Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22978 |
| ensemblid | ENSG00000076685.19 |
| hgncid | 8022 |
| symbol | NT5C2 |
| name | 5'-nucleotidase, cytosolic II |
| refseq_nuc | NM_001351169.2 |
| refseq_prot | NP_001338098.1 |
| ensembl_nuc | ENST00000404739.8 |
| ensembl_prot | ENSP00000383960.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 103088038 |
| end | 103193272 |
| strand | - |
| ver | v1.2 |
| region | chr10:103088038-103193272 |
| region5000 | chr10:103083038-103198272 |
| regionname0 | NT5C2_chr10_103088038_103193272 |
| regionname5000 | NT5C2_chr10_103083038_103198272 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 561 | 308 | 64 | 51 | 143 | 10 | 38 | 113 | NT5C2_chr10_103083038_103198272 | NT5C2 | MSTSW others(556): Show |
chr10 | 103083038 | 103198272 |
| a0002 | 0/0 | 561 | 31 | 2 | 11 | 16 | 2 | 0 | 11 | NT5C2_chr10_103083038_103198272 | NT5C2 | MSASW others(556): Show |
chr10 | 103083038 | 103198272 |
| a0003 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | MSTSW others(556): Show |
chr10 | 103083038 | 103198272 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1683 | 172 | 27 | 33 | 84 | 5 | 21 | NT5C2_chr10_103083038_103198272 | NT5C2 | ATGTC others(1678): Show |
chr10 | 103083038 | 103198272 | ||
| a0001c0002 | 0/0 | 1683 | 136 | 37 | 18 | 59 | 5 | 17 | NT5C2_chr10_103083038_103198272 | NT5C2 | ATGTC others(1678): Show |
chr10 | 103083038 | 103198272 | ||
| a0002c0003 | 0/0 | 1683 | 31 | 2 | 11 | 16 | 2 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | ATGTC others(1678): Show |
chr10 | 103083038 | 103198272 | ||
| a0003c0004 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | ATGTC others(1678): Show |
chr10 | 103083038 | 103198272 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3525 | 94 | 26 | 17 | 37 | 3 | 11 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0001t0002 | 1/1 | 3525 | 63 | 1 | 12 | 36 | 2 | 10 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0001t0005 | 0/0 | 3525 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0001t0007 | 0/0 | 3525 | 8 | 0 | 0 | 8 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0001t0011 | 0/0 | 3525 | 2 | 0 | 2 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0001t0012 | 0/0 | 3525 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0001t0016 | 0/0 | 3525 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0001t0018 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0002t0003 | 0/0 | 3525 | 62 | 4 | 9 | 42 | 0 | 7 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0002t0004 | 0/0 | 3525 | 16 | 10 | 2 | 0 | 2 | 2 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0002t0005 | 0/0 | 3525 | 25 | 13 | 5 | 4 | 3 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0002t0006 | 0/0 | 3525 | 17 | 0 | 2 | 9 | 0 | 6 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0002t0008 | 0/0 | 3525 | 7 | 7 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0002t0009 | 0/0 | 3525 | 3 | 0 | 0 | 3 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0002t0010 | 0/0 | 3525 | 2 | 0 | 0 | 0 | 0 | 2 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0002t0013 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0002t0014 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0002t0015 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0001c0002t0017 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0002c0003t0004 | 0/0 | 3525 | 31 | 2 | 11 | 16 | 2 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| a0003c0004t0005 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | AGTTG others(3520): Show |
chr10 | 103083038 | 103198272 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0261 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0007g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0011g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0011g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0012g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0016g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0001t0018g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0008g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0009g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0009g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0009g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0010g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0010g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0014g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0001c0002t0017g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0002c0003t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| a0003c0004t0005g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0301 | EUR | FIN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00408 | hp2 | a0001 | c0002 | t0006 | g0192 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00544 | hp2 | a0001 | c0002 | t0003 | g0027 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00558 | hp1 | a0001 | c0001 | t0018 | g0255 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00558 | hp2 | a0001 | c0001 | t0007 | g0145 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00597 | hp2 | a0003 | c0004 | t0005 | g0335 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00609 | hp1 | a0001 | c0002 | t0006 | g0186 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00609 | hp2 | a0002 | c0003 | t0004 | g0003 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00621 | hp2 | a0002 | c0003 | t0004 | g0218 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00639 | hp1 | a0002 | c0003 | t0004 | g0223 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00639 | hp2 | a0001 | c0002 | t0005 | g0332 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00642 | hp1 | a0002 | c0003 | t0004 | g0233 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00673 | hp1 | a0002 | c0003 | t0004 | g0235 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00673 | hp2 | a0001 | c0002 | t0005 | g0327 | EAS | CHS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00733 | hp1 | a0001 | c0001 | t0011 | g0287 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00733 | hp2 | a0002 | c0003 | t0004 | g0241 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00735 | hp1 | a0002 | c0003 | t0004 | g0221 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00735 | hp2 | a0001 | c0002 | t0004 | g0021 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00738 | hp1 | a0001 | c0002 | t0005 | g0328 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0048 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01070 | hp2 | a0001 | c0002 | t0006 | g0190 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01071 | hp1 | a0001 | c0002 | t0006 | g0191 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01099 | hp1 | a0002 | c0003 | t0004 | g0220 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01106 | hp2 | a0001 | c0001 | t0016 | g0126 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0018 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0050 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01169 | hp2 | a0001 | c0002 | t0005 | g0323 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01243 | hp1 | a0001 | c0002 | t0005 | g0309 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01255 | hp2 | a0002 | c0003 | t0004 | g0226 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01257 | hp1 | a0002 | c0003 | t0004 | g0002 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01258 | hp2 | a0002 | c0003 | t0004 | g0002 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01358 | hp2 | a0001 | c0002 | t0003 | g0068 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01433 | hp1 | a0001 | c0001 | t0011 | g0305 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0060 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01496 | hp1 | a0002 | c0003 | t0004 | g0230 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01515 | hp1 | a0001 | c0002 | t0005 | g0330 | EUR | IBS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0290 | EUR | IBS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01516 | hp1 | a0001 | c0002 | t0004 | g0020 | EUR | IBS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01517 | hp1 | a0001 | c0002 | t0005 | g0331 | EUR | IBS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01517 | hp2 | a0001 | c0002 | t0004 | g0019 | EUR | IBS | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01884 | hp2 | a0001 | c0002 | t0008 | g0211 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01928 | hp2 | a0001 | c0001 | t0012 | g0111 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01943 | hp1 | a0001 | c0002 | t0003 | g0061 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01952 | hp2 | a0001 | c0002 | t0005 | g0324 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0066 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02004 | hp2 | a0001 | c0002 | t0003 | g0062 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02027 | hp2 | a0002 | c0003 | t0004 | g0240 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02040 | hp1 | a0001 | c0002 | t0006 | g0193 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02071 | hp2 | a0001 | c0002 | t0017 | g0067 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02074 | hp1 | a0001 | c0001 | t0007 | g0141 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02074 | hp2 | a0001 | c0002 | t0003 | g0055 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0057 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0026 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02135 | hp2 | a0002 | c0003 | t0004 | g0237 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02145 | hp2 | a0001 | c0002 | t0008 | g0215 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02155 | hp1 | a0001 | c0002 | t0003 | g0054 | EAS | CDX | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02257 | hp1 | a0001 | c0002 | t0008 | g0207 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0063 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02258 | hp1 | a0001 | c0002 | t0005 | g0319 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02258 | hp2 | a0001 | c0002 | t0015 | g0014 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0044 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02280 | hp1 | a0002 | c0003 | t0004 | g0225 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0046 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02300 | hp2 | a0002 | c0003 | t0004 | g0227 | AMR | PEL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02523 | hp1 | a0001 | c0001 | t0007 | g0140 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02523 | hp2 | a0001 | c0002 | t0006 | g0189 | EAS | KHV | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0206 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02622 | hp2 | a0001 | c0002 | t0008 | g0213 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02647 | hp1 | a0001 | c0002 | t0008 | g0216 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02647 | hp2 | a0001 | c0002 | t0005 | g0334 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02683 | hp1 | a0001 | c0002 | t0006 | g0188 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0262 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0022 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0070 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02735 | hp2 | a0001 | c0002 | t0006 | g0200 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0051 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02809 | hp2 | a0001 | c0002 | t0005 | g0321 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02818 | hp2 | a0001 | c0002 | t0005 | g0318 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02896 | hp1 | a0001 | c0002 | t0004 | g0202 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0185 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02970 | hp1 | a0001 | c0002 | t0005 | g0315 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0012 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0071 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03041 | hp2 | a0001 | c0002 | t0005 | g0311 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03098 | hp2 | a0001 | c0002 | t0005 | g0310 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03139 | hp1 | a0001 | c0002 | t0005 | g0317 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03195 | hp2 | a0001 | c0002 | t0013 | g0197 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03225 | hp1 | a0001 | c0002 | t0005 | g0308 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03225 | hp2 | a0001 | c0002 | t0008 | g0212 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0312 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03490 | hp1 | a0001 | c0002 | t0004 | g0016 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0069 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03492 | hp1 | a0001 | c0002 | t0004 | g0017 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0279 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03516 | hp1 | a0001 | c0002 | t0005 | g0313 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0015 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0275 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0037 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03831 | hp1 | a0001 | c0002 | t0006 | g0204 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0047 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0052 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03942 | hp1 | a0001 | c0002 | t0010 | g0007 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03942 | hp2 | a0001 | c0002 | t0006 | g0196 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG04115 | hp1 | a0001 | c0002 | t0006 | g0201 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG04115 | hp2 | a0001 | c0002 | t0010 | g0043 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG04184 | hp1 | a0001 | c0002 | t0006 | g0199 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0059 | SAS | STU | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18522 | hp1 | a0001 | c0002 | t0008 | g0214 | AFR | YRI | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18612 | hp1 | a0001 | c0001 | t0007 | g0139 | EAS | CHB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0036 | EAS | CHB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18747 | hp1 | a0001 | c0002 | t0006 | g0205 | EAS | CHB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18747 | hp2 | a0001 | c0002 | t0003 | g0049 | EAS | CHB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0038 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18941 | hp2 | a0002 | c0003 | t0004 | g0219 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18947 | hp2 | a0001 | c0002 | t0005 | g0329 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18950 | hp1 | a0002 | c0003 | t0004 | g0238 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18951 | hp2 | a0001 | c0002 | t0003 | g0085 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18957 | hp1 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18957 | hp2 | a0001 | c0001 | t0007 | g0173 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18960 | hp2 | a0001 | c0002 | t0005 | g0325 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18961 | hp1 | a0001 | c0002 | t0003 | g0086 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18962 | hp1 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18963 | hp2 | a0002 | c0003 | t0004 | g0229 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18965 | hp2 | a0002 | c0003 | t0004 | g0239 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18968 | hp2 | a0001 | c0002 | t0003 | g0078 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18971 | hp2 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0322 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18975 | hp2 | a0001 | c0002 | t0003 | g0058 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18977 | hp1 | a0001 | c0002 | t0006 | g0187 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18978 | hp1 | a0001 | c0002 | t0003 | g0080 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18981 | hp1 | a0001 | c0002 | t0003 | g0064 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18981 | hp2 | a0001 | c0001 | t0007 | g0138 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18982 | hp1 | a0001 | c0002 | t0003 | g0041 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18985 | hp1 | a0001 | c0002 | t0003 | g0077 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0242 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18990 | hp2 | a0001 | c0002 | t0009 | g0029 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18992 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0167 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18994 | hp2 | a0002 | c0003 | t0004 | g0234 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA18995 | hp2 | a0002 | c0003 | t0004 | g0236 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19004 | hp2 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19005 | hp1 | a0002 | c0003 | t0004 | g0228 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19005 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19007 | hp2 | a0001 | c0002 | t0006 | g0198 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19009 | hp1 | a0001 | c0001 | t0007 | g0163 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19009 | hp2 | a0001 | c0002 | t0003 | g0065 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19011 | hp1 | a0002 | c0003 | t0004 | g0217 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19030 | hp1 | a0001 | c0002 | t0014 | g0087 | AFR | LWK | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0203 | AFR | LWK | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19043 | hp2 | a0001 | c0002 | t0004 | g0011 | AFR | LWK | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19054 | hp1 | a0001 | c0002 | t0009 | g0030 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19055 | hp2 | a0001 | c0002 | t0003 | g0056 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19057 | hp2 | a0001 | c0002 | t0003 | g0053 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19058 | hp2 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19064 | hp1 | a0001 | c0002 | t0003 | g0072 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19067 | hp1 | a0001 | c0002 | t0005 | g0314 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0074 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19076 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19077 | hp1 | a0001 | c0002 | t0006 | g0195 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19077 | hp2 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19078 | hp1 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19081 | hp2 | a0001 | c0002 | t0003 | g0039 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19082 | hp2 | a0001 | c0002 | t0003 | g0075 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19083 | hp1 | a0002 | c0003 | t0004 | g0010 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19083 | hp2 | a0001 | c0002 | t0003 | g0035 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0042 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19084 | hp2 | a0001 | c0002 | t0006 | g0194 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19086 | hp1 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19086 | hp2 | a0002 | c0003 | t0004 | g0006 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19087 | hp1 | a0001 | c0002 | t0003 | g0084 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19089 | hp1 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA19090 | hp2 | a0001 | c0002 | t0009 | g0031 | EAS | JPT | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ASW | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA20129 | hp2 | a0001 | c0002 | t0003 | g0079 | AFR | ASW | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA20752 | hp1 | a0002 | c0003 | t0004 | g0222 | EUR | TSI | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA20805 | hp1 | a0001 | c0002 | t0005 | g0320 | EUR | TSI | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA20805 | hp2 | a0002 | c0003 | t0004 | g0231 | EUR | TSI | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01123 | hp1 | a0002 | c0003 | t0004 | g0224 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02109 | hp2 | a0001 | c0002 | t0004 | g0013 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02486 | hp1 | a0002 | c0003 | t0004 | g0232 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0326 | AFR | USA | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | USA | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA21309 | hp1 | a0001 | c0002 | t0005 | g0333 | AFR | LWK | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| NA21309 | hp2 | a0001 | c0002 | t0003 | g0076 | AFR | LWK | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0261 | REF | REF | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0288 | REF | REF | NT5C2_chr10_103083038_103198272 | NT5C2 | chr10 | 103083038 | 103198272 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:103093298 | T | C | 1 | a0003 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.1000A>G | p.Thr334Ala | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/19 | 1205/3525 | 1000/1686 | 334/561 | chr10 | 103093298 | |||
| chr10:103174952 | T | C | 1 | a0002 | 31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
missense_variant | MODERATE | c.7A>G | p.Thr3Ala | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/19 | 212/3525 | 7/1686 | 3/561 | chr10 | 103174952 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:103089711 | G | A | 2 | a0001c0002 a0002c0003 |
167 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(164): Show |
synonymous_variant | LOW | c.1647C>T | p.Asp549Asp | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 1852/3525 | 1647/1686 | 549/561 | chr10 | 103089711 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:103088298 | C | G | 1 | a0001c0001t0018 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1374G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 1374 | chr10 | 103088298 | ||||||
| chr10:103088366 | G | A | 14 | a0001c0001t0005 a0001c0002t0003 a0001c0002t0004 others(11): Show |
170 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1306C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 1306 | chr10 | 103088366 | ||||||
| chr10:103088502 | A | G | 1 | a0001c0001t0007 | 8 | HG00558.hp2 HG02074.hp1 HG02523.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1170T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 1170 | chr10 | 103088502 | ||||||
| chr10:103088661 | A | T | 1 | a0001c0002t0014 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1011T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 1011 | chr10 | 103088661 | ||||||
| chr10:103088673 | C | T | 4 | a0001c0002t0003 a0001c0002t0009 a0001c0002t0010 others(1): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*999G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 999 | chr10 | 103088673 | ||||||
| chr10:103088693 | T | G | 1 | a0001c0002t0015 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*979A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 979 | chr10 | 103088693 | ||||||
| chr10:103088791 | T | C | 1 | a0001c0002t0017 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*881A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 881 | chr10 | 103088791 | ||||||
| chr10:103089087 | A | T | 2 | a0001c0002t0006 a0001c0002t0013 |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*585T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 585 | chr10 | 103089087 | ||||||
| chr10:103089098 | A | T | 2 | a0001c0002t0006 a0001c0002t0013 |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*574T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 574 | chr10 | 103089098 | ||||||
| chr10:103089150 | A | G | 1 | a0001c0002t0008 | 7 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*522T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 522 | chr10 | 103089150 | ||||||
| chr10:103089254 | G | A | 1 | a0001c0002t0013 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*418C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 418 | chr10 | 103089254 | ||||||
| chr10:103089359 | G | C | 6 | a0001c0001t0011 a0001c0001t0016 a0001c0002t0003 others(3): Show |
71 | HG00544.hp2 HG00733.hp1 HG01069.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*313C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 313 | chr10 | 103089359 | ||||||
| chr10:103089387 | A | C | 2 | a0001c0002t0006 a0001c0002t0013 |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*285T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 285 | chr10 | 103089387 | ||||||
| chr10:103089457 | C | G | 1 | a0001c0001t0012 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*215G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 215 | chr10 | 103089457 | ||||||
| chr10:103089528 | A | G | 1 | a0001c0002t0009 | 3 | NA18990.hp2 NA19054.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*144T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 19/19 | 144 | chr10 | 103089528 | ||||||
| chr10:103181189 | T | C | 4 | a0001c0002t0003 a0001c0002t0009 a0001c0002t0010 others(1): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-29A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/19 | chr10 | 103181189 | |||||||
| chr10:103181263 | C | T | 1 | a0001c0002t0010 | 2 | HG03942.hp1 HG04115.hp2 |
5_prime_UTR_variant | MODIFIER | c.-103G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/19 | 6305 | chr10 | 103181263 | ||||||
| chr10:103193250 | C | G | 18 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(15): Show |
274 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(271): Show |
5_prime_UTR_variant | MODIFIER | c.-183G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/19 | 18292 | chr10 | 103193250 | ||||||
| chr10:103193264 | C | A | 3 | a0001c0001t0005 a0001c0002t0005 a0003c0004t0005 |
28 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-197G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/19 | 18306 | chr10 | 103193264 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:103089948 | G | A | 3 | a0001c0002t0006g0188 a0001c0002t0006g0190 a0001c0002t0006g0191 |
3 | HG01070.hp2 HG01071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1450-40C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 18/18 | chr10 | 103089948 | |||||||
| chr10:103090304 | A | G | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1449+307T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 18/18 | chr10 | 103090304 | |||||||
| chr10:103090398 | T | C | 2 | a0001c0002t0003g0070 a0001c0002t0003g0071 |
2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1449+213A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 18/18 | chr10 | 103090398 | |||||||
| chr10:103090419 | A | C | 1 | a0001c0002t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1449+192T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 18/18 | chr10 | 103090419 | |||||||
| chr10:103090811 | T | G | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.1273-24A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 17/18 | chr10 | 103090811 | |||||||
| chr10:103090812 | C | T | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.1273-25G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 17/18 | chr10 | 103090812 | |||||||
| chr10:103090861 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1273-74G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 17/18 | chr10 | 103090861 | |||||||
| chr10:103090863 | A | C | 13 | a0002c0003t0004g0002 a0002c0003t0004g0221 a0002c0003t0004g0222 others(10): Show |
14 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1272+73T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 17/18 | chr10 | 103090863 | |||||||
| chr10:103090864 | TAATA | T | 12 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(9): Show |
12 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1272+68_1272+71del others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 17/18 | chr10 | 103090864 | |||||||
| chr10:103090875 | G | A | 183 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(180): Show |
186 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(183): Show |
intron_variant | MODIFIER | c.1272+61C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 17/18 | chr10 | 103090875 | |||||||
| chr10:103091064 | T | C | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1212-68A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091064 | |||||||
| chr10:103091066 | A | G | 1 | a0001c0002t0008g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1212-70T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091066 | |||||||
| chr10:103091078 | A | G | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1212-82T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091078 | |||||||
| chr10:103091207 | T | C | 1 | a0001c0001t0002g0268 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1212-211A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091207 | |||||||
| chr10:103091346 | G | T | 1 | a0001c0002t0006g0193 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1211+218C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091346 | |||||||
| chr10:103091349 | C | CT | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
69 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.1211+214dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091349 | |||||||
| chr10:103091367 | C | T | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1211+197G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091367 | |||||||
| chr10:103091384 | C | T | 1 | a0002c0003t0004g0236 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1211+180G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091384 | |||||||
| chr10:103091517 | G | A | 1 | a0001c0001t0002g0249 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1211+47C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091517 | |||||||
| chr10:103091528 | G | A | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1211+36C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091528 | |||||||
| chr10:103091544 | G | T | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1211+20C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 16/18 | chr10 | 103091544 | |||||||
| chr10:103091639 | G | T | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1160-24C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091639 | |||||||
| chr10:103091643 | G | A | 17 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(14): Show |
17 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1160-28C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091643 | |||||||
| chr10:103091730 | A | G | 2 | a0001c0001t0002g0303 a0001c0001t0002g0304 |
