Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 283927 |
| ensemblid | ENSG00000140876.11 |
| hgncid | 8054 |
| symbol | NUDT7 |
| name | nudix hydrolase 7 |
| refseq_nuc | NM_001105663.3 |
| refseq_prot | NP_001099133.1 |
| ensembl_nuc | ENST00000268533.9 |
| ensembl_prot | ENSP00000268533.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 77722514 |
| end | 77742260 |
| strand | + |
| ver | v1.2 |
| region | chr16:77722514-77742260 |
| region5000 | chr16:77717514-77747260 |
| regionname0 | NUDT7_chr16_77722514_77742260 |
| regionname5000 | NUDT7_chr16_77717514_77747260 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 238 | 290 | 79 | 56 | 114 | 10 | 29 | 81 | NUDT7_chr16_77717514_77747260 | NUDT7 | MSRLG others(233): Show |
chr16 | 77717514 | 77747260 |
| a0002 | 0/0 | 238 | 106 | 7 | 12 | 68 | 3 | 16 | 54 | NUDT7_chr16_77717514_77747260 | NUDT7 | MSRLG others(233): Show |
chr16 | 77717514 | 77747260 |
| a0003 | 0/0 | 238 | 51 | 6 | 6 | 34 | 3 | 2 | 31 | NUDT7_chr16_77717514_77747260 | NUDT7 | MSRLG others(233): Show |
chr16 | 77717514 | 77747260 |
| a0004 | 0/0 | 7 | 6 | 0 | 6 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | MSRLG others(2): Show |
chr16 | 77717514 | 77747260 |
| a0005 | 0/0 | 238 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | MSRLG others(233): Show |
chr16 | 77717514 | 77747260 |
| a0006 | 0/0 | 238 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | MSRLG others(233): Show |
chr16 | 77717514 | 77747260 |
| a0007 | 0/0 | 238 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | MSRLG others(233): Show |
chr16 | 77717514 | 77747260 |
| a0008 | 0/0 | 238 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | MSRLG others(233): Show |
chr16 | 77717514 | 77747260 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 714 | 286 | 76 | 56 | 113 | 10 | 29 | NUDT7_chr16_77717514_77747260 | NUDT7 | ATGTC others(709): Show |
chr16 | 77717514 | 77747260 | ||
| a0001c0006 | 0/0 | 714 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | ATGTC others(709): Show |
chr16 | 77717514 | 77747260 | ||
| a0001c0011 | 0/0 | 714 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | ATGTC others(709): Show |
chr16 | 77717514 | 77747260 | ||
| a0001c0013 | 0/0 | 714 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | ATGTC others(709): Show |
chr16 | 77717514 | 77747260 | ||
| a0002c0002 | 0/0 | 714 | 105 | 7 | 12 | 68 | 2 | 16 | NUDT7_chr16_77717514_77747260 | NUDT7 | ATGTC others(709): Show |
chr16 | 77717514 | 77747260 | ||
| a0002c0009 | 0/0 | 714 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | ATGTC others(709): Show |
chr16 | 77717514 | 77747260 | ||
| a0003c0003 | 0/0 | 714 | 51 | 6 | 6 | 34 | 3 | 2 | NUDT7_chr16_77717514_77747260 | NUDT7 | ATGTC others(709): Show |
chr16 | 77717514 | 77747260 | ||
| a0004c0004 | 0/0 | 714 | 6 | 0 | 6 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | ATGTC others(709): Show |
chr16 | 77717514 | 77747260 | ||
| a0005c0005 | 0/0 | 714 | 4 | 4 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | ATGTC others(709): Show |
chr16 | 77717514 | 77747260 | ||
| a0006c0007 | 0/0 | 714 | 2 | 0 | 0 | 0 | 0 | 2 | NUDT7_chr16_77717514_77747260 | NUDT7 | ATGTC others(709): Show |
chr16 | 77717514 | 77747260 | ||
| a0007c0008 | 0/0 | 714 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | ATGTC others(709): Show |
chr16 | 77717514 | 77747260 | ||
| a0007c0012 | 0/0 | 714 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | ATGTC others(709): Show |
chr16 | 77717514 | 77747260 | ||
| a0008c0010 | 0/0 | 714 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | ATGTC others(709): Show |
chr16 | 77717514 | 77747260 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1096 | 147 | 59 | 23 | 50 | 3 | 11 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0001c0001t0002 | 0/1 | 1096 | 130 | 12 | 30 | 63 | 7 | 17 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0001c0001t0003 | 0/0 | 1096 | 6 | 5 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0001c0001t0005 | 0/0 | 1096 | 3 | 0 | 2 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0001c0006t0001 | 0/0 | 1096 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0001c0006t0003 | 0/0 | 1096 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0001c0011t0006 | 0/0 | 1096 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0001c0013t0002 | 0/0 | 1096 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0002c0002t0001 | 0/0 | 1096 | 103 | 7 | 12 | 67 | 1 | 16 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0002c0002t0002 | 0/0 | 1096 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0002c0002t0007 | 0/0 | 1096 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0002c0009t0001 | 0/0 | 1096 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0003c0003t0001 | 0/0 | 1096 | 45 | 0 | 6 | 34 | 3 | 2 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0003c0003t0004 | 0/0 | 1096 | 6 | 6 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0004c0004t0001 | 0/0 | 1096 | 6 | 0 | 6 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0005c0005t0002 | 0/0 | 1096 | 3 | 3 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0005c0005t0008 | 0/0 | 1096 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0006c0007t0001 | 0/0 | 1096 | 2 | 0 | 0 | 0 | 0 | 2 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0007c0008t0002 | 0/0 | 1096 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0007c0012t0001 | 0/0 | 1096 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| a0008c0010t0002 | 0/0 | 1096 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | GCTCT others(1091): Show |
chr16 | 77717514 | 77747260 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0063 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0066 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0001 | 0/0 | 22 | 0 | 6 | 13 | 2 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0004 | 0/0 | 10 | 0 | 1 | 7 | 0 | 2 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0014 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0062 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0069 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0005g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0006t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0006t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0011t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0001c0013t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0002 | 0/0 | 16 | 0 | 1 | 13 | 0 | 2 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0005 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0010 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0065 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0067 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0068 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0002t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0002c0009t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0003 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0031 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0003c0003t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0004c0004t0001g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0004c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0005c0005t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0005c0005t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0005c0005t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0005c0005t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0006c0007t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0007c0008t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0007c0012t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| a0008c0010t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0140 | EUR | GBR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0003 | EUR | GBR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0019 | EUR | FIN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0081 | EUR | FIN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0125 | EUR | FIN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | CHS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00733 | hp1 | a0003 | c0003 | t0001 | g0087 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01070 | hp1 | a0004 | c0004 | t0001 | g0215 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0134 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0272 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0252 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0285 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01243 | hp1 | a0003 | c0003 | t0001 | g0031 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0281 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01358 | hp2 | a0004 | c0004 | t0001 | g0003 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0265 | EUR | IBS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0031 | EUR | IBS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0031 | EUR | IBS | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01884 | hp1 | a0001 | c0006 | t0003 | g0269 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0288 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0088 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01975 | hp2 | a0004 | c0004 | t0001 | g0003 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01978 | hp2 | a0004 | c0004 | t0001 | g0003 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0168 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01993 | hp2 | a0003 | c0003 | t0001 | g0247 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02027 | hp2 | a0003 | c0003 | t0001 | g0210 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02055 | hp2 | a0003 | c0003 | t0004 | g0149 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02074 | hp1 | a0003 | c0003 | t0001 | g0172 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02129 | hp2 | a0002 | c0002 | t0007 | g0041 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02145 | hp2 | a0003 | c0003 | t0004 | g0061 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02148 | hp1 | a0004 | c0004 | t0001 | g0003 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | CDX | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02155 | hp2 | a0001 | c0013 | t0002 | g0009 | EAS | CDX | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CDX | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CDX | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0143 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02258 | hp2 | a0005 | c0005 | t0008 | g0287 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02300 | hp2 | a0004 | c0004 | t0001 | g0003 | AMR | PEL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0275 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02622 | hp2 | a0005 | c0005 | t0002 | g0256 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0286 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0080 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0092 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0116 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02809 | hp1 | a0003 | c0003 | t0004 | g0146 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02818 | hp1 | a0001 | c0006 | t0001 | g0156 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02818 | hp2 | a0003 | c0003 | t0004 | g0003 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0262 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0195 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0228 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03453 | hp1 | a0001 | c0011 | t0006 | g0290 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03490 | hp1 | a0006 | c0007 | t0001 | g0035 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03492 | hp2 | a0006 | c0007 | t0001 | g0035 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03516 | hp2 | a0005 | c0005 | t0002 | g0155 | AFR | ESN | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0282 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0284 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0093 | SAS | STU | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03704 | hp2 | a0007 | c0008 | t0002 | g0136 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0067 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0126 | SAS | BEB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | BEB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0283 | SAS | BEB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | BEB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | BEB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0094 | SAS | BEB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | STU | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0067 | SAS | STU | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0109 | SAS | STU | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | CHB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | YRI | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18906 | hp2 | a0005 | c0005 | t0002 | g0191 | AFR | YRI | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0202 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18947 | hp1 | a0003 | c0003 | t0001 | g0253 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18949 | hp1 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18956 | hp1 | a0007 | c0012 | t0001 | g0104 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18956 | hp2 | a0003 | c0003 | t0001 | g0205 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18957 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18960 | hp2 | a0003 | c0003 | t0001 | g0060 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18963 | hp1 | a0003 | c0003 | t0001 | g0251 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18963 | hp2 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18968 | hp2 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18975 | hp2 | a0003 | c0003 | t0001 | g0060 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18983 | hp1 | a0003 | c0003 | t0001 | g0173 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18984 | hp1 | a0003 | c0003 | t0001 | g0214 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18985 | hp1 | a0003 | c0003 | t0001 | g0050 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18988 | hp1 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18988 | hp2 | a0003 | c0003 | t0001 | g0023 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18994 | hp2 | a0003 | c0003 | t0001 | g0071 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18997 | hp2 | a0003 | c0003 | t0001 | g0023 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19004 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19006 | hp2 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19007 | hp2 | a0008 | c0010 | t0002 | g0203 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19009 | hp1 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19011 | hp2 | a0003 | c0003 | t0001 | g0090 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19030 | hp2 | a0003 | c0003 | t0004 | g0148 | AFR | LWK | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | LWK | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19057 | hp2 | a0003 | c0003 | t0001 | g0209 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19060 | hp1 | a0003 | c0003 | t0001 | g0120 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19062 | hp2 | a0003 | c0003 | t0001 | g0130 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19066 | hp2 | a0003 | c0003 | t0001 | g0050 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19076 | hp2 | a0003 | c0003 | t0001 | g0023 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19078 | hp2 | a0003 | c0003 | t0001 | g0061 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19087 | hp2 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19090 | hp1 | a0003 | c0003 | t0001 | g0178 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0278 | AFR | YRI | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ASW | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ASW | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA20805 | hp2 | a0002 | c0009 | t0001 | g0279 | EUR | TSI | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0224 | SAS | GIH | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0041 | SAS | GIH | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | CLM | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02109 | hp2 | a0003 | c0003 | t0004 | g0003 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | MSL | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | USA | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | USA | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | USA | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | USA | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | LWK | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0072 | REF | REF | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0237 | REF | REF | NUDT7_chr16_77717514_77747260 | NUDT7 | chr16 | 77717514 | 77747260 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:77722604 | G | T | 1 | a0004 | 6 | HG01070.hp1 HG01358.hp2 HG01975.hp2 others(3): Show |
stop_gained | HIGH | c.22G>T | p.Glu8* | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/4 | 91/1096 | 22/717 | 8/238 | chr16 | 77722604 | |||
| chr16:77722616 | A | G | 1 | a0006 | 2 | HG03490.hp1 HG03492.hp2 |
missense_variant&splice_region_variant | MODERATE | c.34A>G | p.Arg12Gly | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/4 | 103/1096 | 34/717 | 12/238 | chr16 | 77722616 | |||
| chr16:77735924 | G | A | 1 | a0007 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.286G>A | p.Glu96Lys | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/4 | 355/1096 | 286/717 | 96/238 | chr16 | 77735924 | |||
| chr16:77735926 | A | C | 1 | a0007 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.288A>C | p.Glu96Asp | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/4 | 357/1096 | 288/717 | 96/238 | chr16 | 77735926 | |||
| chr16:77735937 | G | A | 2 | a0002 a0006 |
108 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(105): Show |
missense_variant | MODERATE | c.299G>A | p.Arg100His | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/4 | 368/1096 | 299/717 | 100/238 | chr16 | 77735937 | |||
| chr16:77735984 | G | C | 1 | a0005 | 4 | HG02258.hp2 HG02622.hp2 HG03516.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.346G>C | p.Asp116His | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/4 | 415/1096 | 346/717 | 116/238 | chr16 | 77735984 | |||
| chr16:77741775 | A | G | 2 | a0003 a0004 |
57 | HG00140.hp1 HG00733.hp1 HG01070.hp1 others(54): Show |
missense_variant | MODERATE | c.542A>G | p.Glu181Gly | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 4/4 | 611/1096 | 542/717 | 181/238 | chr16 | 77741775 | |||
| chr16:77741866 | G | C | 1 | a0008 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.633G>C | p.Glu211Asp | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 4/4 | 702/1096 | 633/717 | 211/238 | chr16 | 77741866 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:77735875 | C | T | 1 | a0001c0013 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.237C>T | p.Asp79Asp | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/4 | 306/1096 | 237/717 | 79/238 | chr16 | 77735875 | |||
| chr16:77741779 | C | T | 1 | a0002c0009 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.546C>T | p.Asp182Asp | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 4/4 | 615/1096 | 546/717 | 182/238 | chr16 | 77741779 | |||
| chr16:77741803 | A | G | 1 | a0001c0011 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.570A>G | p.Gly190Gly | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 4/4 | 639/1096 | 570/717 | 190/238 | chr16 | 77741803 | |||
| chr16:77741809 | G | T | 1 | a0001c0011 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.576G>T | p.Thr192Thr | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 4/4 | 645/1096 | 576/717 | 192/238 | chr16 | 77741809 | |||
| chr16:77741881 | T | C | 1 | a0001c0006 | 2 | HG01884.hp1 HG02818.hp1 |
synonymous_variant | LOW | c.648T>C | p.Leu216Leu | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 4/4 | 717/1096 | 648/717 | 216/238 | chr16 | 77741881 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:77722536 | C | G | 2 | a0001c0001t0003 a0001c0006t0003 |
7 | HG01109.hp2 HG01884.hp1 HG02809.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-47C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/4 | 47 | chr16 | 77722536 | ||||||
| chr16:77722564 | A | G | 1 | a0005c0005t0008 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-19A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/4 | 19 | chr16 | 77722564 | ||||||
| chr16:77742006 | G | A | 2 | a0001c0011t0006 a0003c0003t0004 |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*56G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 4/4 | 56 | chr16 | 77742006 | ||||||
| chr16:77742007 | T | G | 1 | a0001c0011t0006 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*57T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 4/4 | 57 | chr16 | 77742007 | ||||||
| chr16:77742020 | A | G | 8 | a0001c0001t0002 a0001c0001t0005 a0001c0013t0002 others(5): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*70A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 4/4 | 70 | chr16 | 77742020 | ||||||
| chr16:77742093 | C | T | 1 | a0001c0011t0006 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*143C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 4/4 | 143 | chr16 | 77742093 | ||||||
| chr16:77742141 | A | G | 1 | a0002c0002t0007 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 4/4 | 191 | chr16 | 77742141 | ||||||
| chr16:77742162 | A | G | 7 | a0001c0001t0002 a0001c0013t0002 a0002c0002t0002 others(4): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*212A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 4/4 | 212 | chr16 | 77742162 | ||||||
| chr16:77742227 | C | G | 1 | a0001c0011t0006 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*277C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 4/4 | 277 | chr16 | 77742227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:77722716 | G | A | 111 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0033 others(108): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.35+99G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77722716 | |||||||
| chr16:77722738 | G | A | 1 | a0003c0003t0004g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35+121G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77722738 | |||||||
| chr16:77722802 | G | C | 1 | a0001c0001t0002g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.35+185G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77722802 | |||||||
| chr16:77722816 | C | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0257 a0001c0001t0001g0258 others(8): Show |
13 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.35+199C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77722816 | |||||||
| chr16:77722878 | T | G | 1 | a0003c0003t0001g0071 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.35+261T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77722878 | |||||||
| chr16:77722916 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.35+299G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77722916 | |||||||
| chr16:77722931 | C | G | 1 | a0001c0001t0001g0292 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.35+314C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77722931 | |||||||
| chr16:77722937 | C | G | 1 | a0002c0002t0001g0291 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.35+320C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77722937 | |||||||
| chr16:77723051 | T | G | 3 | a0001c0001t0001g0021 a0003c0003t0004g0148 a0003c0003t0004g0149 |
5 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.35+434T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723051 | |||||||
| chr16:77723122 | T | C | 1 | a0003c0003t0001g0073 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.35+505T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723122 | |||||||
| chr16:77723137 | TC | T | 106 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0022 others(103): Show |
149 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.35+522delC | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 77723137 | ||||||
| chr16:77723189 | T | C | 2 | a0001c0001t0001g0229 a0002c0002t0001g0228 |
2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.35+572T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723189 | |||||||
| chr16:77723244 | C | G | 30 | a0001c0001t0001g0059 a0001c0001t0001g0211 a0001c0001t0001g0212 others(27): Show |
45 | HG00140.hp1 HG00544.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.35+627C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723244 | |||||||
| chr16:77723247 | C | T | 1 | a0002c0002t0001g0145 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.35+630C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723247 | |||||||
| chr16:77723249 | G | A | 2 | a0003c0003t0001g0209 a0003c0003t0001g0210 |
2 | HG02027.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.35+632G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723249 | |||||||
| chr16:77723297 | A | G | 1 | a0001c0001t0002g0069 | 2 | HG00639.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.35+680A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723297 | |||||||
| chr16:77723365 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.35+748A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723365 | |||||||
| chr16:77723374 | G | A | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG03098.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.35+757G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723374 | |||||||
| chr16:77723374 | G | T | 112 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0033 others(109): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.35+757G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723374 | |||||||
| chr16:77723401 | GC | G | 5 | a0001c0001t0001g0232 a0001c0001t0002g0062 a0001c0001t0002g0230 others(2): Show |
6 | HG02615.hp2 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+785delC | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723401 | |||||||
| chr16:77723428 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.35+811A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723428 | |||||||
| chr16:77723493 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.35+876G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723493 | |||||||
| chr16:77723592 | C | CT | 25 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0063 others(22): Show |
36 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.35+993dupT | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 77723592 | ||||||
| chr16:77723592 | C | CTTT | 19 | a0001c0001t0001g0021 a0001c0001t0001g0157 a0001c0001t0001g0158 others(16): Show |
21 | HG01070.hp1 HG01515.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.35+991_35+993dupTT others(1): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 77723592 | ||||||
| chr16:77723592 | C | CTTTT | 85 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0024 others(82): Show |
121 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.35+990_35+993dupTT others(2): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 77723592 | ||||||
| chr16:77723592 | C | CTTTTT | 41 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0055 others(38): Show |
53 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.35+989_35+993dupTT others(3): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 77723592 | ||||||
| chr16:77723592 | CT | C | 72 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0040 others(69): Show |
129 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.35+993delT | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 77723592 | ||||||
