ASW | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0133 | EUR | TSI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20805 | hp2 | a0001 | c0001 | t0017 | g0292 | EUR | TSI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0051 | SAS | GIH | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | GIH | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01123 | hp2 | a0001 | c0001 | t0007 | g0268 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0130 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0147 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0105 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0108 | AFR | USA | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG06807 | hp2 | a0001 | c0001 | t0037 | g0275 | AFR | USA | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | USA | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | USA | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA21309 | hp1 | a0001 | c0003 | t0014 | g0063 | AFR | LWK | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | LWK | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0031 | g0052 | REF | REF | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0142 | REF | REF | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116106254 | A | G | 1 | a0003 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.104A>G | p.Asn35Ser | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/12 | 182/6919 | 104/1368 | 35/455 | chr6 | 116106254 | |||
| chr6:116238243 | T | G | 1 | a0002 | 2 | HG01168.hp1 HG01192.hp1 |
missense_variant | MODERATE | c.978T>G | p.Ser326Arg | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 10/12 | 1056/6919 | 978/1368 | 326/455 | chr6 | 116238243 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116117881 | A | G | 1 | a0001c0003 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.465A>G | p.Thr155Thr | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/12 | 543/6919 | 465/1368 | 155/455 | chr6 | 116117881 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116100890 | C | T | 1 | a0001c0001t0039 | 1 | HG01993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-41C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/12 | 41 | chr6 | 116100890 | ||||||
| chr6:116244341 | G | A | 8 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(5): Show |
101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*317G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 317 | chr6 | 116244341 | ||||||
| chr6:116244562 | C | A | 15 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(12): Show |
99 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*538C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 538 | chr6 | 116244562 | ||||||
| chr6:116244799 | A | G | 2 | a0001c0001t0010 a0001c0001t0033 |
8 | HG01074.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*775A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 775 | chr6 | 116244799 | ||||||
| chr6:116245033 | CTATT | C | 8 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(5): Show |
101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1012_*1015delTTTA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1012 | INFO_REALIGN_3_PRIME | chr6 | 116245033 | |||||
| chr6:116245042 | G | A | 9 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(6): Show |
102 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1018G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1018 | chr6 | 116245042 | ||||||
| chr6:116245275 | G | A | 1 | a0001c0001t0017 | 2 | HG02280.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1251G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1251 | chr6 | 116245275 | ||||||
| chr6:116245473 | C | CA | 2 | a0001c0001t0011 a0001c0001t0021 |
5 | HG01168.hp2 HG01169.hp2 HG02735.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1457dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1458 | INFO_REALIGN_3_PRIME | chr6 | 116245473 | |||||
| chr6:116245617 | A | C | 1 | a0001c0001t0020 | 2 | HG02735.hp2 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1593A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1593 | chr6 | 116245617 | ||||||
| chr6:116245653 | G | T | 1 | a0001c0001t0032 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1629G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1629 | chr6 | 116245653 | ||||||
| chr6:116245802 | CT | C | 9 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(6): Show |
102 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1780delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1780 | INFO_REALIGN_3_PRIME | chr6 | 116245802 | |||||
| chr6:116245885 | T | C | 8 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(5): Show |
101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1861T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1861 | chr6 | 116245885 | ||||||
| chr6:116246011 | A | C | 1 | a0001c0001t0030 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1987A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1987 | chr6 | 116246011 | ||||||
| chr6:116246267 | T | G | 1 | a0001c0001t0034 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2243T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2243 | chr6 | 116246267 | ||||||
| chr6:116246298 | C | T | 1 | a0001c0001t0029 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2274C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2274 | chr6 | 116246298 | ||||||
| chr6:116246362 | T | C | 1 | a0001c0001t0017 | 2 | HG02280.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2338T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2338 | chr6 | 116246362 | ||||||
| chr6:116246468 | T | TAC | 2 | a0001c0001t0013 a0001c0001t0023 |
5 | HG01243.hp2 HG01891.hp2 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2469_*2470dupAC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | |||||
| chr6:116246468 | T | TACAC | 5 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(2): Show |
97 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2467_*2470dupACAC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | |||||
| chr6:116246468 | T | TACACAC | 4 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0015 others(1): Show |
15 | HG00639.hp1 HG00738.hp1 HG01361.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2465_*2470dupACAC others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | |||||
| chr6:116246468 | T | TACACACA others(1): Show |
3 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0027 |
43 | HG00408.hp2 HG00558.hp2 HG01081.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2463_*2470dupACAC others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | |||||
| chr6:116246468 | T | TACACACA others(3): Show |
5 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0020 others(2): Show |
30 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2461_*2470dupACAC others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | |||||
| chr6:116246468 | T | TACACACA others(5): Show |
4 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0010 others(1): Show |
27 | HG00642.hp2 HG01496.hp1 HG01884.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2459_*2470dupACAC others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | |||||
| chr6:116246468 | T | TACACACA others(7): Show |
3 | a0001c0001t0009 a0001c0001t0030 a0001c0001t0035 |
9 | HG02717.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2457_*2470dupACAC others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | |||||
| chr6:116246468 | T | TACACACA others(9): Show |
1 | a0001c0001t0026 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2455_*2470dupACAC others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | |||||
| chr6:116246468 | T | TACACACA others(11): Show |
1 | a0001c0001t0033 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2453_*2470dupACAC others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | |||||
| chr6:116246468 | T | TACACACA others(13): Show |
1 | a0001c0001t0016 | 2 | HG01891.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2451_*2470dupACAC others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | |||||
| chr6:116246468 | T | TACACACA others(15): Show |
1 | a0001c0001t0025 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2449_*2470dupACAC others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | |||||
| chr6:116246468 | TAC | T | 2 | a0001c0001t0017 a0001c0001t0038 |
3 | HG02280.hp1 HG02896.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2469_*2470delAC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2469 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | |||||
| chr6:116246523 | A | C | 5 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0025 others(2): Show |
12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2499A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2499 | chr6 | 116246523 | ||||||
| chr6:116246535 | T | C | 1 | a0001c0001t0020 | 2 | HG02735.hp2 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2511T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2511 | chr6 | 116246535 | ||||||
| chr6:116246986 | A | T | 1 | a0001c0001t0020 | 2 | HG02735.hp2 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2962A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2962 | chr6 | 116246986 | ||||||
| chr6:116247610 | A | C | 8 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(5): Show |
101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3586A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 3586 | chr6 | 116247610 | ||||||
| chr6:116247664 | T | A | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3640T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 3640 | chr6 | 116247664 | ||||||
| chr6:116247752 | G | T | 8 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(5): Show |
101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3728G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 3728 | chr6 | 116247752 | ||||||
| chr6:116247821 | CTT | C | 8 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(5): Show |
101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3798_*3799delTT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 3798 | chr6 | 116247821 | ||||||
| chr6:116248123 | A | C | 1 | a0001c0001t0037 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4099A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 4099 | chr6 | 116248123 | ||||||
| chr6:116248123 | A | G | 1 | a0001c0001t0034 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4099A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 4099 | chr6 | 116248123 | ||||||
| chr6:116248138 | A | C | 5 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0025 others(2): Show |
12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4114A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 4114 | chr6 | 116248138 | ||||||
| chr6:116248314 | G | A | 1 | a0001c0001t0019 | 2 | HG01515.hp1 HG01934.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4290G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 4290 | chr6 | 116248314 | ||||||
| chr6:116248770 | G | A | 5 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0025 others(2): Show |
12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4746G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 4746 | chr6 | 116248770 | ||||||
| chr6:116248799 | A | T | 1 | a0001c0001t0027 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4775A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 4775 | chr6 | 116248799 | ||||||
| chr6:116249173 | GCTCT | G | 8 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(5): Show |
101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*5152_*5155delCTCT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 5152 | INFO_REALIGN_3_PRIME | chr6 | 116249173 | |||||
| chr6:116249180 | A | C | 1 | a0001c0001t0036 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5156A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 5156 | chr6 | 116249180 | ||||||
| chr6:116249275 | TTTAA | T | 1 | a0001c0001t0012 | 4 | NA18941.hp1 NA18968.hp2 NA19007.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5256_*5259delTTAA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 5256 | INFO_REALIGN_3_PRIME | chr6 | 116249275 | |||||
| chr6:116249325 | A | G | 16 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(13): Show |
101 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*5301A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 5301 | chr6 | 116249325 | ||||||
| chr6:116249360 | C | T | 1 | a0001c0001t0021 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5336C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 5336 | chr6 | 116249360 | ||||||
| chr6:116249434 | T | C | 9 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(6): Show |
102 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*5410T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 5410 | chr6 | 116249434 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116101118 | C | G | 56 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(53): Show |
56 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.93+95C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101118 | |||||||
| chr6:116101299 | T | C | 1 | a0001c0001t0027g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.93+276T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101299 | |||||||
| chr6:116101310 | T | A | 65 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0002g0049 others(62): Show |
67 | HG00408.hp2 HG00558.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.93+287T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101310 | |||||||
| chr6:116101371 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0148 others(128): Show |
134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.93+348C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101371 | |||||||
| chr6:116101380 | A | C | 1 | a0001c0001t0020g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.93+357A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101380 | |||||||
| chr6:116101446 | AT | A | 27 | a0001c0001t0001g0074 a0001c0001t0002g0004 a0001c0001t0002g0005 others(24): Show |
29 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.93+431delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 116101446 | ||||||
| chr6:116101553 | A | G | 2 | a0001c0001t0002g0291 a0001c0001t0017g0292 |
2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.93+530A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101553 | |||||||
| chr6:116101601 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.93+578A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101601 | |||||||
| chr6:116101684 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0092 others(149): Show |
155 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.93+661G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101684 | |||||||
| chr6:116101718 | G | A | 2 | a0001c0001t0007g0244 a0001c0001t0014g0245 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.93+695G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101718 | |||||||
| chr6:116101737 | T | C | 2 | a0001c0001t0006g0011 a0001c0001t0006g0012 |
2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.93+714T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101737 | |||||||
| chr6:116101765 | C | A | 1 | a0001c0001t0001g0013 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.93+742C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101765 | |||||||
| chr6:116102081 | T | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(214): Show |
222 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.93+1058T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102081 | |||||||
| chr6:116102136 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(216): Show |
224 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.93+1113T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102136 | |||||||
| chr6:116102214 | GGCACCCG others(9): Show |
G | 12 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(9): Show |
12 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.93+1198_93+1213del others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 116102214 | ||||||
| chr6:116102289 | C | T | 1 | a0001c0001t0032g0234 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.93+1266C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102289 | |||||||
| chr6:116102316 | A | T | 2 | a0001c0001t0006g0011 a0001c0001t0006g0012 |
2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.93+1293A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102316 | |||||||
| chr6:116102609 | A | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.93+1586A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102609 | |||||||
| chr6:116102628 | CAA | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0233 |
5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+1606_93+1607del others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102628 | |||||||
| chr6:116102856 | G | A | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.93+1833G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102856 | |||||||
| chr6:116103113 | C | T | 2 | a0001c0001t0007g0244 a0001c0001t0014g0245 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.93+2090C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103113 | |||||||
| chr6:116103321 | C | CCACTGTT others(23): Show |
2 | a0001c0001t0003g0231 a0001c0001t0020g0230 |
2 | HG02132.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.93+2306_93+2335dup others(30): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 116103321 | ||||||
| chr6:116103399 | C | T | 2 | a0001c0001t0007g0244 a0001c0001t0014g0245 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.93+2376C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103399 | |||||||
| chr6:116103461 | T | C | 23 | a0001c0001t0001g0148 a0001c0001t0002g0237 a0001c0001t0002g0238 others(20): Show |
23 | HG01074.hp1 HG01106.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.93+2438T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103461 | |||||||
| chr6:116103490 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(171): Show |
177 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.93+2467C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103490 | |||||||
| chr6:116103551 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(174): Show |
180 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.93+2528T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103551 | |||||||
| chr6:116103560 | C | T | 2 | a0001c0001t0007g0244 a0001c0001t0014g0245 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.93+2537C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103560 | |||||||
| chr6:116103650 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.94-2594A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103650 | |||||||
| chr6:116104031 | T | G | 3 | a0001c0001t0002g0049 a0001c0001t0004g0051 a0001c0001t0029g0050 |
3 | HG01099.hp2 HG01106.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.94-2213T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104031 | |||||||
| chr6:116104165 | G | A | 9 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(6): Show |
9 | HG02615.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.94-2079G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104165 | |||||||
| chr6:116104253 | T | C | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.94-1991T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104253 | |||||||
| chr6:116104260 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.94-1984C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104260 | |||||||
| chr6:116104336 | A | T | 1 | a0001c0001t0035g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.94-1908A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104336 | |||||||
| chr6:116104442 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(176): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.94-1802T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104442 | |||||||
| chr6:116104443 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.94-1801G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104443 | |||||||
| chr6:116104465 | A | G | 9 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(6): Show |
9 | HG02615.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.94-1779A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104465 | |||||||
| chr6:116104554 | A | G | 1 | a0001c0001t0003g0231 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.94-1690A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104554 | |||||||
| chr6:116104833 | T | C | 10 | a0001c0001t0004g0248 a0001c0001t0004g0251 a0001c0001t0004g0253 others(7): Show |
10 | HG00639.hp1 HG00741.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.94-1411T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104833 | |||||||
| chr6:116104907 | G | C | 1 | a0001c0001t0001g0257 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.94-1337G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104907 | |||||||
| chr6:116105002 | A | T | 24 | a0001c0001t0002g0049 a0001c0001t0002g0053 a0001c0001t0002g0055 others(21): Show |
24 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.94-1242A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116105002 | |||||||
| chr6:116105246 | C | T | 1 | a0001c0001t0014g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-998C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116105246 | |||||||
| chr6:116105271 | G | A | 4 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | NA18947.hp2 NA19067.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-973G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116105271 | |||||||
| chr6:116105819 | C | T | 5 | a0001c0001t0010g0102 a0001c0001t0010g0103 a0001c0001t0010g0104 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-425C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116105819 | |||||||
| chr6:116105870 | T | G | 1 | a0001c0001t0010g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-374T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116105870 | |||||||
| chr6:116106207 | G | A | 1 | a0001c0001t0003g0014 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.94-37G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116106207 | |||||||
| chr6:116106343 | CT | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(189): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.185+27delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116106343 | ||||||
| chr6:116106343 | CTT | C | 15 | a0001c0001t0001g0156 a0001c0001t0002g0049 a0001c0001t0002g0053 others(12): Show |
15 | HG00741.hp1 HG01069.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.185+26_185+27delTT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116106343 | ||||||
| chr6:116106410 | A | G | 2 | a0001c0001t0009g0144 a0001c0001t0014g0143 |
2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.185+75A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116106410 | |||||||
| chr6:116106497 | T | C | 1 | a0001c0001t0029g0050 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.185+162T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116106497 | |||||||
| chr6:116106631 | A | G | 2 | a0001c0001t0007g0244 a0001c0001t0014g0245 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.185+296A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116106631 | |||||||
| chr6:116106651 | G | A | 174 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0119 others(171): Show |
179 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.185+316G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116106651 | |||||||
| chr6:116106983 | G | A | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.185+648G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116106983 | |||||||
| chr6:116107044 | T | C | 21 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0124 others(18): Show |
21 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.185+709T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116107044 | |||||||
| chr6:116107274 | G | A | 1 | a0001c0001t0014g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.185+939G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116107274 | |||||||
| chr6:116107423 | C | A | 2 | a0001c0001t0002g0291 a0001c0001t0017g0292 |
2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.186-941C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116107423 | |||||||
| chr6:116107471 | C | T | 1 | a0001c0001t0002g0273 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.186-893C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116107471 | |||||||
| chr6:116107540 | T | TTTTTA | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(104): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.186-779_186-775dup others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | ||||||
| chr6:116107540 | T | TTTTTATT others(3): Show |
17 | a0001c0001t0001g0119 a0001c0001t0001g0145 a0001c0001t0001g0146 others(14): Show |
17 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.186-784_186-775dup others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | ||||||
| chr6:116107540 | T | TTTTTATT others(8): Show |
10 | a0001c0001t0002g0109 a0001c0001t0003g0111 a0001c0001t0009g0107 others(7): Show |
10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.186-789_186-775dup others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | ||||||
| chr6:116107540 | T | TTTTTATT others(13): Show |
3 | a0001c0001t0002g0106 a0001c0001t0010g0102 a0001c0001t0010g0242 |
3 | HG02451.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.186-794_186-775dup others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | ||||||
| chr6:116107540 | TTTTTA | T | 45 | a0001c0001t0001g0074 a0001c0001t0001g0220 a0001c0001t0002g0004 others(42): Show |
47 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.186-779_186-775del others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | ||||||
| chr6:116107540 | TTTTTATT others(3): Show |
T | 28 | a0001c0001t0002g0049 a0001c0001t0002g0053 a0001c0001t0002g0055 others(25): Show |
28 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.186-784_186-775del others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | ||||||
| chr6:116107540 | TTTTTATT others(8): Show |
T | 6 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(3): Show |
6 | HG01192.hp2 HG01243.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-789_186-775del others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | ||||||
| chr6:116107560 | A | ATTTTCT | 5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(2): Show |
5 | HG01175.hp2 HG01993.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-800_186-799ins others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107560 | ||||||
| chr6:116107642 | G | A | 1 | a0001c0001t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.186-722G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116107642 | |||||||
| chr6:116107672 | A | G | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.186-692A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116107672 | |||||||
| chr6:116107990 | A | ATG | 3 | a0001c0001t0001g0217 a0001c0001t0015g0287 a0001c0001t0035g0290 |
3 | HG02683.hp1 HG03225.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.186-356_186-355dup others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107990 | ||||||
| chr6:116107990 | ATGTGTGT others(1): Show |
A | 26 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(23): Show |
26 | HG01074.hp1 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.186-362_186-355del others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107990 | ||||||
| chr6:116108242 | A | G | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-122A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116108242 | |||||||
| chr6:116108460 | T | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(176): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.257+25T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116108460 | |||||||
| chr6:116108468 | A | G | 22 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(19): Show |
22 | HG01074.hp1 HG01106.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.257+33A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116108468 | |||||||
| chr6:116108801 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(176): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.257+366A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116108801 | |||||||
| chr6:116108812 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.257+377G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116108812 | |||||||
| chr6:116109219 | G | A | 141 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0119 others(138): Show |
146 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.257+784G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109219 | |||||||
| chr6:116109284 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.257+849C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109284 | |||||||
| chr6:116109370 | G | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(174): Show |
180 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.257+935G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109370 | |||||||
| chr6:116109537 | A | G | 27 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(24): Show |
27 | HG01074.hp1 HG01106.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.257+1102A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109537 | |||||||
| chr6:116109575 | T | C | 2 | a0001c0001t0006g0011 a0001c0001t0006g0012 |
2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.257+1140T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109575 | |||||||
| chr6:116109640 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(176): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.257+1205G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109640 | |||||||
| chr6:116109720 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.258-1130C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109720 | |||||||
| chr6:116109817 | C | T | 7 | a0001c0001t0010g0100 a0001c0001t0010g0101 a0001c0001t0010g0102 others(4): Show |
7 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.258-1033C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109817 | |||||||
| chr6:116109858 | AAACTACA others(27): Show |
A | 1 | a0001c0001t0014g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.258-969_258-936del others(34): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 116109858 | ||||||
| chr6:116109877 | A | G | 1 | a0001c0001t0007g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.258-973A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109877 | |||||||
| chr6:116109995 | A | G | 9 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0124 others(6): Show |
9 | HG01891.hp2 HG02257.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.258-855A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109995 | |||||||
| chr6:116110095 | C | T | 22 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(19): Show |
22 | HG01074.hp1 HG01106.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.258-755C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110095 | |||||||
| chr6:116110209 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(176): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.258-641G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110209 | |||||||
| chr6:116110263 | C | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(174): Show |
180 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.258-587C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110263 | |||||||
| chr6:116110329 | C | T | 1 | a0001c0001t0018g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.258-521C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110329 | |||||||
| chr6:116110453 | C | T | 1 | a0001c0001t0032g0234 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.258-397C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110453 | |||||||
| chr6:116110706 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258-144A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110706 | |||||||
| chr6:116110740 | C | A | 1 | a0001c0001t0003g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.258-110C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110740 | |||||||
| chr6:116111038 | C | G | 1 | a0001c0001t0002g0272 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.364+82C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111038 | |||||||
| chr6:116111274 | C | T | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.364+318C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111274 | |||||||
| chr6:116111431 | A | G | 2 | a0001c0001t0007g0140 a0001c0001t0038g0141 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.364+475A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111431 | |||||||
| chr6:116111473 | T | G | 23 | a0001c0001t0002g0055 a0001c0001t0002g0237 a0001c0001t0002g0238 others(20): Show |
23 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.364+517T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111473 | |||||||
| chr6:116111489 | A | G | 23 | a0001c0001t0002g0055 a0001c0001t0002g0237 a0001c0001t0002g0238 others(20): Show |
23 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.364+533A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111489 | |||||||
| chr6:116111540 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(153): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.364+584T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111540 | |||||||
| chr6:116111680 | G | A | 1 | a0001c0001t0020g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.364+724G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111680 | |||||||
| chr6:116111826 | A | G | 7 | a0001c0001t0001g0137 a0001c0001t0001g0139 a0001c0001t0005g0134 others(4): Show |
7 | HG00642.hp2 HG02922.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.364+870A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111826 | |||||||
| chr6:116111861 | G | C | 2 | a0001c0001t0007g0244 a0001c0001t0014g0245 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.364+905G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111861 | |||||||
| chr6:116111901 | A | T | 2 | a0001c0001t0001g0215 a0001c0001t0020g0230 |
2 | HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.364+945A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111901 | |||||||
| chr6:116112102 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(150): Show |
156 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.364+1146C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116112102 | |||||||
| chr6:116112172 | G | A | 10 | a0001c0001t0004g0248 a0001c0001t0004g0251 a0001c0001t0004g0253 others(7): Show |
10 | HG00639.hp1 HG00741.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.364+1216G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116112172 | |||||||
| chr6:116112383 | C | A | 1 | a0001c0001t0020g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.364+1427C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116112383 | |||||||
| chr6:116112475 | C | T | 2 | a0001c0001t0004g0255 a0001c0001t0008g0256 |
2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.364+1519C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116112475 | |||||||
| chr6:116112793 | A | T | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.364+1837A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116112793 | |||||||
| chr6:116112920 | A | G | 1 | a0001c0001t0020g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.364+1964A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116112920 | |||||||
| chr6:116113252 | A | C | 4 | a0001c0001t0002g0291 a0001c0001t0005g0278 a0001c0001t0008g0147 others(1): Show |
4 | HG01981.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+2296A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116113252 | |||||||
| chr6:116113454 | G | A | 23 | a0001c0001t0002g0055 a0001c0001t0002g0237 a0001c0001t0002g0238 others(20): Show |
23 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.365-2237G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116113454 | |||||||
| chr6:116113752 | G | C | 10 | a0001c0001t0004g0248 a0001c0001t0004g0251 a0001c0001t0004g0253 others(7): Show |
10 | HG00639.hp1 HG00741.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-1939G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116113752 | |||||||
| chr6:116113809 | G | A | 3 | a0001c0001t0010g0102 a0001c0001t0010g0103 a0001c0001t0010g0104 |
3 | HG01884.hp1 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-1882G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116113809 | |||||||
| chr6:116114355 | A | C | 23 | a0001c0001t0002g0049 a0001c0001t0002g0053 a0001c0001t0002g0056 others(20): Show |
23 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.365-1336A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114355 | |||||||
| chr6:116114397 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.365-1294C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114397 | |||||||
| chr6:116114430 | C | T | 8 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0284 others(5): Show |
8 | HG00738.hp1 HG01081.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.365-1261C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114430 | |||||||
| chr6:116114431 | G | A | 1 | a0001c0001t0006g0006 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.365-1260G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114431 | |||||||
| chr6:116114478 | T | G | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.365-1213T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114478 | |||||||
| chr6:116114531 | GGGGGA | G | 22 | a0001c0001t0002g0055 a0001c0001t0002g0237 a0001c0001t0002g0238 others(19): Show |
22 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.365-1155_365-1151d others(7): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 116114531 | ||||||
| chr6:116114532 | GGGGA | G | 58 | a0001c0001t0001g0137 a0001c0001t0001g0139 a0001c0001t0001g0151 others(55): Show |
61 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.365-1155_365-1152d others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 116114532 | ||||||
| chr6:116114533 | GGGA | G | 41 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0002g0004 others(38): Show |
43 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.365-1155_365-1153d others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 116114533 | ||||||
| chr6:116114536 | A | G | 4 | a0001c0001t0005g0278 a0001c0001t0007g0244 a0001c0001t0014g0245 others(1): Show |
4 | HG02809.hp1 HG02818.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-1155A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114536 | |||||||
| chr6:116114538 | G | A | 16 | a0001c0001t0002g0049 a0001c0001t0002g0053 a0001c0001t0002g0056 others(13): Show |
16 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.365-1153G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114538 | |||||||
| chr6:116114539 | G | C | 2 | a0001c0001t0006g0006 a0001c0001t0018g0127 |
3 | HG02451.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.365-1152G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114539 | |||||||
| chr6:116114541 | G | T | 1 | a0001c0001t0014g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.365-1150G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114541 | |||||||
| chr6:116114575 | T | C | 161 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0074 others(158): Show |
166 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.365-1116T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114575 | |||||||
