Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 169714 |
| ensemblid | ENSG00000165661.18 |
| hgncid | 30249 |
| symbol | QSOX2 |
| name | quiescin sulfhydryl oxidase 2 |
| refseq_nuc | NM_181701.4 |
| refseq_prot | NP_859052.3 |
| ensembl_nuc | ENST00000358701.10 |
| ensembl_prot | ENSP00000351536.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 136206333 |
| end | 136245812 |
| strand | - |
| ver | v1.2 |
| region | chr9:136206333-136245812 |
| region5000 | chr9:136201333-136250812 |
| regionname0 | QSOX2_chr9_136206333_136245812 |
| regionname5000 | QSOX2_chr9_136201333_136250812 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 698 | 326 | 89 | 64 | 122 | 11 | 38 | 86 | QSOX2_chr9_136201333_136250812 | QSOX2 | MAAAG others(693): Show |
chr9 | 136201333 | 136250812 |
| a0002 | 0/0 | 698 | 58 | 2 | 3 | 44 | 3 | 6 | 34 | QSOX2_chr9_136201333_136250812 | QSOX2 | MAAAG others(693): Show |
chr9 | 136201333 | 136250812 |
| a0003 | 0/0 | 698 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | MAAAG others(693): Show |
chr9 | 136201333 | 136250812 |
| a0004 | 0/0 | 698 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | MAAAG others(693): Show |
chr9 | 136201333 | 136250812 |
| a0005 | 0/0 | 698 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | MAAAG others(693): Show |
chr9 | 136201333 | 136250812 |
| a0006 | 0/0 | 698 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | MAAAG others(693): Show |
chr9 | 136201333 | 136250812 |
| a0007 | 0/0 | 698 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | MAAAG others(693): Show |
chr9 | 136201333 | 136250812 |
| a0008 | 0/0 | 698 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | MAAAG others(693): Show |
chr9 | 136201333 | 136250812 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2094 | 124 | 54 | 26 | 28 | 1 | 14 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0002 | 0/1 | 2094 | 120 | 17 | 21 | 60 | 4 | 17 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0004 | 0/0 | 2094 | 43 | 0 | 14 | 17 | 6 | 6 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0005 | 0/0 | 2094 | 12 | 9 | 2 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0006 | 0/0 | 2094 | 10 | 0 | 0 | 10 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0007 | 0/0 | 2094 | 4 | 0 | 1 | 2 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0008 | 0/0 | 2094 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0011 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0012 | 0/0 | 2094 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0013 | 0/0 | 2094 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0014 | 0/0 | 2094 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0015 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0017 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0019 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0020 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0023 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0024 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0001c0026 | 0/0 | 2094 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0002c0003 | 0/0 | 2094 | 57 | 2 | 3 | 43 | 3 | 6 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0002c0016 | 0/0 | 2094 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0003c0010 | 0/0 | 2094 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0004c0009 | 0/0 | 2094 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0005c0025 | 0/0 | 2094 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0006c0022 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0007c0021 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 | ||
| a0008c0018 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ATGGC others(2089): Show |
chr9 | 136201333 | 136250812 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4530 | 6 | 1 | 3 | 1 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0002 | 0/0 | 4526 | 3 | 1 | 0 | 1 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4521): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0004 | 0/0 | 4527 | 32 | 8 | 2 | 13 | 1 | 8 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0005 | 0/0 | 4529 | 23 | 4 | 10 | 7 | 0 | 2 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0007 | 0/0 | 4528 | 15 | 9 | 5 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4523): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0008 | 0/0 | 4527 | 11 | 10 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0010 | 0/0 | 4527 | 7 | 7 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0011 | 0/0 | 4528 | 7 | 6 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4523): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0014 | 0/0 | 4527 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0015 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0017 | 0/0 | 4529 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0020 | 0/0 | 4528 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4523): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0021 | 0/0 | 4528 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4523): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0026 | 0/0 | 4513 | 2 | 0 | 0 | 1 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4508): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0029 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0031 | 1/0 | 4501 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4496): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0032 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0033 | 0/0 | 4528 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4523): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0034 | 0/0 | 4529 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0047 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0051 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4521): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0053 | 0/0 | 4528 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4523): Show |
chr9 | 136201333 | 136250812 |
| a0001c0001t0054 | 0/0 | 4515 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4510): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0001 | 0/0 | 4530 | 58 | 6 | 12 | 27 | 1 | 12 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0002 | 0/0 | 4526 | 7 | 0 | 0 | 7 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4521): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0004 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0005 | 0/0 | 4529 | 3 | 0 | 1 | 1 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0006 | 0/0 | 4531 | 18 | 1 | 0 | 14 | 1 | 2 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4526): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0010 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0012 | 0/0 | 4528 | 6 | 5 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4523): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0013 | 0/0 | 4527 | 4 | 0 | 0 | 3 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0014 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0018 | 0/0 | 4531 | 3 | 0 | 3 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4526): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0022 | 0/0 | 4530 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0023 | 0/0 | 4530 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0024 | 0/0 | 4530 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0025 | 0/0 | 4531 | 2 | 0 | 1 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4526): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0035 | 0/0 | 4529 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0037 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0038 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0039 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0040 | 0/0 | 4530 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0042 | 0/1 | 4526 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4521): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0045 | 0/0 | 4531 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4526): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0046 | 0/0 | 4531 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4526): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0049 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0002t0050 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0001c0004t0003 | 0/0 | 4527 | 36 | 0 | 9 | 15 | 6 | 6 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0004t0004 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0004t0016 | 0/0 | 4528 | 3 | 0 | 2 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4523): Show |
chr9 | 136201333 | 136250812 |
| a0001c0004t0019 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0004t0027 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0004t0028 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0005t0001 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0005t0004 | 0/0 | 4527 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0005t0005 | 0/0 | 4529 | 6 | 3 | 2 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0001c0005t0008 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0005t0017 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0001c0006t0009 | 0/0 | 4530 | 9 | 0 | 0 | 9 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0006t0044 | 0/0 | 4531 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4526): Show |
chr9 | 136201333 | 136250812 |
| a0001c0007t0003 | 0/0 | 4527 | 3 | 0 | 0 | 2 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0007t0004 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0008t0013 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0008t0041 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4526): Show |
chr9 | 136201333 | 136250812 |
| a0001c0011t0048 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0012t0002 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4521): Show |
chr9 | 136201333 | 136250812 |
| a0001c0013t0003 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0014t0001 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0015t0005 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0001c0017t0011 | 0/0 | 4528 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4523): Show |
chr9 | 136201333 | 136250812 |
| a0001c0019t0036 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0001c0020t0003 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0001c0023t0030 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0001c0024t0002 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4521): Show |
chr9 | 136201333 | 136250812 |
| a0001c0026t0005 | 0/0 | 4529 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0002c0003t0001 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| a0002c0003t0002 | 0/0 | 4526 | 47 | 1 | 3 | 35 | 3 | 5 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4521): Show |
chr9 | 136201333 | 136250812 |
| a0002c0003t0005 | 0/0 | 4529 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0002c0003t0006 | 0/0 | 4531 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4526): Show |
chr9 | 136201333 | 136250812 |
| a0002c0003t0014 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0002c0003t0015 | 0/0 | 4527 | 3 | 0 | 0 | 2 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0002c0003t0043 | 0/0 | 4531 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4526): Show |
chr9 | 136201333 | 136250812 |
| a0002c0003t0052 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4521): Show |
chr9 | 136201333 | 136250812 |
| a0002c0016t0002 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4521): Show |
chr9 | 136201333 | 136250812 |
| a0003c0010t0007 | 0/0 | 4528 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4523): Show |
chr9 | 136201333 | 136250812 |
| a0004c0009t0004 | 0/0 | 4527 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0005c0025t0002 | 0/0 | 4526 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4521): Show |
chr9 | 136201333 | 136250812 |
| a0006c0022t0005 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4524): Show |
chr9 | 136201333 | 136250812 |
| a0007c0021t0019 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4522): Show |
chr9 | 136201333 | 136250812 |
| a0008c0018t0001 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | ACTTC others(4525): Show |