| chr16:77723592 | CTT | C | 9 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0076 others(6): Show |
15 | HG00544.hp2 HG01993.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.35+992_35+993delTT | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 77723592 | ||||||
| chr16:77723606 | T | G | 4 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0075 others(1): Show |
9 | HG00408.hp1 HG00741.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.35+989T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723606 | |||||||
| chr16:77723631 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.35+1014C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723631 | |||||||
| chr16:77723648 | A | G | 1 | a0001c0001t0002g0144 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.35+1031A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723648 | |||||||
| chr16:77723661 | G | C | 1 | a0005c0005t0008g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.35+1044G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723661 | |||||||
| chr16:77723726 | G | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0002c0002t0001g0080 others(2): Show |
6 | HG00280.hp2 HG01074.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+1109G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723726 | |||||||
| chr16:77723736 | C | T | 2 | a0001c0001t0002g0206 a0005c0005t0002g0155 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.35+1119C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723736 | |||||||
| chr16:77723821 | A | G | 62 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0024 others(59): Show |
93 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.35+1204A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723821 | |||||||
| chr16:77723938 | T | A | 1 | a0001c0001t0001g0266 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35+1321T>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723938 | |||||||
| chr16:77723950 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.35+1333G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723950 | |||||||
| chr16:77723956 | C | G | 36 | a0001c0001t0001g0066 a0001c0001t0001g0232 a0001c0001t0001g0264 others(33): Show |
41 | HG00609.hp1 HG00738.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.35+1339C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723956 | |||||||
| chr16:77723984 | G | A | 265 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(262): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.35+1367G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723984 | |||||||
| chr16:77723991 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0183 |
4 | HG02895.hp1 HG02897.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.35+1374C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77723991 | |||||||
| chr16:77724000 | G | A | 1 | a0001c0001t0002g0118 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.35+1383G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724000 | |||||||
| chr16:77724026 | T | G | 1 | a0001c0001t0001g0266 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.36-1405T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724026 | |||||||
| chr16:77724039 | A | C | 1 | a0002c0002t0001g0145 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.36-1392A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724039 | |||||||
| chr16:77724053 | C | A | 8 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0260 others(5): Show |
8 | HG02572.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.36-1378C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724053 | |||||||
| chr16:77724151 | G | C | 1 | a0001c0006t0001g0156 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.36-1280G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724151 | |||||||
| chr16:77724247 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.36-1184C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724247 | |||||||
| chr16:77724346 | T | G | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG03098.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.36-1085T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724346 | |||||||
| chr16:77724381 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.36-1050C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724381 | |||||||
| chr16:77724435 | C | CT | 76 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(73): Show |
97 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-983dupT | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr16 | 77724435 | ||||||
| chr16:77724551 | G | A | 32 | a0001c0001t0001g0066 a0001c0001t0001g0264 a0001c0001t0001g0265 others(29): Show |
36 | HG00609.hp1 HG00738.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.36-880G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724551 | |||||||
| chr16:77724566 | G | C | 47 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0001g0232 others(44): Show |
54 | HG00609.hp1 HG00738.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.36-865G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724566 | |||||||
| chr16:77724589 | G | T | 30 | a0001c0001t0001g0066 a0001c0001t0001g0264 a0001c0001t0001g0265 others(27): Show |
34 | HG00609.hp1 HG00738.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.36-842G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724589 | |||||||
| chr16:77724613 | C | T | 2 | a0001c0001t0002g0206 a0005c0005t0002g0155 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.36-818C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724613 | |||||||
| chr16:77724725 | A | G | 30 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(27): Show |
43 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.36-706A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724725 | |||||||
| chr16:77724730 | C | G | 47 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0001g0232 others(44): Show |
54 | HG00609.hp1 HG00738.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.36-701C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724730 | |||||||
| chr16:77724733 | T | C | 47 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0001g0232 others(44): Show |
54 | HG00609.hp1 HG00738.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.36-698T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724733 | |||||||
| chr16:77724738 | C | T | 1 | a0003c0003t0004g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.36-693C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724738 | |||||||
| chr16:77724789 | C | T | 47 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0001g0232 others(44): Show |
54 | HG00609.hp1 HG00738.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.36-642C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724789 | |||||||
| chr16:77724805 | T | C | 47 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0001g0232 others(44): Show |
54 | HG00609.hp1 HG00738.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.36-626T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724805 | |||||||
| chr16:77724858 | G | A | 29 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(26): Show |
42 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.36-573G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724858 | |||||||
| chr16:77724869 | T | C | 24 | a0001c0001t0001g0059 a0001c0001t0001g0216 a0001c0001t0001g0218 others(21): Show |
39 | HG00140.hp1 HG00544.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.36-562T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724869 | |||||||
| chr16:77724911 | A | G | 1 | a0002c0002t0001g0116 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.36-520A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77724911 | |||||||
| chr16:77725048 | T | G | 31 | a0001c0001t0001g0066 a0001c0001t0001g0264 a0001c0001t0001g0265 others(28): Show |
35 | HG00609.hp1 HG00738.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.36-383T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77725048 | |||||||
| chr16:77725072 | G | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0234 a0001c0001t0001g0235 |
5 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.36-359G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77725072 | |||||||
| chr16:77725154 | C | T | 47 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0001g0232 others(44): Show |
54 | HG00609.hp1 HG00738.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.36-277C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77725154 | |||||||
| chr16:77725189 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.36-242T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77725189 | |||||||
| chr16:77725239 | T | C | 61 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0024 others(58): Show |
92 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.36-192T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77725239 | |||||||
| chr16:77725248 | T | C | 3 | a0001c0001t0001g0084 a0002c0002t0001g0005 a0002c0002t0001g0145 |
10 | HG00423.hp1 HG01261.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.36-183T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77725248 | |||||||
| chr16:77725264 | C | A | 29 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(26): Show |
42 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.36-167C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77725264 | |||||||
| chr16:77725282 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0184 |
3 | HG00738.hp2 HG01346.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.36-149T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77725282 | |||||||
| chr16:77725289 | T | C | 3 | a0001c0001t0001g0085 a0002c0002t0001g0016 a0003c0003t0001g0071 |
5 | HG02040.hp1 NA18972.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.36-142T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77725289 | |||||||
| chr16:77725418 | G | C | 2 | a0001c0001t0002g0206 a0005c0005t0002g0155 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.36-13G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 1/3 | chr16 | 77725418 | |||||||
| chr16:77725661 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0002g0114 |
2 | HG02698.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.189+77A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77725661 | |||||||
| chr16:77725715 | A | G | 27 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0001g0257 others(24): Show |
33 | HG00738.hp1 HG01192.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.189+131A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77725715 | |||||||
| chr16:77725755 | A | C | 8 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.189+171A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77725755 | |||||||
| chr16:77725816 | G | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0183 |
4 | HG02895.hp1 HG02897.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+232G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77725816 | |||||||
| chr16:77725873 | G | C | 6 | a0001c0001t0002g0086 a0001c0001t0002g0119 a0001c0001t0002g0121 others(3): Show |
6 | HG02135.hp2 NA18948.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+289G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77725873 | |||||||
| chr16:77725943 | C | G | 8 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0260 others(5): Show |
8 | HG02572.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+359C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77725943 | |||||||
| chr16:77726096 | C | T | 1 | a0001c0006t0001g0156 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.189+512C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726096 | |||||||
| chr16:77726195 | T | G | 1 | a0003c0003t0001g0162 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.189+611T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726195 | |||||||
| chr16:77726260 | T | C | 163 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(160): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.189+676T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726260 | |||||||
| chr16:77726353 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.189+769G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726353 | |||||||
| chr16:77726518 | T | C | 60 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(57): Show |
81 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.189+934T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726518 | |||||||
| chr16:77726534 | A | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(56): Show |
80 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.189+950A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726534 | |||||||
| chr16:77726537 | A | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(56): Show |
80 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.189+953A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726537 | |||||||
| chr16:77726597 | C | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0055 a0001c0001t0001g0151 others(11): Show |
19 | HG00280.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.189+1013C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726597 | |||||||
| chr16:77726661 | G | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0183 a0002c0002t0001g0054 |
6 | HG02895.hp1 HG02897.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+1077G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726661 | |||||||
| chr16:77726713 | C | T | 35 | a0001c0001t0001g0026 a0001c0001t0001g0112 a0001c0001t0001g0150 others(32): Show |
45 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.189+1129C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726713 | |||||||
| chr16:77726742 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.189+1158A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726742 | |||||||
| chr16:77726867 | G | C | 146 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(143): Show |
199 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.189+1283G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726867 | |||||||