| chr6:116114632 | C | T | 102 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0137 others(99): Show |
107 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.365-1059C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114632 | |||||||
| chr6:116114648 | G | A | 25 | a0001c0001t0002g0055 a0001c0001t0002g0237 a0001c0001t0002g0238 others(22): Show |
25 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.365-1043G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114648 | |||||||
| chr6:116114794 | G | A | 103 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0137 others(100): Show |
108 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.365-897G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114794 | |||||||
| chr6:116114854 | G | A | 2 | a0001c0001t0007g0244 a0001c0001t0014g0245 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.365-837G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114854 | |||||||
| chr6:116114974 | A | G | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.365-717A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114974 | |||||||
| chr6:116115156 | G | T | 2 | a0001c0001t0006g0011 a0001c0001t0006g0012 |
2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.365-535G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116115156 | |||||||
| chr6:116115234 | A | ATTTGTC | 196 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0119 others(193): Show |
201 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.365-455_365-454ins others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 116115234 | ||||||
| chr6:116115257 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.365-434A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116115257 | |||||||
| chr6:116115370 | T | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.365-321T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116115370 | |||||||
| chr6:116115433 | A | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.365-258A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116115433 | |||||||
| chr6:116115679 | G | T | 1 | a0001c0001t0007g0244 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.365-12G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116115679 | |||||||
| chr6:116115781 | A | T | 18 | a0001c0001t0003g0009 a0001c0001t0003g0286 a0001c0001t0004g0157 others(15): Show |
18 | HG00099.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.444+11A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116115781 | |||||||
| chr6:116115849 | A | G | 13 | a0001c0001t0001g0280 a0001c0001t0003g0289 a0001c0001t0006g0006 others(10): Show |
14 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.444+79A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116115849 | |||||||
| chr6:116116124 | G | A | 52 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0098 others(49): Show |
54 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.444+354G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116124 | |||||||
| chr6:116116164 | G | A | 2 | a0001c0001t0018g0274 a0001c0001t0035g0290 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.444+394G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116164 | |||||||
| chr6:116116343 | T | TAAAAATA others(305): Show |
1 | a0001c0001t0001g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.444+591_444+592ins others(312): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr6 | 116116343 | ||||||
| chr6:116116343 | T | TAAAAATA others(347): Show |
2 | a0001c0001t0001g0121 a0001c0001t0024g0122 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.444+591_444+592ins others(354): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr6 | 116116343 | ||||||
| chr6:116116365 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.444+595C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116365 | |||||||
| chr6:116116418 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.444+648C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116418 | |||||||
| chr6:116116421 | A | G | 4 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0006g0054 others(1): Show |
4 | NA18971.hp2 NA18978.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+651A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116421 | |||||||
| chr6:116116428 | A | G | 57 | a0001c0001t0001g0074 a0001c0001t0001g0280 a0001c0001t0002g0004 others(54): Show |
60 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.444+658A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116428 | |||||||
| chr6:116116458 | A | G | 53 | a0001c0001t0001g0074 a0001c0001t0001g0280 a0001c0001t0002g0004 others(50): Show |
56 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.444+688A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116458 | |||||||
| chr6:116116566 | C | T | 2 | a0001c0001t0003g0289 a0001c0001t0006g0118 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.444+796C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116566 | |||||||
| chr6:116116709 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.444+939A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116709 | |||||||
| chr6:116116752 | T | C | 53 | a0001c0001t0001g0074 a0001c0001t0001g0280 a0001c0001t0002g0004 others(50): Show |
56 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.444+982T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116752 | |||||||
| chr6:116116753 | G | A | 2 | a0001c0001t0018g0274 a0001c0001t0035g0290 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.444+983G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116753 | |||||||
| chr6:116116877 | G | A | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.445-984G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116877 | |||||||
| chr6:116117151 | T | C | 3 | a0001c0001t0013g0069 a0001c0001t0013g0070 a0001c0001t0013g0071 |
3 | HG02615.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.445-710T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117151 | |||||||
| chr6:116117162 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.445-699A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117162 | |||||||
| chr6:116117199 | A | G | 57 | a0001c0001t0001g0074 a0001c0001t0001g0280 a0001c0001t0002g0004 others(54): Show |
60 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-662A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117199 | |||||||
| chr6:116117203 | A | G | 1 | a0001c0001t0010g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.445-658A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117203 | |||||||
| chr6:116117242 | T | C | 1 | a0001c0001t0003g0021 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.445-619T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117242 | |||||||
| chr6:116117397 | A | G | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.445-464A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117397 | |||||||
| chr6:116117506 | T | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0233 |
5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-355T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117506 | |||||||
| chr6:116117549 | T | C | 1 | a0001c0001t0004g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.445-312T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117549 | |||||||
| chr6:116117600 | G | A | 1 | a0001c0001t0035g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.445-261G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117600 | |||||||
| chr6:116117602 | C | G | 1 | a0001c0001t0002g0049 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.445-259C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117602 | |||||||
| chr6:116117797 | G | A | 2 | a0001c0001t0018g0274 a0001c0001t0035g0290 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.445-64G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117797 | |||||||
| chr6:116117972 | A | G | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+27A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116117972 | |||||||
| chr6:116117997 | G | T | 1 | a0001c0001t0002g0218 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.529+52G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116117997 | |||||||
| chr6:116118015 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.529+70A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118015 | |||||||
| chr6:116118057 | A | G | 181 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0137 others(178): Show |
186 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.529+112A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118057 | |||||||
| chr6:116118155 | T | C | 2 | a0001c0001t0007g0244 a0001c0001t0014g0245 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.529+210T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118155 | |||||||
| chr6:116118331 | G | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+386G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118331 | |||||||
| chr6:116118411 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.529+466A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118411 | |||||||
| chr6:116118494 | G | A | 2 | a0001c0001t0018g0274 a0001c0001t0035g0290 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+549G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118494 | |||||||
| chr6:116118581 | C | CAT | 143 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0137 others(140): Show |
148 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.529+637_529+638ins others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116118581 | ||||||
| chr6:116118807 | T | G | 7 | a0001c0001t0003g0002 a0001c0001t0003g0022 a0001c0001t0003g0023 others(4): Show |
8 | NA18947.hp1 NA18957.hp1 NA19003.hp1 others(5): Show |
intron_variant | MODIFIER | c.529+862T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118807 | |||||||
| chr6:116118844 | A | C | 57 | a0001c0001t0001g0074 a0001c0001t0001g0280 a0001c0001t0002g0004 others(54): Show |
60 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.529+899A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118844 | |||||||
| chr6:116119031 | T | C | 2 | a0001c0001t0018g0274 a0001c0001t0035g0290 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+1086T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119031 | |||||||
| chr6:116119047 | C | T | 14 | a0001c0001t0002g0049 a0001c0001t0002g0053 a0001c0001t0004g0051 others(11): Show |
14 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+1102C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119047 | |||||||
| chr6:116119048 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.529+1103G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119048 | |||||||
| chr6:116119657 | C | T | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+1712C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119657 | |||||||
| chr6:116119756 | A | T | 1 | a0001c0001t0020g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.529+1811A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119756 | |||||||
| chr6:116119757 | A | AT | 11 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(8): Show |
11 | HG01099.hp2 HG01106.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+1822dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116119757 | ||||||
| chr6:116119758 | T | A | 1 | a0001c0001t0020g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.529+1813T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119758 | |||||||
| chr6:116119827 | A | G | 3 | a0001c0001t0002g0049 a0001c0001t0004g0051 a0001c0001t0029g0050 |
3 | HG01099.hp2 HG01106.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.529+1882A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119827 | |||||||
| chr6:116119916 | T | C | 2 | a0001c0001t0004g0157 a0001c0001t0004g0183 |
2 | NA18991.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.529+1971T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119916 | |||||||
| chr6:116119960 | C | T | 1 | a0001c0001t0003g0045 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.529+2015C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119960 | |||||||
| chr6:116120066 | T | TGGG | 285 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(282): Show |
293 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.529+2122_529+2123i others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116120066 | ||||||
| chr6:116120076 | C | G | 1 | a0001c0001t0001g0220 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.529+2131C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120076 | |||||||
| chr6:116120189 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.529+2244C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120189 | |||||||
| chr6:116120265 | A | G | 2 | a0001c0001t0018g0274 a0001c0001t0035g0290 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+2320A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120265 | |||||||
| chr6:116120281 | A | G | 1 | a0001c0001t0002g0271 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.529+2336A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120281 | |||||||
| chr6:116120295 | C | A | 1 | a0001c0001t0003g0022 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.529+2350C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120295 | |||||||
| chr6:116120307 | C | G | 5 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(2): Show |
5 | HG00738.hp1 HG02258.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+2362C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120307 | |||||||
| chr6:116120483 | C | G | 77 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0055 others(74): Show |
79 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.529+2538C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120483 | |||||||
| chr6:116121383 | G | T | 1 | a0001c0001t0006g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.529+3438G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116121383 | |||||||
| chr6:116121491 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.529+3546C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116121491 | |||||||
| chr6:116121734 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+3789C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116121734 | |||||||
| chr6:116121972 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.529+4027C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116121972 | |||||||
| chr6:116122145 | A | G | 2 | a0001c0001t0018g0274 a0001c0001t0035g0290 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+4200A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122145 | |||||||
| chr6:116122175 | A | G | 2 | a0001c0001t0007g0244 a0001c0001t0014g0245 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.529+4230A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122175 | |||||||
| chr6:116122191 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.529+4246A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122191 | |||||||
| chr6:116122221 | T | C | 1 | a0001c0001t0003g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.529+4276T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122221 | |||||||
| chr6:116122376 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0184 |
2 | NA18991.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.529+4431G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122376 | |||||||
| chr6:116122385 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.529+4440G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122385 | |||||||
| chr6:116122572 | T | A | 143 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0137 others(140): Show |
148 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.529+4627T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122572 | |||||||
| chr6:116122577 | C | A | 23 | a0001c0001t0002g0055 a0001c0001t0002g0237 a0001c0001t0002g0238 others(20): Show |
23 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.529+4632C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122577 | |||||||
| chr6:116122672 | G | A | 2 | a0001c0001t0018g0274 a0001c0001t0035g0290 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+4727G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122672 | |||||||
| chr6:116122849 | A | C | 3 | a0001c0001t0016g0116 a0001c0001t0016g0117 a0001c0001t0025g0115 |
3 | HG01891.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.529+4904A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122849 | |||||||
| chr6:116122901 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.529+4956A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122901 | |||||||
| chr6:116122903 | A | C | 1 | a0001c0001t0006g0138 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.529+4958A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122903 | |||||||
| chr6:116122922 | G | C | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+4977G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122922 | |||||||
| chr6:116122954 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+5009G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122954 | |||||||
| chr6:116123005 | A | C | 51 | a0001c0001t0001g0074 a0001c0001t0001g0280 a0001c0001t0002g0004 others(48): Show |
54 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.529+5060A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123005 | |||||||
| chr6:116123215 | A | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+5270A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123215 | |||||||
| chr6:116123444 | T | A | 143 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0137 others(140): Show |
148 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.529+5499T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123444 | |||||||
| chr6:116123486 | G | A | 1 | a0001c0001t0003g0026 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.529+5541G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123486 | |||||||
| chr6:116123630 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+5685T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123630 | |||||||
| chr6:116123734 | A | G | 2 | a0001c0001t0003g0016 a0001c0001t0003g0044 |
2 | NA18942.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.529+5789A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123734 | |||||||
| chr6:116123922 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+5977G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123922 | |||||||
| chr6:116123990 | A | G | 23 | a0001c0001t0002g0055 a0001c0001t0002g0237 a0001c0001t0002g0238 others(20): Show |
23 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.529+6045A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123990 | |||||||
| chr6:116124016 | G | A | 1 | a0001c0003t0014g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.529+6071G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124016 | |||||||
| chr6:116124106 | T | A | 1 | a0001c0001t0001g0257 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.529+6161T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124106 | |||||||
| chr6:116124560 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+6615A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124560 | |||||||
| chr6:116124733 | A | G | 1 | a0001c0001t0002g0270 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.529+6788A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124733 | |||||||
| chr6:116124792 | T | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+6847T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124792 | |||||||
| chr6:116124842 | G | A | 1 | a0001c0001t0003g0017 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.529+6897G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124842 | |||||||
| chr6:116124851 | T | C | 1 | a0001c0001t0002g0072 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.529+6906T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124851 | |||||||
| chr6:116124852 | G | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+6907G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124852 | |||||||
| chr6:116124887 | G | T | 1 | a0001c0001t0002g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.529+6942G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124887 | |||||||
| chr6:116125009 | A | G | 1 | a0001c0001t0003g0002 | 2 | NA18957.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.529+7064A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125009 | |||||||
| chr6:116125035 | A | T | 1 | a0001c0001t0001g0280 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.529+7090A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125035 | |||||||
| chr6:116125143 | A | G | 1 | a0001c0001t0010g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.529+7198A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125143 | |||||||
| chr6:116125199 | C | T | 1 | a0001c0001t0004g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.529+7254C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125199 | |||||||
| chr6:116125235 | G | A | 8 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+7290G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125235 | |||||||
| chr6:116125296 | A | G | 1 | a0001c0001t0017g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.529+7351A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125296 | |||||||
| chr6:116125326 | C | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+7381C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125326 | |||||||
| chr6:116125413 | A | G | 143 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0137 others(140): Show |
148 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.529+7468A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125413 | |||||||
| chr6:116125470 | A | C | 2 | a0001c0001t0018g0274 a0001c0001t0035g0290 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+7525A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125470 | |||||||
| chr6:116125562 | AT | A | 9 | a0001c0001t0001g0280 a0001c0001t0006g0158 a0001c0001t0007g0128 others(6): Show |
9 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+7619delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116125562 | ||||||
| chr6:116125936 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+7991C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125936 | |||||||
| chr6:116125952 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.529+8007C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125952 | |||||||
| chr6:116126193 | C | G | 53 | a0001c0001t0001g0074 a0001c0001t0001g0280 a0001c0001t0002g0004 others(50): Show |
56 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.529+8248C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126193 | |||||||
| chr6:116126355 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+8410C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126355 | |||||||
| chr6:116126411 | A | G | 19 | a0001c0001t0002g0049 a0001c0001t0002g0053 a0001c0001t0004g0051 others(16): Show |
19 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.529+8466A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126411 | |||||||
| chr6:116126449 | G | A | 1 | a0001c0001t0006g0006 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.529+8504G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126449 | |||||||
| chr6:116126799 | G | T | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+8854G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126799 | |||||||
| chr6:116126859 | A | G | 5 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(2): Show |
5 | HG02109.hp2 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+8914A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126859 | |||||||
| chr6:116126859 | A | T | 2 | a0001c0001t0007g0244 a0001c0001t0014g0245 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.529+8914A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126859 | |||||||
| chr6:116126934 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.529+8989A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126934 | |||||||
| chr6:116126957 | G | A | 5 | a0001c0001t0002g0098 a0001c0001t0005g0095 a0001c0001t0005g0097 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+9012G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126957 | |||||||
| chr6:116127117 | G | T | 1 | a0001c0001t0002g0277 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.529+9172G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116127117 | |||||||
| chr6:116127196 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.529+9251A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116127196 | |||||||
| chr6:116127333 | A | G | 1 | a0001c0001t0002g0005 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.529+9388A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116127333 | |||||||
| chr6:116127480 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+9535A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116127480 | |||||||
| chr6:116127813 | G | A | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+9868G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116127813 | |||||||
| chr6:116128157 | A | G | 9 | a0001c0001t0001g0280 a0001c0001t0006g0158 a0001c0001t0007g0128 others(6): Show |
9 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+10212A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128157 | |||||||
| chr6:116128185 | G | T | 1 | a0001c0001t0005g0133 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.529+10240G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128185 | |||||||
| chr6:116128192 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+10247T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128192 | |||||||
| chr6:116128342 | C | T | 2 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
2 | HG01258.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.529+10397C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128342 | |||||||
| chr6:116128393 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.529+10448A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128393 | |||||||
| chr6:116128541 | A | G | 1 | a0001c0001t0003g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.529+10596A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128541 | |||||||
| chr6:116128566 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+10621T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128566 | |||||||
| chr6:116128720 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.529+10775C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128720 | |||||||
| chr6:116128814 | G | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+10869G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128814 | |||||||
| chr6:116129033 | C | A | 1 | a0001c0001t0002g0073 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.529+11088C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129033 | |||||||
| chr6:116129043 | T | C | 3 | a0001c0001t0020g0230 a0001c0001t0020g0236 a0001c0001t0033g0241 |
3 | HG01074.hp1 HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+11098T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129043 | |||||||
| chr6:116129153 | A | T | 3 | a0001c0001t0007g0244 a0001c0001t0018g0274 a0001c0001t0035g0290 |
3 | HG02145.hp1 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+11208A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129153 | |||||||
| chr6:116129252 | T | C | 1 | a0001c0001t0010g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.529+11307T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129252 | |||||||
| chr6:116129515 | A | G | 4 | a0001c0001t0011g0090 a0001c0001t0011g0091 a0001c0001t0011g0211 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+11570A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129515 | |||||||
| chr6:116129592 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.529+11647T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129592 | |||||||
| chr6:116129615 | C | A | 3 | a0001c0001t0007g0244 a0001c0001t0018g0274 a0001c0001t0035g0290 |
3 | HG02145.hp1 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+11670C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129615 | |||||||
| chr6:116129909 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.529+11964G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129909 | |||||||
| chr6:116129976 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+12031A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129976 | |||||||
| chr6:116130050 | A | G | 14 | a0001c0001t0001g0280 a0001c0001t0003g0289 a0001c0001t0006g0006 others(11): Show |
15 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.529+12105A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130050 | |||||||
| chr6:116130194 | T | C | 1 | a0001c0001t0003g0014 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.529+12249T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130194 | |||||||
| chr6:116130279 | A | G | 56 | a0001c0001t0001g0280 a0001c0001t0002g0004 a0001c0001t0002g0005 others(53): Show |
59 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.529+12334A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130279 | |||||||
| chr6:116130339 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+12394G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130339 | |||||||
| chr6:116130349 | T | C | 93 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0055 others(90): Show |
95 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.529+12404T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130349 | |||||||
| chr6:116130449 | G | GT | 20 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(17): Show |
22 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.529+12512dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116130449 | ||||||
| chr6:116130553 | G | T | 1 | a0001c0001t0001g0259 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.529+12608G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130553 | |||||||
| chr6:116130658 | T | G | 7 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.529+12713T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130658 | |||||||
| chr6:116130703 | A | G | 7 | a0001c0001t0001g0162 a0001c0001t0001g0179 a0001c0001t0001g0222 others(4): Show |
7 | HG01192.hp2 HG01243.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.529+12758A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130703 | |||||||
| chr6:116130776 | A | G | 1 | a0001c0001t0007g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.529+12831A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130776 | |||||||
| chr6:116130921 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.529+12976G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130921 | |||||||
| chr6:116130991 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+13046G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130991 | |||||||
| chr6:116131040 | T | G | 149 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0001g0280 others(146): Show |
154 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.529+13095T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131040 | |||||||
| chr6:116131106 | C | T | 2 | a0001c0001t0004g0157 a0001c0001t0004g0183 |
2 | NA18991.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.529+13161C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131106 | |||||||
| chr6:116131112 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+13167T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131112 | |||||||
| chr6:116131223 | A | G | 2 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
2 | HG01258.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.529+13278A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131223 | |||||||
| chr6:116131261 | G | A | 4 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | NA18947.hp2 NA19067.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+13316G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131261 | |||||||
| chr6:116131270 | A | G | 1 | a0001c0001t0006g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.529+13325A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131270 | |||||||
| chr6:116131355 | T | G | 1 | a0001c0001t0018g0274 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+13410T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131355 | |||||||
| chr6:116131383 | T | C | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+13438T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131383 | |||||||
| chr6:116131385 | T | C | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+13440T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131385 | |||||||
| chr6:116131398 | A | G | 23 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(20): Show |
25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.529+13453A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131398 | |||||||
| chr6:116131434 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+13489A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131434 | |||||||
| chr6:116131495 | C | A | 150 | a0001c0001t0001g0031 a0001c0001t0001g0280 a0001c0001t0002g0004 others(147): Show |
155 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.529+13550C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131495 | |||||||
| chr6:116131870 | A | G | 1 | a0001c0001t0008g0010 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.529+13925A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131870 | |||||||
| chr6:116131878 | A | G | 2 | a0001c0001t0019g0149 a0001c0001t0019g0150 |
2 | HG01515.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.529+13933A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131878 | |||||||
| chr6:116132003 | T | A | 3 | a0001c0001t0013g0069 a0001c0001t0013g0070 a0001c0001t0013g0071 |
3 | HG02615.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.529+14058T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132003 | |||||||
| chr6:116132068 | T | C | 20 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(17): Show |
22 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.529+14123T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132068 | |||||||
| chr6:116132144 | G | T | 1 | a0001c0001t0004g0043 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.529+14199G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132144 | |||||||
| chr6:116132666 | G | C | 1 | a0001c0001t0002g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.529+14721G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132666 | |||||||
| chr6:116132805 | C | G | 1 | a0001c0001t0002g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.529+14860C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132805 | |||||||
| chr6:116132825 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0210 a0001c0001t0034g0279 |
3 | HG02074.hp2 HG03130.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.529+14880C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132825 | |||||||
| chr6:116132880 | A | T | 1 | a0001c0001t0002g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.529+14935A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132880 | |||||||
| chr6:116133007 | T | C | 3 | a0001c0001t0003g0016 a0001c0001t0003g0027 a0001c0001t0003g0044 |
3 | NA18942.hp2 NA18983.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.529+15062T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133007 | |||||||
| chr6:116133028 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.529+15083G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133028 | |||||||
| chr6:116133262 | C | G | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+15317C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133262 | |||||||
| chr6:116133297 | C | A | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+15352C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133297 | |||||||
| chr6:116133425 | G | A | 196 | a0001c0001t0001g0031 a0001c0001t0001g0119 a0001c0001t0001g0121 others(193): Show |
201 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.529+15480G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133425 | |||||||
| chr6:116133459 | G | A | 1 | a0001c0001t0005g0247 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.529+15514G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133459 | |||||||
| chr6:116133496 | C | T | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+15551C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133496 | |||||||
| chr6:116133514 | C | T | 3 | a0001c0001t0006g0006 a0001c0001t0014g0245 a0001c0001t0018g0274 |
4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+15569C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133514 | |||||||
| chr6:116133521 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+15576G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133521 | |||||||
| chr6:116133583 | C | T | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+15638C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133583 | |||||||
| chr6:116133714 | G | C | 2 | a0001c0001t0007g0268 a0001c0001t0007g0269 |
2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.529+15769G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133714 | |||||||
| chr6:116133768 | A | G | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+15823A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133768 | |||||||
| chr6:116133823 | C | G | 1 | a0001c0001t0006g0138 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.529+15878C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133823 | |||||||
| chr6:116133916 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+15971T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133916 | |||||||
| chr6:116134239 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.529+16294A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134239 | |||||||
| chr6:116134385 | T | A | 91 | a0001c0001t0001g0031 a0001c0001t0002g0055 a0001c0001t0002g0098 others(88): Show |
93 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.529+16440T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134385 | |||||||
| chr6:116134490 | A | C | 1 | a0001c0003t0014g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.529+16545A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134490 | |||||||
| chr6:116134550 | T | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+16605T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134550 | |||||||
| chr6:116134630 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.529+16685A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134630 | |||||||
| chr6:116134745 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.529+16800G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134745 | |||||||
| chr6:116134902 | A | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG03654.hp1 HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.529+16957A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134902 | |||||||
| chr6:116134937 | A | G | 48 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(45): Show |
50 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.529+16992A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134937 | |||||||
| chr6:116135052 | T | C | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+17107T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135052 | |||||||
| chr6:116135172 | G | A | 153 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0005 others(150): Show |
158 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.529+17227G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135172 | |||||||
| chr6:116135341 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+17396T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135341 | |||||||
| chr6:116135385 | AT | A | 4 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0006g0054 others(1): Show |