chr9 | 136201333 | 136250812 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0007g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0008g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0008g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0008g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0010g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0010g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0010g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0010g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0010g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0010g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0011g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0011g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0011g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0014g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0014g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0015g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0017g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0020g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0020g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0021g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0021g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0026g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0026g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0029g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0031g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0032g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0033g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0034g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0047g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0051g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0053g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0001t0054g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0005g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0012g0012 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0012g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0013g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0013g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0013g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0014g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0018g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0018g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0018g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0022g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0022g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0023g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0023g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0024g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0025g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0025g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0035g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0037g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0038g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0039g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0040g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0042g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0045g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0046g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0049g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0002t0050g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0002 | 0/0 | 7 | 0 | 2 | 1 | 2 | 2 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0006 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0016g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0016g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0016g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0019g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0027g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0004t0028g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0005t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0005t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0005t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0005t0005g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0005t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0005t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0005t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0005t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0005t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0005t0017g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0006t0009g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0006t0009g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0006t0009g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0006t0009g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0006t0009g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0006t0044g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0007t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0007t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0007t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0007t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0008t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0008t0041g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0011t0048g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0012t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0013t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0014t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0015t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0017t0011g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0019t0036g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0020t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0023t0030g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0024t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0001c0026t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0001 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0010 | 0/0 | 4 | 0 | 0 | 1 | 2 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0014g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0015g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0015g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0015g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0043g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0003t0052g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0002c0016t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0003c0010t0007g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0004c0009t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0004c0009t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0005c0025t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0006c0022t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0007c0021t0019g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| a0008c0018t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0003 | g0159 | EUR | GBR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0064 | EUR | GBR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00140 | hp1 | a0001 | c0004 | t0003 | g0088 | EUR | GBR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00140 | hp2 | a0001 | c0002 | t0006 | g0071 | EUR | GBR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00280 | hp1 | a0003 | c0010 | t0007 | g0035 | EUR | FIN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00280 | hp2 | a0001 | c0004 | t0003 | g0002 | EUR | FIN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0266 | EUR | FIN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00323 | hp2 | a0001 | c0004 | t0003 | g0002 | EUR | FIN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00408 | hp2 | a0001 | c0002 | t0004 | g0109 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00423 | hp1 | a0001 | c0002 | t0006 | g0093 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00423 | hp2 | a0002 | c0003 | t0052 | g0238 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00438 | hp1 | a0001 | c0002 | t0006 | g0050 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00438 | hp2 | a0002 | c0003 | t0002 | g0246 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00544 | hp1 | a0002 | c0003 | t0043 | g0242 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00544 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00558 | hp2 | a0001 | c0004 | t0003 | g0022 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00609 | hp2 | a0001 | c0004 | t0016 | g0100 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00621 | hp1 | a0001 | c0002 | t0035 | g0066 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00621 | hp2 | a0001 | c0014 | t0001 | g0114 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00639 | hp1 | a0001 | c0004 | t0003 | g0054 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00642 | hp1 | a0001 | c0002 | t0024 | g0024 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00642 | hp2 | a0001 | c0004 | t0003 | g0006 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00673 | hp2 | a0002 | c0003 | t0002 | g0005 | EAS | CHS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0212 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0221 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00741 | hp1 | a0001 | c0004 | t0003 | g0053 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG00741 | hp2 | a0001 | c0001 | t0033 | g0175 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0179 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01070 | hp1 | a0001 | c0001 | t0017 | g0037 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01070 | hp2 | a0001 | c0004 | t0003 | g0103 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0038 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01074 | hp2 | a0001 | c0001 | t0008 | g0033 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01081 | hp1 | a0001 | c0001 | t0017 | g0037 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0214 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01099 | hp2 | a0001 | c0004 | t0016 | g0099 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0190 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01109 | hp2 | a0001 | c0002 | t0012 | g0012 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01167 | hp1 | a0001 | c0005 | t0005 | g0030 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0038 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01168 | hp1 | a0002 | c0003 | t0002 | g0289 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01168 | hp2 | a0001 | c0002 | t0018 | g0116 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01169 | hp1 | a0002 | c0003 | t0002 | g0286 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01169 | hp2 | a0001 | c0005 | t0005 | g0030 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01175 | hp1 | a0005 | c0025 | t0002 | g0172 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01175 | hp2 | a0001 | c0004 | t0028 | g0092 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01192 | hp1 | a0001 | c0002 | t0046 | g0123 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01192 | hp2 | a0001 | c0004 | t0016 | g0097 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0274 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01255 | hp1 | a0001 | c0004 | t0003 | g0052 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01255 | hp2 | a0001 | c0002 | t0018 | g0128 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01261 | hp1 | a0001 | c0004 | t0003 | g0002 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01261 | hp2 | a0001 | c0001 | t0015 | g0203 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01346 | hp2 | a0002 | c0003 | t0002 | g0287 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0213 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01358 | hp2 | a0001 | c0002 | t0024 | g0024 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01361 | hp1 | a0001 | c0002 | t0018 | g0042 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01361 | hp2 | a0001 | c0002 | t0025 | g0133 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01496 | hp1 | a0001 | c0007 | t0004 | g0162 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01496 | hp2 | a0001 | c0001 | t0011 | g0003 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01515 | hp1 | a0002 | c0003 | t0002 | g0283 | EUR | IBS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01515 | hp2 | a0001 | c0004 | t0003 | g0020 | EUR | IBS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01516 | hp1 | a0002 | c0003 | t0002 | g0010 | EUR | IBS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01516 | hp2 | a0003 | c0010 | t0007 | g0035 | EUR | IBS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01517 | hp1 | a0001 | c0004 | t0003 | g0020 | EUR | IBS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01517 | hp2 | a0002 | c0003 | t0002 | g0010 | EUR | IBS | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01884 | hp1 | a0004 | c0009 | t0004 | g0305 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01891 | hp2 | a0001 | c0023 | t0030 | g0298 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0219 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0217 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01952 | hp2 | a0001 | c0004 | t0027 | g0089 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01978 | hp1 | a0001 | c0004 | t0003 | g0087 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01978 | hp2 | a0001 | c0004 | t0004 | g0060 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02004 | hp1 | a0001 | c0004 | t0003 | g0127 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02015 | hp2 | a0001 | c0006 | t0009 | g0028 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02040 | hp1 | a0002 | c0003 | t0002 | g0235 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02040 | hp2 | a0002 | c0003 | t0002 | g0291 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02055 | hp1 | a0001 | c0001 | t0029 | g0189 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0201 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02056 | hp1 | a0002 | c0003 | t0002 | g0010 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02056 | hp2 | a0001 | c0002 | t0006 | g0078 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02071 | hp1 | a0001 | c0026 | t0005 | g0306 