| chr16:77726940 | G | T | 106 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(103): Show |
145 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.189+1356G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726940 | |||||||
| chr16:77726947 | C | CATGGCAG | 40 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0049 others(37): Show |
54 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.189+1365_189+1371d others(9): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77726947 | ||||||
| chr16:77726949 | T | TGGCAGAC | 105 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(102): Show |
144 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.189+1371_189+1372i others(9): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77726949 | ||||||
| chr16:77726981 | C | G | 105 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(102): Show |
144 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.189+1397C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77726981 | |||||||
| chr16:77727042 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.189+1458G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727042 | |||||||
| chr16:77727068 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.189+1484A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727068 | |||||||
| chr16:77727111 | A | C | 159 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(156): Show |
213 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.189+1527A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727111 | |||||||
| chr16:77727161 | G | A | 1 | a0005c0005t0008g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.189+1577G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727161 | |||||||
| chr16:77727200 | G | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0055 others(12): Show |
22 | HG01891.hp1 HG02280.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.189+1616G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727200 | |||||||
| chr16:77727214 | T | G | 44 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(41): Show |
61 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.189+1630T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727214 | |||||||
| chr16:77727382 | C | T | 117 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(114): Show |
157 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.189+1798C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727382 | |||||||
| chr16:77727414 | TCTGAGC | T | 117 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(114): Show |
157 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.189+1832_189+1837d others(8): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77727414 | ||||||
| chr16:77727433 | C | G | 1 | a0001c0001t0003g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.189+1849C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727433 | |||||||
| chr16:77727435 | G | A | 1 | a0002c0002t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.189+1851G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727435 | |||||||
| chr16:77727460 | C | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0055 others(12): Show |
22 | HG01891.hp1 HG02280.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.189+1876C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727460 | |||||||
| chr16:77727469 | G | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(113): Show |
156 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.189+1885G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727469 | |||||||
| chr16:77727471 | G | A | 1 | a0001c0001t0002g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.189+1887G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727471 | |||||||
| chr16:77727474 | A | C | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | HG00099.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.189+1890A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727474 | |||||||
| chr16:77727501 | A | G | 116 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(113): Show |
156 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.189+1917A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727501 | |||||||
| chr16:77727511 | C | G | 116 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(113): Show |
156 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.189+1927C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727511 | |||||||
| chr16:77727520 | G | T | 88 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0051 others(85): Show |
118 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.189+1936G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727520 | |||||||
| chr16:77727534 | G | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0055 others(12): Show |
22 | HG01891.hp1 HG02280.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.189+1950G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727534 | |||||||
| chr16:77727549 | A | G | 1 | a0001c0001t0001g0022 | 3 | NA18973.hp2 NA19002.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.189+1965A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727549 | |||||||
| chr16:77727577 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0183 a0001c0001t0001g0213 others(1): Show |
7 | HG02895.hp1 HG02897.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+1993G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727577 | |||||||
| chr16:77727577 | G | T | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.189+1993G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727577 | |||||||
| chr16:77727623 | G | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0055 others(12): Show |
22 | HG01891.hp1 HG02280.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.189+2039G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727623 | |||||||
| chr16:77727675 | C | T | 1 | a0002c0002t0001g0016 | 3 | NA18972.hp1 NA18978.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.189+2091C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727675 | |||||||
| chr16:77727805 | C | T | 2 | a0001c0001t0001g0232 a0003c0003t0001g0251 |
2 | HG02723.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.189+2221C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727805 | |||||||
| chr16:77727812 | G | A | 1 | a0001c0006t0001g0156 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.189+2228G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727812 | |||||||
| chr16:77727878 | A | AAAAT | 115 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(112): Show |
155 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(152): Show |
intron_variant | MODIFIER | c.189+2295_189+2296i others(6): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77727878 | ||||||
| chr16:77727880 | T | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(112): Show |
155 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(152): Show |
intron_variant | MODIFIER | c.189+2296T>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727880 | |||||||
| chr16:77727977 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.189+2393T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77727977 | |||||||
| chr16:77728064 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.189+2480A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728064 | |||||||
| chr16:77728132 | C | G | 116 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(113): Show |
156 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.189+2548C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728132 | |||||||
| chr16:77728190 | C | T | 44 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(41): Show |
61 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.189+2606C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728190 | |||||||
| chr16:77728242 | C | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0175 a0001c0001t0001g0198 others(2): Show |
7 | HG02055.hp1 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+2658C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728242 | |||||||
| chr16:77728251 | C | G | 110 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0021 others(107): Show |
149 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.189+2667C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728251 | |||||||
| chr16:77728287 | C | T | 43 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0051 others(40): Show |
56 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+2703C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728287 | |||||||
| chr16:77728359 | A | G | 43 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(40): Show |
60 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.189+2775A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728359 | |||||||
| chr16:77728395 | G | C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0051 others(26): Show |
38 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.189+2811G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728395 | |||||||
| chr16:77728507 | G | C | 1 | a0001c0001t0002g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.189+2923G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728507 | |||||||
| chr16:77728602 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.189+3018G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728602 | |||||||
| chr16:77728635 | A | G | 45 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0051 others(42): Show |
58 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.189+3051A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728635 | |||||||
| chr16:77728647 | C | T | 2 | a0005c0005t0002g0155 a0005c0005t0008g0287 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.189+3063C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728647 | |||||||
| chr16:77728672 | A | G | 34 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0085 others(31): Show |
44 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.189+3088A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728672 | |||||||
| chr16:77728675 | G | A | 1 | a0001c0001t0001g0063 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.189+3091G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728675 | |||||||
| chr16:77728723 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.189+3139C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728723 | |||||||
| chr16:77728854 | A | C | 2 | a0005c0005t0002g0155 a0005c0005t0008g0287 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.189+3270A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728854 | |||||||
| chr16:77728902 | CCA | C | 78 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0059 others(75): Show |
105 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.189+3322_189+3323d others(4): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77728902 | ||||||
| chr16:77728935 | C | A | 44 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(41): Show |
61 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.189+3351C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728935 | |||||||
| chr16:77728941 | C | T | 1 | a0001c0001t0005g0109 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.189+3357C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728941 | |||||||
| chr16:77728985 | G | C | 44 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(41): Show |
61 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.189+3401G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77728985 | |||||||
| chr16:77729236 | C | A | 2 | a0001c0001t0002g0012 a0001c0001t0002g0089 |
5 | NA18969.hp2 NA18972.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+3652C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729236 | |||||||
| chr16:77729321 | A | ATCTC | 15 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0167 others(12): Show |
17 | HG00733.hp1 HG01952.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.189+3738_189+3739i others(6): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77729321 | ||||||
| chr16:77729358 | T | G | 92 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0049 others(89): Show |
124 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.189+3774T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729358 | |||||||
| chr16:77729359 | T | A | 2 | a0005c0005t0002g0155 a0005c0005t0008g0287 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.189+3775T>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729359 | |||||||
| chr16:77729432 | C | T | 43 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(40): Show |
60 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.189+3848C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729432 | |||||||
| chr16:77729468 | T | G | 7 | a0001c0001t0001g0196 a0001c0001t0003g0262 a0001c0001t0003g0268 others(4): Show |
7 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+3884T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729468 | |||||||
| chr16:77729669 | T | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0235 a0001c0001t0003g0263 |
5 | HG02280.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+4085T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729669 | |||||||
| chr16:77729698 | A | G | 46 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(43): Show |
63 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.189+4114A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729698 | |||||||
| chr16:77729768 | T | G | 116 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0042 others(113): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.189+4184T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729768 | |||||||
| chr16:77729795 | A | G | 46 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(43): Show |
63 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.189+4211A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729795 | |||||||
| chr16:77729847 | T | TAAAA | 46 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(43): Show |
63 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.189+4263_189+4264i others(6): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729847 | |||||||