4 | NA18971.hp2 NA18978.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+17448delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135385 | ||||||
| chr6:116135420 | A | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+17475A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135420 | |||||||
| chr6:116135431 | T | C | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+17486T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135431 | |||||||
| chr6:116135440 | C | T | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+17495C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135440 | |||||||
| chr6:116135441 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+17496A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135441 | |||||||
| chr6:116135478 | T | C | 1 | a0001c0001t0006g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.529+17533T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135478 | |||||||
| chr6:116135557 | C | A | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+17612C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135557 | |||||||
| chr6:116135730 | A | G | 1 | a0001c0001t0002g0089 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.529+17785A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135730 | |||||||
| chr6:116135734 | T | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+17789T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135734 | |||||||
| chr6:116135781 | T | C | 3 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 |
3 | NA18947.hp1 NA19088.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.529+17836T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135781 | |||||||
| chr6:116135834 | G | GAT | 33 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0093 others(30): Show |
35 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.529+17927_529+1792 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135834 | G | GATAT | 21 | a0001c0001t0001g0007 a0001c0001t0001g0094 a0001c0001t0001g0137 others(18): Show |
22 | HG00741.hp1 HG01106.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.529+17925_529+1792 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135834 | G | GATATATA others(3): Show |
4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | HG00558.hp1 HG03704.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+17919_529+1792 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135834 | G | GATATATA others(5): Show |
1 | a0001c0001t0001g0228 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.529+17917_529+1792 others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135834 | G | GATATATA others(53): Show |
1 | a0001c0001t0014g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.529+17903_529+1790 others(64): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135834 | GAT | G | 18 | a0001c0001t0001g0169 a0001c0001t0001g0186 a0001c0001t0001g0187 others(15): Show |
18 | HG01175.hp2 HG01346.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.529+17927_529+1792 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135834 | GATAT | G | 41 | a0001c0001t0001g0031 a0001c0001t0002g0098 a0001c0001t0003g0002 others(38): Show |
43 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.529+17925_529+1792 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135834 | GATATAT | G | 29 | a0001c0001t0002g0055 a0001c0001t0002g0246 a0001c0001t0002g0261 others(26): Show |
29 | HG00099.hp2 HG00741.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.529+17923_529+1792 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135834 | GATATATA others(1): Show |
G | 7 | a0001c0001t0001g0280 a0001c0001t0002g0263 a0001c0001t0002g0264 others(4): Show |
7 | HG02055.hp2 HG04199.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.529+17921_529+1792 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135834 | GATATATA others(3): Show |
G | 3 | a0001c0001t0002g0262 a0001c0001t0020g0230 a0001c0001t0020g0236 |
3 | HG02735.hp2 HG03654.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.529+17919_529+1792 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135834 | GATATATA others(7): Show |
G | 13 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(10): Show |
13 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.529+17915_529+1792 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135834 | GATATATA others(9): Show |
G | 2 | a0001c0001t0001g0220 a0001c0001t0009g0107 |
2 | HG02809.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.529+17913_529+1792 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135834 | GATATATA others(17): Show |
G | 1 | a0001c0001t0002g0089 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.529+17905_529+1792 others(28): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135834 | GATATATA others(21): Show |
G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0163 others(9): Show |
12 | HG00438.hp2 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.529+17901_529+1792 others(32): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | ||||||
| chr6:116135847 | A | ATGTATAT others(59): Show |
1 | a0001c0001t0018g0274 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+17903_529+1790 others(70): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135847 | ||||||
| chr6:116135847 | A | ATGTATAT others(55): Show |
1 | a0001c0001t0006g0006 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.529+17903_529+1790 others(66): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135847 | ||||||
| chr6:116135847 | A | G | 22 | a0001c0001t0002g0005 a0001c0001t0002g0067 a0001c0001t0002g0068 others(19): Show |
23 | HG00280.hp1 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.529+17902A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135847 | |||||||
| chr6:116135848 | TATATATA others(19): Show |
T | 1 | a0001c0001t0036g0136 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.529+17905_529+1793 others(30): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135848 | ||||||
| chr6:116135849 | A | G | 11 | a0001c0001t0006g0118 a0001c0001t0006g0158 a0001c0001t0007g0128 others(8): Show |
11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+17904A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135849 | |||||||
| chr6:116135852 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+17907T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135852 | |||||||
| chr6:116135853 | A | G | 11 | a0001c0001t0003g0289 a0001c0001t0006g0118 a0001c0001t0006g0158 others(8): Show |
11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+17908A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135853 | |||||||
| chr6:116135857 | A | G | 1 | a0001c0001t0003g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.529+17912A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135857 | |||||||
| chr6:116135864 | T | C | 1 | a0001c0001t0003g0021 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.529+17919T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135864 | |||||||
| chr6:116135864 | TATATATA others(3): Show |
T | 3 | a0001c0001t0002g0277 a0001c0001t0015g0282 a0001c0001t0015g0287 |
3 | HG00738.hp1 HG02486.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.529+17921_529+1793 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135864 | ||||||
| chr6:116135866 | T | C | 5 | a0001c0001t0003g0021 a0001c0001t0003g0030 a0001c0001t0005g0134 others(2): Show |
5 | HG03239.hp2 HG04115.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+17921T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135866 | |||||||
| chr6:116135866 | TATATATA others(1): Show |
T | 8 | a0001c0001t0001g0165 a0001c0001t0002g0056 a0001c0001t0002g0057 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.529+17923_529+1793 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135866 | ||||||
| chr6:116135868 | T | C | 66 | a0001c0001t0001g0031 a0001c0001t0002g0098 a0001c0001t0003g0002 others(63): Show |
68 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.529+17923T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135868 | |||||||
| chr6:116135868 | TATATAC | T | 4 | a0001c0001t0007g0244 a0001c0001t0010g0100 a0001c0001t0010g0101 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+17925_529+1793 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135868 | ||||||
| chr6:116135870 | T | C | 89 | a0001c0001t0001g0031 a0001c0001t0002g0055 a0001c0001t0002g0098 others(86): Show |
91 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.529+17925T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135870 | |||||||
| chr6:116135870 | TATAC | T | 15 | a0001c0001t0001g0125 a0001c0001t0001g0145 a0001c0001t0001g0146 others(12): Show |
16 | HG02451.hp2 HG02559.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.529+17927_529+1793 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135870 | ||||||
| chr6:116135872 | T | C | 107 | a0001c0001t0001g0031 a0001c0001t0002g0055 a0001c0001t0002g0098 others(104): Show |
109 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.529+17927T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135872 | |||||||
| chr6:116135872 | T | TATATACA others(5): Show |
1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+17928_529+1792 others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135872 | ||||||
| chr6:116135872 | TAC | T | 34 | a0001c0001t0001g0119 a0001c0001t0001g0161 a0001c0001t0001g0177 others(31): Show |
34 | HG00280.hp1 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.529+17933_529+1793 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135872 | ||||||
| chr6:116135874 | C | T | 22 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0126 others(19): Show |
24 | HG00642.hp1 HG00642.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.529+17929C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135874 | |||||||
| chr6:116135880 | T | C | 1 | a0001c0001t0027g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.529+17935T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135880 | |||||||
| chr6:116135884 | C | T | 1 | a0001c0001t0027g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.529+17939C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135884 | |||||||
| chr6:116135903 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.529+17958A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135903 | |||||||
| chr6:116136099 | C | T | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+18154C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116136099 | |||||||
| chr6:116136312 | G | T | 5 | a0001c0001t0010g0102 a0001c0001t0010g0103 a0001c0001t0010g0104 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+18367G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116136312 | |||||||
| chr6:116136468 | G | GT | 90 | a0001c0001t0001g0031 a0001c0001t0002g0055 a0001c0001t0002g0098 others(87): Show |
92 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.529+18531dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116136468 | ||||||
| chr6:116136476 | T | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+18531T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116136476 | |||||||
| chr6:116136511 | C | T | 1 | a0001c0001t0002g0262 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.529+18566C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116136511 | |||||||
| chr6:116136551 | G | T | 1 | a0001c0001t0010g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.529+18606G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116136551 | |||||||
| chr6:116136767 | G | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+18822G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116136767 | |||||||
| chr6:116137005 | A | C | 2 | a0001c0001t0002g0065 a0001c0001t0002g0066 |
2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.529+19060A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116137005 | |||||||
| chr6:116137254 | T | C | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+19309T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116137254 | |||||||
| chr6:116137807 | C | T | 2 | a0001c0001t0007g0268 a0001c0001t0007g0269 |
2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.529+19862C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116137807 | |||||||
| chr6:116137855 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+19910A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116137855 | |||||||
| chr6:116137952 | G | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+20007G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116137952 | |||||||
| chr6:116138027 | A | G | 154 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0005 others(151): Show |
159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+20082A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138027 | |||||||
| chr6:116138046 | C | CCCG | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+20104_529+2010 others(7): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116138046 | ||||||
| chr6:116138048 | C | T | 5 | a0001c0001t0002g0098 a0001c0001t0005g0095 a0001c0001t0005g0097 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+20103C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138048 | |||||||
| chr6:116138105 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+20160A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138105 | |||||||
| chr6:116138195 | C | T | 91 | a0001c0001t0001g0031 a0001c0001t0002g0055 a0001c0001t0002g0098 others(88): Show |
93 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.529+20250C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138195 | |||||||
| chr6:116138324 | A | C | 1 | a0001c0001t0035g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.529+20379A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138324 | |||||||
| chr6:116138607 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.529+20662A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138607 | |||||||
| chr6:116138614 | T | C | 2 | a0001c0001t0003g0026 a0001c0001t0003g0048 |
2 | NA18962.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.529+20669T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138614 | |||||||
| chr6:116138703 | A | G | 1 | a0001c0001t0003g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.529+20758A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138703 | |||||||
| chr6:116138772 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+20827T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138772 | |||||||
| chr6:116139032 | A | G | 1 | a0001c0001t0004g0043 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.529+21087A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139032 | |||||||
| chr6:116139099 | A | C | 18 | a0001c0001t0003g0009 a0001c0001t0003g0286 a0001c0001t0004g0157 others(15): Show |
18 | HG00099.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.529+21154A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139099 | |||||||
| chr6:116139101 | A | C | 18 | a0001c0001t0003g0009 a0001c0001t0003g0286 a0001c0001t0004g0157 others(15): Show |
18 | HG00099.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.529+21156A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139101 | |||||||
| chr6:116139177 | T | C | 13 | a0001c0001t0002g0049 a0001c0001t0002g0053 a0001c0001t0004g0051 others(10): Show |
13 | HG00642.hp2 HG00741.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.529+21232T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139177 | |||||||
| chr6:116139256 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+21311A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139256 | |||||||
| chr6:116139493 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+21548A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139493 | |||||||
| chr6:116139571 | A | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+21626A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139571 | |||||||
| chr6:116139657 | T | C | 11 | a0001c0001t0003g0289 a0001c0001t0006g0118 a0001c0001t0006g0158 others(8): Show |
11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+21712T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139657 | |||||||
| chr6:116139670 | A | G | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+21725A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139670 | |||||||
| chr6:116139926 | G | A | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+21981G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139926 | |||||||
| chr6:116140032 | T | C | 1 | a0001c0001t0039g0075 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.529+22087T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140032 | |||||||
| chr6:116140241 | C | A | 23 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(20): Show |
25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.529+22296C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140241 | |||||||
| chr6:116140314 | T | C | 176 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0005 others(173): Show |
181 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.529+22369T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140314 | |||||||
| chr6:116140335 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.529+22390C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140335 | |||||||
| chr6:116140393 | C | T | 11 | a0001c0001t0003g0289 a0001c0001t0006g0118 a0001c0001t0006g0158 others(8): Show |
11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+22448C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140393 | |||||||
| chr6:116140398 | A | G | 1 | a0001c0003t0014g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.529+22453A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140398 | |||||||
| chr6:116140451 | G | A | 67 | a0001c0001t0001g0031 a0001c0001t0002g0098 a0001c0001t0003g0002 others(64): Show |
69 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.529+22506G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140451 | |||||||
| chr6:116140465 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+22520A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140465 | |||||||
| chr6:116140475 | C | T | 16 | a0001c0001t0002g0004 a0001c0001t0002g0067 a0001c0001t0002g0073 others(13): Show |
17 | HG00642.hp1 HG00738.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.529+22530C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140475 | |||||||
| chr6:116140812 | G | A | 1 | a0001c0001t0003g0048 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.529+22867G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140812 | |||||||
| chr6:116140920 | A | C | 154 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0005 others(151): Show |
159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+22975A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140920 | |||||||
| chr6:116140947 | T | C | 3 | a0001c0001t0013g0069 a0001c0001t0013g0070 a0001c0001t0013g0071 |
3 | HG02615.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.529+23002T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140947 | |||||||
| chr6:116140995 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.529+23050A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140995 | |||||||
| chr6:116141112 | C | T | 1 | a0001c0001t0018g0274 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+23167C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141112 | |||||||
| chr6:116141263 | A | AT | 14 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(11): Show |
14 | HG01884.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+23330dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141263 | ||||||
| chr6:116141397 | T | C | 1 | a0001c0001t0003g0286 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.529+23452T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141397 | |||||||
| chr6:116141489 | T | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+23544T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141489 | |||||||
| chr6:116141601 | A | G | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+23656A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141601 | |||||||
| chr6:116141629 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+23684T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141629 | |||||||
| chr6:116141759 | G | GT | 10 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 others(7): Show |
10 | HG00099.hp2 HG01891.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+23826dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141759 | ||||||
| chr6:116141786 | C | T | 1 | a0001c0001t0005g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.529+23841C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141786 | |||||||
| chr6:116141798 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+23853T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141798 | |||||||
| chr6:116141849 | GTC | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02896.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.529+23906_529+2390 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141849 | ||||||
| chr6:116141885 | A | AAC | 44 | a0001c0001t0001g0119 a0001c0001t0001g0124 a0001c0001t0001g0125 others(41): Show |
45 | HG00280.hp1 HG00738.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.529+23981_529+2398 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | ||||||
| chr6:116141885 | A | AACAC | 19 | a0001c0001t0001g0121 a0001c0001t0001g0148 a0001c0001t0001g0186 others(16): Show |
20 | HG00642.hp1 HG00642.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.529+23979_529+2398 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | ||||||
| chr6:116141885 | A | AACACAC | 14 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(11): Show |
14 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.529+23977_529+2398 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | ||||||
| chr6:116141885 | A | AACACACA others(1): Show |
8 | a0001c0001t0001g0126 a0001c0001t0002g0277 a0001c0001t0003g0289 others(5): Show |
8 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+23975_529+2398 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | ||||||
| chr6:116141885 | A | AACACACA others(7): Show |
1 | a0001c0001t0009g0110 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.529+23969_529+2398 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | ||||||
| chr6:116141885 | A | AACACACA others(9): Show |
4 | a0001c0001t0003g0111 a0001c0001t0009g0276 a0001c0001t0009g0288 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+23967_529+2398 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | ||||||
| chr6:116141885 | A | AACACACA others(11): Show |
5 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0009g0107 others(2): Show |
5 | HG02630.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+23965_529+2398 others(22): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | ||||||
| chr6:116141885 | A | AACACACA others(13): Show |
1 | a0001c0001t0009g0112 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.529+23963_529+2398 others(24): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | ||||||
| chr6:116141885 | AAC | A | 7 | a0001c0001t0001g0093 a0001c0001t0001g0137 a0001c0001t0001g0179 others(4): Show |
7 | HG01074.hp2 HG02071.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.529+23981_529+2398 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | ||||||
| chr6:116141885 | AACAC | A | 28 | a0001c0001t0001g0196 a0001c0001t0002g0073 a0001c0001t0002g0237 others(25): Show |
28 | HG00323.hp1 HG00323.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.529+23979_529+2398 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | ||||||
| chr6:116141885 | AACACAC | A | 63 | a0001c0001t0001g0031 a0001c0001t0001g0188 a0001c0001t0001g0189 others(60): Show |
65 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.529+23977_529+2398 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | ||||||
| chr6:116141915 | C | A | 3 | a0001c0001t0002g0291 a0001c0001t0017g0062 a0001c0001t0017g0292 |
3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.529+23970C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141915 | |||||||
| chr6:116141926 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.529+23981A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141926 | |||||||
| chr6:116142059 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0024g0122 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.529+24114T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142059 | |||||||
| chr6:116142085 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.529+24140A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142085 | |||||||
| chr6:116142155 | T | A | 117 | a0001c0001t0001g0031 a0001c0001t0002g0055 a0001c0001t0002g0056 others(114): Show |
119 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.529+24210T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142155 | |||||||
| chr6:116142179 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.529+24234T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142179 | |||||||
| chr6:116142238 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.529+24293G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142238 | |||||||
| chr6:116142284 | C | CT | 8 | a0001c0001t0002g0098 a0001c0001t0005g0095 a0001c0001t0005g0097 others(5): Show |
8 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.529+24348dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116142284 | ||||||
| chr6:116142589 | CTG | C | 11 | a0001c0001t0003g0289 a0001c0001t0006g0118 a0001c0001t0006g0158 others(8): Show |
11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+24648_529+2464 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116142589 | ||||||
| chr6:116142724 | T | C | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+24779T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142724 | |||||||
| chr6:116142931 | A | C | 17 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(14): Show |
18 | HG01891.hp1 HG02145.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.529+24986A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142931 | |||||||
| chr6:116142985 | A | G | 1 | a0001c0001t0004g0051 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.529+25040A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142985 | |||||||
| chr6:116143056 | A | T | 23 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(20): Show |
25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.529+25111A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143056 | |||||||
| chr6:116143069 | C | T | 91 | a0001c0001t0001g0031 a0001c0001t0002g0055 a0001c0001t0002g0098 others(88): Show |
93 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.529+25124C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143069 | |||||||
| chr6:116143100 | A | G | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+25155A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143100 | |||||||
| chr6:116143113 | G | A | 2 | a0001c0001t0004g0255 a0001c0001t0008g0256 |
2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.529+25168G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143113 | |||||||
| chr6:116143250 | C | T | 6 | a0001c0001t0003g0015 a0001c0001t0003g0029 a0001c0001t0003g0042 others(3): Show |
6 | HG02055.hp2 HG02895.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.529+25305C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143250 | |||||||
| chr6:116143337 | A | G | 1 | a0001c0001t0003g0025 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.529+25392A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143337 | |||||||
| chr6:116143405 | T | C | 154 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0005 others(151): Show |
159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+25460T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143405 | |||||||
| chr6:116143406 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+25461G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143406 | |||||||
| chr6:116143507 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.529+25562C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143507 | |||||||
| chr6:116143667 | T | C | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+25722T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143667 | |||||||
| chr6:116144177 | A | G | 1 | a0001c0001t0005g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.529+26232A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144177 | |||||||
| chr6:116144241 | C | T | 1 | a0001c0001t0003g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.529+26296C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144241 | |||||||
| chr6:116144257 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.529+26312C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144257 | |||||||
| chr6:116144271 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+26326G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144271 | |||||||
| chr6:116144277 | C | T | 1 | a0001c0001t0007g0244 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.529+26332C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144277 | |||||||
| chr6:116144280 | A | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+26335A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144280 | |||||||
| chr6:116144366 | T | C | 3 | a0001c0001t0002g0291 a0001c0001t0017g0062 a0001c0001t0017g0292 |
3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.529+26421T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144366 | |||||||
| chr6:116144451 | ATGT | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0092 others(57): Show |
63 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.529+26510_529+2651 others(7): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116144451 | ||||||
| chr6:116144466 | A | G | 3 | a0001c0001t0007g0129 a0001c0001t0007g0130 a0001c0001t0007g0131 |
3 | HG02559.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.529+26521A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144466 | |||||||
| chr6:116144489 | G | A | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+26544G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144489 | |||||||
| chr6:116144495 | G | A | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+26550G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144495 | |||||||
| chr6:116144499 | C | CA | 7 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 others(4): Show |
7 | HG02809.hp2 NA18947.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.529+26568dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116144499 | ||||||
| chr6:116144499 | CA | C | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01081.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.529+26568delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116144499 | ||||||
| chr6:116144512 | A | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+26567A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144512 | |||||||
| chr6:116144525 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.529+26580G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144525 | |||||||
| chr6:116144575 | T | C | 1 | a0001c0001t0006g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.529+26630T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144575 | |||||||
| chr6:116144648 | G | A | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+26703G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144648 | |||||||
| chr6:116144807 | G | A | 1 | a0001c0001t0002g0005 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.529+26862G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144807 | |||||||
| chr6:116144914 | G | A | 8 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+26969G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144914 | |||||||
| chr6:116145021 | T | G | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+27076T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145021 | |||||||
| chr6:116145064 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+27119T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145064 | |||||||
| chr6:116145066 | T | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0156 others(10): Show |
16 | HG00558.hp1 NA18942.hp1 NA18957.hp2 others(13): Show |
intron_variant | MODIFIER | c.529+27121T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145066 | |||||||
| chr6:116145091 | T | C | 8 | a0001c0001t0006g0158 a0001c0001t0007g0128 a0001c0001t0007g0129 others(5): Show |
8 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+27146T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145091 | |||||||
| chr6:116145194 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.529+27249C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145194 | |||||||
| chr6:116145217 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+27272A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145217 | |||||||
| chr6:116145506 | G | A | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+27561G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145506 | |||||||
| chr6:116145681 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.529+27736C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145681 | |||||||
| chr6:116145827 | G | A | 23 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(20): Show |
25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.529+27882G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145827 | |||||||
| chr6:116145941 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+27996A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145941 | |||||||
| chr6:116145948 | C | G | 1 | a0001c0001t0001g0281 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.529+28003C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145948 | |||||||
| chr6:116146013 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+28068C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146013 | |||||||
| chr6:116146133 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+28188A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146133 | |||||||
| chr6:116146211 | G | A | 1 | a0001c0001t0010g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.529+28266G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146211 | |||||||
| chr6:116146262 | C | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+28317C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146262 | |||||||
| chr6:116146543 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.529+28598T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146543 | |||||||
| chr6:116146565 | A | C | 3 | a0001c0001t0006g0006 a0001c0001t0014g0245 a0001c0001t0018g0274 |
4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+28620A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146565 | |||||||
| chr6:116146608 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+28663A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146608 | |||||||
| chr6:116146726 | C | G | 1 | a0001c0001t0010g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.529+28781C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146726 | |||||||
| chr6:116146817 | T | G | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+28872T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146817 | |||||||
| chr6:116146827 | A | G | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+28882A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146827 | |||||||
| chr6:116147000 | A | AAT | 175 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0005 others(172): Show |
180 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.529+29068_529+2906 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116147000 | ||||||
| chr6:116147049 | G | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0030 a0001c0001t0007g0244 others(1): Show |
4 | HG02818.hp1 HG03225.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+29104G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147049 | |||||||
| chr6:116147113 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.529+29168A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147113 | |||||||
| chr6:116147152 | A | T | 34 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(31): Show |
36 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.529+29207A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147152 | |||||||
| chr6:116147247 | G | A | 1 | a0001c0001t0008g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.529+29302G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147247 | |||||||
| chr6:116147336 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+29391G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147336 | |||||||
| chr6:116147456 | A | T | 2 | a0001c0001t0003g0009 a0001c0001t0008g0010 |
2 | NA19002.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.529+29511A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147456 | |||||||
| chr6:116147495 | A | T | 1 | a0001c0001t0001g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.529+29550A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147495 | |||||||
| chr6:116147815 | G | A | 7 | a0001c0001t0003g0002 a0001c0001t0003g0022 a0001c0001t0003g0023 others(4): Show |
8 | NA18947.hp1 NA18957.hp1 NA19003.hp1 others(5): Show |
intron_variant | MODIFIER | c.529+29870G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147815 | |||||||
| chr6:116147850 | G | A | 1 | a0001c0001t0005g0133 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.529+29905G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147850 | |||||||
| chr6:116147941 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.529+29996G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147941 | |||||||
| chr6:116147984 | C | CA | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+30051dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116147984 | ||||||
| chr6:116147999 | T | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+30054T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147999 | |||||||
| chr6:116148000 | G | T | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+30055G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148000 | |||||||
| chr6:116148046 | G | T | 1 | a0001c0001t0018g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.529+30101G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148046 | |||||||
| chr6:116148089 | G | A | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+30144G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148089 | |||||||
| chr6:116148146 | A | G | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+30201A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148146 | |||||||
| chr6:116148213 | T | G | 2 | a0001c0001t0003g0009 a0001c0001t0008g0010 |
2 | NA19002.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.529+30268T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148213 | |||||||
| chr6:116148252 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0092 others(54): Show |
60 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.529+30307A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148252 | |||||||
| chr6:116148288 | T | C | 14 | a0001c0001t0002g0055 a0001c0001t0002g0261 a0001c0001t0002g0262 others(11): Show |
14 | HG01515.hp1 HG01934.hp1 HG03688.hp1 others(11): Show |
intron_variant | MODIFIER | c.529+30343T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148288 | |||||||
| chr6:116148338 | A | C | 1 | a0001c0001t0010g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.529+30393A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148338 | |||||||
| chr6:116148421 | A | G | 154 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0005 others(151): Show |
159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+30476A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148421 | |||||||