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02071 | hp2 | a0001 | c0007 | t0003 | g0137 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02074 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02080 | hp1 | a0001 | c0002 | t0006 | g0135 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02080 | hp2 | a0001 | c0002 | t0006 | g0149 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02083 | hp1 | a0001 | c0005 | t0005 | g0297 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02083 | hp2 | a0001 | c0013 | t0003 | g0098 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02129 | hp1 | a0001 | c0001 | t0032 | g0295 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02129 | hp2 | a0001 | c0007 | t0003 | g0095 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02132 | hp1 | a0001 | c0002 | t0006 | g0111 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02135 | hp1 | a0001 | c0002 | t0006 | g0043 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0252 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02145 | hp2 | a0001 | c0002 | t0038 | g0084 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | CDX | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | CDX | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02165 | hp1 | a0001 | c0001 | t0026 | g0307 | EAS | CDX | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02165 | hp2 | a0002 | c0003 | t0002 | g0241 | EAS | CDX | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0032 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02258 | hp1 | a0001 | c0001 | t0053 | g0303 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0195 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02280 | hp1 | a0001 | c0002 | t0049 | g0110 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02280 | hp2 | a0006 | c0022 | t0005 | g0276 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02293 | hp1 | a0001 | c0002 | t0005 | g0148 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0223 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0215 | AMR | PEL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02451 | hp1 | a0001 | c0015 | t0005 | g0136 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02451 | hp2 | a0001 | c0002 | t0050 | g0083 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02523 | hp1 | a0001 | c0004 | t0003 | g0063 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02572 | hp2 | a0001 | c0001 | t0010 | g0176 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0178 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02615 | hp1 | a0001 | c0017 | t0011 | g0168 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02615 | hp2 | a0001 | c0008 | t0041 | g0049 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0057 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02630 | hp2 | a0001 | c0002 | t0014 | g0124 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02647 | hp1 | a0001 | c0002 | t0012 | g0012 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0250 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02698 | hp1 | a0001 | c0004 | t0003 | g0006 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02698 | hp2 | a0001 | c0007 | t0003 | g0126 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0255 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02723 | hp2 | a0001 | c0020 | t0003 | g0171 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02738 | hp1 | a0002 | c0003 | t0002 | g0010 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0077 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02809 | hp2 | a0001 | c0002 | t0012 | g0046 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0278 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0300 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0251 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0131 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02896 | hp1 | a0001 | c0005 | t0005 | g0183 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02896 | hp2 | a0001 | c0001 | t0010 | g0253 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02897 | hp1 | a0001 | c0005 | t0005 | g0184 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0299 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02922 | hp2 | a0007 | c0021 | t0019 | g0170 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0281 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0273 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02970 | hp1 | a0004 | c0009 | t0004 | g0304 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02970 | hp2 | a0001 | c0005 | t0004 | g0186 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0280 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0033 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03041 | hp1 | a0008 | c0018 | t0001 | g0169 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0198 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03098 | hp1 | a0001 | c0002 | t0012 | g0044 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03098 | hp2 | a0001 | c0001 | t0020 | g0196 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0279 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0032 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03139 | hp1 | a0001 | c0001 | t0014 | g0249 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03195 | hp2 | a0001 | c0002 | t0010 | g0041 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0243 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03209 | hp2 | a0002 | c0003 | t0014 | g0245 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03225 | hp2 | a0001 | c0011 | t0048 | g0091 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03239 | hp1 | a0002 | c0003 | t0002 | g0244 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03239 | hp2 | a0001 | c0004 | t0003 | g0006 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03453 | hp1 | a0001 | c0005 | t0008 | g0199 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03453 | hp2 | a0001 | c0001 | t0020 | g0282 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03486 | hp1 | a0001 | c0002 | t0012 | g0045 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03486 | hp2 | a0001 | c0005 | t0005 | g0181 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0209 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03490 | hp2 | a0001 | c0004 | t0003 | g0002 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0211 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | ESN | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0173 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | GWD | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0206 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03669 | hp1 | a0001 | c0002 | t0006 | g0090 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03669 | hp2 | a0001 | c0002 | t0005 | g0074 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0265 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03688 | hp2 | a0001 | c0004 | t0003 | g0101 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0257 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03710 | hp1 | a0001 | c0002 | t0006 | g0132 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0262 | SAS | PJL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03831 | hp1 | a0002 | c0003 | t0002 | g0228 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03831 | hp2 | a0001 | c0001 | t0026 | g0308 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0025 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0269 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03927 | hp1 | a0002 | c0003 | t0002 | g0284 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03927 | hp2 | a0001 | c0004 | t0003 | g0006 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03942 | hp1 | a0002 | c0003 | t0015 | g0285 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0263 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG04115 | hp1 | a0001 | c0002 | t0025 | g0129 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0086 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG04184 | hp1 | a0002 | c0003 | t0002 | g0288 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG04184 | hp2 | a0001 | c0004 | t0003 | g0002 | SAS | BEB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG04199 | hp1 | a0001 | c0001 | t0007 | g0220 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0258 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0073 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0069 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0015 | SAS | STU | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0174 | AFR | YRI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0275 | AFR | YRI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18612 | hp1 | a0001 | c0012 | t0002 | g0094 | EAS | CHB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18612 | hp2 | a0001 | c0001 | t0034 | g0216 | EAS | CHB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18906 | hp1 | a0001 | c0005 | t0004 | g0191 | AFR | YRI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0193 | AFR | YRI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18941 | hp1 | a0002 | c0003 | t0002 | g0294 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18942 | hp2 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18944 | hp2 | a0001 | c0004 | t0003 | g0022 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18946 | hp1 | a0001 | c0004 | t0003 | g0014 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18946 | hp2 | a0001 | c0006 | t0009 | g0107 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18947 | hp1 | a0002 | c0003 | t0002 | g0230 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18947 | hp2 | a0001 | c0002 | t0006 | g0139 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18948 | hp2 | a0001 | c0002 | t0022 | g0119 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18952 | hp1 | a0002 | c0003 | t0002 | g0005 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18952 | hp2 | a0001 | c0006 | t0044 | g0147 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18954 | hp1 | a0001 | c0004 | t0019 | g0104 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18959 | hp1 | a0002 | c0003 | t0002 | g0036 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18961 | hp1 | a0002 | c0003 | t0002 | g0232 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18962 | hp1 | a0001 | c0006 | t0009 | g0144 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18962 | hp2 | a0002 | c0016 | t0002 | g0161 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18963 | hp1 | a0001 | c0002 | t0022 | g0115 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18963 | hp2 | a0002 | c0003 | t0002 | g0293 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18964 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18965 | hp1 | a0001 | c0002 | t0006 | g0142 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18965 | hp2 | a0002 | c0003 | t0002 | g0005 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18966 | hp2 | a0002 | c0003 | t0002 | g0204 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18967 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18968 | hp1 | a0002 | c0003 | t0002 | g0005 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18968 | hp2 | a0001 | c0002 | t0039 | g0145 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18973 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18977 | hp1 | a0001 | c0004 | t0003 | g0059 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18977 | hp2 | a0001 | c0002 | t0013 | g0120 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18979 | hp1 | a0001 | c0004 | t0003 | g0048 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18983 | hp1 | a0001 | c0002 | t0006 | g0112 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18983 | hp2 | a0001 | c0002 | t0006 | g0146 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18985 | hp1 | a0001 | c0002 | t0006 | g0051 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18985 | hp2 | a0001 | c0004 | t0003 | g0014 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18986 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18986 | hp2 | a0001 | c0004 | t0003 | g0106 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18988 | hp1 | a0001 | c0006 | t0009 | g0007 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18988 | hp2 | a0002 | c0003 | t0015 | g0239 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18990 | hp1 | a0001 | c0006 | t0009 | g0007 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18990 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18992 | hp1 | a0002 | c0003 | t0006 | g0218 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18992 | hp2 | a0002 | c0003 | t0005 | g0236 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18998 | hp1 | a0001 | c0002 | t0013 | g0023 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19000 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19000 | hp2 | a0001 | c0001 | t0021 | g0268 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19004 | hp1 | a0002 | c0003 | t0002 | g0233 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19005 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19007 | hp1 | a0001 | c0004 | t0003 | g0138 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19007 | hp2 | a0001 | c0006 | t0009 | g0007 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19009 | hp1 | a0002 | c0003 | t0002 | g0231 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19010 | hp1 | a0001 | c0006 | t0009 | g0028 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19010 | hp2 | a0001 | c0002 | t0005 | g0113 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19011 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19030 | hp1 | a0001 | c0001 | t0047 | g0234 | AFR | LWK | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0301 | AFR | LWK | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19043 | hp1 | a0001 | c0019 | t0036 | g0254 | AFR | LWK | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0207 | AFR | LWK | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19057 | hp1 | a0002 | c0003 | t0002 | g0036 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19057 | hp2 | a0001 | c0001 | t0054 | g0309 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19058 | hp1 | a0001 | c0006 | t0009 | g0157 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19058 | hp2 | a0001 | c0001 | t0021 | g0177 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19064 | hp2 | a0001 | c0002 | t0013 | g0023 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19065 | hp2 | a0001 | c0002 | t0037 | g0160 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19066 | hp1 | a0001 | c0004 | t0003 | g0062 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19068 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19070 | hp1 | a0002 | c0003 | t0002 | g0240 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19070 | hp2 | a0001 | c0006 | t0009 | g0007 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19078 | hp1 | a0002 | c0003 | t0015 | g0205 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19078 | hp2 | a0001 | c0002 | t0006 | g0154 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19079 | hp1 | a0001 | c0004 | t0003 | g0108 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19079 | hp2 | a0002 | c0003 | t0002 | g0005 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19081 | hp1 | a0001 | c0004 | t0003 | g0058 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19084 | hp1 | a0001 | c0004 | t0003 | g0014 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19084 | hp2 | a0002 | c0003 | t0006 | g0237 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19085 | hp1 | a0001 | c0004 | t0003 | g0105 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19085 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19087 | hp1 | a0002 | c0003 | t0002 | g0227 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19087 | hp2 | a0001 | c0002 | t0023 | g0067 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19088 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19088 | hp2 | a0001 | c0002 | t0023 | g0061 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19090 | hp1 | a0001 | c0002 | t0006 | g0153 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19090 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0197 | AFR | YRI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA19240 | hp2 | a0001 | c0008 | t0013 | g0047 | AFR | YRI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA20752 | hp1 | a0001 | c0002 | t0013 | g0122 | EUR | TSI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA20752 | hp2 | a0001 | c0002 | t0045 | g0076 | EUR | TSI | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0180 | SAS | GIH | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA20905 | hp2 | a0001 | c0002 | t0040 | g0075 | SAS | GIH | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG01123 | hp2 | a0001 | c0004 | t0003 | g0002 | AMR | CLM | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0192 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02109 | hp2 | a0001 | c0005 | t0004 | g0187 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02486 | hp1 | a0001 | c0005 | t0017 | g0182 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0226 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0248 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0194 | AFR | ACB | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03471 | hp1 | a0001 | c0001 | t0051 | g0202 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG03471 | hp2 | a0001 | c0002 | t0012 | g0012 | AFR | MSL | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG06807 | hp1 | a0002 | c0003 | t0002 | g0277 | AFR | USA | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0200 | AFR | USA | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA18955 | hp2 | a0002 | c0003 | t0001 | g0292 | EAS | JPT | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0302 | AFR | LWK | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| NA21309 | hp2 | a0001 | c0024 | t0002 | g0229 | AFR | LWK | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0042 | g0085 | REF | REF | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0031 | g0272 | REF | REF | QSOX2_chr9_136201333_136250812 | QSOX2 | chr9 | 136201333 | 136250812 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:136208898 | T | C | 1 | a0006 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.1927A>G | p.Lys643Glu | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1936/4501 | 1927/2097 | 643/698 | chr9 | 136208898 | |||
| chr9:136209255 | G | A | 1 | a0005 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.1570C>T | p.Arg524Trp | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1579/4501 | 1570/2097 | 524/698 | chr9 | 136209255 | |||
| chr9:136211431 | G | A | 1 | a0007 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1382C>T | p.Ala461Val | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/12 | 1391/4501 | 1382/2097 | 461/698 | chr9 | 136211431 | |||
| chr9:136215249 | C | T | 1 | a0004 | 2 | HG01884.hp1 HG02970.hp1 |
missense_variant | MODERATE | c.1265G>A | p.Arg422Gln | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/12 | 1274/4501 | 1265/2097 | 422/698 | chr9 | 136215249 | |||
| chr9:136218710 | G | A | 1 | a0003 | 2 | HG00280.hp1 HG01516.hp2 |
missense_variant | MODERATE | c.1055C>T | p.Thr352Met | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/12 | 1064/4501 | 1055/2097 | 352/698 | chr9 | 136218710 | |||
| chr9:136226827 | T | C | 2 | a0002 a0005 |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
missense_variant | MODERATE | c.376A>G | p.Lys126Glu | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/12 | 385/4501 | 376/2097 | 126/698 | chr9 | 136226827 | |||
| chr9:136245599 | C | G | 1 | a0008 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.205G>C | p.Gly69Arg | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/12 | 214/4501 | 205/2097 | 69/698 | chr9 | 136245599 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:136208821 | G | A | 1 | a0001c0006 | 10 | HG02015.hp2 NA18946.hp2 NA18952.hp2 others(7): Show |
synonymous_variant | LOW | c.2004C>T | p.Tyr668Tyr | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 2013/4501 | 2004/2097 | 668/698 | chr9 | 136208821 | |||
| chr9:136208887 | G | A | 1 | a0001c0013 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1938C>T | p.Gly646Gly | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1947/4501 | 1938/2097 | 646/698 | chr9 | 136208887 | |||
| chr9:136208959 | T | C | 5 | a0001c0004 a0001c0007 a0001c0013 others(2): Show |
50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
synonymous_variant | LOW | c.1866A>G | p.Pro622Pro | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1875/4501 | 1866/2097 | 622/698 | chr9 | 136208959 | |||
| chr9:136209043 | G | A | 1 | a0001c0014 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.1782C>T | p.Leu594Leu | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1791/4501 | 1782/2097 | 594/698 | chr9 | 136209043 | |||
| chr9:136211406 | G | A | 1 | a0001c0023 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1407C>T | p.Tyr469Tyr | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/12 | 1416/4501 | 1407/2097 | 469/698 | chr9 | 136211406 | |||
| chr9:136216639 | G | A | 1 | a0001c0015 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1170C>T | p.Pro390Pro | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/12 | 1179/4501 | 1170/2097 | 390/698 | chr9 | 136216639 | |||
| chr9:136218808 | C | T | 3 | a0001c0004 a0001c0012 a0001c0013 |
45 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(42): Show |
splice_region_variant&synonymous_variant | LOW | c.957G>A | p.Lys319Lys | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/12 | 966/4501 | 957/2097 | 319/698 | chr9 | 136218808 | |||
| chr9:136219113 | A | G | 5 | a0001c0005 a0001c0008 a0001c0020 others(2): Show |
17 | HG01167.hp1 HG01169.hp2 HG02083.hp1 others(14): Show |
synonymous_variant | LOW | c.873T>C | p.Asp291Asp | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 7/12 | 882/4501 | 873/2097 | 291/698 | chr9 | 136219113 | |||
| chr9:136219137 | C | T | 1 | a0001c0019 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.849G>A | p.Ser283Ser | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 7/12 | 858/4501 | 849/2097 | 283/698 | chr9 | 136219137 | |||
| chr9:136221813 | C | G | 1 | a0001c0011 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.804G>C | p.Ser268Ser | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/12 | 813/4501 | 804/2097 | 268/698 | chr9 | 136221813 | |||
| chr9:136224020 | G | A | 1 | a0001c0024 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.571C>T | p.Leu191Leu | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 4/12 | 580/4501 | 571/2097 | 191/698 | chr9 | 136224020 | |||
| chr9:136245561 | C | A | 1 | a0001c0026 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.243G>T | p.Ala81Ala | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/12 | 252/4501 | 243/2097 | 81/698 | chr9 | 136245561 | |||
| chr9:136245699 | C | G | 1 | a0001c0017 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.105G>C | p.Arg35Arg | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/12 | 114/4501 | 105/2097 | 35/698 | chr9 | 136245699 | |||
| chr9:136245780 | C | T | 11 | a0001c0002 a0001c0004 a0001c0006 others(8): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
synonymous_variant | LOW | c.24G>A | p.Val8Val | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/12 | 33/4501 | 24/2097 | 8/698 | chr9 | 136245780 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:136206370 | C | T | 1 | a0001c0002t0037 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2358G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 2358 | chr9 | 136206370 | ||||||
| chr9:136206537 | A | T | 3 | a0001c0001t0026 a0001c0001t0032 a0001c0001t0054 |
4 | HG02129.hp1 HG02165.hp1 HG03831.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2191T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 2191 | chr9 | 136206537 | ||||||
| chr9:136206567 | A | G | 2 | a0001c0002t0022 a0001c0002t0037 |
3 | NA18948.hp2 NA18963.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2161T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 2161 | chr9 | 136206567 | ||||||
| chr9:136206624 | T | C | 2 | a0001c0001t0011 a0001c0017t0011 |
8 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2104A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 2104 | chr9 | 136206624 | ||||||
| chr9:136206668 | AC | A | 3 | a0001c0002t0024 a0001c0002t0038 a0001c0002t0046 |
4 | HG00642.hp1 HG01192.hp1 HG01358.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2059delG | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 2059 | chr9 | 136206668 | ||||||
| chr9:136206799 | G | A | 2 | a0001c0006t0009 a0001c0006t0044 |
10 | HG02015.hp2 NA18946.hp2 NA18952.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1929C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1929 | chr9 | 136206799 | ||||||
| chr9:136206885 | A | C | 3 | a0001c0001t0014 a0001c0002t0014 a0002c0003t0014 |
4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1843T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1843 | chr9 | 136206885 | ||||||
| chr9:136207087 | G | A | 1 | a0001c0001t0051 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1641C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1641 | chr9 | 136207087 | ||||||
| chr9:136207096 | G | A | 2 | a0001c0002t0024 a0001c0002t0046 |
3 | HG00642.hp1 HG01192.hp1 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1632C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1632 | chr9 | 136207096 | ||||||
| chr9:136207227 | A | G | 42 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(39): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*1501T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1501 | chr9 | 136207227 | ||||||
| chr9:136207266 | T | C | 1 | a0001c0002t0039 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1462A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1462 | chr9 | 136207266 | ||||||
| chr9:136207342 | G | A | 2 | a0001c0002t0040 a0001c0002t0045 |
2 | NA20752.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1386C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1386 | chr9 | 136207342 | ||||||
| chr9:136207359 | TCTCATAC others(5): Show |
T | 1 | a0001c0001t0054 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1357_*1368delTGTG others(8): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1357 | chr9 | 136207359 | ||||||
| chr9:136207359 | TCTCATAC others(7): Show |