2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1160-115T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091730 | |||||||
| chr10:103091787 | T | A | 4 | a0002c0003t0004g0217 a0002c0003t0004g0218 a0002c0003t0004g0219 others(1): Show |
4 | HG00621.hp2 HG00673.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-172A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091787 | |||||||
| chr10:103091853 | C | A | 1 | a0001c0001t0002g0244 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1160-238G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091853 | |||||||
| chr10:103091854 | A | C | 1 | a0001c0001t0002g0244 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1160-239T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091854 | |||||||
| chr10:103091855 | C | A | 1 | a0001c0001t0002g0244 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1160-240G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103091855 | |||||||
| chr10:103092132 | T | C | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1160-517A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092132 | |||||||
| chr10:103092155 | C | T | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1160-540G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092155 | |||||||
| chr10:103092245 | T | C | 45 | a0001c0001t0002g0245 a0001c0001t0002g0247 a0001c0001t0002g0248 others(42): Show |
45 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1160-630A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092245 | |||||||
| chr10:103092342 | G | T | 1 | a0001c0001t0002g0247 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1160-727C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092342 | |||||||
| chr10:103092358 | A | ATGTC | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.1160-747_1160-744d others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092358 | |||||||
| chr10:103092409 | T | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1159+730A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092409 | |||||||
| chr10:103092453 | G | A | 1 | a0001c0002t0015g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1159+686C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092453 | |||||||
| chr10:103092496 | T | C | 1 | a0002c0003t0004g0241 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1159+643A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092496 | |||||||
| chr10:103092560 | AATG | A | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159+576_1159+578d others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092560 | |||||||
| chr10:103092609 | G | C | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1159+530C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092609 | |||||||
| chr10:103092662 | A | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1159+477T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092662 | |||||||
| chr10:103092749 | G | C | 7 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | NA18943.hp2 NA18945.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.1159+390C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092749 | |||||||
| chr10:103092772 | G | A | 1 | a0001c0001t0002g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1159+367C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092772 | |||||||
| chr10:103092776 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1159+363A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092776 | |||||||
| chr10:103092813 | G | A | 1 | a0001c0002t0003g0034 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1159+326C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092813 | |||||||
| chr10:103092891 | G | A | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1159+248C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092891 | |||||||
| chr10:103092902 | A | AAACTT | 112 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(109): Show |
114 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1159+232_1159+236d others(7): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103092902 | |||||||
| chr10:103093001 | AG | A | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.1159+137delC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 15/18 | chr10 | 103093001 | |||||||
| chr10:103093360 | C | T | 1 | a0001c0002t0015g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.989-51G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093360 | |||||||
| chr10:103093533 | A | G | 11 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(8): Show |
11 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.989-224T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093533 | |||||||
| chr10:103093536 | C | G | 1 | a0001c0001t0001g0172 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.989-227G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093536 | |||||||
| chr10:103093569 | A | C | 2 | a0002c0003t0004g0238 a0002c0003t0004g0239 |
2 | NA18950.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.989-260T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093569 | |||||||
| chr10:103093650 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0182 |
2 | HG01192.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.988+322G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093650 | |||||||
| chr10:103093739 | A | G | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.988+233T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093739 | |||||||
| chr10:103093746 | A | T | 23 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(20): Show |
23 | HG00408.hp1 HG00642.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.988+226T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093746 | |||||||
| chr10:103093820 | T | C | 13 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0108 others(10): Show |
13 | HG01106.hp1 HG01928.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.988+152A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 14/18 | chr10 | 103093820 | |||||||
| chr10:103094145 | G | A | 3 | a0001c0002t0003g0061 a0001c0002t0003g0062 a0001c0002t0003g0063 |
3 | HG01943.hp1 HG02004.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.922-107C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 13/18 | chr10 | 103094145 | |||||||
| chr10:103094239 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.921+109G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 13/18 | chr10 | 103094239 | |||||||
| chr10:103094247 | T | TA | 41 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0016 others(38): Show |
41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.921+100dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 13/18 | chr10 | 103094247 | |||||||
| chr10:103094505 | G | A | 2 | a0002c0003t0004g0002 a0002c0003t0004g0222 |
3 | HG01257.hp1 HG01258.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.814-50C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094505 | |||||||
| chr10:103094599 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.814-144C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094599 | |||||||
| chr10:103094605 | C | T | 1 | a0001c0001t0002g0276 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.814-150G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094605 | |||||||
| chr10:103094687 | T | G | 1 | a0001c0001t0002g0285 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.814-232A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094687 | |||||||
| chr10:103094880 | C | CA | 255 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(252): Show |
259 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.814-426dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094880 | |||||||
| chr10:103094880 | C | CAA | 52 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0104 others(49): Show |
53 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.814-427_814-426dup others(2): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094880 | |||||||
| chr10:103094880 | CAAAA | C | 6 | a0001c0001t0001g0121 a0001c0002t0008g0211 a0001c0002t0008g0212 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.814-429_814-426del others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103094880 | |||||||
| chr10:103095012 | T | TA | 181 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(178): Show |
184 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(181): Show |
intron_variant | MODIFIER | c.814-558dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095012 | |||||||
| chr10:103095060 | A | G | 1 | a0001c0001t0002g0299 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.814-605T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095060 | |||||||
| chr10:103095101 | C | T | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.814-646G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095101 | |||||||
| chr10:103095289 | T | C | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.813+650A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095289 | |||||||
| chr10:103095424 | A | T | 1 | a0001c0002t0008g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.813+515T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095424 | |||||||
| chr10:103095504 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0170 |
2 | HG01243.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.813+435A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095504 | |||||||
| chr10:103095510 | C | T | 5 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0019 others(2): Show |
5 | HG00735.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+429G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095510 | |||||||
| chr10:103095521 | C | T | 53 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 others(50): Show |
55 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.813+418G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095521 | |||||||
| chr10:103095530 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.813+409T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095530 | |||||||
| chr10:103095836 | T | C | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.813+103A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095836 | |||||||
| chr10:103095860 | C | T | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.813+79G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095860 | |||||||
| chr10:103095899 | T | C | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.813+40A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095899 | |||||||
| chr10:103095913 | G | A | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.813+26C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095913 | |||||||
| chr10:103095920 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.813+19T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 12/18 | chr10 | 103095920 | |||||||
| chr10:103096304 | A | G | 1 | a0002c0003t0004g0236 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.772-324T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096304 | |||||||
| chr10:103096343 | A | C | 4 | a0001c0002t0003g0069 a0001c0002t0003g0070 a0001c0002t0003g0071 others(1): Show |
4 | HG02735.hp1 HG03017.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.772-363T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096343 | |||||||
| chr10:103096405 | G | A | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.772-425C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096405 | |||||||
| chr10:103096525 | T | C | 1 | a0001c0002t0004g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.772-545A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096525 | |||||||
| chr10:103096794 | C | T | 1 | a0001c0002t0003g0038 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.771+497G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096794 | |||||||
| chr10:103096845 | C | CA | 61 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0107 others(58): Show |
62 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.771+445dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096845 | |||||||
| chr10:103096845 | C | CAA | 17 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(14): Show |
17 | HG03540.hp1 HG04115.hp1 NA18940.hp1 others(14): Show |
intron_variant | MODIFIER | c.771+444_771+445dup others(2): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096845 | |||||||
| chr10:103096845 | C | CAAA | 27 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0098 others(24): Show |
29 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.771+443_771+445dup others(3): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096845 | |||||||
| chr10:103096845 | C | CAAAA | 8 | a0002c0003t0004g0217 a0002c0003t0004g0218 a0002c0003t0004g0219 others(5): Show |
8 | HG00621.hp2 HG00642.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.771+442_771+445dup others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096845 | |||||||
| chr10:103096845 | CA | C | 28 | a0001c0001t0002g0290 a0001c0001t0002g0304 a0001c0001t0005g0316 others(25): Show |
28 | HG00597.hp2 HG00673.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.771+445delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103096845 | |||||||
| chr10:103097007 | CAA | C | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.771+282_771+283del others(2): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 11/18 | chr10 | 103097007 | |||||||
| chr10:103097448 | GA | G | 53 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 others(50): Show |
55 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.688-75delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103097448 | |||||||
| chr10:103097461 | A | C | 53 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 others(50): Show |
55 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.688-87T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103097461 | |||||||
| chr10:103097477 | C | A | 29 | a0002c0003t0004g0002 a0002c0003t0004g0003 a0002c0003t0004g0006 others(26): Show |
31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.688-103G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103097477 | |||||||
| chr10:103097555 | T | A | 1 | a0001c0002t0015g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.688-181A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103097555 | |||||||
| chr10:103097766 | A | C | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.688-392T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103097766 | |||||||
| chr10:103097869 | A | C | 2 | a0001c0001t0001g0171 a0001c0001t0012g0111 |
2 | HG01928.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.688-495T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103097869 | |||||||
| chr10:103098184 | T | TA | 18 | a0001c0001t0001g0151 a0001c0001t0001g0181 a0001c0001t0002g0005 others(15): Show |
19 | HG01257.hp2 HG01361.hp1 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.687+746dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103098184 | |||||||
| chr10:103098199 | T | C | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.687+732A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103098199 | |||||||
| chr10:103098237 | A | G | 15 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0005g0308 others(12): Show |
15 | HG00597.hp2 HG00673.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.687+694T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103098237 | |||||||
| chr10:103098387 | G | T | 29 | a0002c0003t0004g0002 a0002c0003t0004g0003 a0002c0003t0004g0006 others(26): Show |
31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.687+544C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103098387 | |||||||
| chr10:103098682 | T | TA | 4 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0049 others(1): Show |
4 | NA18747.hp2 NA18957.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.687+248dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103098682 | |||||||
| chr10:103098793 | T | C | 1 | a0001c0002t0003g0046 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.687+138A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 10/18 | chr10 | 103098793 | |||||||
| chr10:103099073 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.634-89G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 9/18 | chr10 | 103099073 | |||||||
| chr10:103099224 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | NA18977.hp2 NA18989.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.634-240G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 9/18 | chr10 | 103099224 | |||||||
| chr10:103099230 | T | G | 1 | a0001c0002t0006g0192 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.634-246A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 9/18 | chr10 | 103099230 | |||||||
| chr10:103099515 | T | C | 3 | a0001c0002t0003g0057 a0001c0002t0003g0058 a0001c0002t0003g0078 |
3 | HG02083.hp1 NA18968.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.633+411A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 9/18 | chr10 | 103099515 | |||||||
| chr10:103100296 | T | A | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.540-277A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 8/18 | chr10 | 103100296 | |||||||
| chr10:103100369 | C | T | 1 | a0001c0001t0002g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.540-350G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 8/18 | chr10 | 103100369 | |||||||
| chr10:103100637 | C | T | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.539+408G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 8/18 | chr10 | 103100637 | |||||||
| chr10:103100638 | T | G | 324 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0088 others(321): Show |
329 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.539+407A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 8/18 | chr10 | 103100638 | |||||||
| chr10:103101444 | G | A | 2 | a0001c0002t0004g0012 a0001c0002t0004g0013 |
2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.390-118C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103101444 | |||||||
| chr10:103101514 | A | AT | 110 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(107): Show |
112 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.390-189dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103101514 | |||||||
| chr10:103101514 | AT | A | 70 | a0001c0001t0001g0104 a0001c0001t0001g0158 a0001c0001t0002g0268 others(67): Show |
71 | HG00544.hp2 HG01069.hp1 HG01358.hp2 others(68): Show |
intron_variant | MODIFIER | c.390-189delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103101514 | |||||||
| chr10:103101666 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0142 a0001c0001t0001g0147 others(1): Show |
5 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.390-340A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103101666 | |||||||
| chr10:103101706 | AT | A | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.390-381delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103101706 | |||||||
| chr10:103101979 | T | G | 11 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(8): Show |
11 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.390-653A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103101979 | |||||||
| chr10:103102045 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0118 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.390-719C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102045 | |||||||
| chr10:103102068 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.390-742A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102068 | |||||||
| chr10:103102186 | C | G | 1 | a0001c0001t0002g0282 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.390-860G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102186 | |||||||
| chr10:103102232 | G | A | 6 | a0001c0002t0003g0039 a0001c0002t0003g0040 a0001c0002t0003g0041 others(3): Show |
6 | NA18971.hp2 NA18982.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.390-906C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102232 | |||||||
| chr10:103102345 | T | C | 1 | a0001c0002t0005g0326 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.390-1019A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102345 | |||||||
| chr10:103102752 | CTAGA | C | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.390-1430_390-1427d others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102752 | |||||||
| chr10:103102756 | A | G | 1 | a0001c0002t0003g0069 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.390-1430T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102756 | |||||||
| chr10:103102757 | T | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.390-1431A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103102757 | |||||||
| chr10:103103083 | G | A | 2 | a0001c0001t0002g0272 a0001c0001t0002g0274 |
2 | NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.390-1757C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103103083 | |||||||
| chr10:103103404 | G | A | 4 | a0001c0001t0002g0245 a0001c0001t0002g0283 a0001c0001t0002g0284 others(1): Show |
4 | NA18945.hp1 NA18953.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.390-2078C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103103404 | |||||||
| chr10:103103523 | T | C | 5 | a0001c0002t0005g0317 a0001c0002t0005g0318 a0001c0002t0005g0319 others(2): Show |
5 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.389+2183A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103103523 | |||||||
| chr10:103103672 | G | A | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+2034C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103103672 | |||||||
| chr10:103104040 | T | C | 1 | a0001c0002t0003g0054 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.389+1666A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104040 | |||||||
| chr10:103104086 | T | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.389+1620A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104086 | |||||||
| chr10:103104157 | TTAACTC | T | 5 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.389+1543_389+1548d others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104157 | |||||||
| chr10:103104291 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.389+1415C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104291 | |||||||
| chr10:103104331 | C | T | 1 | a0001c0002t0008g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.389+1375G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104331 | |||||||
| chr10:103104436 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.389+1270A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104436 | |||||||
| chr10:103104532 | G | A | 1 | a0001c0002t0010g0043 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.389+1174C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104532 | |||||||
| chr10:103104857 | C | G | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.389+849G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104857 | |||||||
| chr10:103104921 | G | A | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.389+785C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103104921 | |||||||
| chr10:103105190 | C | T | 1 | a0001c0001t0007g0139 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.389+516G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103105190 | |||||||
| chr10:103105318 | T | C | 13 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0026 others(10): Show |
13 | HG01978.hp2 HG02071.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.389+388A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103105318 | |||||||
| chr10:103105390 | G | C | 6 | a0001c0002t0003g0039 a0001c0002t0003g0040 a0001c0002t0003g0041 others(3): Show |
6 | NA18971.hp2 NA18982.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.389+316C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 6/18 | chr10 | 103105390 | |||||||
| chr10:103105990 | T | G | 1 | a0001c0002t0005g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.294-189A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 5/18 | chr10 | 103105990 | |||||||
| chr10:103106122 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.294-321C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 5/18 | chr10 | 103106122 | |||||||
| chr10:103106305 | C | T | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.293+284G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 5/18 | chr10 | 103106305 | |||||||
| chr10:103106929 | C | T | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.176-223G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103106929 | |||||||
| chr10:103106956 | T | C | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-250A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103106956 | |||||||
| chr10:103106989 | C | T | 1 | a0001c0002t0005g0309 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.176-283G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103106989 | |||||||
| chr10:103107058 | G | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.176-352C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107058 | |||||||
| chr10:103107106 | C | T | 173 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(170): Show |
177 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(174): Show |
intron_variant | MODIFIER | c.176-400G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107106 | |||||||
| chr10:103107201 | A | G | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.176-495T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107201 | |||||||
| chr10:103107412 | T | C | 1 | a0001c0001t0002g0306 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.176-706A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107412 | |||||||
| chr10:103107415 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.176-709G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107415 | |||||||
| chr10:103107449 | C | T | 40 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0016 others(37): Show |
40 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.176-743G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107449 | |||||||
| chr10:103107676 | A | C | 1 | a0001c0002t0008g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.176-970T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107676 | |||||||
| chr10:103107882 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0170 |
2 | HG01243.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.176-1176G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107882 | |||||||
| chr10:103107929 | C | T | 72 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(69): Show |
73 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.176-1223G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107929 | |||||||
| chr10:103107938 | T | G | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.176-1232A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107938 | |||||||
| chr10:103107950 | T | C | 1 | a0001c0002t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.176-1244A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107950 | |||||||
| chr10:103107952 | C | T | 1 | a0001c0001t0002g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.176-1246G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103107952 | |||||||
| chr10:103108189 | C | T | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.176-1483G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103108189 | |||||||
| chr10:103108433 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.176-1727A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103108433 | |||||||
| chr10:103108527 | A | G | 2 | a0001c0002t0003g0027 a0001c0002t0003g0035 |
2 | HG00544.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.176-1821T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103108527 | |||||||
| chr10:103108999 | C | T | 1 | a0001c0002t0003g0050 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.176-2293G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103108999 | |||||||
| chr10:103109080 | C | T | 3 | a0001c0002t0004g0018 a0001c0002t0004g0022 a0001c0002t0004g0023 |
3 | HG01109.hp2 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.176-2374G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109080 | |||||||
| chr10:103109102 | G | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.176-2396C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109102 | |||||||
| chr10:103109107 | C | T | 1 | a0001c0002t0003g0078 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.176-2401G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109107 | |||||||
| chr10:103109174 | A | G | 1 | a0002c0003t0004g0228 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.176-2468T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109174 | |||||||
| chr10:103109277 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.176-2571T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109277 | |||||||
| chr10:103109281 | T | C | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-2575A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109281 | |||||||
| chr10:103109313 | T | C | 1 | a0001c0001t0002g0297 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.176-2607A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109313 | |||||||
| chr10:103109518 | T | C | 1 | a0001c0002t0013g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.176-2812A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109518 | |||||||
| chr10:103109694 | C | T | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-2988G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109694 | |||||||
| chr10:103109774 | C | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0105 others(46): Show |
50 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.176-3068G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103109774 | |||||||
| chr10:103110239 | T | G | 1 | a0001c0002t0005g0315 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.176-3533A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103110239 | |||||||
| chr10:103110461 | G | A | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-3755C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103110461 | |||||||
| chr10:103110518 | A | AT | 7 | a0001c0001t0001g0135 a0001c0001t0001g0152 a0001c0001t0001g0162 others(4): Show |
7 | HG00738.hp2 HG01070.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-3813dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103110518 | |||||||
| chr10:103110580 | C | A | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-3874G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103110580 | |||||||
| chr10:103110779 | AAACTCCT others(8): Show |
A | 1 | a0001c0002t0006g0188 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.176-4088_176-4074d others(17): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103110779 | |||||||
| chr10:103110934 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.176-4228G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103110934 | |||||||