| chr6:116148429 | A | G | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+30484A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148429 | |||||||
| chr6:116148540 | T | C | 3 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0260 |
3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.529+30595T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148540 | |||||||
| chr6:116148583 | A | G | 1 | a0001c0001t0008g0040 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.529+30638A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148583 | |||||||
| chr6:116148594 | T | C | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+30649T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148594 | |||||||
| chr6:116148740 | C | T | 1 | a0001c0001t0003g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.529+30795C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148740 | |||||||
| chr6:116149288 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.529+31343A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149288 | |||||||
| chr6:116149398 | A | G | 154 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0005 others(151): Show |
159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+31453A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149398 | |||||||
| chr6:116149462 | A | G | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+31517A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149462 | |||||||
| chr6:116149604 | T | G | 16 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(13): Show |
16 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.529+31659T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149604 | |||||||
| chr6:116149723 | T | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02896.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.529+31778T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149723 | |||||||
| chr6:116149880 | C | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0210 others(2): Show |
5 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+31935C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149880 | |||||||
| chr6:116149894 | G | A | 3 | a0001c0001t0006g0006 a0001c0001t0014g0245 a0001c0001t0018g0274 |
4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+31949G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149894 | |||||||
| chr6:116149909 | G | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+31964G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149909 | |||||||
| chr6:116149915 | T | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+31970T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149915 | |||||||
| chr6:116150207 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+32262T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150207 | |||||||
| chr6:116150233 | C | T | 1 | a0001c0001t0011g0182 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.529+32288C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150233 | |||||||
| chr6:116150247 | C | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+32302C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150247 | |||||||
| chr6:116150266 | G | GT | 17 | a0001c0001t0001g0139 a0001c0001t0001g0154 a0001c0001t0001g0207 others(14): Show |
17 | HG00642.hp2 HG01099.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.529+32331dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116150266 | ||||||
| chr6:116150434 | G | A | 1 | a0001c0001t0003g0286 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.529+32489G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150434 | |||||||
| chr6:116150537 | G | A | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+32592G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150537 | |||||||
| chr6:116150595 | G | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+32650G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150595 | |||||||
| chr6:116150636 | G | A | 2 | a0001c0001t0019g0149 a0001c0001t0019g0150 |
2 | HG01515.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.529+32691G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150636 | |||||||
| chr6:116150656 | A | G | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+32711A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150656 | |||||||
| chr6:116150761 | G | A | 2 | a0001c0001t0002g0237 a0001c0001t0002g0243 |
2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.529+32816G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150761 | |||||||
| chr6:116151071 | T | G | 1 | a0001c0001t0002g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.529+33126T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151071 | |||||||
| chr6:116151079 | TGAATTTG others(11): Show |
T | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+33143_529+3316 others(22): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116151079 | ||||||
| chr6:116151082 | A | G | 1 | a0001c0001t0005g0247 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.529+33137A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151082 | |||||||
| chr6:116151105 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.529+33160C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151105 | |||||||
| chr6:116151154 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+33209C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151154 | |||||||
| chr6:116151416 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+33471C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151416 | |||||||
| chr6:116151449 | A | G | 3 | a0001c0001t0016g0116 a0001c0001t0016g0117 a0001c0001t0025g0115 |
3 | HG01891.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.529+33504A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151449 | |||||||
| chr6:116151542 | C | T | 23 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(20): Show |
25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.529+33597C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151542 | |||||||
| chr6:116151594 | A | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+33649A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151594 | |||||||
| chr6:116151605 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+33660G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151605 | |||||||
| chr6:116151746 | A | C | 69 | a0001c0001t0001g0031 a0001c0001t0002g0098 a0001c0001t0003g0002 others(66): Show |
71 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.529+33801A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151746 | |||||||
| chr6:116152025 | A | T | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+34080A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152025 | |||||||
| chr6:116152104 | G | T | 19 | a0001c0001t0002g0055 a0001c0001t0002g0237 a0001c0001t0002g0238 others(16): Show |
19 | HG01515.hp1 HG01934.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.529+34159G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152104 | |||||||
| chr6:116152130 | C | A | 4 | a0001c0001t0003g0002 a0001c0001t0003g0023 a0001c0001t0003g0024 others(1): Show |
5 | NA18947.hp1 NA18957.hp1 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+34185C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152130 | |||||||
| chr6:116152371 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+34426G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152371 | |||||||
| chr6:116152483 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.529+34538A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152483 | |||||||
| chr6:116152616 | C | G | 1 | a0001c0001t0001g0013 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.529+34671C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152616 | |||||||
| chr6:116152694 | T | C | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+34749T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152694 | |||||||
| chr6:116152776 | C | A | 11 | a0001c0001t0003g0289 a0001c0001t0006g0118 a0001c0001t0006g0158 others(8): Show |
11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+34831C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152776 | |||||||
| chr6:116152781 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+34836C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152781 | |||||||
| chr6:116153323 | A | G | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+35378A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153323 | |||||||
| chr6:116153340 | GTT | G | 152 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0005 others(149): Show |
157 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.529+35399_529+3540 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116153340 | ||||||
| chr6:116153366 | A | G | 4 | a0001c0001t0010g0102 a0001c0001t0010g0103 a0001c0001t0010g0104 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+35421A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153366 | |||||||
| chr6:116153421 | T | G | 1 | a0001c0001t0002g0229 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.529+35476T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153421 | |||||||
| chr6:116153624 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.529+35679G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153624 | |||||||
| chr6:116153648 | A | G | 1 | a0001c0001t0004g0254 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.529+35703A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153648 | |||||||
| chr6:116153737 | T | C | 22 | a0001c0001t0002g0055 a0001c0001t0002g0237 a0001c0001t0002g0238 others(19): Show |
22 | HG01515.hp1 HG01934.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.529+35792T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153737 | |||||||
| chr6:116153874 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.529+35929G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153874 | |||||||
| chr6:116153913 | G | A | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+35968G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153913 | |||||||
| chr6:116154029 | CT | C | 28 | a0001c0001t0001g0176 a0001c0001t0001g0186 a0001c0001t0001g0219 others(25): Show |
29 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.529+36102delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116154029 | ||||||
| chr6:116154085 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+36140A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154085 | |||||||
| chr6:116154088 | A | G | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02258.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.529+36143A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154088 | |||||||
| chr6:116154129 | G | A | 2 | a0001c0001t0004g0255 a0001c0001t0008g0256 |
2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.529+36184G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154129 | |||||||
| chr6:116154169 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.529+36224A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154169 | |||||||
| chr6:116154325 | G | A | 1 | a0001c0001t0003g0046 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.529+36380G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154325 | |||||||
| chr6:116154327 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.529+36382G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154327 | |||||||
| chr6:116154359 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+36414C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154359 | |||||||
| chr6:116154394 | T | G | 154 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0005 others(151): Show |
159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+36449T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154394 | |||||||
| chr6:116154431 | G | C | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+36486G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154431 | |||||||
| chr6:116154658 | AT | A | 37 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(34): Show |
40 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.529+36715delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116154658 | ||||||
| chr6:116154751 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+36806A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154751 | |||||||
| chr6:116154904 | A | G | 8 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+36959A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154904 | |||||||
| chr6:116155093 | C | T | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02258.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.529+37148C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155093 | |||||||
| chr6:116155182 | C | G | 7 | a0001c0001t0010g0100 a0001c0001t0010g0101 a0001c0001t0010g0102 others(4): Show |
7 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.529+37237C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155182 | |||||||
| chr6:116155246 | TTA | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0281 a0001c0001t0023g0123 |
3 | HG01891.hp2 HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.529+37306_529+3730 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116155246 | ||||||
| chr6:116155251 | T | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0281 a0001c0001t0023g0123 |
3 | HG01891.hp2 HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.529+37306T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155251 | |||||||
| chr6:116155409 | A | T | 1 | a0001c0001t0001g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.529+37464A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155409 | |||||||
| chr6:116155410 | T | C | 2 | a0001c0001t0003g0289 a0001c0001t0006g0118 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.529+37465T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155410 | |||||||
| chr6:116155437 | G | A | 19 | a0001c0001t0002g0055 a0001c0001t0002g0237 a0001c0001t0002g0238 others(16): Show |
19 | HG01515.hp1 HG01934.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.529+37492G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155437 | |||||||
| chr6:116155516 | G | A | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+37571G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155516 | |||||||
| chr6:116155541 | C | T | 3 | a0001c0001t0002g0291 a0001c0001t0017g0062 a0001c0001t0017g0292 |
3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.529+37596C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155541 | |||||||
| chr6:116155605 | G | A | 1 | a0003c0004t0002g0076 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.529+37660G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155605 | |||||||
| chr6:116155709 | T | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+37764T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155709 | |||||||
| chr6:116155721 | C | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0156 |
3 | NA18942.hp1 NA19065.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.529+37776C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155721 | |||||||
| chr6:116155752 | T | TA | 9 | a0001c0001t0001g0094 a0001c0001t0001g0201 a0001c0001t0003g0020 others(6): Show |
9 | HG01346.hp2 HG02280.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+37827dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116155752 | ||||||
| chr6:116155752 | TA | T | 46 | a0001c0001t0001g0074 a0001c0001t0001g0145 a0001c0001t0001g0146 others(43): Show |
46 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.529+37827delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116155752 | ||||||
| chr6:116155776 | G | A | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+37831G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155776 | |||||||
| chr6:116155844 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.529+37899G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155844 | |||||||
| chr6:116156115 | C | T | 154 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0005 others(151): Show |
159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+38170C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156115 | |||||||
| chr6:116156330 | A | C | 20 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(17): Show |
22 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.529+38385A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156330 | |||||||
| chr6:116156334 | C | G | 1 | a0001c0001t0001g0176 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.529+38389C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156334 | |||||||
| chr6:116156355 | C | T | 152 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0005 others(149): Show |
156 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.529+38410C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156355 | |||||||
| chr6:116156457 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.529+38512C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156457 | |||||||
| chr6:116156547 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.529+38602G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156547 | |||||||
| chr6:116156753 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0219 |
2 | NA18940.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.529+38808C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156753 | |||||||
| chr6:116156826 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.529+38881C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156826 | |||||||
| chr6:116156890 | T | G | 1 | a0001c0001t0001g0169 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.529+38945T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156890 | |||||||
| chr6:116156936 | C | A | 2 | a0001c0001t0002g0267 a0001c0001t0002g0272 |
2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.529+38991C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156936 | |||||||
| chr6:116156937 | A | G | 2 | a0001c0001t0002g0267 a0001c0001t0002g0272 |
2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.529+38992A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156937 | |||||||
| chr6:116157024 | C | T | 153 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0005 others(150): Show |
158 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.529+39079C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157024 | |||||||
| chr6:116157150 | T | C | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+39205T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157150 | |||||||
| chr6:116157315 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+39370C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157315 | |||||||
| chr6:116157341 | C | T | 1 | a0001c0001t0010g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.529+39396C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157341 | |||||||
| chr6:116157367 | A | G | 1 | a0001c0001t0008g0040 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.529+39422A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157367 | |||||||
| chr6:116157558 | G | A | 2 | a0001c0001t0007g0244 a0001c0001t0035g0290 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+39613G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157558 | |||||||
| chr6:116157718 | A | T | 2 | a0001c0001t0003g0021 a0001c0001t0003g0030 |
2 | NA18973.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.529+39773A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157718 | |||||||
| chr6:116157779 | C | T | 1 | a0001c0001t0007g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.529+39834C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157779 | |||||||
| chr6:116157788 | C | G | 93 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0055 others(90): Show |
95 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.529+39843C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157788 | |||||||
| chr6:116158008 | G | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+40063G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158008 | |||||||
| chr6:116158086 | C | G | 1 | a0001c0001t0002g0083 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.529+40141C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158086 | |||||||
| chr6:116158138 | A | C | 1 | a0001c0001t0002g0083 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.529+40193A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158138 | |||||||
| chr6:116158219 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.529+40274A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158219 | |||||||
| chr6:116158618 | A | G | 1 | a0001c0001t0005g0134 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.529+40673A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158618 | |||||||
| chr6:116158793 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+40848T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158793 | |||||||
| chr6:116158834 | G | A | 2 | a0001c0001t0033g0241 a0001c0001t0034g0279 |
2 | HG01074.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.529+40889G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158834 | |||||||
| chr6:116159145 | C | A | 10 | a0001c0001t0001g0092 a0001c0001t0001g0190 a0001c0001t0001g0196 others(7): Show |
10 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(7): Show |
intron_variant | MODIFIER | c.529+41200C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159145 | |||||||
| chr6:116159154 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+41209A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159154 | |||||||
| chr6:116159295 | A | G | 180 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0004 others(177): Show |
185 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.529+41350A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159295 | |||||||
| chr6:116159456 | C | T | 2 | a0001c0001t0015g0282 a0001c0001t0015g0287 |
2 | HG00738.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.529+41511C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159456 | |||||||
| chr6:116159574 | G | A | 3 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0260 |
3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.529+41629G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159574 | |||||||
| chr6:116159724 | A | G | 1 | a0001c0001t0007g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.529+41779A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159724 | |||||||
| chr6:116159782 | C | T | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+41837C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159782 | |||||||
| chr6:116159870 | T | C | 11 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(8): Show |
11 | HG02615.hp1 HG02630.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+41925T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159870 | |||||||
| chr6:116159909 | T | G | 1 | a0001c0001t0005g0247 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.529+41964T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159909 | |||||||
| chr6:116160107 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+42162T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160107 | |||||||
| chr6:116160371 | T | A | 1 | a0001c0001t0015g0287 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.529+42426T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160371 | |||||||
| chr6:116160437 | TC | T | 3 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0260 |
3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.529+42494delC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116160437 | ||||||
| chr6:116160467 | G | A | 4 | a0001c0001t0011g0090 a0001c0001t0011g0091 a0001c0001t0011g0211 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+42522G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160467 | |||||||
| chr6:116160526 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+42581C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160526 | |||||||
| chr6:116160576 | A | G | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+42631A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160576 | |||||||
| chr6:116160701 | G | T | 1 | a0001c0001t0003g0048 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.529+42756G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160701 | |||||||
| chr6:116160779 | T | A | 2 | a0001c0001t0009g0108 a0001c0001t0030g0113 |
2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.529+42834T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160779 | |||||||
| chr6:116160780 | A | T | 2 | a0001c0001t0009g0108 a0001c0001t0030g0113 |
2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.529+42835A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160780 | |||||||
| chr6:116160907 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+42962T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160907 | |||||||
| chr6:116160936 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0258 |
2 | HG02074.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.529+42991C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160936 | |||||||
| chr6:116160943 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+42998G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160943 | |||||||
| chr6:116161152 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+43207G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161152 | |||||||
| chr6:116161198 | G | A | 2 | a0001c0001t0003g0009 a0001c0001t0008g0010 |
2 | NA19002.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.529+43253G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161198 | |||||||
| chr6:116161260 | A | G | 1 | a0001c0001t0036g0136 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.529+43315A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161260 | |||||||
| chr6:116161395 | A | G | 4 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0277 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+43450A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161395 | |||||||
| chr6:116161724 | C | T | 11 | a0001c0001t0003g0289 a0001c0001t0006g0118 a0001c0001t0006g0158 others(8): Show |
11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+43779C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161724 | |||||||
| chr6:116161770 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0233 |
5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+43825A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161770 | |||||||
| chr6:116161775 | TAATTTGA others(7): Show |
T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0210 |
3 | HG02074.hp2 HG02132.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.529+43831_529+4384 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161775 | |||||||
| chr6:116161784 | G | A | 157 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0004 others(154): Show |
162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.529+43839G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161784 | |||||||
| chr6:116161851 | T | C | 34 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(31): Show |
36 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.529+43906T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161851 | |||||||
| chr6:116161894 | A | G | 1 | a0001c0001t0012g0168 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.529+43949A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161894 | |||||||
| chr6:116161979 | TA | T | 4 | a0001c0001t0002g0079 a0001c0001t0002g0080 a0002c0002t0002g0081 others(1): Show |
4 | HG01168.hp1 HG01192.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+44037delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116161979 | ||||||
| chr6:116162355 | A | T | 1 | a0001c0001t0004g0214 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.529+44410A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162355 | |||||||
| chr6:116162443 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.529+44498A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162443 | |||||||
| chr6:116162523 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.529+44578T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162523 | |||||||
| chr6:116162641 | A | T | 20 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0237 others(17): Show |
20 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.529+44696A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162641 | |||||||
| chr6:116162847 | G | A | 94 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0049 others(91): Show |
96 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.529+44902G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162847 | |||||||
| chr6:116162943 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0137 |
2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.529+44998T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162943 | |||||||
| chr6:116162955 | G | A | 1 | a0001c0001t0015g0287 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.529+45010G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162955 | |||||||
| chr6:116163075 | C | G | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+45130C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163075 | |||||||
| chr6:116163082 | G | A | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+45137G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163082 | |||||||
| chr6:116163106 | G | A | 1 | a0001c0001t0007g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.529+45161G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163106 | |||||||
| chr6:116163126 | C | CAAAAA | 11 | a0001c0001t0002g0098 a0001c0001t0003g0046 a0001c0001t0003g0231 others(8): Show |
11 | HG01243.hp2 HG01884.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.529+45193_529+4519 others(9): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163126 | ||||||
| chr6:116163126 | C | CAAAAAA | 65 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0053 others(62): Show |
67 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.529+45192_529+4519 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163126 | ||||||
| chr6:116163126 | C | CAAAAAAA | 9 | a0001c0001t0002g0085 a0001c0001t0003g0014 a0001c0001t0003g0020 others(6): Show |
9 | HG01346.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+45191_529+4519 others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163126 | ||||||
| chr6:116163135 | A | AATAT | 28 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(25): Show |
31 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.529+45191_529+4519 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163135 | ||||||
| chr6:116163135 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0160 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.529+45191_529+4519 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163135 | ||||||
| chr6:116163135 | A | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0208 |
2 | HG00558.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.529+45190A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163135 | |||||||
| chr6:116163135 | AAAAAAAA others(9): Show |
A | 8 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0210 others(5): Show |
8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.529+45192_529+4520 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163135 | ||||||
| chr6:116163137 | A | AATAT | 10 | a0001c0001t0001g0094 a0001c0001t0001g0190 a0001c0001t0001g0196 others(7): Show |
10 | HG00323.hp1 HG02300.hp2 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+45193_529+4519 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163137 | ||||||
| chr6:116163137 | A | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(41): Show |
47 | HG00408.hp1 HG00558.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.529+45192A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163137 | |||||||
| chr6:116163139 | A | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(82): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.529+45194A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163139 | |||||||
| chr6:116163141 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(21): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0009g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.529+45197_529+4519 others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAAAAAA others(4): Show |
12 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(9): Show |
12 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.529+45197_529+4519 others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0009g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAAAAAT | 16 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(13): Show |
18 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.529+45197_529+4519 others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAAAAAT others(6): Show |
1 | a0001c0001t0002g0277 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.529+45197_529+4519 others(17): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAAAATA others(11): Show |
1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(22): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAAAATA others(23): Show |
1 | a0001c0001t0002g0291 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.529+45197_529+4519 others(34): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAAAATA others(39): Show |
1 | a0001c0001t0017g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(50): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAAAT | 7 | a0001c0001t0002g0055 a0001c0001t0002g0237 a0001c0001t0002g0238 others(4): Show |
7 | HG01515.hp1 HG01934.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.529+45197_529+4519 others(9): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAAATAT | 9 | a0001c0001t0002g0049 a0001c0001t0002g0261 a0001c0001t0002g0262 others(6): Show |
9 | HG01099.hp2 NA18953.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.529+45197_529+4519 others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAAATAT others(6): Show |
1 | a0001c0001t0002g0056 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(17): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAATATA others(3): Show |
1 | a0001c0001t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.529+45197_529+4519 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAATATA others(7): Show |
1 | a0001c0001t0002g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAATATA others(9): Show |
1 | a0001c0001t0037g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.529+45197_529+4519 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAATATA others(13): Show |
2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.529+45197_529+4519 others(24): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAAATATA others(19): Show |
1 | a0001c0001t0017g0292 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.529+45197_529+4519 others(30): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAATATAT others(4): Show |
3 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0059 |
3 | HG01884.hp2 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.529+45197_529+4519 others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AAATATAT others(6): Show |
1 | a0001c0001t0002g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(17): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AATATATA others(3): Show |
1 | a0001c0001t0018g0274 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+45209_529+4521 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AATATATA others(11): Show |
3 | a0001c0001t0001g0119 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02896.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.529+45201_529+4521 others(22): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AATATATA others(13): Show |
3 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0023g0123 |
3 | HG01891.hp2 HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.529+45199_529+4521 others(24): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | AATATATA others(15): Show |
1 | a0001c0001t0001g0281 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.529+45197_529+4521 others(26): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | ||||||
| chr6:116163141 | A | ATATATAT | 5 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(2): Show |
5 | HG02559.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+45196_529+4519 others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163141 | |||||||
| chr6:116163141 | A | ATATATAT others(12): Show |
1 | a0001c0001t0024g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.529+45196_529+4519 others(23): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163141 | |||||||
| chr6:116163141 | A | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(87): Show |
93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.529+45196A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163141 | |||||||
| chr6:116163143 | T | A | 63 | a0001c0001t0002g0098 a0001c0001t0003g0002 a0001c0001t0003g0003 others(60): Show |
65 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.529+45198T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163143 | |||||||
| chr6:116163145 | T | A | 6 | a0001c0001t0003g0016 a0001c0001t0003g0044 a0001c0001t0003g0231 others(3): Show |
6 | HG01884.hp1 HG02132.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.529+45200T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163145 | |||||||
| chr6:116163147 | T | A | 1 | a0001c0001t0003g0231 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.529+45202T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163147 | |||||||
| chr6:116163197 | A | G | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+45252A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163197 | |||||||
| chr6:116163240 | T | G | 1 | a0001c0001t0010g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.529+45295T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163240 | |||||||
| chr6:116163290 | A | G | 1 | a0001c0001t0018g0274 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+45345A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163290 | |||||||
| chr6:116163354 | G | T | 2 | a0002c0002t0002g0081 a0002c0002t0002g0082 |
2 | HG01168.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.529+45409G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163354 | |||||||
| chr6:116163437 | T | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0233 |
5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+45492T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163437 | |||||||
| chr6:116163546 | T | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0233 |
5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+45601T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163546 | |||||||
| chr6:116163714 | G | A | 1 | a0001c0001t0018g0274 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+45769G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163714 | |||||||
| chr6:116163905 | T | C | 11 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(8): Show |
11 | HG02615.hp1 HG02630.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+45960T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163905 | |||||||
| chr6:116163957 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+46012G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163957 | |||||||
| chr6:116163957 | G | C | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+46012G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163957 | |||||||
| chr6:116164256 | T | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+46311T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164256 | |||||||
| chr6:116164325 | T | G | 1 | a0001c0001t0005g0133 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.529+46380T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164325 | |||||||