T | 1 | a0001c0001t0026 | 2 | HG02165.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1355_*1368delTGTG others(10): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1355 | chr9 | 136207359 | ||||||
| chr9:136207364 | T | TAC | 7 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0010 others(4): Show |
14 | HG01243.hp1 HG02451.hp1 HG02717.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1362_*1363dupGT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | ||||||
| chr9:136207364 | T | TACAC | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(5): Show |
17 | HG01167.hp1 HG01169.hp2 HG01261.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1360_*1363dupGTGT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | ||||||
| chr9:136207364 | T | TACACAC | 23 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(20): Show |
83 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1358_*1363dupGTGT others(2): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | ||||||
| chr9:136207364 | T | TACACACA others(1): Show |
7 | a0001c0001t0007 a0001c0001t0010 a0001c0002t0002 others(4): Show |
11 | HG00558.hp2 HG01884.hp1 HG02056.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1356_*1363dupGTGT others(4): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | ||||||
| chr9:136207364 | T | TACACACA others(3): Show |
6 | a0001c0001t0010 a0001c0001t0014 a0002c0003t0002 others(3): Show |
7 | HG02559.hp1 HG02886.hp2 HG03139.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1354_*1363dupGTGT others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | ||||||
| chr9:136207364 | T | TACACACA others(5): Show |
1 | a0001c0002t0002 | 4 | NA18954.hp2 NA18971.hp2 NA18975.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1352_*1363dupGTGT others(8): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | ||||||
| chr9:136207364 | T | TACACACA others(9): Show |
1 | a0001c0002t0002 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1348_*1363dupGTGT others(12): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1363 | chr9 | 136207364 | ||||||
| chr9:136207364 | TAC | T | 15 | a0001c0001t0020 a0001c0002t0001 a0001c0002t0006 others(12): Show |
47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1362_*1363delGT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1362 | chr9 | 136207364 | ||||||
| chr9:136207364 | TACAC | T | 36 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(33): Show |
151 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*1360_*1363delGTGT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1360 | chr9 | 136207364 | ||||||
| chr9:136207364 | TACACAC | T | 7 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0017 others(4): Show |
9 | HG01070.hp1 HG01081.hp1 HG01891.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1358_*1363delGTGT others(2): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1358 | chr9 | 136207364 | ||||||
| chr9:136207364 | TACACACA others(3): Show |
T | 2 | a0001c0002t0001 a0002c0003t0002 |
2 | HG06807.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1354_*1363delGTGT others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1354 | chr9 | 136207364 | ||||||
| chr9:136207374 | C | T | 1 | a0001c0001t0054 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1354G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1354 | chr9 | 136207374 | ||||||
| chr9:136207376 | C | T | 1 | a0001c0001t0026 | 2 | HG02165.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1352G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1352 | chr9 | 136207376 | ||||||
| chr9:136207566 | C | T | 1 | a0001c0002t0035 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1162G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1162 | chr9 | 136207566 | ||||||
| chr9:136207605 | A | C | 86 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(83): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
3_prime_UTR_variant | MODIFIER | c.*1123T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1123 | chr9 | 136207605 | ||||||
| chr9:136207625 | C | G | 6 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0033 others(3): Show |
13 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1103G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 1103 | chr9 | 136207625 | ||||||
| chr9:136207749 | G | T | 1 | a0001c0001t0032 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 979 | chr9 | 136207749 | ||||||
| chr9:136207754 | G | C | 2 | a0001c0002t0023 a0001c0002t0035 |
3 | HG00621.hp1 NA19087.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*974C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 974 | chr9 | 136207754 | ||||||
| chr9:136207781 | G | A | 1 | a0001c0004t0028 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*947C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 947 | chr9 | 136207781 | ||||||
| chr9:136207782 | C | T | 3 | a0001c0008t0041 a0001c0011t0048 a0001c0019t0036 |
3 | HG02615.hp2 HG03225.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*946G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 946 | chr9 | 136207782 | ||||||
| chr9:136207855 | C | A | 1 | a0002c0003t0052 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*873G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 873 | chr9 | 136207855 | ||||||
| chr9:136207939 | G | A | 1 | a0001c0001t0053 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*789C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 789 | chr9 | 136207939 | ||||||
| chr9:136208072 | G | C | 1 | a0001c0004t0028 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*656C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 656 | chr9 | 136208072 | ||||||
| chr9:136208081 | C | G | 6 | a0001c0001t0008 a0001c0001t0026 a0001c0001t0029 others(3): Show |
17 | HG01074.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*647G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 647 | chr9 | 136208081 | ||||||
| chr9:136208139 | AAC | A | 2 | a0001c0001t0004 a0001c0005t0004 |
9 | HG01069.hp2 HG01106.hp1 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*587_*588delGT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 587 | chr9 | 136208139 | ||||||
| chr9:136208192 | C | T | 2 | a0001c0004t0019 a0007c0021t0019 |
2 | HG02922.hp2 NA18954.hp1 |
3_prime_UTR_variant | MODIFIER | c.*536G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 536 | chr9 | 136208192 | ||||||
| chr9:136208218 | C | A | 1 | a0001c0001t0020 | 2 | HG03098.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*510G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 510 | chr9 | 136208218 | ||||||
| chr9:136208242 | C | G | 1 | a0001c0001t0034 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*486G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 486 | chr9 | 136208242 | ||||||
| chr9:136208252 | G | A | 2 | a0001c0001t0008 a0001c0005t0008 |
12 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*476C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 476 | chr9 | 136208252 | ||||||
| chr9:136208284 | A | G | 1 | a0001c0001t0020 | 2 | HG03098.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*444T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 444 | chr9 | 136208284 | ||||||
| chr9:136208289 | A | AGTGGAGG others(21): Show |
1 | a0001c0023t0030 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*438_*439insCCACCT others(22): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 438 | chr9 | 136208289 | ||||||
| chr9:136208291 | T | TGGAGGGT others(22): Show |
1 | a0001c0001t0047 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436_*437insCCCCGA others(23): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | ||||||
| chr9:136208291 | T | TGGAGGGT others(19): Show |
36 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(33): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*437insCCACCT others(20): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | ||||||
| chr9:136208291 | T | TGGAGGGT others(20): Show |
12 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0015 others(9): Show |
44 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*437insCCCACC others(21): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | ||||||
| chr9:136208291 | T | TGGAGGGT others(21): Show |
12 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0034 others(9): Show |
42 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*437insCCCCAC others(22): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | ||||||
| chr9:136208291 | T | TGGAGGGT others(22): Show |
1 | a0001c0011t0048 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*436_*437insGCCCCA others(23): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | ||||||
| chr9:136208291 | T | TGGAGGGT others(22): Show |
15 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0022 others(12): Show |
87 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*437insCCCCCA others(23): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | ||||||
| chr9:136208291 | T | TGGAGGGT others(23): Show |
9 | a0001c0002t0006 a0001c0002t0018 a0001c0002t0024 others(6): Show |
31 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*437insCCCCCC others(24): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | ||||||
| chr9:136208291 | T | TGGAGGGT others(24): Show |
1 | a0001c0002t0046 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436_*437insCCCCCC others(25): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 436 | chr9 | 136208291 | ||||||
| chr9:136208294 | G | C | 2 | a0001c0002t0025 a0001c0002t0049 |
3 | HG01361.hp2 HG02280.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*434C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 434 | chr9 | 136208294 | ||||||
| chr9:136208313 | G | C | 1 | a0001c0002t0050 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*415C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 415 | chr9 | 136208313 | ||||||
| chr9:136208314 | G | T | 1 | a0001c0001t0029 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*414C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 414 | chr9 | 136208314 | ||||||
| chr9:136208524 | T | C | 1 | a0001c0002t0012 | 6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*204A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 204 | chr9 | 136208524 | ||||||
| chr9:136208567 | C | T | 9 | a0001c0004t0003 a0001c0004t0016 a0001c0004t0019 others(6): Show |
48 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*161G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 161 | chr9 | 136208567 | ||||||
| chr9:136208568 | GT | G | 11 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0051 others(8): Show |
67 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*159delA | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 159 | chr9 | 136208568 | ||||||
| chr9:136208607 | C | T | 2 | a0001c0004t0027 a0001c0004t0028 |
2 | HG01175.hp2 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*121G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 121 | chr9 | 136208607 | ||||||
| chr9:136208628 | T | G | 1 | a0001c0001t0053 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 100 | chr9 | 136208628 | ||||||
| chr9:136208673 | C | T | 2 | a0001c0001t0008 a0001c0005t0008 |
12 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*55G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 12/12 | 55 | chr9 | 136208673 | ||||||
| chr9:136245807 | G | A | 2 | a0001c0001t0026 a0001c0001t0054 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
5_prime_UTR_variant | MODIFIER | c.-4C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/12 | 4 | chr9 | 136245807 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:136209329 | C | T | 2 | a0001c0001t0004g0262 a0001c0001t0004g0263 |
2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1550-54G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209329 | |||||||
| chr9:136209485 | C | T | 1 | a0001c0001t0029g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1550-210G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209485 | |||||||
| chr9:136209519 | G | T | 1 | a0001c0001t0007g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1550-244C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209519 | |||||||
| chr9:136209528 | C | T | 1 | a0001c0001t0053g0303 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1550-253G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209528 | |||||||
| chr9:136209543 | C | T | 2 | a0001c0001t0020g0196 a0001c0001t0020g0282 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1550-268G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209543 | |||||||
| chr9:136209672 | C | A | 9 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(6): Show |
12 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1550-397G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209672 | |||||||
| chr9:136209724 | C | T | 36 | a0001c0002t0001g0143 a0001c0004t0003g0002 a0001c0004t0003g0006 others(33): Show |
49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1550-449G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209724 | |||||||
| chr9:136209737 | G | T | 130 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(127): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1550-462C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209737 | |||||||
| chr9:136209765 | T | C | 7 | a0001c0001t0007g0193 a0001c0001t0007g0194 a0001c0001t0007g0195 others(4): Show |