| chr10:103111044 | T | A | 3 | a0001c0002t0004g0018 a0001c0002t0004g0022 a0001c0002t0004g0023 |
3 | HG01109.hp2 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.176-4338A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103111044 | |||||||
| chr10:103111045 | A | G | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.176-4339T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103111045 | |||||||
| chr10:103111438 | A | G | 4 | a0001c0001t0002g0245 a0001c0001t0002g0283 a0001c0001t0002g0284 others(1): Show |
4 | NA18945.hp1 NA18953.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-4732T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103111438 | |||||||
| chr10:103111447 | A | G | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-4741T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103111447 | |||||||
| chr10:103111522 | T | G | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-4816A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103111522 | |||||||
| chr10:103111604 | A | G | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.176-4898T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103111604 | |||||||
| chr10:103112396 | T | C | 1 | a0001c0001t0007g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.176-5690A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112396 | |||||||
| chr10:103112454 | C | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0155 |
2 | HG02071.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.176-5748G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112454 | |||||||
| chr10:103112710 | C | G | 4 | a0001c0002t0006g0196 a0001c0002t0006g0199 a0001c0002t0006g0200 others(1): Show |
4 | HG02735.hp2 HG03831.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-6004G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112710 | |||||||
| chr10:103112718 | C | T | 1 | a0001c0002t0004g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.176-6012G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112718 | |||||||
| chr10:103112790 | A | T | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.176-6084T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112790 | |||||||
| chr10:103112906 | A | C | 1 | a0001c0002t0008g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.176-6200T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112906 | |||||||
| chr10:103112927 | A | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-6221T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112927 | |||||||
| chr10:103112988 | TTAAA | T | 8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG03834.hp2 NA18943.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-6286_176-6283d others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103112988 | |||||||
| chr10:103113062 | C | A | 2 | a0001c0002t0003g0027 a0001c0002t0003g0035 |
2 | HG00544.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.176-6356G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113062 | |||||||
| chr10:103113247 | A | G | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-6541T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113247 | |||||||
| chr10:103113289 | GAAT | G | 8 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 others(5): Show |
8 | HG01081.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.176-6586_176-6584d others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113289 | |||||||
| chr10:103113374 | A | G | 3 | a0001c0002t0006g0188 a0001c0002t0006g0190 a0001c0002t0006g0191 |
3 | HG01070.hp2 HG01071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.176-6668T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113374 | |||||||
| chr10:103113416 | T | C | 1 | a0001c0002t0008g0213 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.176-6710A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113416 | |||||||
| chr10:103113495 | TA | T | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-6790delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113495 | |||||||
| chr10:103113496 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.176-6790T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113496 | |||||||
| chr10:103113500 | T | G | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-6794A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113500 | |||||||
| chr10:103113674 | G | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0142 a0001c0001t0001g0147 others(4): Show |
8 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.176-6968C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103113674 | |||||||
| chr10:103114004 | G | C | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-7298C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114004 | |||||||
| chr10:103114085 | C | G | 1 | a0001c0002t0008g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.176-7379G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114085 | |||||||
| chr10:103114213 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0118 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.176-7507C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114213 | |||||||
| chr10:103114302 | C | T | 1 | a0001c0001t0002g0248 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.176-7596G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114302 | |||||||
| chr10:103114396 | G | A | 1 | a0001c0002t0003g0034 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.176-7690C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114396 | |||||||
| chr10:103114403 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.176-7697A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114403 | |||||||
| chr10:103114532 | T | C | 1 | a0001c0002t0004g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.176-7826A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114532 | |||||||
| chr10:103114601 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.176-7895T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114601 | |||||||
| chr10:103114852 | A | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0184 |
2 | HG01192.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.176-8146T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103114852 | |||||||
| chr10:103115128 | C | T | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-8422G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115128 | |||||||
| chr10:103115158 | T | C | 1 | a0001c0002t0008g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.176-8452A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115158 | |||||||
| chr10:103115321 | G | C | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.176-8615C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115321 | |||||||
| chr10:103115327 | G | A | 32 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 others(29): Show |
34 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.176-8621C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115327 | |||||||
| chr10:103115376 | T | C | 1 | a0001c0002t0003g0033 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.176-8670A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115376 | |||||||
| chr10:103115379 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0146 |
2 | HG00642.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.176-8673C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115379 | |||||||
| chr10:103115399 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.176-8693G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115399 | |||||||
| chr10:103115442 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0123 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.176-8736C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115442 | |||||||
| chr10:103115547 | A | C | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.176-8841T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115547 | |||||||
| chr10:103115574 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.176-8868T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115574 | |||||||
| chr10:103115683 | A | G | 2 | a0001c0002t0006g0196 a0001c0002t0006g0199 |
2 | HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.176-8977T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115683 | |||||||
| chr10:103115782 | T | C | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-9076A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115782 | |||||||
| chr10:103115853 | T | C | 1 | a0001c0002t0003g0075 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.176-9147A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103115853 | |||||||
| chr10:103116564 | A | G | 7 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | NA18943.hp2 NA18945.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.176-9858T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116564 | |||||||
| chr10:103116586 | T | C | 1 | a0001c0002t0004g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.176-9880A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116586 | |||||||
| chr10:103116587 | C | CT | 89 | a0001c0001t0001g0179 a0001c0001t0005g0316 a0001c0001t0005g0322 others(86): Show |
91 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.176-9882dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116587 | |||||||
| chr10:103116587 | C | CTT | 11 | a0001c0002t0005g0308 a0001c0002t0005g0309 a0001c0002t0005g0310 others(8): Show |
11 | HG01243.hp1 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.176-9883_176-9882d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116587 | |||||||
| chr10:103116587 | C | T | 1 | a0001c0002t0004g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.176-9881G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116587 | |||||||
| chr10:103116822 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0002t0003g0052 |
3 | HG03927.hp2 NA18943.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.176-10116C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116822 | |||||||
| chr10:103116833 | C | T | 1 | a0001c0002t0015g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.176-10127G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103116833 | |||||||
| chr10:103117084 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.176-10378G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117084 | |||||||
| chr10:103117109 | T | C | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.176-10403A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117109 | |||||||
| chr10:103117278 | T | C | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.176-10572A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117278 | |||||||
| chr10:103117545 | T | C | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-10839A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117545 | |||||||
| chr10:103117648 | AAAC | A | 32 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 others(29): Show |
34 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.176-10945_176-1094 others(7): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117648 | |||||||
| chr10:103117845 | T | C | 7 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0128 others(4): Show |
7 | HG01928.hp2 HG01952.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-11139A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117845 | |||||||
| chr10:103117902 | T | A | 1 | a0001c0002t0004g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.176-11196A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103117902 | |||||||
| chr10:103118070 | A | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0123 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.176-11364T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118070 | |||||||
| chr10:103118253 | A | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-11547T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118253 | |||||||
| chr10:103118361 | C | CT | 14 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(11): Show |
14 | HG02135.hp1 HG03834.hp2 HG04199.hp2 others(11): Show |
intron_variant | MODIFIER | c.176-11656dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118361 | |||||||
| chr10:103118361 | C | CTT | 96 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(93): Show |
98 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.176-11657_176-1165 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118361 | |||||||
| chr10:103118677 | T | G | 1 | a0001c0002t0006g0200 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.176-11971A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118677 | |||||||
| chr10:103118697 | G | A | 41 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0016 others(38): Show |
41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.176-11991C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118697 | |||||||
| chr10:103118782 | T | C | 2 | a0001c0002t0004g0019 a0001c0002t0004g0020 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.176-12076A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118782 | |||||||
| chr10:103118786 | C | T | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.176-12080G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118786 | |||||||
| chr10:103118805 | T | C | 10 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0028 others(7): Show |
10 | HG01978.hp2 NA18747.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.176-12099A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118805 | |||||||
| chr10:103118937 | A | C | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.176-12231T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118937 | |||||||
| chr10:103118989 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.176-12283A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103118989 | |||||||
| chr10:103119085 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0132 |
2 | NA18973.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.176-12379C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119085 | |||||||
| chr10:103119175 | G | A | 1 | a0001c0002t0003g0066 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.176-12469C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119175 | |||||||
| chr10:103119292 | C | T | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.176-12586G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119292 | |||||||
| chr10:103119343 | T | C | 1 | a0001c0002t0005g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.176-12637A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119343 | |||||||
| chr10:103119645 | G | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-12939C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119645 | |||||||
| chr10:103119804 | CA | C | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.176-13099delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119804 | |||||||
| chr10:103119862 | G | C | 3 | a0001c0002t0004g0202 a0001c0002t0004g0203 a0001c0002t0004g0206 |
3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.176-13156C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103119862 | |||||||
| chr10:103120041 | G | A | 4 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-13335C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120041 | |||||||
| chr10:103120090 | C | A | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-13384G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120090 | |||||||
| chr10:103120098 | C | CA | 68 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(65): Show |
69 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.176-13393dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120098 | |||||||
| chr10:103120099 | A | G | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.176-13393T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120099 | |||||||
| chr10:103120364 | A | T | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-13658T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120364 | |||||||
| chr10:103120479 | T | C | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.176-13773A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120479 | |||||||
| chr10:103120672 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.176-13966G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120672 | |||||||
| chr10:103120856 | C | A | 1 | a0001c0001t0002g0284 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.176-14150G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103120856 | |||||||
| chr10:103121016 | A | G | 4 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-14310T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121016 | |||||||
| chr10:103121199 | T | C | 2 | a0001c0001t0002g0263 a0001c0001t0002g0279 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.176-14493A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121199 | |||||||
| chr10:103121249 | G | A | 6 | a0001c0002t0005g0308 a0001c0002t0005g0309 a0001c0002t0005g0310 others(3): Show |
6 | HG01243.hp1 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-14543C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121249 | |||||||
| chr10:103121278 | T | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-14572A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121278 | |||||||
| chr10:103121294 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.176-14588A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121294 | |||||||
| chr10:103121645 | T | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-14939A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121645 | |||||||
| chr10:103121993 | A | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.176-15287T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103121993 | |||||||
| chr10:103122019 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.176-15313G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103122019 | |||||||
| chr10:103122080 | G | A | 1 | a0001c0002t0008g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.176-15374C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103122080 | |||||||
| chr10:103122160 | C | G | 1 | a0001c0002t0004g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.176-15454G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103122160 | |||||||
| chr10:103122350 | C | T | 4 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(1): Show |
4 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-15644G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103122350 | |||||||
| chr10:103122730 | G | T | 1 | a0001c0002t0004g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.176-16024C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103122730 | |||||||
| chr10:103122972 | A | G | 1 | a0001c0002t0003g0084 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.176-16266T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103122972 | |||||||
| chr10:103123156 | G | A | 28 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0005g0308 others(25): Show |
28 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.175+16250C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123156 | |||||||
| chr10:103123267 | C | A | 1 | a0001c0001t0002g0248 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.175+16139G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123267 | |||||||
| chr10:103123513 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.175+15893G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123513 | |||||||
| chr10:103123529 | T | C | 1 | a0001c0001t0002g0275 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.175+15877A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123529 | |||||||
| chr10:103123580 | A | G | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+15826T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123580 | |||||||
| chr10:103123702 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.175+15704G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123702 | |||||||
| chr10:103123737 | C | T | 4 | a0001c0002t0006g0196 a0001c0002t0006g0199 a0001c0002t0006g0200 others(1): Show |
4 | HG02735.hp2 HG03831.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+15669G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123737 | |||||||
| chr10:103123847 | T | TG | 42 | a0001c0001t0002g0247 a0001c0001t0005g0316 a0001c0001t0005g0322 others(39): Show |
42 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.175+15558dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123847 | |||||||
| chr10:103123855 | GA | G | 14 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(11): Show |
14 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(11): Show |
intron_variant | MODIFIER | c.175+15550delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123855 | |||||||
| chr10:103123856 | A | G | 5 | a0001c0002t0004g0012 a0001c0002t0004g0185 a0001c0002t0005g0334 others(2): Show |
5 | HG02647.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+15550T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123856 | |||||||
| chr10:103123893 | A | G | 111 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(108): Show |
113 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.175+15513T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123893 | |||||||
| chr10:103123988 | C | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | NA18989.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.175+15418G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103123988 | |||||||
| chr10:103124055 | C | T | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+15351G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124055 | |||||||
| chr10:103124076 | CTT | C | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+15328_175+1532 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124076 | |||||||
| chr10:103124105 | C | T | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.175+15301G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124105 | |||||||
| chr10:103124185 | G | T | 1 | a0002c0003t0004g0237 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.175+15221C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124185 | |||||||
| chr10:103124211 | AT | A | 116 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(113): Show |
118 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.175+15194delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124211 | |||||||
| chr10:103124237 | G | T | 2 | a0001c0002t0004g0016 a0001c0002t0004g0017 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.175+15169C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124237 | |||||||
| chr10:103124305 | C | T | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+15101G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124305 | |||||||
| chr10:103124451 | T | C | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+14955A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124451 | |||||||
| chr10:103124798 | T | C | 2 | a0001c0002t0003g0045 a0001c0002t0003g0065 |
2 | NA18954.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.175+14608A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124798 | |||||||
| chr10:103124872 | T | TTAA | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+14531_175+1453 others(7): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103124872 | |||||||
| chr10:103125005 | T | C | 1 | a0001c0001t0002g0262 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.175+14401A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125005 | |||||||
| chr10:103125094 | T | C | 2 | a0001c0002t0004g0016 a0001c0002t0004g0017 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.175+14312A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125094 | |||||||
| chr10:103125191 | TC | T | 3 | a0001c0002t0004g0202 a0001c0002t0004g0203 a0001c0002t0004g0206 |
3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.175+14214delG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125191 | |||||||
| chr10:103125265 | C | T | 2 | a0001c0002t0004g0012 a0001c0002t0004g0013 |
2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.175+14141G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125265 | |||||||
| chr10:103125296 | T | TA | 16 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(13): Show |
16 | HG02135.hp1 HG03834.hp2 HG03942.hp2 others(13): Show |
intron_variant | MODIFIER | c.175+14109dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125296 | |||||||
| chr10:103125296 | TA | T | 7 | a0001c0001t0011g0287 a0001c0002t0005g0317 a0001c0002t0005g0318 others(4): Show |
7 | HG00733.hp1 HG02040.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+14109delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125296 | |||||||
| chr10:103125573 | A | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+13833T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103125573 | |||||||
| chr10:103126061 | G | A | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+13345C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126061 | |||||||
| chr10:103126211 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0183 |
3 | HG01109.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.175+13195C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126211 | |||||||
| chr10:103126268 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.175+13138C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126268 | |||||||
| chr10:103126431 | C | G | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+12975G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126431 | |||||||
| chr10:103126483 | G | A | 1 | a0002c0003t0004g0221 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.175+12923C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126483 | |||||||
| chr10:103126545 | C | G | 4 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0005g0327 others(1): Show |
4 | HG00597.hp2 HG00673.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+12861G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126545 | |||||||
| chr10:103126591 | C | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+12815G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126591 | |||||||
| chr10:103126617 | G | A | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+12789C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126617 | |||||||
| chr10:103126655 | A | G | 1 | a0001c0002t0004g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175+12751T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126655 | |||||||
| chr10:103126776 | G | T | 82 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(79): Show |
84 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.175+12630C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126776 | |||||||
| chr10:103126778 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.175+12628A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126778 | |||||||
| chr10:103126792 | G | A | 1 | a0001c0002t0003g0075 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.175+12614C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126792 | |||||||
| chr10:103126855 | A | G | 4 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0172 others(1): Show |
4 | HG01106.hp1 NA18954.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+12551T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126855 | |||||||
| chr10:103126864 | T | A | 1 | a0001c0002t0003g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.175+12542A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103126864 | |||||||
| chr10:103127009 | T | C | 1 | a0001c0001t0002g0251 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.175+12397A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127009 | |||||||
| chr10:103127085 | T | C | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.175+12321A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127085 | |||||||
| chr10:103127384 | G | A | 3 | a0001c0002t0003g0061 a0001c0002t0003g0062 a0001c0002t0003g0063 |
3 | HG01943.hp1 HG02004.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.175+12022C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127384 | |||||||
| chr10:103127406 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0172 |
2 | NA18965.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.175+12000A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127406 | |||||||
| chr10:103127742 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0122 |
3 | HG03041.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.175+11664C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127742 | |||||||
| chr10:103127760 | G | A | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+11646C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127760 | |||||||
| chr10:103127769 | G | A | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+11637C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127769 | |||||||
| chr10:103127777 | C | T | 1 | a0001c0002t0015g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+11629G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127777 | |||||||
| chr10:103127786 | G | C | 1 | a0001c0002t0004g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+11620C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127786 | |||||||
| chr10:103127819 | G | A | 1 | a0001c0002t0004g0206 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.175+11587C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127819 | |||||||
| chr10:103127852 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.175+11554C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103127852 | |||||||
| chr10:103128044 | T | TCTCTCC | 48 | a0001c0001t0002g0248 a0001c0001t0002g0259 a0001c0001t0002g0267 others(45): Show |
49 | HG01433.hp2 HG01943.hp1 HG01978.hp2 others(46): Show |
intron_variant | MODIFIER | c.175+11356_175+1136 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | |||||||
| chr10:103128044 | T | TCTCTCCC others(5): Show |
8 | a0001c0002t0003g0036 a0001c0002t0003g0037 a0001c0002t0003g0050 others(5): Show |
8 | HG01167.hp1 HG02083.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+11350_175+1136 others(16): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | |||||||
| chr10:103128044 | T | TCTCTCCC others(11): Show |
2 | a0001c0002t0003g0058 a0001c0002t0017g0067 |
2 | HG02071.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.175+11344_175+1136 others(22): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | |||||||
| chr10:103128044 | TCTCTCC | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0101 others(80): Show |
84 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.175+11356_175+1136 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | |||||||
| chr10:103128044 | TCTCTCCC others(5): Show |
T | 87 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(84): Show |
88 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.175+11350_175+1136 others(16): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | |||||||
| chr10:103128044 | TCTCTCCC others(11): Show |