| chr16:77729867 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.189+4283T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729867 | |||||||
| chr16:77729903 | A | ATAT | 5 | a0001c0001t0002g0062 a0001c0001t0002g0206 a0001c0001t0002g0230 others(2): Show |
6 | HG02615.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+4319_189+4320i others(5): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729903 | |||||||
| chr16:77729905 | T | TACA | 5 | a0001c0001t0002g0062 a0001c0001t0002g0206 a0001c0001t0002g0230 others(2): Show |
6 | HG02615.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+4322_189+4323i others(5): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77729905 | ||||||
| chr16:77729907 | T | C | 5 | a0001c0001t0002g0062 a0001c0001t0002g0206 a0001c0001t0002g0230 others(2): Show |
6 | HG02615.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+4323T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729907 | |||||||
| chr16:77729951 | ACTCACAT others(25): Show |
A | 51 | a0001c0001t0001g0021 a0001c0001t0001g0059 a0001c0001t0001g0163 others(48): Show |
70 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.189+4387_189+4418d others(34): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77729951 | ||||||
| chr16:77729969 | T | TACCACAC others(57): Show |
1 | a0001c0001t0001g0264 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.189+4393_189+4394i others(66): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77729969 | ||||||
| chr16:77729978 | C | T | 35 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0022 others(32): Show |
54 | HG00642.hp1 HG00735.hp2 HG01192.hp1 others(51): Show |
intron_variant | MODIFIER | c.189+4394C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77729978 | |||||||
| chr16:77730024 | G | T | 35 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0079 others(32): Show |
45 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.189+4440G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730024 | |||||||
| chr16:77730092 | G | A | 54 | a0001c0001t0001g0021 a0001c0001t0001g0059 a0001c0001t0001g0163 others(51): Show |
73 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.189+4508G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730092 | |||||||
| chr16:77730124 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.189+4540C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730124 | |||||||
| chr16:77730169 | C | G | 46 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(43): Show |
63 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.189+4585C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730169 | |||||||
| chr16:77730197 | C | A | 52 | a0001c0001t0001g0021 a0001c0001t0001g0059 a0001c0001t0001g0163 others(49): Show |
71 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.189+4613C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730197 | |||||||
| chr16:77730197 | C | T | 15 | a0001c0001t0001g0042 a0001c0001t0001g0105 a0001c0001t0001g0229 others(12): Show |
22 | HG00280.hp1 HG01099.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.189+4613C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730197 | |||||||
| chr16:77730219 | C | T | 219 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(216): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(358): Show |
intron_variant | MODIFIER | c.189+4635C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730219 | |||||||
| chr16:77730220 | G | A | 3 | a0001c0001t0001g0235 a0001c0001t0003g0262 a0001c0001t0003g0268 |
3 | HG02630.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.189+4636G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730220 | |||||||
| chr16:77730230 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.189+4646C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730230 | |||||||
| chr16:77730284 | C | T | 52 | a0001c0001t0001g0021 a0001c0001t0001g0059 a0001c0001t0001g0163 others(49): Show |
71 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.189+4700C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730284 | |||||||
| chr16:77730628 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.189+5044G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730628 | |||||||
| chr16:77730659 | T | C | 3 | a0001c0001t0001g0234 a0005c0005t0002g0191 a0005c0005t0002g0256 |
3 | HG02486.hp1 HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.189+5075T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730659 | |||||||
| chr16:77730715 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.190-5113T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730715 | |||||||
| chr16:77730738 | A | G | 9 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0110 others(6): Show |
10 | HG01109.hp2 HG01433.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.190-5090A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730738 | |||||||
| chr16:77730775 | G | C | 45 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(42): Show |
62 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.190-5053G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730775 | |||||||
| chr16:77730788 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.190-5040G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730788 | |||||||
| chr16:77730808 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.190-5020G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730808 | |||||||
| chr16:77730814 | C | G | 167 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0033 others(164): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.190-5014C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730814 | |||||||
| chr16:77730925 | A | T | 160 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(157): Show |
245 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.190-4903A>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730925 | |||||||
| chr16:77730927 | A | ATTT | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-4894_190-4892d others(5): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77730927 | ||||||
| chr16:77730936 | T | A | 1 | a0001c0001t0001g0157 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.190-4892T>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77730936 | |||||||
| chr16:77731156 | C | A | 48 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(45): Show |
66 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.190-4672C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77731156 | |||||||
| chr16:77731157 | T | C | 184 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(181): Show |
280 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.190-4671T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77731157 | |||||||
| chr16:77731198 | C | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0171 a0001c0001t0001g0192 |
5 | HG02451.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-4630C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77731198 | |||||||
| chr16:77731310 | A | G | 2 | a0001c0001t0001g0273 a0002c0002t0001g0274 |
2 | HG00609.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.190-4518A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77731310 | |||||||
| chr16:77731339 | GATGGACC | G | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-4479_190-4473d others(9): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77731339 | ||||||
| chr16:77731445 | G | T | 48 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(45): Show |
66 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.190-4383G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77731445 | |||||||
| chr16:77731533 | A | G | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-4295A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77731533 | |||||||
| chr16:77731559 | A | T | 1 | a0001c0001t0001g0240 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.190-4269A>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77731559 | |||||||
| chr16:77731685 | A | G | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-4143A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77731685 | |||||||
| chr16:77731758 | C | A | 1 | a0003c0003t0001g0073 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.190-4070C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77731758 | |||||||
| chr16:77731849 | G | GA | 6 | a0001c0001t0001g0192 a0001c0001t0001g0276 a0002c0002t0001g0096 others(3): Show |
6 | HG02622.hp2 HG02717.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-3970dupA | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77731849 | ||||||
| chr16:77731923 | A | G | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-3905A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77731923 | |||||||
| chr16:77732003 | A | T | 29 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0033 others(26): Show |
36 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.190-3825A>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732003 | |||||||
| chr16:77732089 | G | A | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-3739G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732089 | |||||||
| chr16:77732197 | G | A | 43 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0028 others(40): Show |
61 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.190-3631G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732197 | |||||||
| chr16:77732258 | T | G | 280 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(277): Show |
437 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(434): Show |
intron_variant | MODIFIER | c.190-3570T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732258 | |||||||
| chr16:77732270 | G | T | 1 | a0001c0001t0002g0275 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.190-3558G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732270 | |||||||
| chr16:77732326 | C | CA | 62 | a0001c0001t0001g0183 a0001c0001t0001g0273 a0001c0001t0001g0280 others(59): Show |
104 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.190-3490dupA | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77732326 | ||||||
| chr16:77732335 | A | AAAAAG | 46 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(43): Show |
64 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.190-3490_190-3489i others(7): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77732335 | ||||||
| chr16:77732362 | A | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0078 a0001c0001t0001g0084 others(2): Show |
6 | HG02015.hp2 NA18940.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-3466A>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732362 | |||||||
| chr16:77732387 | A | G | 187 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(184): Show |
283 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.190-3441A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732387 | |||||||
| chr16:77732564 | G | A | 1 | a0001c0001t0002g0045 | 2 | NA19000.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.190-3264G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732564 | |||||||
| chr16:77732598 | C | T | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-3230C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732598 | |||||||
| chr16:77732604 | C | T | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-3224C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732604 | |||||||
| chr16:77732644 | A | G | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-3184A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732644 | |||||||
| chr16:77732645 | C | G | 1 | a0002c0002t0001g0285 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.190-3183C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732645 | |||||||
| chr16:77732656 | T | A | 46 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(43): Show |
64 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.190-3172T>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732656 | |||||||
| chr16:77732681 | A | G | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-3147A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732681 | |||||||
| chr16:77732693 | A | T | 3 | a0002c0002t0001g0092 a0002c0002t0001g0116 a0002c0002t0001g0224 |
3 | HG02735.hp2 HG02738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.190-3135A>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732693 | |||||||
| chr16:77732743 | A | G | 64 | a0001c0001t0001g0046 a0001c0001t0001g0105 a0001c0001t0001g0216 others(61): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.190-3085A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732743 | |||||||
| chr16:77732747 | C | G | 1 | a0001c0001t0002g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.190-3081C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732747 | |||||||
| chr16:77732753 | G | A | 1 | a0002c0002t0001g0201 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.190-3075G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732753 | |||||||
| chr16:77732773 | CTGT | C | 3 | a0001c0001t0001g0276 a0005c0005t0002g0191 a0005c0005t0002g0256 |
3 | HG02622.hp2 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.190-3049_190-3047d others(5): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77732773 | ||||||
| chr16:77732789 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.190-3039C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732789 | |||||||
| chr16:77732825 | C | CTG | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-3001_190-3000d others(4): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77732825 | ||||||
| chr16:77732861 | G | A | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-2967G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732861 | |||||||
| chr16:77732863 | T | C | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-2965T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732863 | |||||||
| chr16:77732945 | C | T | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-2883C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732945 | |||||||