11 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1550-490A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209765 | |||||||
| chr9:136209828 | C | T | 2 | a0001c0001t0004g0269 a0001c0001t0010g0251 |
2 | HG02886.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1550-553G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209828 | |||||||
| chr9:136209925 | C | T | 3 | a0004c0009t0004g0304 a0004c0009t0004g0305 a0007c0021t0019g0170 |
3 | HG01884.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1550-650G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209925 | |||||||
| chr9:136209926 | G | A | 108 | a0001c0001t0002g0247 a0001c0001t0002g0264 a0001c0001t0002g0296 others(105): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1550-651C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209926 | |||||||
| chr9:136209930 | G | A | 7 | a0001c0001t0005g0040 a0001c0001t0005g0278 a0001c0005t0005g0030 others(4): Show |
9 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1550-655C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209930 | |||||||
| chr9:136209947 | G | A | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1550-672C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209947 | |||||||
| chr9:136209963 | G | A | 1 | a0001c0001t0020g0282 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1550-688C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209963 | |||||||
| chr9:136209990 | A | G | 1 | a0001c0006t0009g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1550-715T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136209990 | |||||||
| chr9:136210101 | G | T | 15 | a0001c0001t0005g0040 a0001c0001t0005g0278 a0001c0001t0007g0193 others(12): Show |
17 | HG01167.hp1 HG01169.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1550-826C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210101 | |||||||
| chr9:136210108 | C | T | 1 | a0001c0001t0005g0278 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1550-833G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210108 | |||||||
| chr9:136210298 | G | C | 84 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(81): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1549+966C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210298 | |||||||
| chr9:136210471 | C | G | 53 | a0001c0001t0004g0011 a0001c0001t0004g0029 a0001c0001t0004g0256 others(50): Show |
70 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.1549+793G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210471 | |||||||
| chr9:136210473 | G | C | 1 | a0001c0002t0018g0116 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1549+791C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210473 | |||||||
| chr9:136210484 | G | C | 1 | a0001c0001t0029g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1549+780C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210484 | |||||||
| chr9:136210498 | C | T | 1 | a0001c0002t0006g0051 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1549+766G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210498 | |||||||
| chr9:136210499 | G | A | 1 | a0001c0005t0001g0192 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1549+765C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210499 | |||||||
| chr9:136210502 | G | A | 6 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0026g0308 others(3): Show |
6 | HG00741.hp2 HG02129.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1549+762C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210502 | |||||||
| chr9:136210532 | C | A | 1 | a0005c0025t0002g0172 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1549+732G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210532 | |||||||
| chr9:136210565 | C | T | 1 | a0001c0004t0003g0105 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1549+699G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210565 | |||||||
| chr9:136210604 | G | A | 21 | a0001c0001t0002g0264 a0001c0001t0004g0011 a0001c0001t0004g0029 others(18): Show |
25 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1549+660C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210604 | |||||||
| chr9:136210611 | A | G | 1 | a0001c0001t0029g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1549+653T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210611 | |||||||
| chr9:136210747 | T | C | 1 | a0001c0002t0038g0084 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1549+517A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210747 | |||||||
| chr9:136210759 | A | G | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1549+505T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210759 | |||||||
| chr9:136210769 | G | T | 1 | a0001c0004t0003g0058 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1549+495C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210769 | |||||||
| chr9:136210813 | T | C | 1 | a0001c0002t0006g0149 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1549+451A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210813 | |||||||
| chr9:136210877 | G | A | 1 | a0001c0001t0029g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1549+387C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210877 | |||||||
| chr9:136210985 | G | C | 37 | a0001c0004t0003g0002 a0001c0004t0003g0006 a0001c0004t0003g0014 others(34): Show |
50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1549+279C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136210985 | |||||||
| chr9:136211061 | A | AAGCCGGG others(9): Show |
7 | a0001c0001t0007g0193 a0001c0001t0007g0194 a0001c0001t0007g0195 others(4): Show |
11 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1549+187_1549+202d others(18): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136211061 | |||||||
| chr9:136211066 | G | A | 1 | a0001c0002t0001g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1549+198C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136211066 | |||||||
| chr9:136211131 | C | T | 1 | a0001c0002t0035g0066 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1549+133G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136211131 | |||||||
| chr9:136211151 | C | T | 1 | a0002c0003t0006g0218 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1549+113G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136211151 | |||||||
| chr9:136211182 | G | A | 17 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(14): Show |
20 | HG00741.hp2 HG01074.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1549+82C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 11/11 | chr9 | 136211182 | |||||||
| chr9:136211480 | C | T | 1 | a0001c0004t0003g0138 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1361-28G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211480 | |||||||
| chr9:136211536 | A | G | 7 | a0001c0001t0007g0255 a0001c0001t0007g0274 a0001c0001t0007g0299 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1361-84T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211536 | |||||||
| chr9:136211633 | C | T | 1 | a0001c0004t0003g0048 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1361-181G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211633 | |||||||
| chr9:136211732 | G | A | 1 | a0001c0001t0005g0223 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1361-280C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211732 | |||||||
| chr9:136211738 | G | A | 1 | a0001c0008t0013g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1361-286C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211738 | |||||||
| chr9:136211758 | G | A | 7 | a0001c0001t0005g0040 a0001c0001t0005g0278 a0001c0005t0005g0030 others(4): Show |
9 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1361-306C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211758 | |||||||
| chr9:136211804 | T | C | 1 | a0001c0001t0047g0234 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-352A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211804 | |||||||
| chr9:136211863 | T | C | 1 | a0001c0001t0029g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1361-411A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211863 | |||||||
| chr9:136211938 | G | A | 1 | a0001c0001t0029g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1361-486C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136211938 | |||||||
| chr9:136212109 | G | A | 56 | a0001c0001t0002g0264 a0001c0001t0004g0011 a0001c0001t0004g0029 others(53): Show |
73 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1361-657C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212109 | |||||||
| chr9:136212244 | C | T | 1 | a0001c0004t0003g0006 | 4 | HG00642.hp2 HG02698.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1361-792G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212244 | |||||||
| chr9:136212515 | C | T | 5 | a0001c0001t0004g0039 a0001c0001t0004g0275 a0001c0001t0004g0279 others(2): Show |
6 | HG01884.hp2 HG02965.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1361-1063G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212515 | |||||||
| chr9:136212528 | G | GAGAGC | 7 | a0001c0001t0007g0255 a0001c0001t0007g0274 a0001c0001t0007g0299 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1361-1081_1361-107 others(9): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212528 | |||||||
| chr9:136212608 | G | A | 1 | a0001c0001t0002g0296 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1361-1156C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212608 | |||||||
| chr9:136212761 | C | A | 1 | a0001c0002t0018g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1361-1309G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212761 | |||||||
| chr9:136212799 | A | T | 3 | a0001c0001t0004g0185 a0001c0001t0004g0188 a0001c0001t0004g0190 |
3 | HG01106.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1361-1347T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136212799 | |||||||
| chr9:136213147 | G | C | 1 | a0001c0001t0005g0215 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1361-1695C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213147 | |||||||
| chr9:136213216 | C | A | 9 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(6): Show |
12 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1361-1764G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213216 | |||||||
| chr9:136213243 | G | GT | 14 | a0001c0001t0011g0003 a0001c0001t0011g0173 a0001c0001t0011g0197 others(11): Show |
16 | HG01106.hp2 HG01496.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1361-1792dupA | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213243 | |||||||
| chr9:136213243 | GT | G | 72 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(69): Show |
88 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.1361-1792delA | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213243 | |||||||
| chr9:136213243 | GTT | G | 58 | a0001c0001t0002g0264 a0001c0001t0004g0011 a0001c0001t0004g0029 others(55): Show |
75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1361-1793_1361-179 others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213243 | |||||||
| chr9:136213243 | GTTTT | G | 8 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 others(5): Show |
11 | HG02165.hp1 HG02738.hp1 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-1795_1361-179 others(8): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213243 | |||||||
| chr9:136213243 | GTTTTT | G | 46 | a0001c0001t0002g0247 a0001c0001t0004g0178 a0001c0001t0004g0179 others(43): Show |
62 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1361-1796_1361-179 others(9): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213243 | |||||||
| chr9:136213243 | GTTTTTT | G | 6 | a0001c0002t0002g0008 a0001c0002t0002g0166 a0001c0002t0006g0154 others(3): Show |
6 | HG01516.hp1 NA18954.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1361-1797_1361-179 others(10): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213243 | |||||||
| chr9:136213255 | T | G | 7 | a0001c0001t0007g0255 a0001c0001t0007g0274 a0001c0001t0007g0299 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1361-1803A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213255 | |||||||
| chr9:136213263 | T | C | 1 | a0001c0008t0013g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1361-1811A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213263 | |||||||
| chr9:136213383 | T | C | 54 | a0001c0001t0002g0247 a0001c0001t0004g0178 a0001c0001t0004g0179 others(51): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1360+1771A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213383 | |||||||
| chr9:136213400 | C | T | 1 | a0001c0001t0004g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1360+1754G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213400 | |||||||
| chr9:136213469 | TTC | T | 3 | a0001c0001t0004g0185 a0001c0001t0004g0188 a0001c0001t0004g0190 |
3 | HG01106.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1360+1683_1360+168 others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213469 | |||||||
| chr9:136213574 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1360+1580G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213574 | |||||||
| chr9:136213658 | C | T | 1 | a0001c0001t0014g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1360+1496G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213658 | |||||||