T | 14 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(11): Show |
14 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.175+11344_175+1136 others(22): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | |||||||
| chr10:103128044 | TCTCTCCC others(17): Show |
T | 1 | a0001c0002t0008g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.175+11338_175+1136 others(28): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128044 | |||||||
| chr10:103128124 | G | C | 1 | a0002c0003t0004g0228 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.175+11282C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128124 | |||||||
| chr10:103128134 | T | C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | HG02602.hp2 HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.175+11272A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128134 | |||||||
| chr10:103128223 | G | A | 1 | a0001c0001t0002g0266 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.175+11183C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128223 | |||||||
| chr10:103128263 | C | T | 1 | a0001c0002t0008g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.175+11143G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128263 | |||||||
| chr10:103128280 | C | T | 13 | a0001c0001t0001g0151 a0001c0001t0001g0181 a0001c0001t0002g0005 others(10): Show |
14 | HG01361.hp1 HG01943.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.175+11126G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128280 | |||||||
| chr10:103128301 | G | A | 4 | a0002c0003t0004g0217 a0002c0003t0004g0218 a0002c0003t0004g0219 others(1): Show |
4 | HG00621.hp2 HG00673.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+11105C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128301 | |||||||
| chr10:103128328 | G | A | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+11078C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128328 | |||||||
| chr10:103128356 | C | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+11050G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128356 | |||||||
| chr10:103128407 | G | A | 1 | a0001c0002t0006g0200 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.175+10999C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128407 | |||||||
| chr10:103128442 | T | G | 40 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0016 others(37): Show |
40 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.175+10964A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128442 | |||||||
| chr10:103128479 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.175+10927C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128479 | |||||||
| chr10:103128483 | A | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+10923T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128483 | |||||||
| chr10:103128486 | A | AC | 4 | a0001c0001t0005g0316 a0001c0002t0003g0077 a0001c0002t0005g0323 others(1): Show |
4 | HG01169.hp2 HG02622.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+10919dupG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128486 | |||||||
| chr10:103128570 | T | G | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+10836A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128570 | |||||||
| chr10:103128577 | T | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+10829A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128577 | |||||||
| chr10:103128598 | C | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0123 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.175+10808G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128598 | |||||||
| chr10:103128703 | C | T | 1 | a0001c0002t0005g0329 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.175+10703G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128703 | |||||||
| chr10:103128715 | G | A | 1 | a0001c0002t0003g0053 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.175+10691C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128715 | |||||||
| chr10:103128717 | C | T | 93 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(90): Show |
95 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.175+10689G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128717 | |||||||
| chr10:103128755 | G | C | 5 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+10651C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128755 | |||||||
| chr10:103128810 | T | G | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+10596A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128810 | |||||||
| chr10:103128859 | CCTCCGCC others(33): Show |
C | 2 | a0001c0001t0002g0303 a0001c0001t0002g0304 |
2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.175+10507_175+1054 others(44): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128859 | |||||||
| chr10:103128864 | G | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+10542C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128864 | |||||||
| chr10:103128891 | G | A | 2 | a0001c0001t0002g0259 a0001c0001t0002g0268 |
2 | HG03017.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.175+10515C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128891 | |||||||
| chr10:103128899 | T | C | 1 | a0001c0002t0003g0062 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.175+10507A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128899 | |||||||
| chr10:103128974 | T | TG | 19 | a0001c0002t0003g0008 a0001c0002t0003g0027 a0001c0002t0003g0046 others(16): Show |
19 | HG00544.hp2 HG00597.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.175+10431_175+1043 others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128974 | |||||||
| chr10:103128974 | TA | T | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+10431delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128974 | |||||||
| chr10:103128975 | A | G | 167 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0003g0004 others(164): Show |
170 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.175+10431T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103128975 | |||||||
| chr10:103129005 | C | T | 5 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+10401G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129005 | |||||||
| chr10:103129041 | C | G | 7 | a0001c0002t0008g0207 a0001c0002t0008g0211 a0001c0002t0008g0212 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+10365G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129041 | |||||||
| chr10:103129064 | G | A | 40 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0016 others(37): Show |
40 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.175+10342C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129064 | |||||||
| chr10:103129085 | GCCCCCCA others(544): Show |
G | 1 | a0001c0001t0001g0151 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.175+9770_175+10320 others(3): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129085 | |||||||
| chr10:103129109 | G | A | 119 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(116): Show |
122 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.175+10297C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129109 | |||||||
| chr10:103129185 | G | A | 1 | a0001c0002t0015g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+10221C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129185 | |||||||
| chr10:103129221 | T | C | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+10185A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129221 | |||||||
| chr10:103129279 | G | A | 3 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0274 |
3 | NA19002.hp2 NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.175+10127C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129279 | |||||||
| chr10:103129288 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.175+10118C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129288 | |||||||
| chr10:103129315 | C | T | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+10091G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129315 | |||||||
| chr10:103129316 | GCCCGGCC others(170): Show |
G | 1 | a0001c0001t0016g0126 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.175+9913_175+10089 others(3): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129316 | |||||||
| chr10:103129347 | T | TG | 14 | a0001c0001t0001g0101 a0001c0001t0001g0112 a0001c0001t0001g0123 others(11): Show |
14 | HG00408.hp2 HG00597.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.175+10058dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129347 | |||||||
| chr10:103129360 | T | C | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10046A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129360 | |||||||
| chr10:103129362 | T | C | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10044A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129362 | |||||||
| chr10:103129382 | G | A | 1 | a0001c0002t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.175+10024C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129382 | |||||||
| chr10:103129385 | T | C | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10021A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129385 | |||||||
| chr10:103129397 | G | T | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10009C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129397 | |||||||
| chr10:103129399 | C | G | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10007G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129399 | |||||||
| chr10:103129399 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.175+10007G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129399 | |||||||
| chr10:103129400 | G | A | 1 | a0001c0002t0005g0328 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.175+10006C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129400 | |||||||
| chr10:103129401 | C | G | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10005G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129401 | |||||||
| chr10:103129402 | C | G | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10004G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129402 | |||||||
| chr10:103129404 | C | G | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+10002G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129404 | |||||||
| chr10:103129413 | C | T | 1 | a0001c0002t0005g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.175+9993G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129413 | |||||||
| chr10:103129414 | G | C | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9992C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129414 | |||||||
| chr10:103129417 | CCTACTGG others(18): Show |
C | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9964_175+9988d others(27): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129417 | |||||||
| chr10:103129440 | TCAGCCCG others(92): Show |
T | 1 | a0001c0002t0005g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.175+9867_175+9965d others(101): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129440 | |||||||
| chr10:103129455 | A | G | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9951T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129455 | |||||||
| chr10:103129473 | A | G | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9933T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129473 | |||||||
| chr10:103129474 | T | TG | 10 | a0001c0001t0001g0133 a0001c0001t0001g0142 a0001c0001t0001g0162 others(7): Show |
10 | HG00609.hp1 HG00642.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+9931dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129474 | |||||||
| chr10:103129480 | G | T | 2 | a0001c0002t0005g0330 a0001c0002t0005g0331 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.175+9926C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129480 | |||||||
| chr10:103129485 | G | GC | 10 | a0001c0001t0001g0123 a0001c0001t0001g0142 a0001c0001t0001g0177 others(7): Show |
10 | HG00597.hp2 HG01516.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.175+9920dupG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129485 | |||||||
| chr10:103129492 | C | T | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9914G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129492 | |||||||
| chr10:103129493 | A | G | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9913T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129493 | |||||||
| chr10:103129505 | G | GCCCCGTC others(348): Show |
1 | a0001c0001t0002g0244 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.175+9900_175+9901i others(357): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129505 | |||||||
| chr10:103129524 | T | G | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9882A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129524 | |||||||
| chr10:103129524 | T | TG | 10 | a0001c0001t0001g0123 a0001c0001t0001g0136 a0001c0001t0001g0142 others(7): Show |
10 | HG00544.hp1 HG00597.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+9881dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129524 | |||||||
| chr10:103129525 | G | GCGCCTCT others(17): Show |
1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9880_175+9881i others(26): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129525 | |||||||
| chr10:103129529 | G | A | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9877C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129529 | |||||||
| chr10:103129530 | G | A | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9876C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129530 | |||||||
| chr10:103129533 | C | G | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9873G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129533 | |||||||
| chr10:103129534 | A | G | 1 | a0001c0002t0004g0021 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.175+9872T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129534 | |||||||
| chr10:103129539 | C | T | 1 | a0001c0002t0006g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175+9867G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129539 | |||||||
| chr10:103129541 | C | CCGCCCGG others(172): Show |
1 | a0001c0002t0005g0323 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.175+9864_175+9865i others(181): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | |||||||
| chr10:103129541 | C | CGCCCGGC others(171): Show |
1 | a0001c0002t0006g0192 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.175+9864_175+9865i others(180): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | |||||||
| chr10:103129541 | C | CGCCCGGC others(173): Show |
1 | a0003c0004t0005g0335 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.175+9864_175+9865i others(182): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | |||||||
| chr10:103129541 | C | CGCCCGGC others(171): Show |
1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+9864_175+9865i others(180): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | |||||||
| chr10:103129541 | C | CGCCCGGC others(172): Show |
2 | a0001c0002t0005g0324 a0002c0003t0004g0235 |
2 | HG00673.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.175+9864_175+9865i others(181): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | |||||||
| chr10:103129541 | C | CGCCCGGC others(172): Show |
3 | a0001c0002t0004g0023 a0001c0002t0005g0334 a0001c0002t0006g0204 |
3 | HG02055.hp2 HG02647.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.175+9864_175+9865i others(181): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | |||||||
| chr10:103129541 | C | CGCCCGGC others(171): Show |
79 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0012 others(76): Show |
81 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.175+9864_175+9865i others(180): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | |||||||
| chr10:103129541 | C | CGCCCGGC others(171): Show |
3 | a0001c0002t0006g0188 a0001c0002t0006g0190 a0001c0002t0006g0191 |
3 | HG01070.hp2 HG01071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.175+9864_175+9865i others(180): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | |||||||
| chr10:103129541 | C | CTGCCCGG others(172): Show |
2 | a0002c0003t0004g0226 a0002c0003t0004g0233 |
2 | HG00642.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.175+9864_175+9865i others(181): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | |||||||
| chr10:103129541 | C | T | 2 | a0001c0002t0005g0319 a0001c0002t0006g0189 |
2 | HG02258.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.175+9865G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129541 | |||||||
| chr10:103129547 | G | GCCAGCCG others(172): Show |
1 | a0002c0003t0004g0010 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.175+9858_175+9859i others(181): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129547 | |||||||
| chr10:103129583 | A | G | 17 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(14): Show |
17 | HG01496.hp1 HG02135.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.175+9823T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129583 | |||||||
| chr10:103129603 | G | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+9803C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129603 | |||||||
| chr10:103129611 | CGGGA | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0142 a0001c0001t0001g0147 others(4): Show |
8 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.175+9791_175+9794d others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129611 | |||||||
| chr10:103129612 | G | A | 1 | a0001c0002t0004g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+9794C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129612 | |||||||
| chr10:103129622 | T | TG | 40 | a0001c0001t0001g0106 a0001c0001t0001g0133 a0001c0001t0001g0162 others(37): Show |
40 | HG00597.hp1 HG00642.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.175+9783dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129622 | |||||||
| chr10:103129622 | T | TGG | 19 | a0001c0001t0005g0322 a0001c0002t0004g0012 a0001c0002t0004g0013 others(16): Show |
19 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.175+9782_175+9783d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129622 | |||||||
| chr10:103129622 | T | TGGG | 27 | a0001c0001t0005g0316 a0001c0002t0004g0185 a0001c0002t0004g0202 others(24): Show |
28 | HG00597.hp2 HG00639.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.175+9781_175+9783d others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129622 | |||||||
| chr10:103129622 | T | TGGGG | 17 | a0001c0002t0004g0203 a0001c0002t0004g0206 a0001c0002t0005g0309 others(14): Show |
18 | HG00609.hp2 HG00735.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.175+9780_175+9783d others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129622 | |||||||
| chr10:103129622 | T | TGGGGGGG others(172): Show |
1 | a0001c0002t0015g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+9783_175+9784i others(181): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129622 | |||||||
| chr10:103129622 | T | TGGGGGGG others(123): Show |
1 | a0001c0002t0005g0326 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.175+9783_175+9784i others(132): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129622 | |||||||
| chr10:103129623 | GGGGGGGG others(298): Show |
G | 1 | a0001c0002t0003g0080 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.175+9478_175+9782d others(2): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129623 | |||||||
| chr10:103129642 | C | T | 15 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(12): Show |
15 | HG01496.hp1 HG02135.hp1 HG03834.hp2 others(12): Show |
intron_variant | MODIFIER | c.175+9764G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129642 | |||||||
| chr10:103129659 | T | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+9747A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129659 | |||||||
| chr10:103129691 | C | T | 33 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(30): Show |
33 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.175+9715G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129691 | |||||||
| chr10:103129711 | G | A | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.175+9695C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129711 | |||||||
| chr10:103129737 | CGTCCGGG others(120): Show |
C | 2 | a0001c0001t0001g0124 a0001c0001t0007g0163 |
2 | HG02922.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.175+9542_175+9668d others(2): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129737 | |||||||
| chr10:103129738 | G | A | 2 | a0001c0001t0001g0118 a0002c0003t0004g0227 |
2 | HG02300.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.175+9668C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129738 | |||||||
| chr10:103129742 | G | A | 1 | a0001c0002t0005g0324 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.175+9664C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129742 | |||||||
| chr10:103129763 | G | GCCCCCCG others(45): Show |
13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+9642_175+9643i others(54): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129763 | |||||||
| chr10:103129763 | G | GCCCCCCG others(48): Show |
1 | a0002c0003t0004g0230 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.175+9642_175+9643i others(57): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129763 | |||||||
| chr10:103129763 | G | GCCCCCCG others(47): Show |
1 | a0001c0002t0004g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.175+9642_175+9643i others(56): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129763 | |||||||
| chr10:103129864 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0088 others(282): Show |
290 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(287): Show |
intron_variant | MODIFIER | c.175+9542A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129864 | |||||||
| chr10:103129880 | GGGGGTGT others(41): Show |
G | 1 | a0001c0002t0003g0042 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.175+9478_175+9525d others(50): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129880 | |||||||
| chr10:103129901 | G | A | 1 | a0001c0001t0002g0260 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.175+9505C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129901 | |||||||
| chr10:103129910 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.175+9496G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129910 | |||||||
| chr10:103129912 | C | A | 4 | a0001c0001t0002g0245 a0001c0001t0002g0283 a0001c0001t0002g0284 others(1): Show |
4 | NA18945.hp1 NA18953.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+9494G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129912 | |||||||
| chr10:103129913 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.175+9493G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129913 | |||||||
| chr10:103129914 | G | A | 17 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(14): Show |
17 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.175+9492C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129914 | |||||||
| chr10:103129928 | T | TG | 81 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(78): Show |
82 | HG00408.hp2 HG00544.hp2 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.175+9477dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129928 | |||||||
| chr10:103129940 | G | GC | 21 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(18): Show |
21 | HG00408.hp1 HG00408.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.175+9465dupG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129940 | |||||||
| chr10:103129947 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.175+9459G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129947 | |||||||
| chr10:103129952 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.175+9454C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103129952 | |||||||
| chr10:103130085 | T | C | 3 | a0001c0002t0004g0202 a0001c0002t0004g0203 a0001c0002t0004g0206 |
3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.175+9321A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130085 | |||||||
| chr10:103130116 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.175+9290T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130116 | |||||||
| chr10:103130205 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.175+9201G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130205 | |||||||
| chr10:103130364 | G | C | 1 | a0001c0002t0015g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+9042C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130364 | |||||||
| chr10:103130379 | A | C | 1 | a0001c0002t0015g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+9027T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130379 | |||||||
| chr10:103130565 | T | A | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+8841A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130565 | |||||||
| chr10:103130566 | A | T | 1 | a0001c0002t0003g0075 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.175+8840T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130566 | |||||||
| chr10:103130583 | T | TA | 178 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(175): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.175+8822dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130583 | |||||||
| chr10:103130583 | TA | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0091 others(75): Show |
79 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.175+8822delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130583 | |||||||
| chr10:103130583 | TAA | T | 11 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0095 others(8): Show |
11 | HG01952.hp2 HG02040.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.175+8821_175+8822d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130583 | |||||||
| chr10:103130635 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.175+8771T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130635 | |||||||
| chr10:103130654 | C | T | 1 | a0001c0002t0003g0028 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.175+8752G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130654 | |||||||
| chr10:103130854 | C | T | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+8552G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103130854 | |||||||
| chr10:103131256 | T | C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | NA18940.hp2 NA18977.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+8150A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103131256 | |||||||
| chr10:103131441 | T | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+7965A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103131441 | |||||||
| chr10:103131458 | G | A | 1 | a0001c0002t0005g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.175+7948C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103131458 | |||||||
| chr10:103131639 | C | G | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+7767G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103131639 | |||||||
| chr10:103131786 | G | A | 3 | a0001c0002t0004g0202 a0001c0002t0004g0203 a0001c0002t0004g0206 |
3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.175+7620C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103131786 | |||||||
| chr10:103132171 | C | T | 3 | a0001c0002t0005g0330 a0001c0002t0005g0331 a0001c0002t0005g0332 |
3 | HG00639.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.175+7235G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132171 | |||||||
| chr10:103132218 | T | C | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+7188A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132218 | |||||||
| chr10:103132242 | A | G | 1 | a0002c0003t0004g0228 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.175+7164T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132242 | |||||||
| chr10:103132393 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.175+7013T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132393 | |||||||
| chr10:103132459 | T | C | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+6947A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132459 | |||||||
| chr10:103132541 | A | G | 1 | a0001c0001t0007g0139 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.175+6865T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132541 | |||||||
| chr10:103132608 | C | T | 1 | a0001c0001t0002g0246 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.175+6798G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132608 | |||||||
| chr10:103132686 | G | A | 1 | a0001c0002t0003g0075 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.175+6720C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132686 | |||||||
| chr10:103132722 | G | C | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.175+6684C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132722 | |||||||
| chr10:103132726 | T | A | 5 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0019 others(2): Show |
5 | HG00735.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+6680A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132726 | |||||||
| chr10:103132929 | G | A | 2 | a0001c0002t0003g0004 a0001c0002t0003g0242 |
3 | NA18988.hp2 NA18992.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.175+6477C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103132929 | |||||||
| chr10:103133210 | C | T | 1 | a0001c0002t0005g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.175+6196G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133210 | |||||||
| chr10:103133211 | C | T | 1 | a0001c0001t0002g0293 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.175+6195G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133211 | |||||||
| chr10:103133273 | C | CTT | 18 | a0001c0001t0001g0151 a0001c0001t0001g0181 a0001c0001t0002g0005 others(15): Show |
19 | HG00558.hp1 HG01257.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.175+6131_175+6132d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133273 | |||||||
| chr10:103133380 | A | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+6026T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133380 | |||||||
| chr10:103133514 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0088 others(285): Show |
293 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.175+5892T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133514 | |||||||
| chr10:103133811 | A | G | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+5595T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133811 | |||||||
| chr10:103133970 | G | T | 1 | a0001c0002t0005g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.175+5436C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103133970 | |||||||