| chr6:116164438 | A | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+46493A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164438 | |||||||
| chr6:116164471 | G | A | 1 | a0001c0001t0004g0248 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.529+46526G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164471 | |||||||
| chr6:116164559 | C | T | 157 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0004 others(154): Show |
162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.529+46614C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164559 | |||||||
| chr6:116164732 | T | G | 3 | a0001c0001t0010g0102 a0001c0001t0010g0103 a0001c0001t0010g0104 |
3 | HG01884.hp1 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.529+46787T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164732 | |||||||
| chr6:116164834 | C | A | 1 | a0001c0001t0018g0274 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+46889C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164834 | |||||||
| chr6:116164927 | T | A | 2 | a0001c0001t0009g0276 a0001c0001t0009g0288 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.529+46982T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164927 | |||||||
| chr6:116164935 | T | A | 1 | a0001c0001t0001g0215 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.529+46990T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164935 | |||||||
| chr6:116164939 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.529+46994A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164939 | |||||||
| chr6:116164989 | C | T | 37 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(34): Show |
40 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.529+47044C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164989 | |||||||
| chr6:116165061 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.529+47116C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165061 | |||||||
| chr6:116165075 | C | T | 2 | a0001c0001t0006g0006 a0001c0001t0014g0245 |
3 | HG02809.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.529+47130C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165075 | |||||||
| chr6:116165098 | G | GAA | 21 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0237 others(18): Show |
21 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.529+47172_529+4717 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | ||||||
| chr6:116165098 | G | GAAA | 81 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0068 others(78): Show |
84 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.529+47171_529+4717 others(7): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | ||||||
| chr6:116165098 | G | GAAAA | 34 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0056 others(31): Show |
36 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.529+47170_529+4717 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | ||||||
| chr6:116165098 | G | GAAAAA | 18 | a0001c0001t0002g0078 a0001c0001t0002g0080 a0001c0001t0002g0083 others(15): Show |
18 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.529+47169_529+4717 others(9): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | ||||||
| chr6:116165098 | G | GAAAAAA | 11 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01106.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.529+47168_529+4717 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | ||||||
| chr6:116165098 | G | GAAAAAAA | 17 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0284 others(14): Show |
17 | HG00642.hp2 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.529+47167_529+4717 others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | ||||||
| chr6:116165098 | G | GAAAAAAA others(1): Show |
9 | a0001c0001t0001g0285 a0001c0001t0002g0053 a0001c0001t0006g0011 others(6): Show |
9 | HG00738.hp1 HG00741.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.529+47166_529+4717 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | ||||||
| chr6:116165098 | GA | G | 6 | a0001c0001t0001g0119 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
6 | HG01168.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+47173delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | ||||||
| chr6:116165121 | A | C | 110 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0049 others(107): Show |
112 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.529+47176A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165121 | |||||||
| chr6:116165265 | G | C | 1 | a0001c0001t0003g0041 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.529+47320G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165265 | |||||||
| chr6:116165293 | A | G | 8 | a0001c0001t0006g0158 a0001c0001t0007g0128 a0001c0001t0007g0129 others(5): Show |
8 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+47348A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165293 | |||||||
| chr6:116165297 | T | A | 94 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0049 others(91): Show |
96 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.529+47352T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165297 | |||||||
| chr6:116165342 | C | T | 1 | a0001c0001t0014g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.529+47397C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165342 | |||||||
| chr6:116165425 | G | A | 3 | a0001c0001t0002g0291 a0001c0001t0017g0062 a0001c0001t0017g0292 |
3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.529+47480G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165425 | |||||||
| chr6:116165481 | G | T | 2 | a0001c0001t0004g0051 a0001c0001t0029g0050 |
2 | HG01106.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.529+47536G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165481 | |||||||
| chr6:116165584 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+47639C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165584 | |||||||
| chr6:116165629 | C | A | 69 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0098 others(66): Show |
71 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.529+47684C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165629 | |||||||
| chr6:116165654 | G | C | 9 | a0001c0001t0006g0158 a0001c0001t0007g0128 a0001c0001t0007g0129 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.529+47709G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165654 | |||||||
| chr6:116165797 | G | T | 2 | a0001c0001t0015g0282 a0001c0001t0015g0287 |
2 | HG00738.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.529+47852G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165797 | |||||||
| chr6:116165996 | C | G | 3 | a0001c0001t0006g0006 a0001c0001t0014g0245 a0001c0001t0018g0274 |
4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+48051C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165996 | |||||||
| chr6:116166052 | T | C | 4 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+48107T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116166052 | |||||||
| chr6:116166053 | A | G | 2 | a0001c0001t0003g0289 a0001c0001t0006g0118 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.529+48108A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116166053 | |||||||
| chr6:116166177 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+48232C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116166177 | |||||||
| chr6:116166419 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+48474A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116166419 | |||||||
| chr6:116166880 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.529+48935G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116166880 | |||||||
| chr6:116167093 | G | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+49148G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167093 | |||||||
| chr6:116167206 | A | AT | 63 | a0001c0001t0001g0139 a0001c0001t0001g0152 a0001c0001t0001g0154 others(60): Show |
65 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.529+49286dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116167206 | ||||||
| chr6:116167206 | A | ATT | 24 | a0001c0001t0001g0178 a0001c0001t0002g0068 a0001c0001t0002g0073 others(21): Show |
24 | HG00639.hp1 HG01069.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.529+49285_529+4928 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116167206 | ||||||
| chr6:116167206 | AT | A | 55 | a0001c0001t0001g0119 a0001c0001t0001g0124 a0001c0001t0001g0125 others(52): Show |
55 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.529+49286delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116167206 | ||||||
| chr6:116167252 | C | T | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+49307C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167252 | |||||||
| chr6:116167374 | G | A | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+49429G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167374 | |||||||
| chr6:116167403 | A | G | 1 | a0001c0001t0006g0138 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.529+49458A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167403 | |||||||
| chr6:116167414 | G | A | 157 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0004 others(154): Show |
162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.529+49469G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167414 | |||||||
| chr6:116167445 | C | T | 10 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0124 others(7): Show |
10 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.529+49500C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167445 | |||||||
| chr6:116167503 | T | C | 2 | a0001c0001t0004g0157 a0001c0001t0004g0183 |
2 | NA18991.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.529+49558T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167503 | |||||||
| chr6:116167551 | G | T | 3 | a0001c0001t0016g0116 a0001c0001t0016g0117 a0001c0001t0025g0115 |
3 | HG01891.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.529+49606G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167551 | |||||||
| chr6:116167581 | A | G | 1 | a0001c0001t0008g0040 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.529+49636A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167581 | |||||||
| chr6:116167646 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.529+49701C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167646 | |||||||
| chr6:116167692 | C | T | 1 | a0001c0001t0007g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.529+49747C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167692 | |||||||
| chr6:116167740 | A | G | 3 | a0001c0001t0002g0291 a0001c0001t0017g0062 a0001c0001t0017g0292 |
3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.529+49795A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167740 | |||||||
| chr6:116167743 | A | G | 180 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0004 others(177): Show |
185 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.529+49798A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167743 | |||||||
| chr6:116167762 | G | A | 20 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(17): Show |
22 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.529+49817G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167762 | |||||||
| chr6:116167762 | G | C | 2 | a0001c0001t0009g0276 a0001c0001t0009g0288 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.529+49817G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167762 | |||||||
| chr6:116167848 | G | C | 1 | a0001c0001t0006g0006 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.529+49903G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167848 | |||||||
| chr6:116167854 | G | A | 2 | a0001c0001t0007g0140 a0001c0001t0038g0141 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.529+49909G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167854 | |||||||
| chr6:116168083 | CT | C | 75 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0188 others(72): Show |
78 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.529+50157delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116168083 | ||||||
| chr6:116168103 | A | T | 9 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0124 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.529+50158A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168103 | |||||||
| chr6:116168175 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+50230A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168175 | |||||||
| chr6:116168314 | T | C | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+50369T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168314 | |||||||
| chr6:116168387 | A | G | 23 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(20): Show |
25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.529+50442A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168387 | |||||||
| chr6:116168450 | A | G | 1 | a0001c0001t0037g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.529+50505A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168450 | |||||||
| chr6:116168628 | A | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+50683A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168628 | |||||||
| chr6:116168691 | T | C | 157 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0004 others(154): Show |
162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.529+50746T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168691 | |||||||
| chr6:116168812 | T | C | 1 | a0001c0001t0003g0018 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.529+50867T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168812 | |||||||
| chr6:116168812 | T | G | 1 | a0001c0001t0003g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.529+50867T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168812 | |||||||
| chr6:116169006 | T | C | 4 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0277 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+51061T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169006 | |||||||
| chr6:116169163 | C | CT | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+51219dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116169163 | ||||||
| chr6:116169173 | CT | C | 3 | a0001c0001t0006g0006 a0001c0001t0014g0245 a0001c0001t0018g0274 |
4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+51232delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116169173 | ||||||
| chr6:116169376 | T | C | 4 | a0001c0001t0003g0014 a0001c0001t0003g0033 a0001c0001t0003g0034 others(1): Show |
4 | NA18940.hp1 NA19004.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+51431T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169376 | |||||||
| chr6:116169396 | C | G | 2 | a0001c0001t0007g0140 a0001c0001t0038g0141 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.529+51451C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169396 | |||||||
| chr6:116169539 | G | A | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-51515G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169539 | |||||||
| chr6:116169566 | C | T | 3 | a0001c0001t0002g0049 a0001c0001t0019g0149 a0001c0001t0019g0150 |
3 | HG01099.hp2 HG01515.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.530-51488C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169566 | |||||||
| chr6:116169660 | T | G | 3 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 |
3 | NA18947.hp1 NA19088.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.530-51394T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169660 | |||||||
| chr6:116169675 | A | G | 23 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0237 others(20): Show |
23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-51379A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169675 | |||||||
| chr6:116169715 | T | A | 2 | a0001c0001t0004g0255 a0001c0001t0008g0256 |
2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.530-51339T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169715 | |||||||
| chr6:116169727 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.530-51327A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169727 | |||||||
| chr6:116169799 | C | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0233 |
5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.530-51255C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169799 | |||||||
| chr6:116170139 | G | A | 65 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0098 others(62): Show |
67 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.530-50915G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170139 | |||||||
| chr6:116170169 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.530-50885G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170169 | |||||||
| chr6:116170170 | G | A | 3 | a0001c0001t0013g0069 a0001c0001t0013g0070 a0001c0001t0013g0071 |
3 | HG02615.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.530-50884G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170170 | |||||||
| chr6:116170245 | TC | T | 34 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(31): Show |
36 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.530-50805delC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116170245 | ||||||
| chr6:116170292 | G | T | 16 | a0001c0001t0003g0009 a0001c0001t0003g0286 a0001c0001t0004g0157 others(13): Show |
16 | HG00099.hp2 HG00741.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.530-50762G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170292 | |||||||
| chr6:116170559 | G | T | 1 | a0001c0001t0004g0253 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.530-50495G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170559 | |||||||
| chr6:116170693 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-50361G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170693 | |||||||
| chr6:116170838 | C | T | 1 | a0001c0001t0003g0231 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.530-50216C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170838 | |||||||
| chr6:116171014 | C | T | 1 | a0001c0001t0018g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.530-50040C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171014 | |||||||
| chr6:116171062 | G | A | 2 | a0001c0001t0002g0291 a0001c0001t0017g0062 |
2 | HG01981.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.530-49992G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171062 | |||||||
| chr6:116171187 | T | C | 23 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0237 others(20): Show |
23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-49867T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171187 | |||||||
| chr6:116171269 | C | T | 23 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0237 others(20): Show |
23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-49785C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171269 | |||||||
| chr6:116171336 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.530-49718G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171336 | |||||||
| chr6:116171337 | T | C | 94 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0049 others(91): Show |
96 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.530-49717T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171337 | |||||||
| chr6:116171395 | A | G | 3 | a0001c0001t0006g0006 a0001c0001t0014g0245 a0001c0001t0018g0274 |
4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-49659A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171395 | |||||||
| chr6:116171553 | A | G | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-49501A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171553 | |||||||
| chr6:116171561 | G | A | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.530-49493G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171561 | |||||||
| chr6:116171562 | G | T | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-49492G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171562 | |||||||
| chr6:116171695 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.530-49359G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171695 | |||||||
| chr6:116172067 | A | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-48987A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116172067 | |||||||
| chr6:116172183 | A | C | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.530-48871A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116172183 | |||||||
| chr6:116172317 | C | CT | 127 | a0001c0001t0001g0031 a0001c0001t0001g0094 a0001c0001t0001g0126 others(124): Show |
131 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.530-48715dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116172317 | ||||||
| chr6:116172317 | C | CTT | 10 | a0001c0001t0002g0239 a0001c0001t0003g0021 a0001c0001t0003g0025 others(7): Show |
10 | HG01192.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.530-48716_530-4871 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116172317 | ||||||
| chr6:116172317 | CT | C | 13 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0065 others(10): Show |
13 | HG01884.hp1 HG01884.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.530-48715delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116172317 | ||||||
| chr6:116172317 | CTT | C | 14 | a0001c0001t0002g0057 a0001c0001t0002g0106 a0001c0001t0002g0109 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-48716_530-4871 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116172317 | ||||||
| chr6:116172367 | G | A | 1 | a0001c0001t0005g0252 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.530-48687G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116172367 | |||||||
| chr6:116172396 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-48658G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116172396 | |||||||
| chr6:116172611 | C | T | 4 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0260 others(1): Show |
4 | HG02717.hp2 HG03239.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-48443C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116172611 | |||||||
| chr6:116172646 | A | G | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.530-48408A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116172646 | |||||||
| chr6:116173201 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-47853A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116173201 | |||||||
| chr6:116173387 | G | A | 1 | a0001c0001t0005g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.530-47667G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116173387 | |||||||
| chr6:116173400 | G | A | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-47654G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116173400 | |||||||
| chr6:116173465 | G | T | 1 | a0001c0001t0003g0193 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.530-47589G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116173465 | |||||||
| chr6:116173674 | T | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-47380T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116173674 | |||||||
| chr6:116173777 | A | G | 188 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0001g0161 others(185): Show |
193 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.530-47277A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116173777 | |||||||
| chr6:116174174 | A | G | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.530-46880A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116174174 | |||||||
| chr6:116174341 | C | T | 2 | a0001c0001t0010g0100 a0001c0001t0010g0101 |
2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.530-46713C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116174341 | |||||||
| chr6:116174442 | A | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-46612A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116174442 | |||||||
| chr6:116174554 | G | T | 137 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0004 others(134): Show |
142 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.530-46500G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116174554 | |||||||
| chr6:116174706 | C | G | 8 | a0001c0001t0006g0158 a0001c0001t0007g0128 a0001c0001t0007g0129 others(5): Show |
8 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.530-46348C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116174706 | |||||||
| chr6:116175001 | G | A | 43 | a0001c0001t0002g0049 a0001c0001t0002g0053 a0001c0001t0002g0055 others(40): Show |
43 | HG00642.hp2 HG00741.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.530-46053G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175001 | |||||||
| chr6:116175387 | T | C | 20 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0237 others(17): Show |
20 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.530-45667T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175387 | |||||||
| chr6:116175412 | G | A | 2 | a0001c0001t0006g0011 a0001c0001t0006g0012 |
2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.530-45642G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175412 | |||||||
| chr6:116175604 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.530-45450C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175604 | |||||||
| chr6:116175619 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-45435T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175619 | |||||||
| chr6:116175736 | A | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-45318A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175736 | |||||||
| chr6:116175762 | T | C | 4 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0006g0054 others(1): Show |
4 | NA18971.hp2 NA18978.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-45292T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175762 | |||||||
| chr6:116176154 | C | T | 66 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0098 others(63): Show |
68 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.530-44900C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116176154 | |||||||
| chr6:116176540 | G | A | 1 | a0001c0001t0035g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.530-44514G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116176540 | |||||||
| chr6:116176737 | A | G | 1 | a0001c0001t0003g0203 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.530-44317A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116176737 | |||||||
| chr6:116177223 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-43831A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177223 | |||||||
| chr6:116177249 | C | T | 3 | a0001c0001t0002g0291 a0001c0001t0017g0062 a0001c0001t0017g0292 |
3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.530-43805C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177249 | |||||||
| chr6:116177277 | C | G | 9 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 others(6): Show |
9 | NA18953.hp2 NA18954.hp1 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.530-43777C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177277 | |||||||
| chr6:116177464 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-43590C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177464 | |||||||
| chr6:116177747 | T | TG | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0259 |
3 | HG01192.hp2 HG01243.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.530-43307_530-4330 others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177747 | |||||||
| chr6:116177842 | G | A | 3 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 |
3 | HG01258.hp1 HG01952.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.530-43212G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177842 | |||||||
| chr6:116177850 | A | G | 1 | a0001c0001t0018g0274 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.530-43204A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177850 | |||||||
| chr6:116177865 | G | A | 4 | a0001c0001t0012g0168 a0001c0001t0012g0170 a0001c0001t0012g0171 others(1): Show |
4 | NA18941.hp1 NA18968.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-43189G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177865 | |||||||
| chr6:116177880 | A | C | 2 | a0001c0001t0007g0140 a0001c0001t0038g0141 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.530-43174A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177880 | |||||||
| chr6:116177949 | A | G | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-43105A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177949 | |||||||
| chr6:116178052 | A | AGT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0092 others(38): Show |
44 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.530-42966_530-4296 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | ||||||
| chr6:116178052 | A | AGTGT | 8 | a0001c0001t0001g0162 a0001c0001t0001g0204 a0001c0001t0001g0215 others(5): Show |
8 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.530-42968_530-4296 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | ||||||
| chr6:116178052 | A | AGTGTGT | 11 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0206 others(8): Show |
11 | HG01074.hp2 HG01192.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.530-42970_530-4296 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | ||||||
| chr6:116178052 | A | AGTGTGTG others(1): Show |
3 | a0001c0001t0006g0158 a0001c0001t0007g0128 a0001c0001t0014g0143 |
3 | HG02886.hp2 HG03453.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.530-42972_530-4296 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | ||||||
| chr6:116178052 | A | AGTGTGTG others(3): Show |
2 | a0001c0001t0001g0226 a0001c0001t0007g0131 |
2 | HG02300.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.530-42974_530-4296 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | ||||||
| chr6:116178052 | AGT | A | 39 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0002g0291 others(36): Show |
40 | HG00558.hp2 HG00639.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.530-42966_530-4296 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | ||||||
| chr6:116178052 | AGTGT | A | 27 | a0001c0001t0001g0031 a0001c0001t0003g0002 a0001c0001t0003g0015 others(24): Show |
29 | HG00099.hp2 HG01081.hp2 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.530-42968_530-4296 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | ||||||
| chr6:116178052 | AGTGTGT | A | 5 | a0001c0001t0001g0137 a0001c0001t0002g0237 a0001c0001t0002g0238 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.530-42970_530-4296 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | ||||||
| chr6:116178052 | AGTGTGTG others(3): Show |
A | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.530-42974_530-4296 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | ||||||
| chr6:116178068 | T | C | 8 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.530-42986T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178068 | |||||||
| chr6:116178070 | TGTGTGTG others(19): Show |
T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-42982_530-4295 others(30): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178070 | ||||||
| chr6:116178080 | T | C | 1 | a0001c0001t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.530-42974T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178080 | |||||||
| chr6:116178082 | T | C | 1 | a0001c0001t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.530-42972T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178082 | |||||||
| chr6:116178082 | TGTGTGTG others(3): Show |
T | 15 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0243 others(12): Show |
15 | HG01099.hp2 HG01515.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.530-42970_530-4296 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178082 | ||||||
| chr6:116178082 | TGTGTGTG others(5): Show |
T | 1 | a0001c0001t0007g0244 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.530-42970_530-4295 others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178082 | ||||||
| chr6:116178084 | T | C | 1 | a0001c0001t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.530-42970T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178084 | |||||||
| chr6:116178084 | TGTGTGCG others(1): Show |
T | 4 | a0001c0001t0008g0256 a0001c0001t0015g0282 a0001c0001t0015g0287 others(1): Show |
4 | HG00738.hp1 HG01934.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-42968_530-4296 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178084 | ||||||
| chr6:116178084 | TGTGTGCG others(5): Show |
T | 1 | a0001c0001t0035g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.530-42968_530-4295 others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178084 | ||||||
| chr6:116178086 | T | C | 3 | a0001c0001t0002g0246 a0001c0001t0005g0135 a0001c0001t0005g0278 |
3 | HG02647.hp2 HG03516.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-42968T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178086 | |||||||
| chr6:116178086 | TGTGC | T | 3 | a0001c0001t0001g0172 a0001c0001t0002g0004 a0001c0001t0036g0136 |
3 | HG00642.hp1 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.530-42966_530-4296 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178086 | ||||||
| chr6:116178086 | TGTGCGCG others(3): Show |
T | 1 | a0001c0001t0002g0053 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.530-42966_530-4295 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178086 | ||||||
| chr6:116178088 | T | C | 8 | a0001c0001t0002g0246 a0001c0001t0003g0009 a0001c0001t0003g0020 others(5): Show |
8 | HG01346.hp2 HG02132.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-42966T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178088 | |||||||
| chr6:116178088 | T | TGTGTGTG others(5): Show |
1 | a0001c0001t0009g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.530-42965_530-4296 others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178088 | ||||||
| chr6:116178088 | TGC | T | 12 | a0001c0001t0001g0074 a0001c0001t0001g0119 a0001c0001t0001g0121 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.530-42952_530-4295 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178088 | ||||||
| chr6:116178090 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(124): Show |
131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.530-42964C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178090 | |||||||
| chr6:116178092 | C | T | 48 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0124 others(45): Show |
49 | HG00280.hp1 HG00408.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.530-42962C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178092 | |||||||
| chr6:116178094 | C | T | 25 | a0001c0001t0001g0187 a0001c0001t0001g0191 a0001c0001t0001g0201 others(22): Show |
25 | HG00280.hp1 HG00408.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.530-42960C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178094 | |||||||
| chr6:116178096 | C | T | 10 | a0001c0001t0002g0067 a0001c0001t0002g0079 a0001c0001t0002g0080 others(7): Show |
10 | HG00738.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.530-42958C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178096 | |||||||
| chr6:116178096 | CGCGCGCG others(1): Show |
C | 10 | a0001c0001t0004g0051 a0001c0001t0006g0054 a0001c0001t0006g0064 others(7): Show |
10 | HG01106.hp1 HG01106.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-42954_530-4294 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178096 | ||||||
| chr6:116178098 | C | T | 11 | a0001c0001t0002g0080 a0001c0001t0002g0084 a0001c0001t0003g0009 others(8): Show |
11 | HG01081.hp1 HG01168.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.530-42956C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178098 | |||||||
| chr6:116178098 | CGCGCGT | C | 6 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0006g0061 others(3): Show |
6 | HG02976.hp2 HG03139.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.530-42952_530-4294 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178098 | ||||||
| chr6:116178100 | C | T | 71 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0098 others(68): Show |
73 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.530-42954C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178100 | |||||||
| chr6:116178102 | C | T | 5 | a0001c0001t0003g0009 a0001c0001t0004g0043 a0001c0001t0005g0134 others(2): Show |
5 | HG02895.hp1 HG03239.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-42952C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178102 | |||||||
| chr6:116178102 | CGT | C | 5 | a0001c0001t0002g0005 a0001c0001t0002g0072 a0001c0001t0002g0086 others(2): Show |
6 | HG01071.hp2 HG01258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.530-42950_530-4294 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178102 | ||||||
| chr6:116178104 | T | C | 37 | a0001c0001t0001g0187 a0001c0001t0001g0191 a0001c0001t0001g0201 others(34): Show |
37 | HG00280.hp1 HG00408.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.530-42950T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178104 | |||||||
| chr6:116178104 | TGC | T | 8 | a0001c0001t0002g0238 a0001c0001t0002g0291 a0001c0001t0004g0255 others(5): Show |
8 | HG01361.hp2 HG01981.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-42948_530-4294 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178104 | ||||||
| chr6:116178106 | C | CGT | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.530-42946_530-4294 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178106 | ||||||
| chr6:116178106 | C | T | 66 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0098 others(63): Show |
68 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.530-42948C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178106 | |||||||
| chr6:116178106 | CGTGCGT | C | 6 | a0001c0001t0002g0004 a0001c0001t0006g0006 a0001c0001t0013g0069 others(3): Show |
8 | HG00642.hp1 HG02809.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.530-42944_530-4293 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178106 | ||||||
| chr6:116178106 | CGTGCGTG others(3): Show |
C | 1 | a0001c0001t0008g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.530-42944_530-4293 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178106 | ||||||
| chr6:116178108 | T | C | 10 | a0001c0001t0002g0067 a0001c0001t0002g0079 a0001c0001t0002g0080 others(7): Show |
10 | HG00738.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.530-42946T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178108 | |||||||
| chr6:116178108 | TGC | T | 29 | a0001c0001t0002g0055 a0001c0001t0002g0106 a0001c0001t0002g0109 others(26): Show |
29 | HG00642.hp2 HG01891.hp1 HG02615.hp1 others(26): Show |
intron_variant | MODIFIER | c.530-42944_530-4294 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178108 | ||||||
| chr6:116178110 | C | CGT | 4 | a0001c0001t0001g0152 a0001c0001t0001g0192 a0001c0001t0001g0223 others(1): Show |
4 | HG01192.hp2 HG03041.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-42921_530-4292 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178110 | ||||||
| chr6:116178110 | C | T | 91 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0049 others(88): Show |
93 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.530-42944C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178110 | |||||||
| chr6:116178110 | CGT | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0119 others(34): Show |
41 | HG00280.hp1 HG00558.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.530-42921_530-4292 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178110 | ||||||
| chr6:116178112 | T | C | 2 | a0001c0001t0002g0067 a0001c0001t0002g0083 |