| chr9:136213663 | C | G | 1 | a0001c0001t0010g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1360+1491G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213663 | |||||||
| chr9:136213728 | C | T | 1 | a0002c0003t0015g0205 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1360+1426G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213728 | |||||||
| chr9:136213746 | G | A | 3 | a0001c0004t0003g0105 a0001c0004t0003g0106 a0001c0004t0016g0100 |
3 | HG00609.hp2 NA18986.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1360+1408C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213746 | |||||||
| chr9:136213921 | C | G | 2 | a0001c0001t0007g0255 a0001c0001t0007g0274 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1360+1233G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213921 | |||||||
| chr9:136213967 | A | AAC | 139 | a0001c0001t0002g0247 a0001c0001t0002g0264 a0001c0001t0002g0296 others(136): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1360+1185_1360+118 others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213967 | |||||||
| chr9:136213988 | C | T | 25 | a0001c0001t0001g0034 a0001c0001t0001g0210 a0001c0001t0001g0224 others(22): Show |
35 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1360+1166G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136213988 | |||||||
| chr9:136214030 | C | T | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1360+1124G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214030 | |||||||
| chr9:136214094 | G | A | 52 | a0001c0001t0002g0247 a0001c0001t0002g0296 a0001c0001t0004g0178 others(49): Show |
76 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1360+1060C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214094 | |||||||
| chr9:136214307 | C | T | 8 | a0001c0001t0007g0255 a0001c0001t0007g0274 a0001c0001t0007g0299 others(5): Show |
8 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1360+847G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214307 | |||||||
| chr9:136214341 | C | T | 8 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(5): Show |
11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+813G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214341 | |||||||
| chr9:136214491 | C | T | 1 | a0001c0014t0001g0114 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1360+663G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214491 | |||||||
| chr9:136214560 | C | T | 1 | a0001c0004t0003g0108 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1360+594G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214560 | |||||||
| chr9:136214733 | C | T | 2 | a0001c0001t0020g0196 a0001c0001t0020g0282 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1360+421G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214733 | |||||||
| chr9:136214756 | G | A | 1 | a0002c0003t0002g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1360+398C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214756 | |||||||
| chr9:136214785 | G | A | 1 | a0001c0001t0010g0273 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1360+369C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214785 | |||||||
| chr9:136214794 | C | T | 4 | a0001c0002t0012g0012 a0001c0002t0012g0044 a0001c0002t0012g0045 others(1): Show |
6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1360+360G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214794 | |||||||
| chr9:136214916 | T | C | 1 | a0001c0001t0053g0303 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+238A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214916 | |||||||
| chr9:136214968 | G | A | 1 | a0001c0024t0002g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1360+186C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214968 | |||||||
| chr9:136214975 | C | T | 2 | a0001c0002t0001g0073 a0001c0002t0001g0077 |
2 | HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1360+179G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 10/11 | chr9 | 136214975 | |||||||
| chr9:136215329 | C | A | 1 | a0001c0002t0001g0117 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1210-25G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136215329 | |||||||
| chr9:136215384 | T | C | 80 | a0001c0001t0004g0185 a0001c0001t0004g0190 a0001c0001t0004g0281 others(77): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1210-80A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136215384 | |||||||
| chr9:136215423 | A | C | 1 | a0001c0002t0001g0167 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1210-119T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136215423 | |||||||
| chr9:136215793 | G | A | 1 | a0001c0002t0006g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1210-489C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136215793 | |||||||
| chr9:136216012 | C | T | 8 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(5): Show |
11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1209+588G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216012 | |||||||
| chr9:136216033 | C | T | 100 | a0001c0001t0002g0247 a0001c0001t0002g0264 a0001c0001t0002g0296 others(97): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1209+567G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216033 | |||||||
| chr9:136216037 | A | T | 1 | a0001c0002t0001g0072 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1209+563T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216037 | |||||||
| chr9:136216070 | G | A | 1 | a0001c0002t0001g0131 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1209+530C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216070 | |||||||
| chr9:136216078 | C | T | 2 | a0001c0008t0013g0047 a0002c0003t0002g0283 |
2 | HG01515.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1209+522G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216078 | |||||||
| chr9:136216079 | G | A | 36 | a0001c0002t0001g0102 a0001c0004t0003g0002 a0001c0004t0003g0006 others(33): Show |
49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1209+521C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216079 | |||||||
| chr9:136216245 | A | C | 9 | a0001c0001t0014g0248 a0001c0001t0014g0249 a0001c0002t0001g0055 others(6): Show |
9 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1209+355T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216245 | |||||||
| chr9:136216292 | C | T | 4 | a0001c0001t0011g0003 a0001c0001t0011g0173 a0001c0001t0011g0197 others(1): Show |
8 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209+308G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216292 | |||||||
| chr9:136216462 | G | A | 19 | a0001c0001t0002g0247 a0001c0001t0002g0296 a0001c0001t0004g0178 others(16): Show |
19 | HG01069.hp2 HG01106.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1209+138C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216462 | |||||||
| chr9:136216478 | A | G | 138 | a0001c0001t0002g0247 a0001c0001t0002g0264 a0001c0001t0002g0296 others(135): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1209+122T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216478 | |||||||
| chr9:136216499 | G | A | 1 | a0001c0001t0007g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1209+101C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216499 | |||||||
| chr9:136216513 | G | A | 36 | a0001c0002t0001g0102 a0001c0004t0003g0002 a0001c0004t0003g0006 others(33): Show |
49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1209+87C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216513 | |||||||
| chr9:136216526 | C | A | 1 | a0001c0001t0004g0266 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1209+74G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 9/11 | chr9 | 136216526 | |||||||
| chr9:136216793 | G | A | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1087-71C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136216793 | |||||||
| chr9:136216852 | A | G | 2 | a0004c0009t0004g0304 a0004c0009t0004g0305 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1087-130T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136216852 | |||||||
| chr9:136216895 | C | A | 2 | a0004c0009t0004g0304 a0004c0009t0004g0305 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1087-173G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136216895 | |||||||
| chr9:136216910 | T | C | 8 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(5): Show |
11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1087-188A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136216910 | |||||||
| chr9:136217138 | G | A | 2 | a0002c0003t0002g0286 a0002c0003t0002g0289 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1087-416C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217138 | |||||||
| chr9:136217161 | G | A | 20 | a0001c0001t0002g0264 a0001c0001t0004g0011 a0001c0001t0004g0029 others(17): Show |
24 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1087-439C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217161 | |||||||
| chr9:136217170 | C | T | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1087-448G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217170 | |||||||
| chr9:136217213 | G | C | 36 | a0001c0002t0001g0102 a0001c0004t0003g0002 a0001c0004t0003g0006 others(33): Show |
49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1087-491C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217213 | |||||||
| chr9:136217229 | C | T | 1 | a0001c0001t0005g0212 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1087-507G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217229 | |||||||
| chr9:136217234 | T | C | 36 | a0001c0002t0001g0102 a0001c0004t0003g0002 a0001c0004t0003g0006 others(33): Show |
49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1087-512A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217234 | |||||||
| chr9:136217362 | G | A | 1 | a0002c0003t0002g0240 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1087-640C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217362 | |||||||
| chr9:136217401 | A | G | 197 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(194): Show |
258 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1087-679T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217401 | |||||||
| chr9:136217417 | G | A | 36 | a0001c0002t0001g0102 a0001c0004t0003g0002 a0001c0004t0003g0006 others(33): Show |
49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1087-695C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217417 | |||||||
| chr9:136217471 | G | A | 4 | a0001c0002t0012g0012 a0001c0002t0012g0044 a0001c0002t0012g0045 others(1): Show |
6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1087-749C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217471 | |||||||
| chr9:136217522 | C | T | 1 | a0001c0002t0025g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1087-800G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217522 | |||||||
| chr9:136217680 | C | G | 196 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(193): Show |
257 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1087-958G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217680 | |||||||
| chr9:136217727 | G | A | 3 | a0001c0004t0003g0101 a0001c0004t0027g0089 a0001c0004t0028g0092 |
3 | HG01175.hp2 HG01952.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1086+952C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217727 | |||||||
| chr9:136217739 | C | T | 9 | a0001c0001t0004g0039 a0001c0001t0004g0275 a0001c0001t0004g0279 others(6): Show |
11 | HG01884.hp2 HG02280.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1086+940G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217739 | |||||||
| chr9:136217741 | G | A | 1 | a0001c0001t0029g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1086+938C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217741 | |||||||
| chr9:136217972 | C | G | 1 | a0001c0001t0010g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1086+707G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136217972 | |||||||
| chr9:136218015 | T | G | 199 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(196): Show |
260 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1086+664A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218015 | |||||||
| chr9:136218024 | T | G | 7 | a0001c0001t0007g0255 a0001c0001t0007g0274 a0001c0001t0007g0299 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1086+655A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218024 | |||||||
| chr9:136218065 | C | T | 1 | a0001c0002t0001g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1086+614G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218065 | |||||||
| chr9:136218304 | C | T | 2 | a0004c0009t0004g0304 a0004c0009t0004g0305 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1086+375G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218304 | |||||||
| chr9:136218325 | C | G | 25 | a0001c0001t0001g0034 a0001c0001t0001g0210 a0001c0001t0001g0224 others(22): Show |
35 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1086+354G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218325 | |||||||
| chr9:136218361 | A | C | 6 | a0001c0001t0007g0255 a0001c0001t0007g0274 a0001c0001t0007g0301 others(3): Show |
6 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1086+318T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218361 | |||||||