| chr10:103134318 | A | G | 3 | a0001c0002t0004g0202 a0001c0002t0004g0203 a0001c0002t0004g0206 |
3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.175+5088T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103134318 | |||||||
| chr10:103134379 | G | A | 6 | a0001c0002t0003g0039 a0001c0002t0003g0040 a0001c0002t0003g0041 others(3): Show |
6 | NA18971.hp2 NA18982.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+5027C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103134379 | |||||||
| chr10:103134379 | G | C | 1 | a0001c0001t0002g0262 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.175+5027C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103134379 | |||||||
| chr10:103135076 | G | A | 1 | a0001c0002t0005g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.175+4330C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135076 | |||||||
| chr10:103135160 | T | C | 1 | a0001c0002t0004g0202 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.175+4246A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135160 | |||||||
| chr10:103135540 | C | T | 28 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0005g0308 others(25): Show |
28 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.175+3866G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135540 | |||||||
| chr10:103135645 | G | A | 2 | a0001c0001t0001g0180 a0001c0002t0004g0206 |
2 | HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.175+3761C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135645 | |||||||
| chr10:103135664 | T | C | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+3742A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135664 | |||||||
| chr10:103135702 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0172 |
2 | NA18965.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.175+3704G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135702 | |||||||
| chr10:103135704 | A | C | 2 | a0001c0001t0002g0272 a0001c0001t0002g0274 |
2 | NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.175+3702T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135704 | |||||||
| chr10:103135712 | C | T | 2 | a0001c0001t0002g0272 a0001c0001t0002g0274 |
2 | NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.175+3694G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135712 | |||||||
| chr10:103135713 | A | G | 2 | a0001c0001t0002g0272 a0001c0001t0002g0274 |
2 | NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.175+3693T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135713 | |||||||
| chr10:103135720 | G | A | 2 | a0001c0001t0002g0272 a0001c0001t0002g0274 |
2 | NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.175+3686C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135720 | |||||||
| chr10:103135736 | T | A | 3 | a0001c0002t0006g0188 a0001c0002t0006g0190 a0001c0002t0006g0191 |
3 | HG01070.hp2 HG01071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.175+3670A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135736 | |||||||
| chr10:103135779 | T | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+3627A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135779 | |||||||
| chr10:103135811 | G | T | 29 | a0002c0003t0004g0002 a0002c0003t0004g0003 a0002c0003t0004g0006 others(26): Show |
31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.175+3595C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103135811 | |||||||
| chr10:103136029 | G | T | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+3377C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136029 | |||||||
| chr10:103136030 | T | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+3376A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136030 | |||||||
| chr10:103136087 | C | CA | 18 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(15): Show |
18 | HG00544.hp2 HG00733.hp1 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.175+3318dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136087 | |||||||
| chr10:103136321 | T | A | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+3085A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136321 | |||||||
| chr10:103136343 | G | A | 3 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 |
3 | HG00735.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.175+3063C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136343 | |||||||
| chr10:103136531 | C | T | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+2875G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136531 | |||||||
| chr10:103136626 | A | AT | 82 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(79): Show |
84 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.175+2779dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136626 | |||||||
| chr10:103136626 | AT | A | 66 | a0001c0001t0001g0152 a0001c0001t0001g0168 a0001c0002t0003g0004 others(63): Show |
67 | HG00544.hp2 HG01069.hp1 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.175+2779delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136626 | |||||||
| chr10:103136628 | T | TA | 22 | a0001c0002t0004g0185 a0001c0002t0004g0202 a0001c0002t0004g0203 others(19): Show |
22 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.175+2777_175+2778i others(3): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136628 | |||||||
| chr10:103136629 | T | A | 7 | a0001c0001t0002g0292 a0001c0002t0006g0195 a0001c0002t0008g0211 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.175+2777A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136629 | |||||||
| chr10:103136729 | G | A | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+2677C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136729 | |||||||
| chr10:103136806 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0088 others(268): Show |
275 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.175+2600T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136806 | |||||||
| chr10:103136908 | C | T | 1 | a0001c0001t0002g0307 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.175+2498G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136908 | |||||||
| chr10:103136913 | G | A | 2 | a0001c0002t0010g0007 a0001c0002t0010g0043 |
2 | HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.175+2493C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136913 | |||||||
| chr10:103136994 | A | T | 11 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(8): Show |
11 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+2412T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103136994 | |||||||
| chr10:103137059 | T | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+2347A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137059 | |||||||
| chr10:103137220 | A | AG | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.175+2185dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137220 | |||||||
| chr10:103137377 | CAA | C | 3 | a0001c0002t0003g0061 a0001c0002t0003g0062 a0001c0002t0003g0063 |
3 | HG01943.hp1 HG02004.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.175+2027_175+2028d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137377 | |||||||
| chr10:103137390 | G | A | 1 | a0001c0001t0002g0250 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.175+2016C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137390 | |||||||
| chr10:103137486 | C | T | 1 | a0001c0002t0005g0324 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.175+1920G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137486 | |||||||
| chr10:103137496 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.175+1910A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137496 | |||||||
| chr10:103137497 | G | T | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.175+1909C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137497 | |||||||
| chr10:103137701 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.175+1705G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137701 | |||||||
| chr10:103137906 | A | C | 1 | a0001c0002t0004g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+1500T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137906 | |||||||
| chr10:103137963 | A | G | 1 | a0001c0001t0002g0249 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.175+1443T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103137963 | |||||||
| chr10:103138013 | C | G | 2 | a0001c0001t0002g0303 a0001c0001t0002g0304 |
2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.175+1393G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138013 | |||||||
| chr10:103138144 | T | C | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+1262A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138144 | |||||||
| chr10:103138228 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0103 others(69): Show |
73 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.175+1178A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138228 | |||||||
| chr10:103138369 | C | T | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+1037G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138369 | |||||||
| chr10:103138371 | T | C | 1 | a0001c0002t0004g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175+1035A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138371 | |||||||
| chr10:103138397 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.175+1009C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138397 | |||||||
| chr10:103138460 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.175+946C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138460 | |||||||
| chr10:103138580 | C | T | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.175+826G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138580 | |||||||
| chr10:103138602 | G | C | 1 | a0001c0001t0002g0269 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.175+804C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138602 | |||||||
| chr10:103138612 | C | A | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+794G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138612 | |||||||
| chr10:103138620 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.175+786A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138620 | |||||||
| chr10:103138665 | G | A | 3 | a0001c0002t0005g0330 a0001c0002t0005g0331 a0001c0002t0005g0332 |
3 | HG00639.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.175+741C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103138665 | |||||||
| chr10:103139007 | C | CA | 12 | a0001c0001t0011g0287 a0001c0002t0004g0011 a0001c0002t0004g0012 others(9): Show |
12 | HG00733.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+398dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 4/18 | chr10 | 103139007 | |||||||
| chr10:103140018 | G | A | 1 | a0001c0002t0003g0077 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.102-539C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140018 | |||||||
| chr10:103140112 | C | T | 35 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 others(32): Show |
37 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.102-633G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140112 | |||||||
| chr10:103140364 | A | AT | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.102-886_102-885ins others(1): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140364 | |||||||
| chr10:103140367 | C | T | 1 | a0001c0002t0003g0061 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.102-888G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140367 | |||||||
| chr10:103140368 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.102-889C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140368 | |||||||
| chr10:103140515 | G | A | 41 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0016 others(38): Show |
41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.102-1036C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140515 | |||||||
| chr10:103140584 | A | G | 1 | a0001c0002t0003g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.102-1105T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140584 | |||||||
| chr10:103140908 | A | G | 1 | a0001c0001t0002g0266 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.102-1429T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103140908 | |||||||
| chr10:103141005 | C | G | 1 | a0001c0001t0002g0273 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.102-1526G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141005 | |||||||
| chr10:103141084 | C | T | 17 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(14): Show |
17 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.102-1605G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141084 | |||||||
| chr10:103141088 | A | T | 1 | a0001c0001t0002g0267 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.102-1609T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141088 | |||||||
| chr10:103141217 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.102-1738C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141217 | |||||||
| chr10:103141274 | A | G | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.102-1795T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141274 | |||||||
| chr10:103141610 | C | T | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-2131G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141610 | |||||||
| chr10:103141734 | T | C | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.102-2255A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141734 | |||||||
| chr10:103141835 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0123 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.102-2356C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141835 | |||||||
| chr10:103141862 | A | G | 6 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0042 others(3): Show |
6 | NA18747.hp2 NA18957.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-2383T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103141862 | |||||||
| chr10:103142182 | G | T | 1 | a0001c0002t0005g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.102-2703C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142182 | |||||||
| chr10:103142408 | A | G | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.102-2929T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142408 | |||||||
| chr10:103142580 | A | T | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.102-3101T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142580 | |||||||
| chr10:103142673 | G | GA | 66 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(63): Show |
67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.102-3195dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142673 | |||||||
| chr10:103142980 | T | C | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.102-3501A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142980 | |||||||
| chr10:103142986 | C | CA | 25 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0098 others(22): Show |
26 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.102-3508dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142986 | |||||||
| chr10:103142987 | A | C | 5 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-3508T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103142987 | |||||||
| chr10:103143584 | G | A | 1 | a0001c0002t0006g0198 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.102-4105C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143584 | |||||||
| chr10:103143602 | A | AT | 8 | a0001c0001t0001g0113 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
8 | HG01123.hp2 HG01257.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-4124dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | |||||||
| chr10:103143602 | A | ATT | 9 | a0001c0001t0001g0134 a0001c0001t0002g0268 a0001c0001t0002g0291 others(6): Show |
9 | HG01943.hp2 HG01978.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.102-4125_102-4124d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | |||||||
| chr10:103143602 | A | ATTT | 5 | a0001c0001t0001g0181 a0001c0001t0002g0005 a0001c0001t0002g0246 others(2): Show |
6 | HG02055.hp1 NA18940.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-4126_102-4124d others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | |||||||
| chr10:103143602 | AT | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0089 others(110): Show |
114 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.102-4124delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | |||||||
| chr10:103143602 | ATT | A | 48 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0110 others(45): Show |
50 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.102-4125_102-4124d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | |||||||
| chr10:103143602 | ATTT | A | 38 | a0001c0001t0005g0322 a0001c0002t0004g0016 a0001c0002t0004g0017 others(35): Show |
38 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.102-4126_102-4124d others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | |||||||
| chr10:103143602 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0002g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.102-4133_102-4124d others(12): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143602 | |||||||
| chr10:103143611 | T | G | 3 | a0001c0002t0003g0061 a0001c0002t0003g0062 a0001c0002t0003g0063 |
3 | HG01943.hp1 HG02004.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.102-4132A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143611 | |||||||
| chr10:103143615 | T | G | 65 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(62): Show |
66 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(63): Show |
intron_variant | MODIFIER | c.102-4136A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143615 | |||||||
| chr10:103143626 | T | G | 1 | a0001c0002t0003g0077 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.102-4147A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143626 | |||||||
| chr10:103143627 | T | G | 66 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(63): Show |
67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.102-4148A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143627 | |||||||
| chr10:103143807 | T | C | 7 | a0001c0002t0008g0207 a0001c0002t0008g0211 a0001c0002t0008g0212 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-4328A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143807 | |||||||
| chr10:103143881 | A | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.102-4402T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143881 | |||||||
| chr10:103143899 | G | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.102-4420C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143899 | |||||||
| chr10:103143909 | C | T | 32 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 others(29): Show |
34 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.102-4430G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103143909 | |||||||
| chr10:103144404 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.102-4925T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103144404 | |||||||
| chr10:103144865 | T | C | 7 | a0001c0002t0008g0207 a0001c0002t0008g0211 a0001c0002t0008g0212 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-5386A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103144865 | |||||||
| chr10:103145085 | G | T | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.102-5606C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103145085 | |||||||
| chr10:103145352 | G | A | 1 | a0001c0002t0003g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.102-5873C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103145352 | |||||||
| chr10:103145645 | G | A | 1 | a0001c0002t0005g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-6166C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103145645 | |||||||
| chr10:103145772 | G | A | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.102-6293C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103145772 | |||||||
| chr10:103145847 | T | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.102-6368A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103145847 | |||||||
| chr10:103145895 | G | A | 1 | a0001c0001t0002g0260 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.102-6416C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103145895 | |||||||
| chr10:103146229 | A | G | 1 | a0001c0002t0006g0198 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.102-6750T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103146229 | |||||||
| chr10:103146360 | A | G | 1 | a0001c0002t0003g0048 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.102-6881T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103146360 | |||||||
| chr10:103146454 | T | C | 66 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(63): Show |
67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.102-6975A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103146454 | |||||||
| chr10:103147235 | T | C | 41 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0016 others(38): Show |
41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.102-7756A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103147235 | |||||||
| chr10:103147276 | G | A | 2 | a0001c0002t0005g0330 a0001c0002t0005g0331 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.102-7797C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103147276 | |||||||
| chr10:103147757 | A | T | 1 | a0001c0002t0005g0329 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.102-8278T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103147757 | |||||||
| chr10:103147914 | C | T | 5 | a0001c0002t0003g0044 a0001c0002t0003g0045 a0001c0002t0003g0046 others(2): Show |
5 | HG02273.hp1 HG02300.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-8435G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103147914 | |||||||
| chr10:103148033 | A | G | 1 | a0001c0002t0004g0206 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.102-8554T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148033 | |||||||
| chr10:103148331 | G | A | 2 | a0001c0002t0005g0330 a0001c0002t0005g0331 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.102-8852C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148331 | |||||||
| chr10:103148496 | C | T | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.102-9017G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148496 | |||||||
| chr10:103148561 | G | A | 2 | a0001c0001t0002g0303 a0001c0001t0002g0304 |
2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.102-9082C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148561 | |||||||
| chr10:103148587 | G | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0184 |
2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.102-9108C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148587 | |||||||
| chr10:103148603 | CA | C | 162 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(159): Show |
165 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(162): Show |
intron_variant | MODIFIER | c.102-9125delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148603 | |||||||
| chr10:103148650 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.102-9171T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148650 | |||||||
| chr10:103148878 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.102-9399C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103148878 | |||||||
| chr10:103149466 | C | T | 6 | a0001c0002t0005g0308 a0001c0002t0005g0309 a0001c0002t0005g0310 others(3): Show |
6 | HG01243.hp1 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-9987G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149466 | |||||||
| chr10:103149582 | T | G | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.102-10103A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149582 | |||||||
| chr10:103149678 | A | C | 4 | a0001c0002t0006g0196 a0001c0002t0006g0199 a0001c0002t0006g0200 others(1): Show |
4 | HG02735.hp2 HG03831.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-10199T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149678 | |||||||
| chr10:103149697 | T | C | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.102-10218A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149697 | |||||||
| chr10:103149803 | A | G | 1 | a0001c0001t0002g0285 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.102-10324T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149803 | |||||||
| chr10:103149841 | C | T | 4 | a0001c0002t0003g0042 a0001c0002t0009g0029 a0001c0002t0009g0030 others(1): Show |
4 | NA18990.hp2 NA19054.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-10362G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149841 | |||||||
| chr10:103149989 | G | GAATATGA others(2): Show |
180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.102-10511_102-1051 others(13): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103149989 | |||||||
| chr10:103150133 | A | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0088 others(284): Show |
292 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(289): Show |
intron_variant | MODIFIER | c.102-10654T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103150133 | |||||||
| chr10:103150166 | G | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0118 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.102-10687C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103150166 | |||||||
| chr10:103150425 | G | A | 1 | a0001c0002t0006g0192 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.102-10946C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103150425 | |||||||
| chr10:103150626 | A | G | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.102-11147T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103150626 | |||||||
| chr10:103151045 | A | C | 1 | a0002c0003t0004g0010 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.102-11566T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151045 | |||||||
| chr10:103151202 | G | A | 66 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(63): Show |
67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.102-11723C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151202 | |||||||
| chr10:103151282 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0134 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.102-11803A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151282 | |||||||
| chr10:103151464 | T | TA | 52 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(49): Show |
52 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.102-11986dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151464 | |||||||
| chr10:103151464 | T | TAA | 41 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(38): Show |
43 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.102-11987_102-1198 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151464 | |||||||
| chr10:103151473 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.102-11994T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151473 | |||||||
| chr10:103151477 | A | AAAC | 16 | a0001c0002t0006g0186 a0001c0002t0006g0188 a0001c0002t0006g0189 others(13): Show |
16 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-12001_102-1199 others(7): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151477 | |||||||
| chr10:103151599 | A | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.102-12120T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151599 | |||||||
| chr10:103151663 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.102-12184G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103151663 | |||||||
| chr10:103152024 | A | G | 1 | a0001c0001t0002g0260 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.102-12545T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103152024 | |||||||
| chr10:103152279 | C | G | 1 | a0001c0002t0005g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.102-12800G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103152279 | |||||||
| chr10:103152492 | C | G | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.102-13013G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103152492 | |||||||
| chr10:103152555 | A | C | 2 | a0001c0001t0007g0145 a0001c0001t0007g0163 |
2 | HG00558.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.102-13076T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103152555 | |||||||
| chr10:103152596 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.102-13117C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103152596 | |||||||
| chr10:103152607 | C | T | 5 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-13128G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103152607 | |||||||
| chr10:103153127 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.102-13648A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103153127 | |||||||
| chr10:103153425 | A | C | 1 | a0002c0003t0004g0010 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.102-13946T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103153425 | |||||||
| chr10:103153720 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.102-14241C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103153720 | |||||||
| chr10:103153895 | C | T | 1 | a0001c0002t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.102-14416G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103153895 | |||||||
| chr10:103153896 | G | A | 65 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(62): Show |
66 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(63): Show |
intron_variant | MODIFIER | c.102-14417C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103153896 | |||||||
| chr10:103154113 | C | T | 179 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(176): Show |
182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.102-14634G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103154113 | |||||||
| chr10:103154183 | T | C | 67 | a0001c0001t0001g0122 a0001c0002t0003g0004 a0001c0002t0003g0008 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.102-14704A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103154183 | |||||||
| chr10:103154264 | G | A | 3 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 |
3 | HG02109.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.102-14785C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103154264 | |||||||
| chr10:103154348 | A | G | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.102-14869T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103154348 | |||||||
| chr10:103154734 | A | T | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.102-15255T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103154734 | |||||||
| chr10:103155165 | T | G | 1 | a0001c0002t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.102-15686A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103155165 | |||||||