2 | HG00738.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.530-42942T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178112 | |||||||
| chr6:116178112 | T | TGC | 9 | a0001c0001t0001g0191 a0001c0001t0001g0201 a0001c0001t0002g0079 others(6): Show |
9 | HG00408.hp1 HG01081.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.530-42941_530-4294 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178112 | ||||||
| chr6:116178114 | T | C | 10 | a0001c0001t0001g0187 a0001c0001t0001g0228 a0001c0001t0006g0158 others(7): Show |
10 | HG01496.hp2 HG02559.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-42940T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178114 | |||||||
| chr6:116178116 | T | C | 3 | a0001c0001t0003g0289 a0001c0001t0006g0118 a0001c0001t0018g0127 |
3 | HG02451.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.530-42938T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178116 | |||||||
| chr6:116178118 | T | C | 1 | a0001c0001t0014g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.530-42936T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178118 | |||||||
| chr6:116178122 | T | C | 1 | a0001c0001t0002g0271 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.530-42932T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178122 | |||||||
| chr6:116178253 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.530-42801A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178253 | |||||||
| chr6:116178306 | T | A | 1 | a0001c0001t0003g0231 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.530-42748T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178306 | |||||||
| chr6:116178311 | G | A | 1 | a0001c0001t0004g0195 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.530-42743G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178311 | |||||||
| chr6:116178377 | T | G | 1 | a0001c0001t0006g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.530-42677T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178377 | |||||||
| chr6:116178415 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-42639C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178415 | |||||||
| chr6:116178675 | T | C | 1 | a0001c0001t0006g0064 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.530-42379T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178675 | |||||||
| chr6:116178704 | T | C | 3 | a0001c0001t0002g0291 a0001c0001t0017g0062 a0001c0001t0017g0292 |
3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.530-42350T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178704 | |||||||
| chr6:116178785 | A | G | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02258.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.530-42269A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178785 | |||||||
| chr6:116178912 | G | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-42142G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178912 | |||||||
| chr6:116179040 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.530-42014G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116179040 | |||||||
| chr6:116179264 | A | G | 94 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0049 others(91): Show |
96 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.530-41790A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116179264 | |||||||
| chr6:116179400 | G | T | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-41654G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116179400 | |||||||
| chr6:116179507 | T | C | 3 | a0001c0001t0013g0069 a0001c0001t0013g0070 a0001c0001t0013g0071 |
3 | HG02615.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.530-41547T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116179507 | |||||||
| chr6:116179726 | T | C | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-41328T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116179726 | |||||||
| chr6:116179875 | C | A | 30 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0003g0002 others(27): Show |
32 | HG00408.hp2 HG00558.hp2 HG02132.hp2 others(29): Show |
intron_variant | MODIFIER | c.530-41179C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116179875 | |||||||
| chr6:116180017 | ATCT | A | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-41035_530-4103 others(7): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116180017 | ||||||
| chr6:116180340 | G | A | 155 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0004 others(152): Show |
160 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.530-40714G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116180340 | |||||||
| chr6:116180413 | G | C | 1 | a0001c0001t0004g0253 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.530-40641G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116180413 | |||||||
| chr6:116180820 | G | A | 157 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0004 others(154): Show |
162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.530-40234G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116180820 | |||||||
| chr6:116180848 | T | A | 157 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0004 others(154): Show |
162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.530-40206T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116180848 | |||||||
| chr6:116180938 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.530-40116G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116180938 | |||||||
| chr6:116181048 | C | A | 4 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-40006C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116181048 | |||||||
| chr6:116181063 | ATTTAC | A | 23 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0237 others(20): Show |
23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-39986_530-3998 others(9): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116181063 | ||||||
| chr6:116181110 | A | G | 2 | a0001c0001t0007g0140 a0001c0001t0038g0141 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.530-39944A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116181110 | |||||||
| chr6:116181242 | A | G | 47 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0056 others(44): Show |
50 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.530-39812A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116181242 | |||||||
| chr6:116181520 | G | A | 1 | a0001c0001t0005g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.530-39534G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116181520 | |||||||
| chr6:116181680 | T | C | 1 | a0001c0001t0007g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.530-39374T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116181680 | |||||||
| chr6:116181775 | C | CTA | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-39275_530-3927 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116181775 | ||||||
| chr6:116181939 | T | A | 1 | a0001c0001t0002g0005 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.530-39115T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116181939 | |||||||
| chr6:116182005 | C | T | 157 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0004 others(154): Show |
162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.530-39049C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182005 | |||||||
| chr6:116182039 | C | T | 2 | a0001c0001t0009g0276 a0001c0001t0009g0288 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.530-39015C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182039 | |||||||
| chr6:116182222 | A | AGAGAGAG others(13): Show |
1 | a0001c0001t0020g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.530-38831_530-3883 others(24): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | A | AGAGAGAG others(15): Show |
1 | a0001c0001t0020g0230 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.530-38831_530-3883 others(26): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | A | AGAGAGTG others(9): Show |
3 | a0001c0001t0002g0264 a0001c0001t0003g0015 a0001c0001t0003g0045 |
3 | HG02965.hp1 NA18522.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.530-38831_530-3883 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | A | AGAGTGTG others(7): Show |
1 | a0001c0001t0004g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.530-38831_530-3883 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | A | AGAGTGTG others(9): Show |
79 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0049 others(76): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.530-38831_530-3883 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | A | AGAGTGTG others(11): Show |
9 | a0001c0001t0003g0002 a0001c0001t0003g0022 a0001c0001t0003g0023 others(6): Show |
10 | HG02896.hp1 HG03098.hp2 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.530-38831_530-3883 others(22): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | A | AGAGTGTG others(13): Show |
1 | a0001c0001t0005g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.530-38831_530-3883 others(24): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | A | AGT | 39 | a0001c0001t0001g0013 a0001c0001t0001g0121 a0001c0001t0001g0124 others(36): Show |
40 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.530-38801_530-3880 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | A | AGTGT | 4 | a0001c0001t0001g0125 a0001c0001t0001g0215 a0001c0001t0002g0004 others(1): Show |
5 | HG00642.hp1 HG01258.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-38803_530-3880 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | A | AGTGTGT | 4 | a0001c0001t0002g0246 a0001c0001t0006g0006 a0001c0001t0014g0245 others(1): Show |
5 | HG02145.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-38805_530-3880 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | A | AGTGTGTG others(3): Show |
14 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0106 others(11): Show |
14 | HG02559.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-38809_530-3880 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | A | AGTGTGTG others(5): Show |
3 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0005g0278 |
3 | HG01884.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.530-38811_530-3880 others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | A | AGTGTGTG others(7): Show |
7 | a0001c0001t0002g0059 a0001c0001t0002g0277 a0001c0001t0003g0289 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.530-38813_530-3880 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | A | AGTGTGTG others(9): Show |
1 | a0001c0001t0002g0056 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.530-38815_530-3880 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | AGT | A | 19 | a0001c0001t0002g0053 a0001c0001t0006g0054 a0001c0001t0006g0061 others(16): Show |
19 | HG00642.hp2 HG00741.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.530-38801_530-3880 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182222 | AGTGTGT | A | 3 | a0001c0001t0002g0084 a0001c0001t0009g0144 a0003c0004t0002g0076 |
3 | HG01081.hp1 HG01361.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.530-38805_530-3880 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | ||||||
| chr6:116182235 | G | A | 90 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0049 others(87): Show |
92 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.530-38819G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182235 | |||||||
| chr6:116182392 | G | A | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-38662G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182392 | |||||||
| chr6:116182526 | C | T | 37 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(34): Show |
40 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.530-38528C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182526 | |||||||
| chr6:116182553 | T | C | 1 | a0001c0001t0003g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.530-38501T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182553 | |||||||
| chr6:116182581 | G | A | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-38473G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182581 | |||||||
| chr6:116182673 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.530-38381T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182673 | |||||||
| chr6:116182746 | TTGCTGAT others(1): Show |
T | 3 | a0001c0001t0006g0006 a0001c0001t0014g0245 a0001c0001t0018g0274 |
4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-38305_530-3829 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182746 | ||||||
| chr6:116183310 | T | C | 93 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0055 others(90): Show |
95 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.530-37744T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116183310 | |||||||
| chr6:116183348 | G | T | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.530-37706G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116183348 | |||||||
| chr6:116183646 | A | T | 1 | a0001c0001t0002g0049 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.530-37408A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116183646 | |||||||
| chr6:116183761 | A | G | 1 | a0001c0001t0021g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.530-37293A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116183761 | |||||||
| chr6:116183783 | T | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-37271T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116183783 | |||||||
| chr6:116183828 | T | C | 1 | a0001c0001t0003g0286 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.530-37226T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116183828 | |||||||
| chr6:116184048 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.530-37006G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184048 | |||||||
| chr6:116184124 | T | C | 1 | a0001c0001t0018g0274 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.530-36930T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184124 | |||||||
| chr6:116184222 | A | G | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.530-36832A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184222 | |||||||
| chr6:116184451 | G | C | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-36603G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184451 | |||||||
| chr6:116184455 | A | G | 1 | a0001c0001t0004g0214 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.530-36599A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184455 | |||||||
| chr6:116184506 | C | T | 37 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(34): Show |
40 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.530-36548C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184506 | |||||||
| chr6:116184574 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0156 others(10): Show |
16 | HG00558.hp1 NA18942.hp1 NA18957.hp2 others(13): Show |
intron_variant | MODIFIER | c.530-36480G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184574 | |||||||
| chr6:116184632 | G | A | 155 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0004 others(152): Show |
160 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.530-36422G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184632 | |||||||
| chr6:116184776 | T | C | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-36278T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184776 | |||||||
| chr6:116184914 | TG | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0156 others(9): Show |
15 | HG00558.hp1 NA18942.hp1 NA18957.hp2 others(12): Show |
intron_variant | MODIFIER | c.530-36137delG | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116184914 | ||||||
| chr6:116185082 | A | T | 45 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0098 others(42): Show |
47 | HG00408.hp2 HG00558.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.530-35972A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185082 | |||||||
| chr6:116185139 | A | C | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-35915A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185139 | |||||||
| chr6:116185212 | A | G | 3 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0260 |
3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-35842A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185212 | |||||||
| chr6:116185387 | A | G | 3 | a0001c0001t0013g0069 a0001c0001t0013g0070 a0001c0001t0013g0071 |
3 | HG02615.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.530-35667A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185387 | |||||||
| chr6:116185437 | C | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-35617C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185437 | |||||||
| chr6:116185441 | T | G | 1 | a0001c0001t0003g0193 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.530-35613T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185441 | |||||||
| chr6:116185558 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-35496C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185558 | |||||||
| chr6:116185655 | G | A | 2 | a0001c0001t0007g0140 a0001c0001t0038g0141 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.530-35399G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185655 | |||||||
| chr6:116185809 | C | A | 1 | a0001c0001t0008g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.530-35245C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185809 | |||||||
| chr6:116186039 | T | C | 1 | a0001c0001t0018g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.530-35015T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186039 | |||||||
| chr6:116186043 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-35011G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186043 | |||||||
| chr6:116186080 | G | A | 3 | a0001c0001t0006g0006 a0001c0001t0014g0245 a0001c0001t0018g0274 |
4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-34974G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186080 | |||||||
| chr6:116186450 | C | T | 1 | a0001c0001t0004g0195 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.530-34604C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186450 | |||||||
| chr6:116186468 | T | C | 10 | a0001c0001t0004g0051 a0001c0001t0006g0011 a0001c0001t0006g0012 others(7): Show |
10 | HG00642.hp2 HG01106.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-34586T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186468 | |||||||
| chr6:116186512 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.530-34542G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186512 | |||||||
| chr6:116186518 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.530-34536C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186518 | |||||||
| chr6:116186642 | T | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-34412T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186642 | |||||||
| chr6:116186660 | G | A | 7 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.530-34394G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186660 | |||||||
| chr6:116187042 | T | C | 65 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0098 others(62): Show |
67 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.530-34012T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187042 | |||||||
| chr6:116187150 | A | G | 23 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0237 others(20): Show |
23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-33904A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187150 | |||||||
| chr6:116187207 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.530-33847T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187207 | |||||||
| chr6:116187275 | G | A | 8 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0210 others(5): Show |
8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-33779G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187275 | |||||||
| chr6:116187349 | A | G | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-33705A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187349 | |||||||
| chr6:116187542 | G | A | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.530-33512G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187542 | |||||||
| chr6:116187595 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-33459A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187595 | |||||||
| chr6:116187597 | G | A | 2 | a0001c0001t0002g0262 a0001c0001t0002g0273 |
2 | NA18954.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.530-33457G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187597 | |||||||
| chr6:116187620 | G | A | 8 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0210 others(5): Show |
8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-33434G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187620 | |||||||
| chr6:116187812 | T | C | 3 | a0001c0001t0006g0006 a0001c0001t0014g0245 a0001c0001t0018g0274 |
4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-33242T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187812 | |||||||
| chr6:116187855 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-33199T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187855 | |||||||
| chr6:116187880 | G | A | 3 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 |
3 | HG01258.hp1 HG01952.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.530-33174G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187880 | |||||||
| chr6:116188137 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.530-32917A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188137 | |||||||
| chr6:116188390 | G | A | 10 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0124 others(7): Show |
10 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.530-32664G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188390 | |||||||
| chr6:116188439 | T | A | 1 | a0001c0001t0003g0041 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.530-32615T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188439 | |||||||
| chr6:116188473 | C | T | 94 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0002g0049 others(91): Show |
96 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.530-32581C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188473 | |||||||
| chr6:116188477 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.530-32577A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188477 | |||||||
| chr6:116188513 | A | G | 4 | a0001c0001t0001g0187 a0001c0001t0001g0204 a0001c0001t0001g0209 others(1): Show |
4 | HG01167.hp2 HG01261.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-32541A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188513 | |||||||
| chr6:116188526 | C | A | 1 | a0001c0001t0003g0041 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.530-32528C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188526 | |||||||
| chr6:116188542 | A | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-32512A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188542 | |||||||
| chr6:116188706 | C | CT | 157 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0001g0201 others(154): Show |
162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.530-32335dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116188706 | ||||||
| chr6:116188888 | G | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-32166G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188888 | |||||||
| chr6:116189177 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.530-31877C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116189177 | |||||||
| chr6:116189229 | A | G | 3 | a0001c0001t0006g0006 a0001c0001t0014g0245 a0001c0001t0018g0274 |
4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-31825A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116189229 | |||||||
| chr6:116189396 | G | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-31658G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116189396 | |||||||
| chr6:116189475 | A | G | 1 | a0001c0001t0002g0273 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.530-31579A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116189475 | |||||||
| chr6:116189779 | C | G | 1 | a0001c0001t0005g0133 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.530-31275C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116189779 | |||||||
| chr6:116189844 | A | G | 4 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0277 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-31210A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116189844 | |||||||
| chr6:116190127 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.530-30927A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116190127 | |||||||
| chr6:116190481 | G | A | 11 | a0001c0001t0003g0289 a0001c0001t0006g0118 a0001c0001t0006g0158 others(8): Show |
11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.530-30573G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116190481 | |||||||
| chr6:116190541 | G | T | 1 | a0001c0001t0002g0218 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.530-30513G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116190541 | |||||||
| chr6:116190861 | A | C | 2 | a0001c0001t0001g0186 a0001c0001t0001g0192 |
2 | NA19002.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.530-30193A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116190861 | |||||||
| chr6:116190956 | A | G | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-30098A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116190956 | |||||||
| chr6:116191032 | C | T | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.530-30022C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191032 | |||||||
| chr6:116191177 | C | G | 1 | a0001c0001t0010g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.530-29877C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191177 | |||||||
| chr6:116191459 | G | A | 2 | a0001c0001t0003g0289 a0001c0001t0006g0118 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.530-29595G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191459 | |||||||
| chr6:116191513 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.530-29541A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191513 | |||||||
| chr6:116191611 | T | C | 7 | a0001c0001t0003g0002 a0001c0001t0003g0022 a0001c0001t0003g0023 others(4): Show |
8 | NA18947.hp1 NA18957.hp1 NA19003.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-29443T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191611 | |||||||
| chr6:116191697 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.530-29357C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191697 | |||||||
| chr6:116191909 | A | G | 1 | a0001c0001t0039g0075 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.530-29145A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191909 | |||||||
| chr6:116191959 | G | C | 3 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0260 |
3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-29095G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191959 | |||||||
| chr6:116192065 | G | T | 1 | a0001c0001t0010g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.530-28989G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192065 | |||||||
| chr6:116192157 | G | A | 1 | a0001c0001t0002g0271 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.530-28897G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192157 | |||||||
| chr6:116192321 | A | G | 2 | a0001c0001t0003g0021 a0001c0001t0003g0030 |
2 | NA18973.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.530-28733A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192321 | |||||||
| chr6:116192350 | C | A | 14 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0003g0111 others(11): Show |
14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-28704C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192350 | |||||||
| chr6:116192501 | T | C | 3 | a0001c0001t0002g0291 a0001c0001t0017g0062 a0001c0001t0017g0292 |
3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.530-28553T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192501 | |||||||
| chr6:116192515 | G | A | 23 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0261 others(20): Show |
24 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.530-28539G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192515 | |||||||
| chr6:116192749 | T | C | 1 | a0001c0001t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.530-28305T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192749 | |||||||
| chr6:116192791 | T | A | 159 | a0001c0001t0001g0031 a0001c0001t0001g0119 a0001c0001t0001g0121 others(156): Show |
164 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.530-28263T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192791 | |||||||
| chr6:116192874 | G | C | 1 | a0001c0001t0033g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.530-28180G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192874 | |||||||
| chr6:116192883 | C | A | 20 | a0001c0001t0001g0119 a0001c0001t0002g0058 a0001c0001t0005g0134 others(17): Show |
20 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.530-28171C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192883 | |||||||
| chr6:116193090 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0031 others(252): Show |
263 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.530-27964A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193090 | |||||||
| chr6:116193104 | T | C | 16 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(13): Show |
16 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.530-27950T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193104 | |||||||
| chr6:116193355 | A | G | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-27699A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193355 | |||||||
| chr6:116193497 | T | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | NA18947.hp2 NA19067.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.530-27557T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193497 | |||||||
| chr6:116193629 | G | A | 188 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0049 others(185): Show |
193 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.530-27425G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193629 | |||||||
| chr6:116193700 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.530-27354A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193700 | |||||||
| chr6:116193765 | TTAAAAA | T | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0049 others(160): Show |
167 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-27282_530-2727 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116193765 | ||||||
| chr6:116193837 | G | A | 1 | a0001c0001t0004g0248 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.530-27217G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193837 | |||||||
| chr6:116193899 | A | G | 2 | a0001c0001t0014g0245 a0001c0001t0018g0274 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-27155A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193899 | |||||||
| chr6:116194029 | A | G | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-27025A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194029 | |||||||
| chr6:116194061 | C | A | 188 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0049 others(185): Show |
193 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.530-26993C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194061 | |||||||
| chr6:116194170 | T | G | 1 | a0001c0001t0004g0254 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.530-26884T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194170 | |||||||
| chr6:116194499 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.530-26555T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194499 | |||||||
| chr6:116194607 | G | A | 1 | a0001c0001t0007g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.530-26447G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194607 | |||||||
| chr6:116194626 | A | G | 8 | a0001c0001t0010g0100 a0001c0001t0010g0101 a0001c0001t0010g0102 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.530-26428A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194626 | |||||||
| chr6:116194662 | A | T | 1 | a0001c0001t0014g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.530-26392A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194662 | |||||||
| chr6:116194721 | G | A | 23 | a0001c0001t0003g0009 a0001c0001t0003g0286 a0001c0001t0004g0155 others(20): Show |
23 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.530-26333G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194721 | |||||||
| chr6:116194779 | G | A | 2 | a0001c0001t0004g0255 a0001c0001t0008g0256 |
2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.530-26275G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194779 | |||||||
| chr6:116194979 | G | A | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-26075G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194979 | |||||||
| chr6:116195282 | C | T | 24 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(21): Show |
25 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.530-25772C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116195282 | |||||||
| chr6:116195687 | G | C | 4 | a0001c0001t0002g0079 a0001c0001t0002g0080 a0002c0002t0002g0081 others(1): Show |
4 | HG01168.hp1 HG01192.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-25367G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116195687 | |||||||
| chr6:116195894 | A | G | 8 | a0001c0001t0010g0100 a0001c0001t0010g0101 a0001c0001t0010g0102 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.530-25160A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116195894 | |||||||
| chr6:116195998 | G | A | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-25056G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116195998 | |||||||
| chr6:116196208 | A | G | 2 | a0001c0001t0010g0100 a0001c0001t0010g0101 |
2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.530-24846A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196208 | |||||||
| chr6:116196244 | T | G | 5 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0210 others(2): Show |
5 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-24810T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196244 | |||||||
| chr6:116196278 | A | G | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-24776A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196278 | |||||||
| chr6:116196445 | T | G | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-24609T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196445 | |||||||
| chr6:116196482 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.530-24572G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196482 | |||||||
| chr6:116196521 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.530-24533G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196521 | |||||||
| chr6:116196588 | A | G | 2 | a0001c0001t0017g0062 a0001c0001t0017g0292 |
2 | HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.530-24466A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196588 | |||||||
| chr6:116196688 | T | C | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-24366T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196688 | |||||||
| chr6:116196772 | A | G | 23 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(20): Show |
23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-24282A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196772 | |||||||
| chr6:116196791 | G | C | 1 | a0001c0001t0017g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.530-24263G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196791 | |||||||
| chr6:116196807 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.530-24247G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196807 | |||||||
| chr6:116196925 | A | G | 23 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(20): Show |
23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-24129A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196925 | |||||||
| chr6:116197032 | C | T | 4 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0006g0054 others(1): Show |
4 | NA18971.hp2 NA18978.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-24022C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116197032 | |||||||
| chr6:116197440 | G | A | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-23614G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116197440 | |||||||
| chr6:116197450 | G | A | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-23604G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116197450 | |||||||
| chr6:116197663 | G | A | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.530-23391G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116197663 | |||||||
| chr6:116197821 | A | G | 1 | a0001c0001t0004g0051 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.530-23233A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116197821 | |||||||
| chr6:116197889 | CAT | C | 24 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(21): Show |
24 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.530-23164_530-2316 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116197889 | |||||||
| chr6:116198030 | A | T | 3 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0260 |
3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-23024A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116198030 | |||||||
| chr6:116198281 | T | C | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0014 others(31): Show |
36 | HG00408.hp2 HG00558.hp2 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.530-22773T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116198281 | |||||||
| chr6:116198408 | A | G | 3 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0260 |
3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-22646A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116198408 | |||||||
| chr6:116198477 | A | C | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-22577A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116198477 | |||||||
| chr6:116199024 | A | G | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-22030A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199024 | |||||||
| chr6:116199150 | G | A | 1 | a0001c0001t0006g0138 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.530-21904G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199150 | |||||||
| chr6:116199185 | C | A | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-21869C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199185 | |||||||
| chr6:116199822 | G | A | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-21232G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199822 | |||||||
| chr6:116199996 | A | AG | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-21058_530-2105 others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199996 | |||||||
| chr6:116199997 | A | AG | 23 | a0001c0001t0002g0238 a0001c0001t0002g0264 a0001c0001t0007g0140 others(20): Show |
23 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.530-21056dupG | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116199997 | ||||||
| chr6:116199997 | A | AGC | 6 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(3): Show |
6 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.530-21056_530-2105 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116199997 | ||||||
| chr6:116199997 | A | AGG | 15 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(12): Show |