| chr16:77732955 | A | G | 280 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(277): Show |
437 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(434): Show |
intron_variant | MODIFIER | c.190-2873A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732955 | |||||||
| chr16:77732973 | C | G | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-2855C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77732973 | |||||||
| chr16:77733034 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.190-2794A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733034 | |||||||
| chr16:77733128 | T | A | 1 | a0001c0001t0002g0097 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.190-2700T>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733128 | |||||||
| chr16:77733158 | C | G | 24 | a0001c0001t0001g0063 a0001c0001t0001g0095 a0001c0001t0001g0117 others(21): Show |
35 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.190-2670C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733158 | |||||||
| chr16:77733180 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.190-2648A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733180 | |||||||
| chr16:77733191 | G | T | 1 | a0002c0002t0001g0067 | 2 | HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.190-2637G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733191 | |||||||
| chr16:77733194 | A | T | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-2634A>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733194 | |||||||
| chr16:77733326 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.190-2502G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733326 | |||||||
| chr16:77733327 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.190-2501C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733327 | |||||||
| chr16:77733386 | A | G | 50 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(47): Show |
70 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.190-2442A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733386 | |||||||
| chr16:77733398 | G | T | 1 | a0007c0008t0002g0136 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.190-2430G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733398 | |||||||
| chr16:77733407 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0235 a0001c0001t0003g0263 others(2): Show |
7 | HG02258.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.190-2421A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733407 | |||||||
| chr16:77733440 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.190-2388C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733440 | |||||||
| chr16:77733492 | T | C | 47 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(44): Show |
67 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-2336T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733492 | |||||||
| chr16:77733497 | G | T | 1 | a0001c0006t0001g0156 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.190-2331G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733497 | |||||||
| chr16:77733521 | A | G | 50 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(47): Show |
70 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.190-2307A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733521 | |||||||
| chr16:77733594 | A | G | 50 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(47): Show |
70 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.190-2234A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733594 | |||||||
| chr16:77733602 | A | G | 29 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0033 others(26): Show |
36 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.190-2226A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733602 | |||||||
| chr16:77733632 | C | T | 31 | a0001c0001t0001g0046 a0001c0001t0001g0216 a0001c0001t0002g0001 others(28): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.190-2196C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733632 | |||||||
| chr16:77733677 | C | A | 1 | a0006c0007t0001g0035 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.190-2151C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733677 | |||||||
| chr16:77733680 | C | G | 50 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(47): Show |
70 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.190-2148C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733680 | |||||||
| chr16:77733692 | G | A | 5 | a0001c0001t0002g0012 a0001c0001t0002g0075 a0001c0001t0002g0089 others(2): Show |
8 | HG00408.hp1 NA18969.hp2 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-2136G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733692 | |||||||
| chr16:77733964 | T | C | 3 | a0001c0001t0001g0232 a0001c0001t0001g0292 a0001c0006t0003g0269 |
3 | HG01884.hp1 HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.190-1864T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733964 | |||||||
| chr16:77733981 | A | G | 3 | a0001c0001t0002g0086 a0001c0001t0002g0123 a0001c0001t0002g0135 |
3 | NA18948.hp2 NA18965.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.190-1847A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77733981 | |||||||
| chr16:77734020 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.190-1808G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734020 | |||||||
| chr16:77734107 | C | T | 3 | a0001c0001t0001g0276 a0005c0005t0002g0191 a0005c0005t0002g0256 |
3 | HG02622.hp2 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.190-1721C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734107 | |||||||
| chr16:77734133 | C | CA | 50 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(47): Show |
70 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.190-1693dupA | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77734133 | ||||||
| chr16:77734133 | C | T | 7 | a0001c0001t0001g0024 a0001c0001t0002g0062 a0001c0001t0002g0193 others(4): Show |
10 | HG02615.hp2 HG02630.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.190-1695C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734133 | |||||||
| chr16:77734138 | C | G | 50 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(47): Show |
70 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.190-1690C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734138 | |||||||
| chr16:77734148 | C | A | 50 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(47): Show |
70 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.190-1680C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734148 | |||||||
| chr16:77734262 | T | C | 2 | a0001c0001t0002g0098 a0001c0001t0002g0129 |
2 | NA18950.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.190-1566T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734262 | |||||||
| chr16:77734299 | T | C | 50 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(47): Show |
70 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.190-1529T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734299 | |||||||
| chr16:77734351 | C | T | 127 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(124): Show |
201 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.190-1477C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734351 | |||||||
| chr16:77734388 | C | T | 24 | a0001c0001t0001g0063 a0001c0001t0001g0095 a0001c0001t0001g0117 others(21): Show |
35 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.190-1440C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734388 | |||||||
| chr16:77734420 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.190-1408G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734420 | |||||||
| chr16:77734475 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.190-1353T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734475 | |||||||
| chr16:77734487 | C | G | 50 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(47): Show |
70 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.190-1341C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734487 | |||||||
| chr16:77734497 | C | G | 14 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0171 others(11): Show |
18 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.190-1331C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734497 | |||||||
| chr16:77734539 | T | C | 50 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(47): Show |
70 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.190-1289T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734539 | |||||||
| chr16:77734587 | A | C | 1 | a0002c0002t0001g0284 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.190-1241A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734587 | |||||||
| chr16:77734595 | G | C | 49 | a0001c0001t0001g0059 a0001c0001t0001g0163 a0001c0001t0001g0165 others(46): Show |
69 | HG00140.hp1 HG00438.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.190-1233G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734595 | |||||||
| chr16:77734712 | A | G | 7 | a0001c0001t0001g0024 a0001c0001t0002g0062 a0001c0001t0002g0193 others(4): Show |
10 | HG02615.hp2 HG02630.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.190-1116A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734712 | |||||||
| chr16:77734717 | T | TA | 9 | a0001c0001t0001g0028 a0001c0001t0001g0171 a0001c0001t0001g0192 others(6): Show |
11 | HG02109.hp1 HG02451.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.190-1105dupA | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr16 | 77734717 | ||||||
| chr16:77734721 | A | G | 1 | a0007c0012t0001g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.190-1107A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734721 | |||||||
| chr16:77734724 | G | A | 1 | a0007c0012t0001g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.190-1104G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734724 | |||||||
| chr16:77734726 | A | G | 1 | a0007c0012t0001g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.190-1102A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734726 | |||||||
| chr16:77734737 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.190-1091C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734737 | |||||||
| chr16:77734787 | G | T | 5 | a0001c0001t0001g0276 a0001c0006t0001g0156 a0001c0006t0003g0269 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-1041G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734787 | |||||||
| chr16:77734793 | A | G | 1 | a0001c0001t0002g0101 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.190-1035A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734793 | |||||||
| chr16:77734809 | A | T | 1 | a0001c0001t0002g0135 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.190-1019A>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734809 | |||||||
| chr16:77734881 | C | T | 5 | a0001c0001t0001g0276 a0001c0006t0001g0156 a0001c0006t0003g0269 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-947C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734881 | |||||||
| chr16:77734943 | A | G | 243 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(240): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.190-885A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734943 | |||||||
| chr16:77734949 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.190-879C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734949 | |||||||
| chr16:77734966 | A | G | 1 | a0007c0012t0001g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.190-862A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734966 | |||||||
| chr16:77734967 | C | A | 1 | a0007c0012t0001g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.190-861C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734967 | |||||||
| chr16:77734968 | T | C | 1 | a0007c0012t0001g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.190-860T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77734968 | |||||||
| chr16:77735005 | C | G | 3 | a0001c0001t0002g0206 a0001c0001t0002g0231 a0001c0001t0002g0233 |
3 | HG02615.hp2 HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.190-823C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735005 | |||||||
| chr16:77735037 | G | A | 1 | a0001c0001t0001g0051 | 2 | HG00735.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.190-791G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735037 | |||||||
| chr16:77735059 | T | A | 1 | a0007c0012t0001g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.190-769T>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735059 | |||||||
| chr16:77735092 | A | C | 6 | a0001c0001t0001g0105 a0001c0001t0001g0183 a0001c0001t0001g0242 others(3): Show |
6 | HG02109.hp1 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-736A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735092 | |||||||
| chr16:77735093 | T | G | 18 | a0001c0001t0001g0024 a0001c0001t0001g0175 a0001c0001t0001g0198 others(15): Show |
22 | HG01884.hp1 HG02055.hp1 HG02615.hp2 others(19): Show |
intron_variant | MODIFIER | c.190-735T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735093 | |||||||
| chr16:77735230 | C | T | 9 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(6): Show |
10 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.190-598C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735230 | |||||||
| chr16:77735231 | G | A | 5 | a0001c0001t0002g0012 a0001c0001t0002g0075 a0001c0001t0002g0089 others(2): Show |
8 | HG00408.hp1 NA18969.hp2 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-597G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735231 | |||||||
| chr16:77735239 | C | A | 21 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0040 others(18): Show |
26 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.190-589C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735239 | |||||||
| chr16:77735358 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.190-470A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735358 | |||||||