| chr10:103155553 | G | A | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.102-16074C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103155553 | |||||||
| chr10:103155613 | C | T | 3 | a0001c0002t0005g0308 a0001c0002t0005g0311 a0001c0002t0005g0312 |
3 | HG03041.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.102-16134G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103155613 | |||||||
| chr10:103155830 | A | G | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.102-16351T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103155830 | |||||||
| chr10:103155864 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.102-16385A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103155864 | |||||||
| chr10:103156361 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.102-16882A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103156361 | |||||||
| chr10:103156530 | G | A | 2 | a0001c0002t0006g0196 a0001c0002t0006g0199 |
2 | HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.102-17051C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103156530 | |||||||
| chr10:103156755 | C | CA | 100 | a0001c0001t0001g0118 a0001c0001t0005g0316 a0001c0001t0005g0322 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.102-17277dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103156755 | |||||||
| chr10:103157100 | T | C | 52 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 others(49): Show |
54 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.102-17621A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157100 | |||||||
| chr10:103157223 | T | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+17635A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157223 | |||||||
| chr10:103157470 | A | T | 11 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(8): Show |
11 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+17388T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157470 | |||||||
| chr10:103157585 | C | A | 29 | a0002c0003t0004g0002 a0002c0003t0004g0003 a0002c0003t0004g0006 others(26): Show |
31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.101+17273G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157585 | |||||||
| chr10:103157628 | A | G | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+17230T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157628 | |||||||
| chr10:103157687 | C | T | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+17171G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157687 | |||||||
| chr10:103157803 | G | A | 3 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 |
3 | HG02109.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.101+17055C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157803 | |||||||
| chr10:103157900 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.101+16958G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103157900 | |||||||
| chr10:103158063 | C | T | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+16795G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158063 | |||||||
| chr10:103158077 | G | GA | 20 | a0001c0001t0001g0151 a0001c0001t0001g0181 a0001c0001t0002g0005 others(17): Show |
21 | HG00558.hp1 HG01257.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.101+16780dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158077 | |||||||
| chr10:103158163 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.101+16695G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158163 | |||||||
| chr10:103158356 | A | T | 2 | a0001c0001t0002g0303 a0001c0001t0002g0304 |
2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.101+16502T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158356 | |||||||
| chr10:103158364 | A | G | 1 | a0001c0001t0002g0248 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101+16494T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158364 | |||||||
| chr10:103158401 | T | C | 1 | a0001c0002t0015g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+16457A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158401 | |||||||
| chr10:103158644 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.101+16214G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158644 | |||||||
| chr10:103158686 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.101+16172C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158686 | |||||||
| chr10:103158817 | TA | T | 149 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(146): Show |
150 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.101+16040delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103158817 | |||||||
| chr10:103159048 | T | C | 1 | a0002c0003t0004g0220 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.101+15810A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159048 | |||||||
| chr10:103159075 | A | C | 1 | a0001c0002t0005g0309 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.101+15783T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159075 | |||||||
| chr10:103159110 | G | C | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.101+15748C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159110 | |||||||
| chr10:103159195 | T | A | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+15663A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159195 | |||||||
| chr10:103159251 | G | GCA | 51 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(48): Show |
51 | HG00280.hp1 HG00597.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.101+15605_101+1560 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | |||||||
| chr10:103159251 | G | GCACA | 19 | a0001c0001t0001g0001 a0001c0001t0001g0127 a0001c0001t0001g0136 others(16): Show |
20 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.101+15603_101+1560 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | |||||||
| chr10:103159251 | G | GCACACA | 3 | a0001c0001t0001g0009 a0001c0001t0001g0144 a0001c0001t0001g0174 |
3 | HG02970.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.101+15601_101+1560 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | |||||||
| chr10:103159251 | GCA | G | 49 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0115 others(46): Show |
51 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.101+15605_101+1560 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | |||||||
| chr10:103159251 | GCACA | G | 84 | a0001c0001t0001g0098 a0001c0001t0001g0209 a0001c0001t0005g0316 others(81): Show |
85 | HG00544.hp2 HG00597.hp2 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.101+15603_101+1560 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | |||||||
| chr10:103159251 | GCACACA | G | 28 | a0001c0001t0002g0245 a0001c0002t0003g0038 a0001c0002t0003g0082 others(25): Show |
28 | HG00408.hp2 HG00609.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.101+15601_101+1560 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | |||||||
| chr10:103159251 | GCACACAC others(1): Show |
G | 15 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(12): Show |
15 | HG02257.hp1 HG02922.hp2 HG03041.hp2 others(12): Show |
intron_variant | MODIFIER | c.101+15599_101+1560 others(12): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | |||||||
| chr10:103159251 | GCACACAC others(5): Show |
G | 2 | a0001c0001t0002g0294 a0001c0002t0004g0015 |
2 | HG03540.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.101+15595_101+1560 others(16): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | |||||||
| chr10:103159251 | GCACACAC others(7): Show |
G | 3 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0274 |
3 | NA19002.hp2 NA19067.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.101+15593_101+1560 others(18): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159251 | |||||||
| chr10:103159516 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.101+15342A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159516 | |||||||
| chr10:103159559 | G | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+15299C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103159559 | |||||||
| chr10:103160179 | T | C | 3 | a0001c0002t0004g0018 a0001c0002t0004g0022 a0001c0002t0004g0023 |
3 | HG01109.hp2 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.101+14679A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160179 | |||||||
| chr10:103160470 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.101+14388T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160470 | |||||||
| chr10:103160475 | A | G | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.101+14383T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160475 | |||||||
| chr10:103160584 | A | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+14274T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160584 | |||||||
| chr10:103160743 | G | A | 1 | a0002c0003t0004g0236 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.101+14115C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160743 | |||||||
| chr10:103160752 | C | T | 34 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 others(31): Show |
36 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.101+14106G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160752 | |||||||
| chr10:103160841 | T | C | 2 | a0001c0002t0003g0008 a0001c0002t0003g0036 |
2 | NA18612.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.101+14017A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103160841 | |||||||
| chr10:103161066 | C | T | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.101+13792G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103161066 | |||||||
| chr10:103161132 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0105 a0001c0001t0001g0144 others(1): Show |
4 | HG01928.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.101+13726A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103161132 | |||||||
| chr10:103161411 | TATG | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02280.hp2 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.101+13444_101+1344 others(7): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103161411 | |||||||
| chr10:103161478 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.101+13380C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103161478 | |||||||
| chr10:103161886 | G | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+12972C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103161886 | |||||||
| chr10:103162070 | C | A | 1 | a0002c0003t0004g0230 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.101+12788G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162070 | |||||||
| chr10:103162102 | G | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+12756C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162102 | |||||||
| chr10:103162185 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.101+12673A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162185 | |||||||
| chr10:103162282 | A | G | 179 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(176): Show |
182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.101+12576T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162282 | |||||||
| chr10:103162305 | C | T | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101+12553G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162305 | |||||||
| chr10:103162373 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.101+12485T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162373 | |||||||
| chr10:103162427 | T | C | 1 | a0002c0003t0004g0225 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.101+12431A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162427 | |||||||
| chr10:103162638 | C | T | 1 | a0001c0001t0002g0250 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.101+12220G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162638 | |||||||
| chr10:103162788 | A | G | 10 | a0001c0002t0003g0032 a0001c0002t0003g0033 a0001c0002t0003g0034 others(7): Show |
10 | NA18951.hp2 NA18962.hp2 NA18990.hp2 others(7): Show |
intron_variant | MODIFIER | c.101+12070T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162788 | |||||||
| chr10:103162789 | T | C | 1 | a0001c0001t0002g0277 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.101+12069A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162789 | |||||||
| chr10:103162989 | G | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0184 |
2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.101+11869C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103162989 | |||||||
| chr10:103163155 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.101+11703A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163155 | |||||||
| chr10:103163322 | T | C | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+11536A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163322 | |||||||
| chr10:103163331 | C | G | 1 | a0001c0001t0002g0247 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.101+11527G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163331 | |||||||
| chr10:103163382 | T | C | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.101+11476A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163382 | |||||||
| chr10:103163655 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.101+11203G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163655 | |||||||
| chr10:103163710 | T | TA | 111 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(108): Show |
113 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.101+11147dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163710 | |||||||
| chr10:103163789 | G | C | 1 | a0001c0002t0003g0033 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.101+11069C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163789 | |||||||
| chr10:103163838 | G | A | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+11020C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163838 | |||||||
| chr10:103163843 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.101+11015G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163843 | |||||||
| chr10:103163860 | C | CAAA | 8 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0093 others(5): Show |
8 | HG03834.hp2 NA18940.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+10995_101+1099 others(7): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163860 | |||||||
| chr10:103163863 | AAAAAAAA others(1): Show |
A | 29 | a0002c0003t0004g0002 a0002c0003t0004g0003 a0002c0003t0004g0006 others(26): Show |
31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.101+10987_101+1099 others(12): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163863 | |||||||
| chr10:103163865 | A | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0168 |
2 | HG03098.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.101+10993T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163865 | |||||||
| chr10:103163870 | AC | A | 123 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0003g0004 others(120): Show |
124 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.101+10987delG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163870 | |||||||
| chr10:103163871 | C | A | 24 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(21): Show |
24 | HG00735.hp2 HG01433.hp2 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.101+10987G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163871 | |||||||
| chr10:103163876 | A | C | 1 | a0001c0001t0001g0125 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.101+10982T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103163876 | |||||||
| chr10:103164051 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.101+10807G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164051 | |||||||
| chr10:103164282 | G | A | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.101+10576C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164282 | |||||||
| chr10:103164311 | G | A | 1 | a0001c0002t0015g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+10547C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164311 | |||||||
| chr10:103164599 | A | G | 1 | a0001c0002t0006g0192 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.101+10259T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164599 | |||||||
| chr10:103164675 | T | C | 1 | a0001c0002t0005g0315 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.101+10183A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164675 | |||||||
| chr10:103164696 | A | C | 1 | a0001c0002t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101+10162T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164696 | |||||||
| chr10:103164697 | A | T | 1 | a0001c0002t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101+10161T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164697 | |||||||
| chr10:103164698 | A | C | 1 | a0001c0002t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101+10160T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103164698 | |||||||
| chr10:103165063 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0105 others(46): Show |
50 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.101+9795C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165063 | |||||||
| chr10:103165081 | G | A | 29 | a0002c0003t0004g0002 a0002c0003t0004g0003 a0002c0003t0004g0006 others(26): Show |
31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.101+9777C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165081 | |||||||
| chr10:103165219 | C | T | 1 | a0001c0002t0003g0054 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.101+9639G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165219 | |||||||
| chr10:103165241 | C | T | 1 | a0001c0002t0005g0329 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.101+9617G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165241 | |||||||
| chr10:103165301 | C | T | 1 | a0001c0002t0004g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.101+9557G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165301 | |||||||
| chr10:103165408 | G | A | 1 | a0001c0001t0002g0306 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.101+9450C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165408 | |||||||
| chr10:103165574 | C | CT | 7 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0251 others(4): Show |
7 | HG01978.hp1 HG03831.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+9283dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165574 | |||||||
| chr10:103165574 | CT | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0088 others(201): Show |
206 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.101+9283delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165574 | |||||||
| chr10:103165574 | CTT | C | 35 | a0001c0001t0001g0113 a0001c0001t0001g0134 a0001c0001t0001g0162 others(32): Show |
37 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.101+9282_101+9283d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165574 | |||||||
| chr10:103165675 | AT | A | 178 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(175): Show |
181 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(178): Show |
intron_variant | MODIFIER | c.101+9182delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165675 | |||||||
| chr10:103165786 | C | G | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.101+9072G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165786 | |||||||
| chr10:103165806 | G | C | 1 | a0001c0002t0005g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.101+9052C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103165806 | |||||||
| chr10:103166028 | G | A | 5 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.101+8830C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166028 | |||||||
| chr10:103166072 | A | C | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.101+8786T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166072 | |||||||
| chr10:103166558 | C | A | 3 | a0001c0002t0006g0188 a0001c0002t0006g0190 a0001c0002t0006g0191 |
3 | HG01070.hp2 HG01071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.101+8300G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166558 | |||||||
| chr10:103166577 | T | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+8281A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166577 | |||||||
| chr10:103166583 | A | G | 1 | a0001c0002t0008g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.101+8275T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166583 | |||||||
| chr10:103166600 | A | C | 8 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 others(5): Show |
8 | HG01081.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.101+8258T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166600 | |||||||
| chr10:103166608 | AAAAC | A | 42 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(39): Show |
44 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.101+8246_101+8249d others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166608 | |||||||
| chr10:103166666 | T | C | 1 | a0001c0002t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101+8192A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166666 | |||||||
| chr10:103166728 | T | C | 13 | a0002c0003t0004g0002 a0002c0003t0004g0221 a0002c0003t0004g0222 others(10): Show |
14 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.101+8130A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166728 | |||||||
| chr10:103166758 | T | A | 1 | a0002c0003t0004g0227 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.101+8100A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166758 | |||||||
| chr10:103166851 | T | C | 1 | a0001c0002t0005g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.101+8007A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103166851 | |||||||
| chr10:103167119 | G | A | 12 | a0001c0002t0005g0314 a0001c0002t0005g0315 a0001c0002t0005g0320 others(9): Show |
12 | HG00639.hp2 HG00738.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.101+7739C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167119 | |||||||
| chr10:103167176 | T | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+7682A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167176 | |||||||
| chr10:103167383 | A | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0179 |
2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.101+7475T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167383 | |||||||
| chr10:103167441 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.101+7417G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167441 | |||||||
| chr10:103167615 | A | T | 1 | a0001c0001t0001g0165 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.101+7243T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167615 | |||||||
| chr10:103167748 | T | TA | 11 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(8): Show |
11 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+7109dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167748 | |||||||
| chr10:103167877 | A | G | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.101+6981T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167877 | |||||||
| chr10:103167939 | T | A | 1 | a0001c0001t0002g0292 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.101+6919A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103167939 | |||||||
| chr10:103168104 | T | TA | 41 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0016 others(38): Show |
41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.101+6753dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103168104 | |||||||
| chr10:103168378 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0174 |
2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.101+6480T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103168378 | |||||||
| chr10:103168407 | G | C | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.101+6451C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103168407 | |||||||
| chr10:103168550 | G | T | 1 | a0001c0002t0004g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.101+6308C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103168550 | |||||||
| chr10:103168956 | T | G | 1 | a0001c0002t0015g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+5902A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103168956 | |||||||
| chr10:103168967 | G | C | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.101+5891C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103168967 | |||||||
| chr10:103169013 | T | A | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+5845A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169013 | |||||||
| chr10:103169014 | TA | T | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+5843delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169014 | |||||||
| chr10:103169072 | T | A | 1 | a0001c0002t0008g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.101+5786A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169072 | |||||||
| chr10:103169154 | A | C | 1 | a0001c0002t0003g0033 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.101+5704T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169154 | |||||||
| chr10:103169157 | T | A | 66 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(63): Show |
67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.101+5701A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169157 | |||||||
| chr10:103169356 | C | A | 41 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0016 others(38): Show |
41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.101+5502G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169356 | |||||||
| chr10:103169367 | A | G | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.101+5491T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169367 | |||||||
| chr10:103169434 | C | T | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.101+5424G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169434 | |||||||
| chr10:103169440 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.101+5418C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169440 | |||||||
| chr10:103169618 | CA | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0103 others(66): Show |
70 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.101+5239delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169618 | |||||||
| chr10:103169687 | A | G | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101+5171T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169687 | |||||||
| chr10:103169798 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.101+5060A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169798 | |||||||
| chr10:103169813 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.101+5045A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169813 | |||||||
| chr10:103169959 | T | C | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.101+4899A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169959 | |||||||
| chr10:103169991 | G | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+4867C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103169991 | |||||||
| chr10:103170377 | C | A | 5 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.101+4481G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170377 | |||||||
| chr10:103170497 | ACACACAC others(5): Show |
A | 2 | a0001c0001t0007g0145 a0001c0001t0007g0163 |
2 | HG00558.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.101+4349_101+4360d others(14): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170497 | |||||||
| chr10:103170526 | CT | C | 86 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(83): Show |
87 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.101+4331delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170526 | |||||||
| chr10:103170526 | CTT | C | 98 | a0001c0001t0001g0098 a0001c0001t0005g0316 a0001c0001t0005g0322 others(95): Show |
100 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.101+4330_101+4331d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170526 | |||||||
| chr10:103170625 | T | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+4233A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170625 | |||||||
| chr10:103170634 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0142 a0001c0001t0001g0147 others(1): Show |
5 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+4224G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170634 | |||||||
| chr10:103170697 | G | GT | 26 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0102 others(23): Show |
26 | HG00408.hp2 HG00609.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+4160dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170697 | |||||||
| chr10:103170729 | C | T | 332 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0088 others(329): Show |
337 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.101+4129G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170729 | |||||||
| chr10:103170770 | G | A | 2 | a0001c0001t0002g0303 a0001c0001t0002g0304 |
2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.101+4088C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170770 | |||||||
| chr10:103170836 | T | C | 3 | a0001c0002t0006g0188 a0001c0002t0006g0190 a0001c0002t0006g0191 |
3 | HG01070.hp2 HG01071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.101+4022A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170836 | |||||||
| chr10:103170879 | C | T | 1 | a0001c0002t0013g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.101+3979G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170879 | |||||||
| chr10:103170925 | C | T | 1 | a0001c0002t0003g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.101+3933G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103170925 | |||||||
| chr10:103171294 | C | T | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+3564G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103171294 | |||||||
| chr10:103171474 | G | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+3384C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103171474 | |||||||
| chr10:103171501 | G | C | 1 | a0001c0001t0007g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.101+3357C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103171501 | |||||||
| chr10:103171827 | G | C | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.101+3031C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103171827 | |||||||
| chr10:103171914 | A | T | 2 | a0001c0002t0003g0047 a0001c0002t0005g0321 |
2 | HG02809.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.101+2944T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103171914 | |||||||
| chr10:103171932 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.101+2926C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103171932 | |||||||
| chr10:103172061 | T | C | 3 | a0002c0003t0004g0226 a0002c0003t0004g0227 a0002c0003t0004g0233 |