16 | HG00642.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.530-21056_530-2105 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116199997 | ||||||
| chr6:116199997 | A | G | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-21057A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199997 | |||||||
| chr6:116199998 | GT | G | 25 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0053 others(22): Show |
27 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.530-21055delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199998 | |||||||
| chr6:116199999 | T | G | 160 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 others(157): Show |
163 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.530-21055T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199999 | |||||||
| chr6:116200001 | G | GC | 77 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(74): Show |
79 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.530-21053_530-2105 others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116200001 | |||||||
| chr6:116200001 | G | T | 23 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0053 others(20): Show |
25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.530-21053G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116200001 | |||||||
| chr6:116200023 | G | A | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-21031G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116200023 | |||||||
| chr6:116200027 | G | A | 188 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0049 others(185): Show |
193 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.530-21027G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116200027 | |||||||
| chr6:116200499 | A | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0192 |
2 | NA19002.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.530-20555A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116200499 | |||||||
| chr6:116200858 | C | A | 188 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0049 others(185): Show |
193 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.530-20196C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116200858 | |||||||
| chr6:116201452 | G | A | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-19602G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116201452 | |||||||
| chr6:116201672 | C | A | 1 | a0001c0001t0003g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.530-19382C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116201672 | |||||||
| chr6:116202103 | T | G | 1 | a0001c0001t0004g0248 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.530-18951T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116202103 | |||||||
| chr6:116202292 | C | T | 1 | a0001c0001t0003g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.530-18762C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116202292 | |||||||
| chr6:116202477 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.530-18577A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116202477 | |||||||
| chr6:116202685 | A | T | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-18369A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116202685 | |||||||
| chr6:116202747 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.530-18307T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116202747 | |||||||
| chr6:116203100 | A | G | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-17954A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203100 | |||||||
| chr6:116203136 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.530-17918A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203136 | |||||||
| chr6:116203154 | T | G | 2 | a0001c0001t0014g0245 a0001c0001t0018g0274 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-17900T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203154 | |||||||
| chr6:116203239 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0177 a0001c0001t0001g0280 |
3 | HG03654.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.530-17815C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203239 | |||||||
| chr6:116203363 | A | G | 2 | a0001c0001t0014g0245 a0001c0001t0018g0274 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-17691A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203363 | |||||||
| chr6:116203440 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.530-17614T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203440 | |||||||
| chr6:116203454 | T | C | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-17600T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203454 | |||||||
| chr6:116203518 | A | G | 5 | a0001c0001t0003g0015 a0001c0001t0003g0029 a0001c0001t0003g0042 others(2): Show |
5 | HG02615.hp1 HG02965.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-17536A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203518 | |||||||
| chr6:116203610 | T | C | 2 | a0001c0001t0003g0016 a0001c0001t0003g0044 |
2 | NA18942.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.530-17444T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203610 | |||||||
| chr6:116203713 | A | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0177 a0001c0001t0001g0280 |
3 | HG03654.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.530-17341A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203713 | |||||||
| chr6:116204106 | C | T | 188 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0049 others(185): Show |
193 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.530-16948C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204106 | |||||||
| chr6:116204113 | A | G | 1 | a0001c0001t0017g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.530-16941A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204113 | |||||||
| chr6:116204138 | A | C | 1 | a0001c0001t0014g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.530-16916A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204138 | |||||||
| chr6:116204260 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-16794A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204260 | |||||||
| chr6:116204346 | T | C | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-16708T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204346 | |||||||
| chr6:116204426 | C | T | 1 | a0001c0001t0007g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.530-16628C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204426 | |||||||
| chr6:116204442 | C | T | 286 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(283): Show |
294 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.530-16612C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204442 | |||||||
| chr6:116204490 | A | G | 2 | a0002c0002t0002g0081 a0002c0002t0002g0082 |
2 | HG01168.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.530-16564A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204490 | |||||||
| chr6:116204589 | A | G | 3 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0260 |
3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-16465A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204589 | |||||||
| chr6:116204605 | G | A | 1 | a0001c0001t0019g0150 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.530-16449G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204605 | |||||||
| chr6:116204757 | C | T | 1 | a0001c0001t0006g0011 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.530-16297C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204757 | |||||||
| chr6:116204768 | T | C | 4 | a0001c0001t0012g0168 a0001c0001t0012g0170 a0001c0001t0012g0171 others(1): Show |
4 | NA18941.hp1 NA18968.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-16286T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204768 | |||||||
| chr6:116205018 | A | G | 1 | a0001c0001t0007g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.530-16036A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205018 | |||||||
| chr6:116205195 | A | T | 2 | a0001c0001t0014g0245 a0001c0001t0018g0274 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-15859A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205195 | |||||||
| chr6:116205246 | T | C | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-15808T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205246 | |||||||
| chr6:116205412 | C | T | 138 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(135): Show |
140 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.530-15642C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205412 | |||||||
| chr6:116205480 | TA | T | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-15572delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116205480 | ||||||
| chr6:116205599 | T | TG | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-15448dupG | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116205599 | ||||||
| chr6:116205754 | T | A | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-15300T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205754 | |||||||
| chr6:116205849 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0219 |
2 | NA18940.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.530-15205A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205849 | |||||||
| chr6:116205957 | A | G | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-15097A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205957 | |||||||
| chr6:116205981 | C | T | 1 | a0001c0001t0003g0048 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.530-15073C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205981 | |||||||
| chr6:116206369 | T | C | 8 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0210 others(5): Show |
8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-14685T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116206369 | |||||||
| chr6:116206422 | T | C | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-14632T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116206422 | |||||||
| chr6:116206571 | T | A | 1 | a0001c0001t0003g0027 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.530-14483T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116206571 | |||||||
| chr6:116206770 | T | C | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-14284T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116206770 | |||||||
| chr6:116206952 | T | C | 2 | a0001c0001t0014g0245 a0001c0001t0018g0274 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-14102T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116206952 | |||||||
| chr6:116207018 | GTC | G | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-14034_530-1403 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116207018 | ||||||
| chr6:116207035 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.530-14019A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207035 | |||||||
| chr6:116207298 | ATAGAGTC | A | 137 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(134): Show |
139 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.530-13753_530-1374 others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116207298 | ||||||
| chr6:116207306 | T | G | 137 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(134): Show |
139 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.530-13748T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207306 | |||||||
| chr6:116207370 | C | CA | 285 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(282): Show |
293 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.530-13676dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116207370 | ||||||
| chr6:116207430 | A | G | 1 | a0001c0001t0010g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.530-13624A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207430 | |||||||
| chr6:116207485 | G | A | 24 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(21): Show |
24 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.530-13569G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207485 | |||||||
| chr6:116207703 | A | G | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-13351A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207703 | |||||||
| chr6:116207816 | C | T | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-13238C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207816 | |||||||
| chr6:116207877 | C | T | 2 | a0001c0001t0014g0245 a0001c0001t0018g0274 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-13177C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207877 | |||||||
| chr6:116207899 | A | G | 2 | a0001c0001t0002g0267 a0001c0001t0002g0272 |
2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.530-13155A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207899 | |||||||
| chr6:116207951 | T | C | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-13103T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207951 | |||||||
| chr6:116208032 | C | CT | 3 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0260 |
3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-13019dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116208032 | ||||||
| chr6:116208529 | G | A | 12 | a0001c0001t0009g0107 a0001c0001t0009g0108 a0001c0001t0009g0110 others(9): Show |
12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.530-12525G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116208529 | |||||||
| chr6:116208845 | G | A | 1 | a0001c0001t0004g0214 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.530-12209G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116208845 | |||||||
| chr6:116209038 | G | C | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-12016G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209038 | |||||||
| chr6:116209141 | C | T | 21 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(18): Show |
21 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.530-11913C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209141 | |||||||
| chr6:116209344 | A | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-11710A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209344 | |||||||
| chr6:116209604 | T | C | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-11450T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209604 | |||||||
| chr6:116209632 | A | G | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-11422A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209632 | |||||||
| chr6:116209693 | G | T | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-11361G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209693 | |||||||
| chr6:116209819 | C | G | 12 | a0001c0001t0009g0107 a0001c0001t0009g0108 a0001c0001t0009g0110 others(9): Show |
12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.530-11235C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209819 | |||||||
| chr6:116210146 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.530-10908C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116210146 | |||||||
| chr6:116210211 | A | G | 1 | a0001c0001t0002g0266 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.530-10843A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116210211 | |||||||
| chr6:116210366 | GA | G | 23 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0053 others(20): Show |
25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.530-10677delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116210366 | ||||||
| chr6:116210438 | G | T | 2 | a0001c0001t0014g0245 a0001c0001t0018g0274 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-10616G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116210438 | |||||||
| chr6:116210465 | A | G | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-10589A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116210465 | |||||||
| chr6:116210745 | AAAAT | A | 23 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0053 others(20): Show |
25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.530-10304_530-1030 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116210745 | ||||||
| chr6:116210781 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.530-10273A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116210781 | |||||||
| chr6:116210905 | G | T | 12 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(9): Show |
13 | HG00642.hp2 HG02717.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.530-10149G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116210905 | |||||||
| chr6:116211052 | A | G | 2 | a0001c0001t0014g0245 a0001c0001t0018g0274 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-10002A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211052 | |||||||
| chr6:116211102 | C | A | 138 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(135): Show |
140 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.530-9952C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211102 | |||||||
| chr6:116211247 | C | T | 12 | a0001c0001t0009g0107 a0001c0001t0009g0108 a0001c0001t0009g0110 others(9): Show |
12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.530-9807C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211247 | |||||||
| chr6:116211267 | C | T | 25 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0053 others(22): Show |
27 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.530-9787C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211267 | |||||||
| chr6:116211696 | C | T | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-9358C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211696 | |||||||
| chr6:116211937 | G | A | 1 | a0001c0001t0013g0071 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.530-9117G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211937 | |||||||
| chr6:116211951 | C | T | 1 | a0001c0001t0006g0006 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.530-9103C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211951 | |||||||
| chr6:116211953 | G | C | 206 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0124 others(203): Show |
211 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.530-9101G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211953 | |||||||
| chr6:116212220 | TATC | T | 12 | a0001c0001t0009g0107 a0001c0001t0009g0108 a0001c0001t0009g0110 others(9): Show |
12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.530-8831_530-8829d others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116212220 | ||||||
| chr6:116212466 | G | A | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.530-8588G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116212466 | |||||||
| chr6:116212848 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.530-8206G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116212848 | |||||||
| chr6:116213065 | G | C | 8 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0210 others(5): Show |
8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-7989G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213065 | |||||||
| chr6:116213083 | A | G | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-7971A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213083 | |||||||
| chr6:116213129 | A | T | 1 | a0001c0001t0004g0254 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.530-7925A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213129 | |||||||
| chr6:116213272 | A | C | 2 | a0001c0001t0010g0100 a0001c0001t0010g0101 |
2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.530-7782A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213272 | |||||||
| chr6:116213434 | C | T | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.530-7620C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213434 | |||||||
| chr6:116213464 | C | G | 1 | a0001c0001t0002g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.530-7590C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213464 | |||||||
| chr6:116213548 | A | G | 23 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(20): Show |
23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-7506A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213548 | |||||||
| chr6:116213665 | T | C | 2 | a0001c0001t0007g0244 a0001c0001t0035g0290 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.530-7389T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213665 | |||||||
| chr6:116213773 | A | G | 1 | a0001c0001t0007g0130 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.530-7281A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213773 | |||||||
| chr6:116213887 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.530-7167T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213887 | |||||||
| chr6:116214081 | T | G | 3 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0260 |
3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-6973T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214081 | |||||||
| chr6:116214217 | C | G | 188 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0049 others(185): Show |
193 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.530-6837C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214217 | |||||||
| chr6:116214240 | T | C | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.530-6814T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214240 | |||||||
| chr6:116214292 | A | G | 7 | a0001c0001t0004g0155 a0001c0001t0004g0164 a0001c0001t0004g0166 others(4): Show |
7 | HG00323.hp2 HG00438.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.530-6762A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214292 | |||||||
| chr6:116214470 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.530-6584A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214470 | |||||||
| chr6:116214535 | C | G | 1 | a0001c0001t0002g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.530-6519C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214535 | |||||||
| chr6:116214808 | C | T | 2 | a0001c0001t0002g0084 a0003c0004t0002g0076 |
2 | HG01081.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.530-6246C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214808 | |||||||
| chr6:116214820 | TA | T | 11 | a0001c0001t0006g0118 a0001c0001t0006g0158 a0001c0001t0007g0128 others(8): Show |
11 | HG02145.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.530-6223delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116214820 | ||||||
| chr6:116215088 | A | G | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-5966A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116215088 | |||||||
| chr6:116215449 | T | A | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-5605T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116215449 | |||||||
| chr6:116215591 | T | A | 1 | a0001c0001t0002g0053 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.530-5463T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116215591 | |||||||
| chr6:116215761 | C | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-5293C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116215761 | |||||||
| chr6:116215861 | G | A | 1 | a0001c0001t0003g0203 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.530-5193G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116215861 | |||||||
| chr6:116215946 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.530-5108G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116215946 | |||||||
| chr6:116216013 | T | A | 1 | a0001c0001t0003g0021 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.530-5041T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216013 | |||||||
| chr6:116216075 | C | G | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-4979C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216075 | |||||||
| chr6:116216155 | A | T | 1 | a0001c0003t0014g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.530-4899A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216155 | |||||||
| chr6:116216326 | T | A | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-4728T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216326 | |||||||
| chr6:116216335 | T | A | 1 | a0001c0001t0008g0040 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.530-4719T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216335 | |||||||
| chr6:116216392 | T | TA | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-4651dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116216392 | ||||||
| chr6:116216568 | T | C | 7 | a0001c0001t0006g0158 a0001c0001t0007g0128 a0001c0001t0007g0129 others(4): Show |
7 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.530-4486T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216568 | |||||||
| chr6:116216587 | A | G | 1 | a0001c0001t0020g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.530-4467A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216587 | |||||||
| chr6:116216743 | A | C | 1 | a0001c0001t0019g0150 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.530-4311A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216743 | |||||||
| chr6:116216851 | C | G | 2 | a0001c0001t0017g0062 a0001c0001t0017g0292 |
2 | HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.530-4203C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216851 | |||||||
| chr6:116216888 | A | G | 1 | a0001c0001t0004g0043 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.530-4166A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216888 | |||||||
| chr6:116217022 | C | T | 4 | a0001c0001t0010g0102 a0001c0001t0010g0103 a0001c0001t0010g0104 others(1): Show |
4 | HG01074.hp1 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-4032C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116217022 | |||||||
| chr6:116217026 | G | A | 1 | a0001c0001t0007g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.530-4028G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116217026 | |||||||
| chr6:116217161 | AATATTCA others(6): Show |
A | 2 | a0001c0001t0003g0193 a0001c0001t0003g0203 |
2 | HG01358.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.530-3891_530-3879d others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116217161 | ||||||
| chr6:116217210 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.530-3844T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116217210 | |||||||
| chr6:116217371 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.530-3683G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116217371 | |||||||
| chr6:116217923 | T | C | 140 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(137): Show |
143 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.530-3131T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116217923 | |||||||
| chr6:116218227 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.530-2827C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218227 | |||||||
| chr6:116218228 | G | A | 99 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(96): Show |
101 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.530-2826G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218228 | |||||||
| chr6:116218469 | G | T | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-2585G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218469 | |||||||
| chr6:116218538 | A | T | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-2516A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218538 | |||||||
| chr6:116218803 | C | A | 3 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0002g0277 |
3 | HG02486.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.530-2251C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218803 | |||||||
| chr6:116218834 | CA | C | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-2219delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218834 | |||||||
| chr6:116218954 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.530-2100G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218954 | |||||||
| chr6:116219041 | G | A | 1 | a0001c0001t0018g0274 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.530-2013G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219041 | |||||||
| chr6:116219232 | C | T | 22 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(19): Show |
24 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.530-1822C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219232 | |||||||
| chr6:116219477 | T | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-1577T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219477 | |||||||
| chr6:116219547 | A | G | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-1507A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219547 | |||||||
| chr6:116219643 | C | T | 3 | a0001c0001t0016g0116 a0001c0001t0016g0117 a0001c0001t0025g0115 |
3 | HG01891.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.530-1411C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219643 | |||||||
| chr6:116219679 | A | G | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-1375A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219679 | |||||||
| chr6:116219719 | G | A | 1 | a0001c0001t0006g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.530-1335G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219719 | |||||||
| chr6:116219894 | G | A | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-1160G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219894 | |||||||
| chr6:116219961 | C | CA | 53 | a0001c0001t0001g0031 a0001c0001t0001g0092 a0001c0001t0001g0093 others(50): Show |
53 | HG00438.hp1 HG00438.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.530-1070dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116219961 | ||||||
| chr6:116219961 | CAA | C | 11 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.530-1071_530-1070d others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116219961 | ||||||
| chr6:116219961 | CAAA | C | 7 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0283 others(4): Show |
7 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.530-1072_530-1070d others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116219961 | ||||||
| chr6:116219974 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.530-1077_530-1067d others(13): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116219974 | ||||||
| chr6:116219983 | AAC | A | 27 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0006g0064 others(24): Show |
27 | HG00642.hp2 HG01074.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.530-1069_530-1068d others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116219983 | ||||||
| chr6:116219984 | AC | A | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0053 others(37): Show |
42 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.530-1069delC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219984 | |||||||
| chr6:116219985 | C | A | 120 | a0001c0001t0002g0004 a0001c0001t0002g0049 a0001c0001t0002g0055 others(117): Show |
122 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.530-1069C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219985 | |||||||
| chr6:116220002 | G | A | 1 | a0001c0001t0007g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.530-1052G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220002 | |||||||
| chr6:116220049 | C | T | 138 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(135): Show |
140 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.530-1005C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220049 | |||||||
| chr6:116220122 | C | CT | 27 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0121 others(24): Show |
27 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.530-909dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | ||||||
| chr6:116220122 | C | CTT | 67 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0017 others(64): Show |
68 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.530-910_530-909dup others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | ||||||
| chr6:116220122 | C | CTTT | 16 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0014 others(13): Show |
17 | HG00438.hp2 HG01175.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.530-911_530-909dup others(3): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | ||||||
| chr6:116220122 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0059 others(2): Show |
5 | HG01884.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-918_530-909dup others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | ||||||
| chr6:116220122 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0002g0066 a0001c0001t0002g0277 |
2 | HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.530-919_530-909dup others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | ||||||
| chr6:116220122 | C | CTTTTTTT others(5): Show |
6 | a0001c0001t0002g0056 a0001c0001t0002g0065 a0001c0001t0002g0106 others(3): Show |
6 | HG02109.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.530-920_530-909dup others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | ||||||
| chr6:116220122 | C | T | 10 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(7): Show |
11 | HG00642.hp2 HG02717.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.530-932C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220122 | |||||||
| chr6:116220122 | CTT | C | 21 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0067 others(18): Show |
23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.530-910_530-909del others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | ||||||
| chr6:116220213 | C | T | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-841C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220213 | |||||||
| chr6:116220221 | A | G | 28 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(25): Show |
30 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.530-833A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220221 | |||||||
| chr6:116220340 | T | C | 187 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0049 others(184): Show |
192 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.530-714T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220340 | |||||||
| chr6:116220384 | C | T | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530-670C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220384 | |||||||
| chr6:116220556 | C | G | 2 | a0001c0001t0002g0098 a0001c0001t0002g0237 |
2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.530-498C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220556 | |||||||
| chr6:116220828 | TAGCC | T | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-222_530-219del others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220828 | ||||||
| chr6:116220844 | T | C | 23 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(20): Show |
23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-210T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220844 | |||||||
| chr6:116220853 | A | G | 8 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0210 others(5): Show |
8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-201A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220853 | |||||||
| chr6:116220865 | T | C | 4 | a0001c0001t0001g0160 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
4 | HG00558.hp1 NA18961.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-189T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220865 | |||||||
| chr6:116221337 | T | C | 25 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0053 others(22): Show |
27 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.704+109T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116221337 | |||||||
| chr6:116221479 | C | G | 1 | a0001c0001t0006g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.704+251C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116221479 | |||||||
| chr6:116221816 | A | G | 1 | a0001c0001t0014g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.704+588A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116221816 | |||||||
| chr6:116221923 | A | T | 1 | a0001c0001t0004g0251 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.704+695A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116221923 | |||||||
| chr6:116222115 | A | G | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.704+887A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222115 | |||||||
| chr6:116222263 | G | T | 1 | a0001c0001t0010g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.705-771G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222263 | |||||||
| chr6:116222442 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.705-592G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222442 | |||||||
| chr6:116222485 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.705-549T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222485 | |||||||
| chr6:116222644 | A | C | 2 | a0001c0001t0010g0100 a0001c0001t0010g0101 |
2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.705-390A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222644 | |||||||
| chr6:116222661 | C | G | 1 | a0001c0001t0002g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.705-373C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222661 | |||||||
| chr6:116222684 | A | G | 162 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(159): Show |
165 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.705-350A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222684 | |||||||
| chr6:116222720 | A | C | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.705-314A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222720 | |||||||
| chr6:116222782 | A | G | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.705-252A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222782 | |||||||
| chr6:116222872 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.705-162A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222872 | |||||||
| chr6:116222892 | T | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0177 a0001c0001t0001g0280 |
3 | HG03654.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.705-142T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222892 | |||||||
| chr6:116222931 | G | A | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.705-103G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222931 | |||||||
| chr6:116223450 | G | T | 1 | a0001c0001t0001g0224 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.802+319G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116223450 | |||||||
| chr6:116223574 | G | A | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.802+443G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116223574 | |||||||
| chr6:116223579 | G | A | 7 | a0001c0001t0004g0155 a0001c0001t0004g0164 a0001c0001t0004g0166 others(4): Show |
7 | HG00323.hp2 HG00438.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+448G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116223579 | |||||||
| chr6:116223587 | T | A | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.802+456T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116223587 | |||||||
| chr6:116224322 | A | G | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.802+1191A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224322 | |||||||
| chr6:116224486 | A | G | 2 | a0001c0001t0010g0100 a0001c0001t0010g0101 |
2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.802+1355A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224486 | |||||||
| chr6:116224545 | G | A | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.802+1414G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224545 | |||||||
| chr6:116224581 | T | C | 1 | a0001c0001t0003g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.802+1450T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224581 | |||||||