| chr16:77735370 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG03927.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.190-458C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735370 | |||||||
| chr16:77735380 | G | T | 23 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0040 others(20): Show |
28 | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.190-448G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735380 | |||||||
| chr16:77735391 | C | T | 85 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(82): Show |
109 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.190-437C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735391 | |||||||
| chr16:77735462 | G | A | 1 | a0001c0001t0003g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.190-366G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735462 | |||||||
| chr16:77735472 | C | T | 269 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(266): Show |
423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.190-356C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735472 | |||||||
| chr16:77735548 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.190-280C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735548 | |||||||
| chr16:77735735 | G | C | 10 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(7): Show |
11 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.190-93G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735735 | |||||||
| chr16:77735750 | C | T | 267 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(264): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.190-78C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735750 | |||||||
| chr16:77735782 | C | G | 37 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(34): Show |
57 | HG00438.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.190-46C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 2/3 | chr16 | 77735782 | |||||||
| chr16:77736000 | G | C | 8 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+14G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736000 | |||||||
| chr16:77736017 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.348+31C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736017 | |||||||
| chr16:77736018 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.348+32G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736018 | |||||||
| chr16:77736023 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG00733.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.348+37C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736023 | |||||||
| chr16:77736175 | A | G | 8 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+189A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736175 | |||||||
| chr16:77736184 | T | C | 1 | a0007c0012t0001g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.348+198T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736184 | |||||||
| chr16:77736185 | C | T | 1 | a0007c0012t0001g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.348+199C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736185 | |||||||
| chr16:77736204 | G | A | 5 | a0001c0001t0001g0232 a0005c0005t0002g0155 a0005c0005t0002g0191 others(2): Show |
5 | HG02258.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+218G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736204 | |||||||
| chr16:77736260 | C | T | 7 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(4): Show |
8 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+274C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736260 | |||||||
| chr16:77736336 | G | C | 8 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+350G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736336 | |||||||
| chr16:77736348 | C | T | 1 | a0001c0001t0002g0246 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.348+362C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736348 | |||||||
| chr16:77736430 | A | G | 1 | a0001c0001t0002g0245 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.348+444A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736430 | |||||||
| chr16:77736453 | G | A | 268 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(265): Show |
420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.348+467G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736453 | |||||||
| chr16:77736475 | G | A | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+489G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736475 | |||||||
| chr16:77736484 | C | T | 1 | a0002c0002t0001g0037 | 2 | NA18954.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.348+498C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736484 | |||||||
| chr16:77736539 | G | C | 2 | a0001c0001t0001g0141 a0001c0001t0003g0272 |
2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.348+553G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736539 | |||||||
| chr16:77736542 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+556T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736542 | |||||||
| chr16:77736571 | C | CAT | 8 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+586_348+587dup others(2): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 77736571 | ||||||
| chr16:77736616 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.348+630C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736616 | |||||||
| chr16:77736634 | AT | A | 9 | a0001c0001t0002g0062 a0001c0001t0002g0135 a0001c0001t0002g0193 others(6): Show |
10 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+659delT | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 77736634 | ||||||
| chr16:77736640 | T | A | 7 | a0001c0001t0001g0232 a0003c0003t0001g0060 a0003c0003t0001g0130 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+654T>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736640 | |||||||
| chr16:77736641 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.348+655T>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736641 | |||||||
| chr16:77736647 | T | G | 8 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+661T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736647 | |||||||
| chr16:77736663 | G | A | 2 | a0002c0002t0001g0143 a0002c0002t0001g0281 |
2 | HG01255.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.348+677G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736663 | |||||||
| chr16:77736721 | C | T | 2 | a0002c0002t0001g0067 a0002c0009t0001g0279 |
3 | HG03710.hp1 HG04204.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.348+735C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736721 | |||||||
| chr16:77736732 | C | G | 2 | a0005c0005t0002g0191 a0005c0005t0002g0256 |
2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.348+746C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736732 | |||||||
| chr16:77736814 | T | A | 1 | a0007c0012t0001g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.348+828T>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736814 | |||||||
| chr16:77736858 | C | T | 7 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(4): Show |
8 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+872C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736858 | |||||||
| chr16:77736882 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.348+896A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736882 | |||||||
| chr16:77736901 | A | C | 1 | a0001c0001t0001g0232 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.348+915A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77736901 | |||||||
| chr16:77737003 | AACCATAG others(8): Show |
A | 1 | a0001c0001t0002g0186 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.348+1050_348+1064d others(17): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 77737003 | ||||||
| chr16:77737015 | CTAGACCA others(38): Show |
C | 1 | a0001c0001t0002g0261 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.348+1040_348+1084d others(47): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 77737015 | ||||||
| chr16:77737030 | CTAGACCA others(23): Show |
C | 7 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(4): Show |
8 | HG02615.hp2 HG02630.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+1055_348+1084d others(32): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 77737030 | ||||||
| chr16:77737036 | CATAGGAA others(8): Show |
C | 5 | a0001c0001t0001g0232 a0005c0005t0002g0155 a0005c0005t0002g0191 others(2): Show |
5 | HG02258.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+1059_348+1073d others(17): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 77737036 | ||||||
| chr16:77737474 | G | A | 3 | a0001c0001t0001g0213 a0001c0006t0001g0156 a0001c0006t0003g0269 |
3 | HG01884.hp1 HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.348+1488G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737474 | |||||||
| chr16:77737474 | GTTT | G | 6 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0106 others(3): Show |
7 | HG01081.hp1 HG01123.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+1496_348+1498d others(5): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 77737474 | ||||||
| chr16:77737482 | T | G | 13 | a0001c0001t0001g0151 a0001c0001t0001g0190 a0001c0001t0002g0062 others(10): Show |
14 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.348+1496T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737482 | |||||||
| chr16:77737484 | T | TG | 6 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0192 others(3): Show |
10 | HG02257.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.348+1499dupG | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 77737484 | ||||||
| chr16:77737488 | G | GTTTT | 7 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(4): Show |
8 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+1504_348+1505i others(6): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 77737488 | ||||||
| chr16:77737488 | G | T | 1 | a0003c0003t0001g0088 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.348+1502G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737488 | |||||||
| chr16:77737491 | G | T | 8 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+1505G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737491 | |||||||
| chr16:77737494 | G | T | 8 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+1508G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737494 | |||||||
| chr16:77737497 | G | T | 8 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+1511G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737497 | |||||||
| chr16:77737497 | GTTT | G | 71 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0040 others(68): Show |
94 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.348+1516_348+1518d others(5): Show |
NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 77737497 | ||||||
| chr16:77737500 | T | G | 48 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(45): Show |
70 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.348+1514T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737500 | |||||||
| chr16:77737507 | C | G | 8 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+1521C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737507 | |||||||
| chr16:77737510 | A | G | 8 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+1524A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737510 | |||||||
| chr16:77737578 | C | T | 2 | a0005c0005t0002g0155 a0005c0005t0008g0287 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.348+1592C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737578 | |||||||
| chr16:77737585 | A | G | 7 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(4): Show |
8 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+1599A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737585 | |||||||
| chr16:77737598 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0169 |
2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.348+1612G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737598 | |||||||
| chr16:77737646 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.348+1660C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737646 | |||||||
| chr16:77737647 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.348+1661G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737647 | |||||||
| chr16:77737737 | A | G | 8 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+1751A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737737 | |||||||
| chr16:77737754 | G | A | 8 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
9 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+1768G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737754 | |||||||
| chr16:77737755 | G | A | 24 | a0001c0001t0001g0117 a0001c0001t0002g0007 a0001c0001t0002g0012 others(21): Show |
42 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.348+1769G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737755 | |||||||
| chr16:77737990 | T | C | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+2004T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77737990 | |||||||
| chr16:77738015 | A | G | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+2029A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738015 | |||||||
| chr16:77738033 | A | G | 7 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(4): Show |
8 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+2047A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738033 | |||||||
| chr16:77738102 | A | G | 40 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(37): Show |
60 | HG00438.hp2 HG00642.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.348+2116A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738102 | |||||||
| chr16:77738151 | C | T | 27 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0040 others(24): Show |
33 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.348+2165C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738151 | |||||||
| chr16:77738185 | G | C | 9 | a0001c0001t0002g0014 a0001c0001t0002g0025 a0001c0001t0002g0038 others(6): Show |