3 | HG00642.hp1 HG01255.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.101+2797A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172061 | |||||||
| chr10:103172082 | T | G | 1 | a0001c0002t0003g0054 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.101+2776A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172082 | |||||||
| chr10:103172100 | C | T | 8 | a0001c0002t0003g0008 a0001c0002t0003g0036 a0001c0002t0003g0044 others(5): Show |
8 | HG02273.hp1 HG02300.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+2758G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172100 | |||||||
| chr10:103172102 | C | T | 8 | a0001c0001t0002g0245 a0001c0001t0002g0257 a0001c0001t0002g0264 others(5): Show |
8 | NA18945.hp1 NA18952.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.101+2756G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172102 | |||||||
| chr10:103172118 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.101+2740C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172118 | |||||||
| chr10:103172134 | T | C | 9 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0112 others(6): Show |
9 | HG01109.hp1 HG02896.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.101+2724A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172134 | |||||||
| chr10:103172166 | C | T | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+2692G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172166 | |||||||
| chr10:103172247 | A | AT | 92 | a0001c0001t0001g0097 a0001c0001t0005g0316 a0001c0001t0005g0322 others(89): Show |
94 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.101+2610dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172247 | |||||||
| chr10:103172247 | A | ATT | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+2609_101+2610d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172247 | |||||||
| chr10:103172249 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.101+2609A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172249 | |||||||
| chr10:103172305 | G | A | 12 | a0001c0002t0005g0314 a0001c0002t0005g0315 a0001c0002t0005g0320 others(9): Show |
12 | HG00639.hp2 HG00738.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.101+2553C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172305 | |||||||
| chr10:103172404 | A | G | 1 | a0001c0002t0004g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101+2454T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172404 | |||||||
| chr10:103172410 | G | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+2448C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172410 | |||||||
| chr10:103172494 | G | A | 1 | a0001c0001t0007g0140 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.101+2364C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172494 | |||||||
| chr10:103172549 | T | C | 5 | a0001c0002t0005g0317 a0001c0002t0005g0318 a0001c0002t0005g0319 others(2): Show |
5 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.101+2309A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172549 | |||||||
| chr10:103172558 | ACTCACGG others(5): Show |
A | 3 | a0001c0002t0004g0202 a0001c0002t0004g0203 a0001c0002t0004g0206 |
3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.101+2288_101+2299d others(14): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172558 | |||||||
| chr10:103172604 | G | A | 4 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.101+2254C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172604 | |||||||
| chr10:103172985 | G | C | 1 | a0001c0002t0006g0198 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.101+1873C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172985 | |||||||
| chr10:103172995 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | NA18943.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.101+1863C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103172995 | |||||||
| chr10:103173482 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.101+1376A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173482 | |||||||
| chr10:103173486 | G | A | 15 | a0002c0003t0004g0003 a0002c0003t0004g0006 a0002c0003t0004g0010 others(12): Show |
16 | HG00609.hp2 HG00621.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.101+1372C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173486 | |||||||
| chr10:103173611 | C | CA | 34 | a0001c0001t0001g0123 a0001c0001t0001g0164 a0001c0001t0002g0245 others(31): Show |
34 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.101+1246dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173611 | |||||||
| chr10:103173611 | C | CAA | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG02683.hp1 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+1245_101+1246d others(4): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173611 | |||||||
| chr10:103173648 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.101+1210G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173648 | |||||||
| chr10:103173692 | C | T | 82 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(79): Show |
84 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.101+1166G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173692 | |||||||
| chr10:103173754 | G | T | 29 | a0002c0003t0004g0002 a0002c0003t0004g0003 a0002c0003t0004g0006 others(26): Show |
31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.101+1104C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173754 | |||||||
| chr10:103173897 | A | G | 41 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0016 others(38): Show |
41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.101+961T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173897 | |||||||
| chr10:103173913 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.101+945G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173913 | |||||||
| chr10:103173922 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0147 |
3 | HG00280.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.101+936G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173922 | |||||||
| chr10:103173964 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.101+894G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103173964 | |||||||
| chr10:103174074 | C | T | 1 | a0001c0002t0003g0072 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.101+784G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174074 | |||||||
| chr10:103174095 | C | CA | 11 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0134 others(8): Show |
11 | HG01069.hp2 HG01071.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.101+762dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174095 | |||||||
| chr10:103174095 | CA | C | 66 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(63): Show |
66 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.101+762delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174095 | |||||||
| chr10:103174164 | C | T | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.101+694G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174164 | |||||||
| chr10:103174178 | G | A | 1 | a0001c0002t0004g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.101+680C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174178 | |||||||
| chr10:103174197 | A | G | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+661T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174197 | |||||||
| chr10:103174222 | C | T | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+636G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174222 | |||||||
| chr10:103174476 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.101+382G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174476 | |||||||
| chr10:103174544 | C | G | 1 | a0002c0003t0004g0220 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.101+314G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174544 | |||||||
| chr10:103174639 | CAA | C | 82 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(79): Show |
84 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.101+217_101+218del others(2): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174639 | |||||||
| chr10:103174732 | G | A | 1 | a0002c0003t0004g0228 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.101+126C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174732 | |||||||
| chr10:103174806 | G | A | 4 | a0001c0001t0002g0262 a0001c0001t0002g0263 a0001c0001t0002g0275 others(1): Show |
4 | HG02683.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.101+52C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 3/18 | chr10 | 103174806 | |||||||
| chr10:103175081 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02280.hp2 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-24-99G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175081 | |||||||
| chr10:103175138 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-24-156G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175138 | |||||||
| chr10:103175195 | C | T | 41 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0016 others(38): Show |
41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-24-213G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175195 | |||||||
| chr10:103175400 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-24-418C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175400 | |||||||
| chr10:103175415 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-24-433A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175415 | |||||||
| chr10:103175517 | G | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.-24-535C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175517 | |||||||
| chr10:103175607 | G | T | 1 | a0001c0002t0013g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-24-625C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175607 | |||||||
| chr10:103175755 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-24-773T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175755 | |||||||
| chr10:103175836 | G | C | 179 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(176): Show |
182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-24-854C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175836 | |||||||
| chr10:103175929 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-24-947C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103175929 | |||||||
| chr10:103176038 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-24-1056T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103176038 | |||||||
| chr10:103176683 | C | T | 2 | a0002c0003t0004g0217 a0002c0003t0004g0219 |
2 | NA18941.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-24-1701G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103176683 | |||||||
| chr10:103176697 | C | A | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24-1715G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103176697 | |||||||
| chr10:103176813 | A | G | 1 | a0001c0002t0006g0192 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-24-1831T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103176813 | |||||||
| chr10:103176922 | T | C | 1 | a0001c0001t0002g0282 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-24-1940A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103176922 | |||||||
| chr10:103176946 | TC | T | 3 | a0001c0002t0006g0196 a0001c0002t0006g0199 a0001c0002t0006g0204 |
3 | HG03831.hp1 HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-24-1965delG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103176946 | |||||||
| chr10:103177051 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-24-2069A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177051 | |||||||
| chr10:103177209 | C | T | 2 | a0001c0002t0004g0012 a0001c0002t0004g0013 |
2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-24-2227G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177209 | |||||||
| chr10:103177232 | A | G | 1 | a0001c0002t0004g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-24-2250T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177232 | |||||||
| chr10:103177343 | G | C | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-24-2361C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177343 | |||||||
| chr10:103177470 | C | T | 1 | a0002c0003t0004g0220 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-24-2488G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177470 | |||||||
| chr10:103177627 | TC | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0105 others(51): Show |
55 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.-24-2646delG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177627 | |||||||
| chr10:103177646 | AGAACAGC others(12): Show |
A | 1 | a0001c0001t0001g0208 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-24-2683_-24-2665d others(21): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177646 | |||||||
| chr10:103177778 | A | T | 1 | a0001c0002t0005g0313 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-24-2796T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103177778 | |||||||
| chr10:103178146 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-25+3039C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178146 | |||||||
| chr10:103178283 | C | T | 1 | a0001c0002t0005g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-25+2902G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178283 | |||||||
| chr10:103178356 | G | A | 1 | a0001c0002t0005g0315 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-25+2829C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178356 | |||||||
| chr10:103178378 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-25+2807G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178378 | |||||||
| chr10:103178456 | T | G | 1 | a0001c0002t0005g0321 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-25+2729A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178456 | |||||||
| chr10:103178833 | C | CA | 81 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(78): Show |
82 | HG00544.hp2 HG00621.hp2 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.-25+2351dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178833 | |||||||
| chr10:103178849 | A | AG | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-25+2335dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178849 | |||||||
| chr10:103178954 | C | CTTTTTTT | 11 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(8): Show |
11 | HG02135.hp1 HG03834.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25+2224_-25+2230d others(9): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178954 | |||||||
| chr10:103178954 | C | CTTTTTTT others(1): Show |
95 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0005g0322 others(92): Show |
97 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.-25+2223_-25+2230d others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178954 | |||||||
| chr10:103178954 | C | CTTTTTTT others(2): Show |
7 | a0001c0001t0005g0316 a0001c0002t0005g0318 a0001c0002t0006g0200 others(4): Show |
7 | HG00597.hp2 HG02257.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25+2222_-25+2230d others(11): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103178954 | |||||||
| chr10:103179105 | T | A | 1 | a0001c0002t0005g0334 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-25+2080A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179105 | |||||||
| chr10:103179109 | C | G | 3 | a0001c0002t0004g0018 a0001c0002t0004g0022 a0001c0002t0004g0023 |
3 | HG01109.hp2 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-25+2076G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179109 | |||||||
| chr10:103179224 | G | A | 1 | a0001c0002t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-25+1961C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179224 | |||||||
| chr10:103179295 | C | T | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-25+1890G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179295 | |||||||
| chr10:103179425 | G | A | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.-25+1760C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179425 | |||||||
| chr10:103179458 | T | C | 67 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(64): Show |
68 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.-25+1727A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179458 | |||||||
| chr10:103179475 | G | A | 41 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0016 others(38): Show |
41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-25+1710C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179475 | |||||||
| chr10:103179526 | A | G | 113 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
115 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.-25+1659T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179526 | |||||||
| chr10:103179633 | T | TA | 7 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25+1551_-25+1552i others(3): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103179633 | |||||||
| chr10:103180126 | C | A | 1 | a0001c0001t0002g0247 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-25+1059G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180126 | |||||||
| chr10:103180397 | G | A | 1 | a0001c0002t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-25+788C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180397 | |||||||
| chr10:103180496 | C | T | 1 | a0001c0002t0003g0059 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-25+689G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180496 | |||||||
| chr10:103180525 | A | C | 2 | a0001c0002t0004g0016 a0001c0002t0004g0017 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-25+660T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180525 | |||||||
| chr10:103180767 | T | C | 1 | a0001c0002t0005g0315 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-25+418A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180767 | |||||||
| chr10:103180902 | C | T | 2 | a0001c0001t0002g0276 a0001c0001t0018g0255 |
2 | HG00558.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-25+283G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180902 | |||||||
| chr10:103180957 | G | A | 3 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0080 |
3 | NA18957.hp1 NA18978.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-25+228C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103180957 | |||||||
| chr10:103181038 | G | A | 4 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0005g0327 others(1): Show |
4 | HG00597.hp2 HG00673.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+147C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103181038 | |||||||
| chr10:103181096 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-25+89G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103181096 | |||||||
| chr10:103181110 | A | G | 8 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(5): Show |
8 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25+75T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103181110 | |||||||
| chr10:103181178 | T | C | 3 | a0001c0002t0003g0026 a0001c0002t0003g0055 a0001c0002t0017g0067 |
3 | HG02071.hp2 HG02074.hp2 HG02129.hp2 |
splice_region_variant&intron_variant | LOW | c.-25+7A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 2/18 | chr10 | 103181178 | |||||||
| chr10:103181335 | C | CA | 72 | a0001c0001t0001g0180 a0001c0001t0002g0254 a0001c0001t0005g0322 others(69): Show |
74 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(71): Show |
splice_region_variant&intron_variant | LOW | c.-168-8dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181335 | |||||||
| chr10:103181349 | AT | A | 3 | a0001c0002t0003g0008 a0001c0002t0003g0028 a0001c0002t0003g0079 |
3 | NA19076.hp2 NA19089.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-168-22delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181349 | |||||||
| chr10:103181350 | T | A | 179 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(176): Show |
182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-168-22A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181350 | |||||||
| chr10:103181355 | A | T | 181 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(178): Show |
184 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.-168-27T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181355 | |||||||
| chr10:103181496 | T | G | 1 | a0001c0002t0003g0054 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-168-168A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181496 | |||||||
| chr10:103181563 | T | C | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-168-235A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181563 | |||||||
| chr10:103181678 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-168-350A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181678 | |||||||
| chr10:103181782 | A | G | 1 | a0001c0002t0008g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-168-454T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181782 | |||||||
| chr10:103181832 | C | T | 181 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(178): Show |
184 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.-168-504G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181832 | |||||||
| chr10:103181992 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-168-664T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103181992 | |||||||
| chr10:103182009 | C | CA | 36 | a0001c0001t0002g0244 a0001c0001t0002g0276 a0001c0001t0018g0255 others(33): Show |
38 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-168-682dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182009 | |||||||
| chr10:103182099 | A | G | 1 | a0001c0002t0008g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-168-771T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182099 | |||||||
| chr10:103182206 | T | C | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-168-878A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182206 | |||||||
| chr10:103182209 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-168-881G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182209 | |||||||
| chr10:103182225 | C | T | 1 | a0001c0002t0003g0042 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-168-897G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182225 | |||||||
| chr10:103182248 | C | T | 4 | a0001c0002t0003g0032 a0001c0002t0009g0029 a0001c0002t0009g0030 others(1): Show |
4 | NA18962.hp2 NA18990.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-168-920G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182248 | |||||||
| chr10:103182454 | T | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0171 a0001c0001t0012g0111 |
3 | HG01928.hp2 HG01952.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-168-1126A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182454 | |||||||
| chr10:103182486 | G | A | 18 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-168-1158C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182486 | |||||||
| chr10:103182487 | T | G | 66 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(63): Show |
67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.-168-1159A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182487 | |||||||
| chr10:103182545 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-168-1217C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182545 | |||||||
| chr10:103182634 | C | CA | 9 | a0001c0002t0003g0061 a0001c0002t0003g0062 a0001c0002t0003g0063 others(6): Show |
9 | HG01943.hp1 HG02004.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-168-1307dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182634 | |||||||
| chr10:103182800 | T | A | 1 | a0001c0001t0002g0248 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-168-1472A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103182800 | |||||||
| chr10:103183248 | A | G | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-168-1920T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183248 | |||||||
| chr10:103183250 | A | G | 11 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(8): Show |
11 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.-168-1922T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183250 | |||||||
| chr10:103183260 | G | GATATAT | 3 | a0001c0002t0004g0021 a0001c0002t0004g0202 a0001c0002t0004g0206 |
3 | HG00735.hp2 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-168-1933_-168-193 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183260 | |||||||
| chr10:103183260 | G | GATATATA others(3): Show |
1 | a0001c0002t0004g0020 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-168-1933_-168-193 others(14): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183260 | |||||||
| chr10:103183260 | G | GATATATA others(5): Show |
1 | a0001c0002t0004g0019 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-168-1933_-168-193 others(16): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183260 | |||||||
| chr10:103183260 | G | GATATATA others(7): Show |
2 | a0001c0002t0004g0018 a0001c0002t0004g0023 |
2 | HG01109.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-168-1933_-168-193 others(18): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183260 | |||||||
| chr10:103183260 | G | GATATATA others(11): Show |
2 | a0001c0002t0004g0016 a0001c0002t0004g0017 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-168-1933_-168-193 others(22): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183260 | |||||||
| chr10:103183261 | T | A | 18 | a0001c0001t0002g0275 a0001c0002t0003g0039 a0001c0002t0003g0040 others(15): Show |
18 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.-168-1933A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183261 | |||||||
| chr10:103183262 | G | GAT | 15 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 others(12): Show |
15 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.-168-1936_-168-193 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GATAT | 33 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0130 others(30): Show |
33 | HG00597.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-168-1938_-168-193 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GATATAT | 25 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(22): Show |
25 | HG00597.hp2 HG01069.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-168-1940_-168-193 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GATATATA others(1): Show |
25 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(22): Show |
25 | HG00280.hp1 HG00408.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-168-1942_-168-193 others(12): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GATATATA others(3): Show |
27 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0001g0101 others(24): Show |
27 | HG00280.hp2 HG00621.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.-168-1944_-168-193 others(14): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GATATATA others(5): Show |
15 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0110 others(12): Show |
15 | HG00558.hp2 HG01928.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-168-1946_-168-193 others(16): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GATATATA others(7): Show |
10 | a0001c0001t0001g0009 a0001c0001t0001g0118 a0001c0001t0001g0119 others(7): Show |
10 | HG02040.hp2 HG02074.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-168-1948_-168-193 others(18): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GATATATA others(9): Show |
5 | a0001c0001t0001g0098 a0001c0001t0001g0117 a0001c0001t0001g0166 others(2): Show |
5 | HG01258.hp1 HG02135.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-168-1950_-168-193 others(20): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GATATATA others(11): Show |
3 | a0001c0001t0001g0116 a0001c0001t0001g0136 a0001c0002t0005g0309 |
3 | HG00544.hp1 HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-168-1952_-168-193 others(22): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GATATATA others(13): Show |
4 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0209 others(1): Show |
4 | HG02280.hp2 HG02602.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-168-1954_-168-193 others(24): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GATATATA others(15): Show |
4 | a0001c0002t0005g0308 a0001c0002t0005g0310 a0001c0002t0005g0311 others(1): Show |
4 | HG03041.hp2 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-168-1956_-168-193 others(26): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GATATATA others(17): Show |
1 | a0001c0001t0007g0173 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-168-1958_-168-193 others(28): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GATATATA others(23): Show |
1 | a0001c0001t0001g0170 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-168-1964_-168-193 others(34): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GTGAT | 6 | a0001c0001t0001g0114 a0001c0001t0001g0123 a0001c0002t0005g0314 others(3): Show |
6 | HG02970.hp1 HG03098.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-168-1935_-168-193 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GTGATAT | 5 | a0001c0002t0005g0323 a0001c0002t0005g0324 a0001c0002t0005g0330 others(2): Show |
5 | HG00639.hp2 HG01169.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-168-1935_-168-193 others(10): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GTGATATA others(5): Show |
1 | a0001c0002t0005g0320 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-168-1935_-168-193 others(16): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | GTGATATA others(9): Show |
1 | a0001c0002t0005g0329 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-168-1935_-168-193 others(20): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | G | T | 18 | a0001c0001t0002g0275 a0001c0002t0003g0039 a0001c0002t0003g0040 others(15): Show |
18 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.-168-1934C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | GAT | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0134 a0001c0001t0001g0182 others(17): Show |
22 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.-168-1936_-168-193 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | GATAT | G | 7 | a0001c0001t0001g0135 a0001c0001t0001g0177 a0001c0002t0004g0011 others(4): Show |
7 | HG00738.hp1 HG01070.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-168-1938_-168-193 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183262 | GATATATA others(7): Show |
G | 17 | a0001c0001t0002g0005 a0001c0001t0002g0244 a0001c0001t0002g0246 others(14): Show |
18 | HG00558.hp1 HG01257.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-168-1948_-168-193 others(18): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183262 | |||||||