| chr6:116224607 | T | C | 2 | a0001c0001t0014g0245 a0001c0001t0018g0274 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.802+1476T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224607 | |||||||
| chr6:116224749 | G | A | 1 | a0001c0001t0003g0039 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.802+1618G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224749 | |||||||
| chr6:116224749 | G | T | 6 | a0001c0001t0002g0098 a0001c0001t0002g0237 a0001c0001t0002g0238 others(3): Show |
6 | HG02109.hp2 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+1618G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224749 | |||||||
| chr6:116224844 | G | A | 8 | a0001c0001t0010g0100 a0001c0001t0010g0101 a0001c0001t0010g0102 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+1713G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224844 | |||||||
| chr6:116225093 | A | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02896.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.802+1962A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225093 | |||||||
| chr6:116225119 | C | T | 138 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(135): Show |
140 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.802+1988C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225119 | |||||||
| chr6:116225330 | T | C | 1 | a0001c0001t0014g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.802+2199T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225330 | |||||||
| chr6:116225371 | A | G | 1 | a0001c0001t0010g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.802+2240A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225371 | |||||||
| chr6:116225380 | A | G | 25 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0053 others(22): Show |
27 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.802+2249A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225380 | |||||||
| chr6:116225689 | G | C | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.802+2558G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225689 | |||||||
| chr6:116225703 | G | T | 4 | a0001c0001t0010g0102 a0001c0001t0010g0103 a0001c0001t0010g0104 others(1): Show |
4 | HG01074.hp1 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+2572G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225703 | |||||||
| chr6:116225761 | A | G | 188 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0049 others(185): Show |
193 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.802+2630A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225761 | |||||||
| chr6:116225803 | A | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02896.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.802+2672A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225803 | |||||||
| chr6:116225806 | G | A | 2 | a0001c0001t0014g0245 a0001c0001t0018g0274 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.802+2675G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225806 | |||||||
| chr6:116225849 | T | A | 1 | a0001c0001t0005g0133 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.802+2718T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225849 | |||||||
| chr6:116225936 | G | C | 5 | a0001c0001t0003g0015 a0001c0001t0003g0029 a0001c0001t0003g0042 others(2): Show |
5 | HG02615.hp1 HG02965.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.802+2805G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225936 | |||||||
| chr6:116226045 | A | T | 23 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(20): Show |
23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.802+2914A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226045 | |||||||
| chr6:116226077 | T | C | 97 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(94): Show |
99 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.802+2946T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226077 | |||||||
| chr6:116226109 | A | G | 16 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(13): Show |
17 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+2978A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226109 | |||||||
| chr6:116226307 | C | T | 1 | a0001c0001t0008g0040 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.802+3176C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226307 | |||||||
| chr6:116226412 | GT | G | 11 | a0001c0001t0009g0107 a0001c0001t0009g0108 a0001c0001t0009g0112 others(8): Show |
11 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+3289delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116226412 | ||||||
| chr6:116226426 | G | A | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.802+3295G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226426 | |||||||
| chr6:116226692 | T | C | 1 | a0001c0001t0037g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.802+3561T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226692 | |||||||
| chr6:116226806 | G | A | 8 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0210 others(5): Show |
8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.802+3675G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226806 | |||||||
| chr6:116226878 | A | C | 1 | a0001c0001t0026g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.802+3747A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226878 | |||||||
| chr6:116227000 | A | G | 2 | a0001c0001t0009g0107 a0001c0001t0009g0144 |
2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.802+3869A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227000 | |||||||
| chr6:116227065 | T | G | 1 | a0001c0001t0002g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.802+3934T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227065 | |||||||
| chr6:116227077 | G | A | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.802+3946G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227077 | |||||||
| chr6:116227281 | ATGT | A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0192 a0001c0001t0001g0220 |
3 | NA18959.hp1 NA19002.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.802+4154_802+4156d others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116227281 | ||||||
| chr6:116227665 | A | ATGAGGTG others(22): Show |
1 | a0001c0001t0014g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.802+4537_802+4565d others(31): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116227665 | ||||||
| chr6:116227728 | T | C | 138 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(135): Show |
140 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.802+4597T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227728 | |||||||
| chr6:116227733 | C | T | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.802+4602C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227733 | |||||||
| chr6:116227781 | G | C | 138 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(135): Show |
140 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.802+4650G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227781 | |||||||
| chr6:116227866 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(95): Show |
101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.802+4735A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227866 | |||||||
| chr6:116227945 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(77): Show |
83 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.802+4814G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227945 | |||||||
| chr6:116227948 | G | A | 16 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(13): Show |
17 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+4817G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227948 | |||||||
| chr6:116228118 | A | C | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.802+4987A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228118 | |||||||
| chr6:116228228 | G | T | 1 | a0001c0001t0006g0011 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.802+5097G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228228 | |||||||
| chr6:116228279 | CG | C | 7 | a0001c0001t0006g0158 a0001c0001t0007g0128 a0001c0001t0007g0129 others(4): Show |
7 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+5150delG | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116228279 | ||||||
| chr6:116228341 | T | G | 1 | a0001c0001t0002g0229 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.802+5210T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228341 | |||||||
| chr6:116228368 | C | A | 1 | a0001c0001t0004g0043 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.802+5237C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228368 | |||||||
| chr6:116228411 | G | A | 2 | a0001c0001t0002g0004 a0001c0001t0034g0279 |
3 | HG00642.hp1 HG03130.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.802+5280G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228411 | |||||||
| chr6:116228452 | G | A | 1 | a0001c0001t0002g0229 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.802+5321G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228452 | |||||||
| chr6:116228508 | CA | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(258): Show |
267 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.802+5388delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116228508 | ||||||
| chr6:116228619 | G | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(77): Show |
83 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.802+5488G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228619 | |||||||
| chr6:116228764 | A | G | 2 | a0001c0001t0003g0193 a0001c0001t0003g0203 |
2 | HG01358.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.802+5633A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228764 | |||||||
| chr6:116228801 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.802+5670C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228801 | |||||||
| chr6:116228968 | G | A | 1 | a0001c0001t0028g0028 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.802+5837G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228968 | |||||||
| chr6:116229010 | G | A | 2 | a0001c0001t0003g0231 a0001c0001t0004g0043 |
2 | HG02132.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.802+5879G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229010 | |||||||
| chr6:116229063 | G | A | 1 | a0001c0001t0003g0014 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.802+5932G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229063 | |||||||
| chr6:116229169 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.802+6038A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229169 | |||||||
| chr6:116229283 | C | T | 2 | a0001c0001t0004g0255 a0001c0001t0008g0256 |
2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.802+6152C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229283 | |||||||
| chr6:116229490 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.802+6359G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229490 | |||||||
| chr6:116229533 | G | A | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.802+6402G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229533 | |||||||
| chr6:116229754 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.802+6623A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229754 | |||||||
| chr6:116229807 | G | C | 10 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0124 others(7): Show |
10 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.802+6676G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229807 | |||||||
| chr6:116229904 | C | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(77): Show |
83 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.802+6773C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229904 | |||||||
| chr6:116229970 | C | G | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.802+6839C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229970 | |||||||
| chr6:116230320 | C | A | 4 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | HG01993.hp1 HG02300.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-6646C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230320 | |||||||
| chr6:116230440 | C | T | 1 | a0001c0001t0003g0203 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.803-6526C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230440 | |||||||
| chr6:116230458 | A | C | 3 | a0001c0001t0010g0102 a0001c0001t0010g0103 a0001c0001t0010g0104 |
3 | HG01884.hp1 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.803-6508A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230458 | |||||||
| chr6:116230475 | C | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(258): Show |
267 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.803-6491C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230475 | |||||||
| chr6:116230836 | G | A | 1 | a0001c0001t0014g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.803-6130G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230836 | |||||||
| chr6:116230914 | A | G | 4 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0006g0054 others(1): Show |
4 | NA18971.hp2 NA18978.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-6052A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230914 | |||||||
| chr6:116230940 | C | T | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.803-6026C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230940 | |||||||
| chr6:116230975 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.803-5991C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230975 | |||||||
| chr6:116231106 | C | CA | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(90): Show |
96 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.803-5840dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116231106 | ||||||
| chr6:116231106 | CA | C | 137 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(134): Show |
140 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.803-5840delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116231106 | ||||||
| chr6:116231106 | CAAAAAAA others(4): Show |
C | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.803-5850_803-5840d others(13): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116231106 | ||||||
| chr6:116231148 | T | TC | 105 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(102): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.803-5809dupC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116231148 | ||||||
| chr6:116231148 | T | TCC | 100 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(97): Show |
101 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.803-5810_803-5809d others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116231148 | ||||||
| chr6:116231148 | T | TCCC | 45 | a0001c0001t0002g0049 a0001c0001t0002g0263 a0001c0001t0002g0265 others(42): Show |
47 | HG00408.hp2 HG00558.hp2 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.803-5811_803-5809d others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116231148 | ||||||
| chr6:116231395 | A | G | 2 | a0001c0001t0007g0268 a0001c0001t0007g0269 |
2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.803-5571A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231395 | |||||||
| chr6:116231588 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.803-5378T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231588 | |||||||
| chr6:116231705 | G | A | 5 | a0001c0001t0004g0051 a0001c0001t0005g0095 a0001c0001t0005g0097 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-5261G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231705 | |||||||
| chr6:116231824 | T | G | 1 | a0001c0001t0002g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.803-5142T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231824 | |||||||
| chr6:116231872 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.803-5094G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231872 | |||||||
| chr6:116231903 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(95): Show |
101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.803-5063G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231903 | |||||||
| chr6:116231933 | G | T | 138 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(135): Show |
140 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.803-5033G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231933 | |||||||
| chr6:116231971 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.803-4995C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231971 | |||||||
| chr6:116232159 | C | CTG | 263 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.803-4806_803-4805i others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116232159 | ||||||
| chr6:116232161 | A | G | 1 | a0001c0001t0005g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.803-4805A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232161 | |||||||
| chr6:116232188 | C | T | 8 | a0001c0001t0010g0100 a0001c0001t0010g0101 a0001c0001t0010g0102 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-4778C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232188 | |||||||
| chr6:116232286 | A | C | 6 | a0001c0001t0001g0093 a0001c0001t0001g0162 a0001c0001t0001g0222 others(3): Show |
6 | HG01192.hp2 HG01243.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-4680A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232286 | |||||||
| chr6:116232348 | A | G | 23 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(20): Show |
23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.803-4618A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232348 | |||||||
| chr6:116232405 | A | C | 1 | a0001c0001t0038g0141 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.803-4561A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232405 | |||||||
| chr6:116232411 | T | A | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.803-4555T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232411 | |||||||
| chr6:116232525 | GA | G | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.803-4434delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116232525 | ||||||
| chr6:116232554 | A | T | 1 | a0001c0001t0001g0169 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.803-4412A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232554 | |||||||
| chr6:116232937 | C | T | 1 | a0001c0001t0023g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803-4029C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232937 | |||||||
| chr6:116233019 | T | C | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
36 | HG00408.hp2 HG00558.hp2 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.803-3947T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116233019 | |||||||
| chr6:116233182 | A | T | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.803-3784A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116233182 | |||||||
| chr6:116233298 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.803-3668T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116233298 | |||||||
| chr6:116233550 | G | A | 4 | a0001c0001t0012g0168 a0001c0001t0012g0170 a0001c0001t0012g0171 others(1): Show |
4 | NA18941.hp1 NA18968.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-3416G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116233550 | |||||||
| chr6:116233625 | A | G | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.803-3341A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116233625 | |||||||
| chr6:116233916 | C | T | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.803-3050C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116233916 | |||||||
| chr6:116233977 | G | GT | 115 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(112): Show |
118 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.803-2971dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116233977 | ||||||
| chr6:116233977 | G | GTT | 106 | a0001c0001t0001g0139 a0001c0001t0001g0152 a0001c0001t0001g0224 others(103): Show |
108 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.803-2972_803-2971d others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116233977 | ||||||
| chr6:116233977 | GT | G | 14 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(11): Show |
14 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.803-2971delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116233977 | ||||||
| chr6:116234012 | C | T | 1 | a0001c0001t0017g0292 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.803-2954C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116234012 | |||||||
| chr6:116234195 | C | T | 1 | a0001c0001t0018g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.803-2771C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116234195 | |||||||
| chr6:116234457 | A | G | 2 | a0001c0001t0010g0100 a0001c0001t0010g0101 |
2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.803-2509A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116234457 | |||||||
| chr6:116234715 | T | C | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.803-2251T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116234715 | |||||||
| chr6:116234813 | C | T | 4 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | HG01993.hp1 HG02300.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-2153C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116234813 | |||||||
| chr6:116234821 | C | T | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.803-2145C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116234821 | |||||||
| chr6:116235035 | GT | G | 12 | a0001c0001t0001g0094 a0001c0001t0003g0034 a0001c0001t0003g0286 others(9): Show |
12 | HG01081.hp2 HG02145.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.803-1913delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116235035 | ||||||
| chr6:116235035 | GTT | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(240): Show |
249 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.803-1914_803-1913d others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116235035 | ||||||
| chr6:116235035 | GTTT | G | 8 | a0001c0001t0002g0263 a0001c0001t0008g0256 a0001c0001t0017g0062 others(5): Show |
8 | HG02280.hp1 HG02630.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-1915_803-1913d others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116235035 | ||||||
| chr6:116235252 | G | T | 2 | a0001c0001t0017g0062 a0001c0001t0017g0292 |
2 | HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.803-1714G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116235252 | |||||||
| chr6:116235279 | G | C | 1 | a0001c0001t0001g0175 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.803-1687G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116235279 | |||||||
| chr6:116235328 | A | G | 21 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(18): Show |
21 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.803-1638A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116235328 | |||||||
| chr6:116235455 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.803-1511A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116235455 | |||||||
| chr6:116235731 | T | C | 1 | a0001c0003t0014g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803-1235T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116235731 | |||||||
| chr6:116235835 | A | G | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.803-1131A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116235835 | |||||||
| chr6:116235900 | A | AGCCAATG | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.803-1065_803-1059d others(9): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116235900 | ||||||
| chr6:116236091 | G | A | 2 | a0001c0001t0003g0193 a0001c0001t0003g0203 |
2 | HG01358.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.803-875G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116236091 | |||||||
| chr6:116236159 | A | G | 2 | a0001c0001t0007g0268 a0001c0001t0007g0269 |
2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.803-807A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116236159 | |||||||
| chr6:116236498 | G | C | 16 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(13): Show |
17 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-468G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116236498 | |||||||
| chr6:116236786 | G | A | 1 | a0001c0001t0002g0005 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.803-180G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116236786 | |||||||
| chr6:116237408 | G | T | 2 | a0001c0001t0014g0245 a0001c0001t0018g0274 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.921+324G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116237408 | |||||||
| chr6:116237445 | C | A | 1 | a0001c0001t0003g0026 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.921+361C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116237445 | |||||||
| chr6:116237576 | G | A | 12 | a0001c0001t0009g0107 a0001c0001t0009g0108 a0001c0001t0009g0110 others(9): Show |
12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.921+492G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116237576 | |||||||
| chr6:116237622 | A | G | 8 | a0001c0001t0010g0100 a0001c0001t0010g0101 a0001c0001t0010g0102 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.921+538A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116237622 | |||||||
| chr6:116237773 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.922-414A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116237773 | |||||||
| chr6:116237799 | A | G | 23 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(20): Show |
23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.922-388A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116237799 | |||||||
| chr6:116238161 | A | G | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.922-26A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116238161 | |||||||
| chr6:116238409 | A | G | 1 | a0001c0001t0007g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1083+61A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 10/11 | chr6 | 116238409 | |||||||
| chr6:116238464 | TA | T | 95 | a0001c0001t0001g0146 a0001c0001t0001g0185 a0001c0001t0001g0206 others(92): Show |
97 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1083+136delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 116238464 | ||||||
| chr6:116238464 | TAA | T | 33 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(30): Show |
33 | HG00639.hp1 HG01074.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1083+135_1083+136d others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 116238464 | ||||||
| chr6:116238464 | TAAAAAAA others(2): Show |
T | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1083+128_1083+136d others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 116238464 | ||||||
| chr6:116238862 | G | C | 114 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(111): Show |
116 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1084-93G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 10/11 | chr6 | 116238862 | |||||||
| chr6:116239168 | T | A | 15 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1252+45T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239168 | |||||||
| chr6:116239255 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1252+132T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239255 | |||||||
| chr6:116239260 | C | A | 1 | a0001c0001t0005g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1252+137C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239260 | |||||||
| chr6:116239558 | C | T | 25 | a0001c0001t0006g0006 a0001c0001t0006g0011 a0001c0001t0006g0012 others(22): Show |
26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.1252+435C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239558 | |||||||
| chr6:116239603 | G | A | 138 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(135): Show |
140 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1252+480G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239603 | |||||||
| chr6:116239645 | G | C | 3 | a0001c0001t0016g0116 a0001c0001t0016g0117 a0001c0001t0025g0115 |
3 | HG01891.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1252+522G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239645 | |||||||
| chr6:116239707 | C | T | 1 | a0001c0001t0008g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1252+584C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239707 | |||||||
| chr6:116239708 | A | G | 138 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(135): Show |
140 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1252+585A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239708 | |||||||
| chr6:116239904 | T | G | 1 | a0001c0001t0002g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1252+781T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239904 | |||||||
| chr6:116239924 | T | C | 25 | a0001c0001t0003g0286 a0001c0001t0004g0155 a0001c0001t0004g0157 others(22): Show |
25 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1252+801T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239924 | |||||||
| chr6:116240015 | G | A | 1 | a0001c0001t0010g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1252+892G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240015 | |||||||
| chr6:116240158 | G | C | 1 | a0001c0001t0002g0005 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1252+1035G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240158 | |||||||
| chr6:116240548 | T | A | 72 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(69): Show |
74 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.1252+1425T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240548 | |||||||
| chr6:116240646 | T | C | 2 | a0001c0001t0006g0011 a0001c0001t0006g0012 |
2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1252+1523T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240646 | |||||||
| chr6:116240751 | G | A | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1252+1628G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240751 | |||||||
| chr6:116240841 | A | G | 2 | a0001c0001t0007g0140 a0001c0001t0038g0141 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1252+1718A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240841 | |||||||
| chr6:116240901 | T | G | 2 | a0001c0001t0007g0268 a0001c0001t0007g0269 |
2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1252+1778T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240901 | |||||||
| chr6:116241010 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(258): Show |
267 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.1252+1887A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241010 | |||||||
| chr6:116241141 | C | CA | 28 | a0001c0001t0001g0207 a0001c0001t0002g0053 a0001c0001t0002g0239 others(25): Show |
29 | HG00642.hp2 HG00741.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1252+2036dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241141 | ||||||
| chr6:116241141 | CA | C | 8 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
8 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1252+2036delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241141 | ||||||
| chr6:116241478 | G | T | 1 | a0001c0001t0008g0010 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1252+2355G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241478 | |||||||
| chr6:116241593 | A | C | 1 | a0001c0001t0005g0247 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1253-2316A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241593 | |||||||
| chr6:116241751 | G | A | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1253-2158G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241751 | |||||||
| chr6:116241792 | G | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0219 |
2 | NA18940.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1253-2117G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241792 | |||||||
| chr6:116241855 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0179 |
2 | HG02071.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1253-2054G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241855 | |||||||
| chr6:116241918 | G | A | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1253-1991G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241918 | |||||||
| chr6:116241921 | TCAAAAAA others(15): Show |
T | 40 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(37): Show |
40 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.1253-1971_1253-195 others(26): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241921 | ||||||
| chr6:116241922 | CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0002g0263 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1253-1972_1253-195 others(27): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241922 | ||||||
| chr6:116241923 | AAAAAAAA others(14): Show |
A | 74 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(71): Show |
76 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1253-1966_1253-194 others(25): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241923 | ||||||
| chr6:116241924 | AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0005g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1253-1970_1253-195 others(24): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241924 | ||||||
| chr6:116241929 | AAAAAAAA others(8): Show |
A | 2 | a0001c0001t0001g0179 a0001c0001t0011g0090 |
2 | HG01169.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1253-1970_1253-195 others(19): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241929 | ||||||
| chr6:116241930 | AAAAAAAA others(7): Show |
A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(79): Show |
84 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1253-1970_1253-195 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241930 | ||||||
| chr6:116241931 | AAAAAAAA others(6): Show |
A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0124 a0001c0001t0001g0125 others(12): Show |
15 | HG00738.hp1 HG01192.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1253-1970_1253-195 others(17): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241931 | ||||||
| chr6:116241933 | AAAAAACA others(4): Show |
A | 16 | a0001c0001t0002g0049 a0001c0001t0002g0098 a0001c0001t0002g0237 others(13): Show |
16 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1253-1970_1253-196 others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241933 | ||||||
| chr6:116241934 | AAAAACAA others(3): Show |
A | 6 | a0001c0001t0002g0055 a0001c0001t0002g0239 a0001c0001t0002g0262 others(3): Show |
6 | HG03098.hp1 HG03130.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.1253-1970_1253-196 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241934 | ||||||
| chr6:116241935 | AAAACAAA others(2): Show |
A | 17 | a0001c0001t0002g0238 a0001c0001t0006g0006 a0001c0001t0006g0011 others(14): Show |
18 | HG00642.hp2 HG01106.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1253-1970_1253-196 others(13): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241935 | ||||||
| chr6:116241936 | AAACAAAA others(1): Show |
A | 9 | a0001c0001t0006g0054 a0001c0001t0006g0061 a0001c0001t0006g0158 others(6): Show |
9 | HG01123.hp2 HG02559.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1253-1970_1253-196 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241936 | ||||||
| chr6:116241944 | C | A | 1 | a0001c0001t0002g0053 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1253-1965C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241944 | |||||||
| chr6:116241944 | CA | C | 12 | a0001c0001t0002g0004 a0001c0001t0002g0078 a0001c0001t0002g0079 others(9): Show |
13 | HG00642.hp1 HG00738.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1253-1950delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241944 | ||||||
| chr6:116241988 | A | C | 1 | a0001c0001t0034g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1253-1921A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241988 | |||||||
| chr6:116242100 | A | G | 163 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0056 others(160): Show |
166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1253-1809A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242100 | |||||||
| chr6:116242380 | T | G | 3 | a0001c0001t0005g0134 a0001c0001t0005g0135 a0001c0001t0005g0260 |
3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1253-1529T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242380 | |||||||
| chr6:116242384 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(258): Show |
267 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.1253-1525A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242384 | |||||||
| chr6:116242401 | A | G | 2 | a0001c0001t0020g0230 a0001c0001t0020g0236 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1253-1508A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242401 | |||||||
| chr6:116242482 | C | CA | 14 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0124 others(11): Show |
14 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1253-1414dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116242482 | ||||||
| chr6:116242494 | A | G | 1 | a0001c0001t0004g0253 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1253-1415A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242494 | |||||||
| chr6:116242604 | C | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.1253-1305C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242604 | |||||||
| chr6:116242662 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(261): Show |
270 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1253-1247T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242662 | |||||||
| chr6:116242762 | G | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(261): Show |
270 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1253-1147G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242762 | |||||||
| chr6:116242808 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1253-1101C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242808 | |||||||
| chr6:116242948 | A | G | 4 | a0001c0001t0011g0090 a0001c0001t0011g0091 a0001c0001t0011g0211 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1253-961A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242948 | |||||||
| chr6:116243022 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1253-887A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116243022 | |||||||
| chr6:116243050 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1253-859G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116243050 | |||||||
| chr6:116243065 | C | T | 12 | a0001c0001t0009g0107 a0001c0001t0009g0108 a0001c0001t0009g0110 others(9): Show |
12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1253-844C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116243065 | |||||||
| chr6:116243066 | G | A | 1 | a0001c0001t0011g0211 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1253-843G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116243066 | |||||||
| chr6:116243225 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(255): Show |
264 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.1253-684A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116243225 | |||||||
| chr6:116243437 | A | AT | 21 | a0001c0001t0002g0049 a0001c0001t0002g0055 a0001c0001t0002g0098 others(18): Show |
21 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.1253-470dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116243437 | ||||||
| chr6:116243839 | CAA | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0233 |
5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.1253-69_1253-68del others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116243839 |