15 | HG00323.hp2 HG00558.hp2 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.348+2199G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738185 | |||||||
| chr16:77738248 | C | A | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+2262C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738248 | |||||||
| chr16:77738254 | TC | T | 4 | a0005c0005t0002g0155 a0005c0005t0002g0191 a0005c0005t0002g0256 others(1): Show |
4 | HG02258.hp2 HG02622.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+2272delC | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr16 | 77738254 | ||||||
| chr16:77738279 | T | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0212 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.348+2293T>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738279 | |||||||
| chr16:77738286 | G | A | 4 | a0005c0005t0002g0155 a0005c0005t0002g0191 a0005c0005t0002g0256 others(1): Show |
4 | HG02258.hp2 HG02622.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+2300G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738286 | |||||||
| chr16:77738303 | A | G | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | NA18971.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.348+2317A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738303 | |||||||
| chr16:77738322 | T | C | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+2336T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738322 | |||||||
| chr16:77738394 | A | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0192 others(1): Show |
8 | HG02280.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+2408A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738394 | |||||||
| chr16:77738425 | T | C | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+2439T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738425 | |||||||
| chr16:77738448 | T | C | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+2462T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738448 | |||||||
| chr16:77738468 | A | G | 1 | a0002c0002t0001g0094 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.348+2482A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738468 | |||||||
| chr16:77738517 | A | T | 37 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(34): Show |
57 | HG00438.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.348+2531A>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738517 | |||||||
| chr16:77738596 | A | G | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+2610A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738596 | |||||||
| chr16:77738608 | G | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0212 |
2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.348+2622G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738608 | |||||||
| chr16:77738610 | C | G | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+2624C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738610 | |||||||
| chr16:77738644 | A | G | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+2658A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738644 | |||||||
| chr16:77738648 | C | T | 3 | a0003c0003t0001g0050 a0003c0003t0001g0205 a0003c0003t0001g0214 |
4 | NA18956.hp2 NA18984.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+2662C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738648 | |||||||
| chr16:77738693 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.348+2707G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738693 | |||||||
| chr16:77738729 | T | C | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+2743T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738729 | |||||||
| chr16:77738732 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0052 |
8 | HG01261.hp2 HG01943.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+2746A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738732 | |||||||
| chr16:77738740 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0192 others(3): Show |
10 | HG02257.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.348+2754G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738740 | |||||||
| chr16:77738749 | G | A | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+2763G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738749 | |||||||
| chr16:77738780 | C | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0235 |
2 | HG01256.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.348+2794C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738780 | |||||||
| chr16:77738869 | G | A | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-2713G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738869 | |||||||
| chr16:77738961 | C | T | 37 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(34): Show |
57 | HG00438.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.349-2621C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738961 | |||||||
| chr16:77738992 | C | T | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-2590C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77738992 | |||||||
| chr16:77739178 | A | G | 7 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(4): Show |
8 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-2404A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739178 | |||||||
| chr16:77739181 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.349-2401A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739181 | |||||||
| chr16:77739380 | A | G | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-2202A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739380 | |||||||
| chr16:77739427 | G | A | 37 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(34): Show |
57 | HG00438.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.349-2155G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739427 | |||||||
| chr16:77739454 | A | G | 274 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(271): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.349-2128A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739454 | |||||||
| chr16:77739513 | A | C | 77 | a0001c0001t0001g0117 a0001c0001t0001g0232 a0001c0001t0002g0001 others(74): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.349-2069A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739513 | |||||||
| chr16:77739561 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0265 |
2 | HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.349-2021T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739561 | |||||||
| chr16:77739576 | T | C | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-2006T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739576 | |||||||
| chr16:77739739 | T | C | 61 | a0001c0001t0001g0260 a0001c0001t0001g0264 a0001c0001t0002g0188 others(58): Show |
110 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.349-1843T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739739 | |||||||
| chr16:77739750 | A | T | 3 | a0003c0003t0001g0050 a0003c0003t0001g0205 a0003c0003t0001g0214 |
4 | NA18956.hp2 NA18984.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-1832A>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739750 | |||||||
| chr16:77739770 | C | G | 1 | a0001c0001t0002g0133 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.349-1812C>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739770 | |||||||
| chr16:77739945 | C | T | 1 | a0001c0001t0002g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.349-1637C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739945 | |||||||
| chr16:77739953 | T | C | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-1629T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739953 | |||||||
| chr16:77739980 | C | A | 9 | a0002c0002t0001g0005 a0002c0002t0001g0036 a0002c0002t0001g0047 others(6): Show |
18 | HG00423.hp1 HG01106.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.349-1602C>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77739980 | |||||||
| chr16:77740099 | T | C | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-1483T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740099 | |||||||
| chr16:77740179 | C | T | 1 | a0001c0001t0003g0271 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.349-1403C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740179 | |||||||
| chr16:77740377 | G | C | 1 | a0001c0001t0002g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349-1205G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740377 | |||||||
| chr16:77740415 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.349-1167C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740415 | |||||||
| chr16:77740486 | A | G | 7 | a0001c0001t0002g0062 a0001c0001t0002g0193 a0001c0001t0002g0206 others(4): Show |
8 | HG02615.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-1096A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740486 | |||||||
| chr16:77740512 | A | G | 205 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(202): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.349-1070A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740512 | |||||||
| chr16:77740567 | T | C | 1 | a0001c0001t0003g0272 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.349-1015T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740567 | |||||||
| chr16:77740584 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0106 others(2): Show |
6 | HG01081.hp1 HG01123.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-998C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740584 | |||||||
| chr16:77740699 | C | T | 1 | a0003c0003t0001g0173 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.349-883C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740699 | |||||||
| chr16:77740763 | G | C | 73 | a0001c0001t0001g0117 a0001c0001t0001g0184 a0001c0001t0002g0001 others(70): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.349-819G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740763 | |||||||
| chr16:77740790 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0235 |
2 | HG01256.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.349-792C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740790 | |||||||
| chr16:77740791 | G | A | 1 | a0001c0001t0001g0020 | 3 | NA18944.hp2 NA18967.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.349-791G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740791 | |||||||
| chr16:77740801 | G | A | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-781G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740801 | |||||||
| chr16:77740828 | G | A | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-754G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740828 | |||||||
| chr16:77740838 | A | G | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-744A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740838 | |||||||
| chr16:77740865 | A | G | 1 | a0002c0002t0001g0082 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.349-717A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740865 | |||||||
| chr16:77740969 | T | C | 2 | a0002c0002t0001g0259 a0002c0002t0001g0278 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.349-613T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740969 | |||||||
| chr16:77740972 | A | G | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-610A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740972 | |||||||
| chr16:77740999 | T | C | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-583T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77740999 | |||||||
| chr16:77741015 | A | C | 1 | a0001c0001t0001g0212 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.349-567A>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741015 | |||||||
| chr16:77741022 | G | A | 40 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(37): Show |
60 | HG00438.hp2 HG00642.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.349-560G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741022 | |||||||
| chr16:77741094 | A | G | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-488A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741094 | |||||||
| chr16:77741102 | G | C | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-480G>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741102 | |||||||
| chr16:77741173 | G | T | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-409G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741173 | |||||||
| chr16:77741282 | C | T | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-300C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741282 | |||||||
| chr16:77741332 | T | C | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-250T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741332 | |||||||
| chr16:77741360 | A | T | 1 | a0001c0001t0002g0132 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.349-222A>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741360 | |||||||
| chr16:77741395 | G | A | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-187G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741395 | |||||||
| chr16:77741408 | G | T | 1 | a0001c0001t0001g0076 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.349-174G>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741408 | |||||||
| chr16:77741455 | A | G | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-127A>G | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741455 | |||||||
| chr16:77741547 | C | T | 1 | a0001c0011t0006g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-35C>T | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741547 | |||||||
| chr16:77741562 | G | A | 114 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(111): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.349-20G>A | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741562 | |||||||
| chr16:77741568 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.349-14T>C | NUDT7 | ENSG00000140876.11 | transcript | ENST00000268533.9 | protein_coding | 3/3 | chr16 | 77741568 |