| chr10:103183267 | A | T | 1 | a0001c0002t0005g0328 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-168-1939T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183267 | |||||||
| chr10:103183268 | T | G | 1 | a0001c0002t0005g0328 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-168-1940A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183268 | |||||||
| chr10:103183275 | A | AATATATA others(22): Show |
1 | a0001c0002t0003g0077 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-168-1948_-168-194 others(33): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183275 | |||||||
| chr10:103183275 | A | ATATATAT others(24): Show |
1 | a0001c0002t0003g0075 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-168-1948_-168-194 others(35): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183275 | |||||||
| chr10:103183275 | A | ATATATAT others(23): Show |
40 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(37): Show |
41 | HG01069.hp1 HG01167.hp1 HG01943.hp1 others(38): Show |
intron_variant | MODIFIER | c.-168-1948_-168-194 others(34): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183275 | |||||||
| chr10:103183275 | A | ATATATAT others(21): Show |
17 | a0001c0002t0003g0034 a0001c0002t0003g0039 a0001c0002t0003g0040 others(14): Show |
17 | HG01358.hp2 HG02083.hp1 HG02735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-168-1948_-168-194 others(32): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183275 | |||||||
| chr10:103183275 | A | ATATATAT others(19): Show |
2 | a0001c0002t0003g0059 a0001c0002t0003g0060 |
2 | HG01433.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-168-1948_-168-194 others(30): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183275 | |||||||
| chr10:103183275 | A | ATATATAT others(21): Show |
1 | a0001c0002t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-168-1948_-168-194 others(32): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183275 | |||||||
| chr10:103183276 | T | TATATATA others(21): Show |
1 | a0001c0002t0003g0036 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-168-1949_-168-194 others(32): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183276 | |||||||
| chr10:103183291 | A | ATTTTATA others(27): Show |
2 | a0001c0002t0003g0027 a0001c0002t0003g0064 |
2 | HG00544.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-168-1964_-168-196 others(38): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183291 | |||||||
| chr10:103183291 | A | C | 63 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(60): Show |
64 | HG01069.hp1 HG01167.hp1 HG01358.hp2 others(61): Show |
intron_variant | MODIFIER | c.-168-1963T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183291 | |||||||
| chr10:103183334 | C | CT | 7 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-168-2007dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183334 | |||||||
| chr10:103183334 | CT | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0101 others(215): Show |
221 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.-168-2007delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183334 | |||||||
| chr10:103183366 | C | T | 1 | a0001c0002t0005g0308 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-168-2038G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183366 | |||||||
| chr10:103183367 | C | A | 1 | a0001c0001t0002g0290 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-168-2039G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183367 | |||||||
| chr10:103183508 | C | CT | 29 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(26): Show |
29 | HG00639.hp2 HG01081.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.-168-2181dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183508 | |||||||
| chr10:103183508 | CT | C | 12 | a0001c0001t0001g0109 a0001c0001t0001g0124 a0001c0001t0001g0172 others(9): Show |
12 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-168-2181delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183508 | |||||||
| chr10:103183585 | A | G | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.-168-2257T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183585 | |||||||
| chr10:103183625 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-168-2297A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183625 | |||||||
| chr10:103183633 | T | C | 22 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(19): Show |
22 | HG00408.hp1 HG00642.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-168-2305A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183633 | |||||||
| chr10:103183661 | C | T | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-168-2333G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183661 | |||||||
| chr10:103183705 | G | C | 1 | a0001c0001t0002g0246 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-168-2377C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183705 | |||||||
| chr10:103183735 | T | C | 1 | a0001c0002t0005g0329 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-168-2407A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183735 | |||||||
| chr10:103183773 | C | T | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.-168-2445G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183773 | |||||||
| chr10:103183865 | G | T | 4 | a0001c0002t0003g0039 a0001c0002t0003g0040 a0001c0002t0003g0041 others(1): Show |
4 | NA18971.hp2 NA18982.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.-168-2537C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183865 | |||||||
| chr10:103183946 | G | GT | 7 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0002g0282 others(4): Show |
7 | HG02027.hp2 HG02486.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.-168-2619dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183946 | |||||||
| chr10:103183950 | T | G | 2 | a0001c0001t0002g0303 a0001c0001t0002g0304 |
2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-168-2622A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103183950 | |||||||
| chr10:103184127 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-168-2799A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184127 | |||||||
| chr10:103184134 | T | C | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.-168-2806A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184134 | |||||||
| chr10:103184229 | T | A | 180 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(177): Show |
183 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.-168-2901A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184229 | |||||||
| chr10:103184236 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0101 others(87): Show |
91 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.-168-2908C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184236 | |||||||
| chr10:103184244 | C | T | 29 | a0002c0003t0004g0002 a0002c0003t0004g0003 a0002c0003t0004g0006 others(26): Show |
31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-168-2916G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184244 | |||||||
| chr10:103184246 | T | C | 1 | a0001c0002t0003g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-168-2918A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184246 | |||||||
| chr10:103184530 | G | A | 3 | a0001c0002t0003g0061 a0001c0002t0003g0062 a0001c0002t0003g0063 |
3 | HG01943.hp1 HG02004.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-168-3202C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184530 | |||||||
| chr10:103184963 | A | G | 29 | a0002c0003t0004g0002 a0002c0003t0004g0003 a0002c0003t0004g0006 others(26): Show |
31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-168-3635T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184963 | |||||||
| chr10:103184987 | C | G | 179 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(176): Show |
182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-168-3659G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103184987 | |||||||
| chr10:103185010 | C | CTG | 179 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(176): Show |
182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-168-3683_-168-368 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185010 | |||||||
| chr10:103185180 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-168-3852C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185180 | |||||||
| chr10:103185182 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-168-3854T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185182 | |||||||
| chr10:103185271 | C | A | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-168-3943G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185271 | |||||||
| chr10:103185344 | T | TA | 80 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0105 others(77): Show |
83 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.-168-4017dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185344 | |||||||
| chr10:103185456 | A | G | 179 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(176): Show |
182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-168-4128T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185456 | |||||||
| chr10:103185550 | A | G | 2 | a0001c0001t0002g0303 a0001c0001t0002g0304 |
2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-168-4222T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185550 | |||||||
| chr10:103185579 | C | T | 1 | a0001c0002t0008g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-168-4251G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185579 | |||||||
| chr10:103185649 | C | CA | 25 | a0001c0001t0001g0090 a0001c0001t0001g0112 a0001c0001t0005g0316 others(22): Show |
25 | HG00597.hp2 HG00673.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-168-4322dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185649 | |||||||
| chr10:103185649 | C | CAA | 11 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
11 | HG03834.hp2 NA18940.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.-168-4323_-168-432 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185649 | |||||||
| chr10:103185663 | A | AAG | 10 | a0001c0002t0003g0077 a0001c0002t0005g0308 a0001c0002t0005g0309 others(7): Show |
10 | HG01243.hp1 HG01515.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.-168-4336_-168-433 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185663 | |||||||
| chr10:103185664 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-168-4336C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185664 | |||||||
| chr10:103185665 | G | A | 11 | a0001c0002t0003g0077 a0001c0002t0005g0308 a0001c0002t0005g0309 others(8): Show |
11 | HG00639.hp2 HG01243.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.-168-4337C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185665 | |||||||
| chr10:103185665 | G | GA | 22 | a0001c0001t0001g0105 a0001c0001t0001g0162 a0001c0001t0001g0164 others(19): Show |
22 | HG00621.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.-168-4338dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185665 | |||||||
| chr10:103185666 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-168-4338T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185666 | |||||||
| chr10:103185706 | G | A | 179 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(176): Show |
182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-168-4378C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185706 | |||||||
| chr10:103185856 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-168-4528T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185856 | |||||||
| chr10:103185918 | T | C | 1 | a0001c0002t0008g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-168-4590A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185918 | |||||||
| chr10:103185977 | T | C | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02135.hp1 HG03834.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.-168-4649A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185977 | |||||||
| chr10:103185994 | C | T | 179 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(176): Show |
182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-168-4666G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103185994 | |||||||
| chr10:103186032 | C | T | 1 | a0001c0002t0003g0037 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-168-4704G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186032 | |||||||
| chr10:103186066 | G | A | 66 | a0001c0002t0003g0004 a0001c0002t0003g0008 a0001c0002t0003g0024 others(63): Show |
67 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.-168-4738C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186066 | |||||||
| chr10:103186099 | T | G | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-168-4771A>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186099 | |||||||
| chr10:103186157 | C | T | 1 | a0001c0001t0012g0111 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-168-4829G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186157 | |||||||
| chr10:103186288 | G | T | 3 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 |
3 | HG02109.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-168-4960C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186288 | |||||||
| chr10:103186469 | C | T | 2 | a0001c0002t0003g0008 a0001c0002t0003g0036 |
2 | NA18612.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-168-5141G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186469 | |||||||
| chr10:103186568 | T | A | 1 | a0001c0002t0003g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-168-5240A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186568 | |||||||
| chr10:103186633 | G | T | 1 | a0001c0002t0003g0035 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-168-5305C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186633 | |||||||
| chr10:103186653 | G | A | 1 | a0002c0003t0004g0220 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-168-5325C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186653 | |||||||
| chr10:103186912 | CA | C | 119 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
122 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(119): Show |
intron_variant | MODIFIER | c.-168-5585delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186912 | |||||||
| chr10:103186929 | A | G | 1 | a0001c0002t0003g0077 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-168-5601T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186929 | |||||||
| chr10:103186970 | G | T | 6 | a0001c0002t0003g0032 a0001c0002t0003g0033 a0001c0002t0003g0034 others(3): Show |
6 | NA18962.hp2 NA18990.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.-168-5642C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186970 | |||||||
| chr10:103186979 | G | A | 1 | a0001c0002t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-168-5651C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186979 | |||||||
| chr10:103186982 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-168-5654C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103186982 | |||||||
| chr10:103187068 | G | A | 1 | a0001c0002t0006g0205 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-168-5740C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187068 | |||||||
| chr10:103187241 | C | G | 1 | a0001c0002t0003g0075 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-168-5913G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187241 | |||||||
| chr10:103187242 | T | A | 1 | a0001c0002t0003g0075 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-168-5914A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187242 | |||||||
| chr10:103187547 | A | T | 1 | a0001c0001t0002g0249 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-169+5689T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187547 | |||||||
| chr10:103187551 | T | TA | 34 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(31): Show |
34 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.-169+5684dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187551 | |||||||
| chr10:103187551 | TA | T | 9 | a0001c0001t0001g0168 a0001c0001t0001g0179 a0001c0001t0001g0182 others(6): Show |
9 | HG01099.hp1 HG01433.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-169+5684delT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187551 | |||||||
| chr10:103187736 | C | G | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-169+5500G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187736 | |||||||
| chr10:103187823 | G | A | 1 | a0001c0002t0005g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-169+5413C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103187823 | |||||||
| chr10:103188153 | G | A | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-169+5083C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188153 | |||||||
| chr10:103188163 | T | C | 3 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 |
3 | HG02109.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-169+5073A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188163 | |||||||
| chr10:103188219 | A | T | 1 | a0001c0002t0008g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-169+5017T>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188219 | |||||||
| chr10:103188666 | C | T | 4 | a0002c0003t0004g0217 a0002c0003t0004g0218 a0002c0003t0004g0219 others(1): Show |
4 | HG00621.hp2 HG00673.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.-169+4570G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188666 | |||||||
| chr10:103188705 | T | A | 1 | a0001c0001t0002g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-169+4531A>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188705 | |||||||
| chr10:103188712 | C | T | 2 | a0001c0002t0004g0016 a0001c0002t0004g0017 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-169+4524G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188712 | |||||||
| chr10:103188858 | C | T | 41 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0016 others(38): Show |
41 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-169+4378G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188858 | |||||||
| chr10:103188955 | T | C | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-169+4281A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188955 | |||||||
| chr10:103188963 | G | C | 4 | a0001c0002t0003g0069 a0001c0002t0003g0070 a0001c0002t0003g0071 others(1): Show |
4 | HG02735.hp1 HG03017.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-169+4273C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188963 | |||||||
| chr10:103188997 | G | C | 5 | a0002c0003t0004g0003 a0002c0003t0004g0006 a0002c0003t0004g0234 others(2): Show |
6 | HG00609.hp2 NA18950.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.-169+4239C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103188997 | |||||||
| chr10:103189038 | TTGTACTA | T | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-169+4191_-169+419 others(11): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189038 | |||||||
| chr10:103189163 | T | C | 3 | a0001c0002t0004g0202 a0001c0002t0004g0203 a0001c0002t0004g0206 |
3 | HG02622.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-169+4073A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189163 | |||||||
| chr10:103189359 | G | A | 179 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(176): Show |
182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-169+3877C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189359 | |||||||
| chr10:103189561 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0178 |
3 | HG02027.hp1 HG02129.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.-169+3675C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189561 | |||||||
| chr10:103189584 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-169+3652C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189584 | |||||||
| chr10:103189604 | C | CA | 50 | a0001c0001t0001g0088 a0001c0001t0001g0098 a0001c0001t0001g0099 others(47): Show |
50 | HG00597.hp2 HG00673.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.-169+3631dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189604 | |||||||
| chr10:103189617 | G | GA | 8 | a0001c0001t0001g0088 a0001c0001t0001g0179 a0001c0001t0001g0180 others(5): Show |
8 | HG00544.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-169+3618dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189617 | |||||||
| chr10:103189817 | C | T | 1 | a0001c0002t0005g0315 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-169+3419G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189817 | |||||||
| chr10:103189952 | G | A | 100 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(97): Show |
102 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-169+3284C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189952 | |||||||
| chr10:103189960 | G | A | 4 | a0001c0001t0002g0245 a0001c0001t0002g0283 a0001c0001t0002g0284 others(1): Show |
4 | NA18945.hp1 NA18953.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.-169+3276C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189960 | |||||||
| chr10:103189970 | G | A | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-169+3266C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189970 | |||||||
| chr10:103189977 | C | T | 4 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.-169+3259G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189977 | |||||||
| chr10:103189997 | C | CT | 101 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0088 others(98): Show |
102 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-169+3238dupA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189997 | |||||||
| chr10:103189997 | C | CTT | 23 | a0001c0001t0001g0089 a0001c0001t0001g0101 a0001c0001t0001g0102 others(20): Show |
24 | HG01109.hp1 HG01255.hp1 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.-169+3237_-169+323 others(6): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189997 | |||||||
| chr10:103189997 | CT | C | 7 | a0001c0001t0002g0245 a0001c0001t0002g0286 a0001c0001t0011g0287 others(4): Show |
7 | HG00733.hp1 HG01069.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.-169+3238delA | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103189997 | |||||||
| chr10:103190000 | T | TC | 4 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 others(1): Show |
4 | HG02109.hp2 HG02976.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-169+3235_-169+323 others(5): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190000 | |||||||
| chr10:103190001 | T | C | 88 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0015 others(85): Show |
90 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.-169+3235A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190001 | |||||||
| chr10:103190002 | T | C | 2 | a0002c0003t0004g0238 a0002c0003t0004g0239 |
2 | NA18950.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.-169+3234A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190002 | |||||||
| chr10:103190024 | A | G | 331 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0088 others(328): Show |
336 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.-169+3212T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190024 | |||||||
| chr10:103190143 | G | C | 13 | a0001c0001t0001g0181 a0001c0001t0002g0005 a0001c0001t0002g0246 others(10): Show |
14 | HG01361.hp2 HG01943.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.-169+3093C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190143 | |||||||
| chr10:103190195 | T | C | 1 | a0001c0002t0004g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-169+3041A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190195 | |||||||
| chr10:103190406 | C | T | 1 | a0001c0001t0002g0248 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-169+2830G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190406 | |||||||
| chr10:103190440 | C | T | 179 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(176): Show |
182 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.-169+2796G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190440 | |||||||
| chr10:103190711 | T | C | 1 | a0002c0003t0004g0240 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-169+2525A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190711 | |||||||
| chr10:103190716 | GC | G | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-169+2519delG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190716 | |||||||
| chr10:103190870 | A | G | 3 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0080 |
3 | NA18957.hp1 NA18978.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-169+2366T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103190870 | |||||||
| chr10:103191382 | C | CA | 7 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(4): Show |
7 | HG00280.hp1 HG01192.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-169+1853dupT | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191382 | |||||||
| chr10:103191393 | AAAAAAGA others(1): Show |
A | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-169+1835_-169+184 others(12): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191393 | |||||||
| chr10:103191395 | AAAAG | A | 17 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(14): Show |
17 | HG00609.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-169+1837_-169+184 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191395 | |||||||
| chr10:103191397 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-169+1839T>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191397 | |||||||
| chr10:103191397 | AAGAG | A | 75 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0004g0011 others(72): Show |
77 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.-169+1835_-169+183 others(8): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191397 | |||||||
| chr10:103191581 | G | T | 1 | a0001c0001t0001g0088 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-169+1655C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191581 | |||||||
| chr10:103191709 | AC | A | 104 | a0001c0001t0005g0316 a0001c0001t0005g0322 a0001c0002t0003g0082 others(101): Show |
106 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.-169+1526delG | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191709 | |||||||
| chr10:103191726 | C | T | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-169+1510G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191726 | |||||||
| chr10:103191731 | C | T | 6 | a0001c0002t0005g0308 a0001c0002t0005g0309 a0001c0002t0005g0310 others(3): Show |
6 | HG01243.hp1 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-169+1505G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191731 | |||||||
| chr10:103191867 | A | C | 1 | a0001c0002t0014g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-169+1369T>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191867 | |||||||
| chr10:103191932 | T | C | 1 | a0001c0002t0008g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-169+1304A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191932 | |||||||
| chr10:103191982 | C | A | 1 | a0001c0002t0008g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-169+1254G>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103191982 | |||||||
| chr10:103192035 | T | C | 1 | a0002c0003t0004g0241 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-169+1201A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192035 | |||||||
| chr10:103192075 | G | A | 1 | a0001c0002t0003g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-169+1161C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192075 | |||||||
| chr10:103192188 | T | C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | HG02602.hp2 HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-169+1048A>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192188 | |||||||
| chr10:103192742 | C | T | 68 | a0001c0001t0002g0247 a0001c0002t0003g0004 a0001c0002t0003g0008 others(65): Show |
69 | HG00544.hp2 HG01069.hp1 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.-169+494G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192742 | |||||||
| chr10:103192822 | G | A | 2 | a0001c0001t0002g0303 a0001c0001t0002g0304 |
2 | HG01257.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-169+414C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192822 | |||||||
| chr10:103192830 | C | G | 8 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(5): Show |
8 | HG00735.hp2 HG01109.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-169+406G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192830 | |||||||
| chr10:103192839 | G | A | 1 | a0001c0001t0011g0305 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-169+397C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192839 | |||||||
| chr10:103192867 | G | C | 6 | a0001c0002t0008g0211 a0001c0002t0008g0212 a0001c0002t0008g0213 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-169+369C>G | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192867 | |||||||
| chr10:103192868 | G | T | 34 | a0001c0002t0004g0011 a0001c0002t0004g0012 a0001c0002t0004g0013 others(31): Show |
36 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.-169+368C>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192868 | |||||||
| chr10:103192875 | G | A | 29 | a0002c0003t0004g0002 a0002c0003t0004g0003 a0002c0003t0004g0006 others(26): Show |
31 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-169+361C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192875 | |||||||
| chr10:103192898 | C | G | 1 | a0002c0003t0004g0006 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-169+338G>C | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192898 | |||||||
| chr10:103192916 | C | CG | 7 | a0001c0001t0001g0009 a0001c0001t0002g0245 a0001c0001t0002g0246 others(4): Show |
7 | HG02970.hp2 HG03942.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.-169+319dupC | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103192916 | |||||||
| chr10:103193036 | G | A | 2 | a0001c0001t0002g0306 a0001c0001t0002g0307 |
2 | NA19011.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-169+200C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103193036 | |||||||
| chr10:103193120 | G | A | 2 | a0001c0002t0003g0004 a0001c0002t0003g0242 |
3 | NA18988.hp2 NA18992.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-169+116C>T | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103193120 | |||||||
| chr10:103193191 | T | TCGCCCGC others(12): Show |
1 | a0001c0001t0001g0243 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-169+26_-169+44dup others(19): Show |
NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103193191 | |||||||
| chr10:103193213 | C | T | 1 | a0001c0001t0002g0244 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-169+23G>A | NT5C2 | ENSG00000076685.19 | transcript | ENST00000404739.8 | protein_coding | 1/18 | chr10 | 103193213 |