| chr9:136218362 | G | GGT | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1086+315_1086+316d others(4): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218362 | |||||||
| chr9:136218444 | A | G | 305 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(302): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.1086+235T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218444 | |||||||
| chr9:136218501 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1086+178G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218501 | |||||||
| chr9:136218515 | G | A | 4 | a0001c0001t0011g0003 a0001c0001t0011g0173 a0001c0001t0011g0197 others(1): Show |
8 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1086+164C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218515 | |||||||
| chr9:136218524 | G | A | 1 | a0002c0003t0002g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1086+155C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218524 | |||||||
| chr9:136218572 | C | T | 1 | a0001c0001t0029g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1086+107G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218572 | |||||||
| chr9:136218611 | G | A | 1 | a0001c0001t0010g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1086+68C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218611 | |||||||
| chr9:136218673 | C | T | 5 | a0001c0001t0008g0032 a0001c0001t0008g0198 a0001c0001t0008g0200 others(2): Show |
6 | HG02055.hp2 HG02257.hp2 HG03041.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1086+6G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 8/11 | chr9 | 136218673 | |||||||
| chr9:136218835 | G | A | 2 | a0004c0009t0004g0304 a0004c0009t0004g0305 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.957-27C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 7/11 | chr9 | 136218835 | |||||||
| chr9:136218930 | C | G | 1 | a0001c0001t0032g0295 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.956+100G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 7/11 | chr9 | 136218930 | |||||||
| chr9:136218989 | C | T | 1 | a0001c0001t0005g0223 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.956+41G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 7/11 | chr9 | 136218989 | |||||||
| chr9:136219175 | G | A | 1 | a0001c0002t0025g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.822-11C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219175 | |||||||
| chr9:136219187 | G | A | 20 | a0001c0001t0007g0193 a0001c0001t0007g0194 a0001c0001t0007g0195 others(17): Show |
26 | HG00741.hp2 HG01109.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.822-23C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219187 | |||||||
| chr9:136219366 | A | G | 4 | a0001c0002t0012g0012 a0001c0002t0012g0044 a0001c0002t0012g0045 others(1): Show |
6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.822-202T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219366 | |||||||
| chr9:136219581 | G | A | 1 | a0001c0002t0038g0084 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.822-417C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219581 | |||||||
| chr9:136219620 | G | A | 2 | a0001c0002t0001g0017 a0001c0002t0001g0065 |
3 | HG01258.hp1 HG01993.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.822-456C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219620 | |||||||
| chr9:136219883 | G | A | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.822-719C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219883 | |||||||
| chr9:136219911 | C | T | 1 | a0001c0001t0007g0300 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.822-747G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219911 | |||||||
| chr9:136219979 | G | A | 1 | a0001c0008t0041g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.822-815C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219979 | |||||||
| chr9:136219985 | T | C | 6 | a0001c0001t0010g0250 a0001c0001t0010g0251 a0001c0001t0010g0252 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.822-821A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136219985 | |||||||
| chr9:136220024 | G | T | 167 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(164): Show |
215 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.822-860C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220024 | |||||||
| chr9:136220078 | C | T | 1 | a0001c0002t0049g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.822-914G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220078 | |||||||
| chr9:136220127 | G | C | 2 | a0001c0004t0003g0087 a0001c0004t0003g0103 |
2 | HG01070.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.822-963C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220127 | |||||||
| chr9:136220160 | T | C | 6 | a0001c0001t0010g0250 a0001c0001t0010g0251 a0001c0001t0010g0252 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.822-996A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220160 | |||||||
| chr9:136220359 | G | A | 1 | a0001c0001t0005g0217 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.822-1195C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220359 | |||||||
| chr9:136220606 | GCCTCACG others(10): Show |
G | 166 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(163): Show |
214 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.821+1173_821+1189d others(19): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220606 | |||||||
| chr9:136220623 | TCCTCACG others(11): Show |
T | 1 | a0001c0001t0001g0224 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.821+1155_821+1172d others(20): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220623 | |||||||
| chr9:136220629 | C | T | 1 | a0001c0002t0006g0142 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.821+1167G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220629 | |||||||
| chr9:136220676 | C | A | 1 | a0002c0003t0002g0294 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.821+1120G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220676 | |||||||
| chr9:136220701 | C | A | 2 | a0001c0002t0001g0118 a0001c0002t0006g0111 |
2 | HG02074.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.821+1095G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220701 | |||||||
| chr9:136220710 | T | A | 1 | a0002c0003t0002g0230 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.821+1086A>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220710 | |||||||
| chr9:136220749 | C | T | 2 | a0001c0020t0003g0171 a0007c0021t0019g0170 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.821+1047G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220749 | |||||||
| chr9:136220766 | G | A | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.821+1030C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220766 | |||||||
| chr9:136220844 | G | A | 2 | a0001c0001t0002g0296 a0001c0001t0032g0295 |
2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.821+952C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220844 | |||||||
| chr9:136220846 | G | T | 1 | a0001c0008t0013g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.821+950C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220846 | |||||||
| chr9:136220909 | T | C | 2 | a0001c0001t0020g0196 a0001c0001t0020g0282 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.821+887A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136220909 | |||||||
| chr9:136221052 | GCAGAGGC others(40): Show |
G | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.821+697_821+743del others(47): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221052 | |||||||
| chr9:136221057 | G | C | 14 | a0001c0001t0002g0296 a0001c0001t0004g0178 a0001c0001t0004g0179 others(11): Show |
14 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.821+739C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221057 | |||||||
| chr9:136221071 | C | G | 1 | a0001c0002t0006g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.821+725G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221071 | |||||||
| chr9:136221103 | AGGCAAAG others(87): Show |
A | 2 | a0001c0001t0020g0196 a0001c0001t0020g0282 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.821+599_821+692del others(94): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221103 | |||||||
| chr9:136221104 | G | C | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.821+692C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221104 | |||||||
| chr9:136221141 | TCCACGCA others(87): Show |
T | 3 | a0001c0001t0010g0251 a0001c0001t0014g0248 a0001c0001t0014g0249 |
3 | HG02559.hp1 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.821+561_821+654del others(94): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221141 | |||||||
| chr9:136221201 | AAAGGGCT others(40): Show |
A | 1 | a0001c0001t0032g0295 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.821+548_821+594del others(47): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221201 | |||||||
| chr9:136221247 | C | T | 3 | a0001c0001t0010g0250 a0001c0001t0010g0252 a0001c0001t0010g0253 |
3 | HG02145.hp1 HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.821+549G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221247 | |||||||
| chr9:136221299 | G | C | 2 | a0001c0020t0003g0171 a0007c0021t0019g0170 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.821+497C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221299 | |||||||
| chr9:136221340 | G | A | 2 | a0002c0003t0002g0227 a0002c0003t0002g0228 |
2 | HG03831.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.821+456C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221340 | |||||||
| chr9:136221495 | C | G | 2 | a0001c0001t0001g0290 a0001c0002t0001g0096 |
2 | HG01069.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.821+301G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221495 | |||||||
| chr9:136221508 | T | C | 1 | a0001c0002t0001g0134 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.821+288A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221508 | |||||||
| chr9:136221561 | G | A | 3 | a0001c0001t0002g0247 a0001c0001t0015g0203 a0001c0001t0051g0202 |
3 | HG01261.hp2 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.821+235C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221561 | |||||||
| chr9:136221621 | A | C | 17 | a0001c0001t0002g0296 a0001c0001t0004g0178 a0001c0001t0004g0179 others(14): Show |
17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.821+175T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221621 | |||||||
| chr9:136221643 | G | A | 6 | a0001c0001t0010g0250 a0001c0001t0010g0251 a0001c0001t0010g0252 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.821+153C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221643 | |||||||
| chr9:136221785 | C | T | 2 | a0001c0005t0005g0297 a0001c0008t0013g0047 |
2 | HG02083.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.821+11G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 6/11 | chr9 | 136221785 | |||||||
| chr9:136222096 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0005g0209 a0001c0001t0005g0211 |
3 | HG02602.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.676-155A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222096 | |||||||
| chr9:136222104 | T | TA | 93 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(90): Show |
128 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.676-164dupT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222104 | |||||||
| chr9:136222144 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.676-203C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222144 | |||||||
| chr9:136222153 | C | T | 1 | a0001c0005t0004g0186 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-212G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222153 | |||||||
| chr9:136222317 | G | A | 2 | a0001c0020t0003g0171 a0007c0021t0019g0170 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.676-376C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222317 | |||||||
| chr9:136222338 | G | A | 1 | a0002c0003t0002g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.676-397C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222338 | |||||||
| chr9:136222345 | C | T | 8 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(5): Show |
11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.676-404G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222345 | |||||||
| chr9:136222462 | T | C | 56 | a0001c0001t0002g0264 a0001c0001t0002g0296 a0001c0001t0004g0011 others(53): Show |
63 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.676-521A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222462 | |||||||
| chr9:136222575 | C | T | 14 | a0001c0001t0002g0296 a0001c0001t0004g0178 a0001c0001t0004g0179 others(11): Show |
14 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.676-634G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222575 | |||||||
| chr9:136222582 | G | A | 1 | a0001c0004t0003g0006 | 4 | HG00642.hp2 HG02698.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-641C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222582 | |||||||
| chr9:136222613 | G | C | 1 | a0001c0002t0001g0118 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.676-672C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222613 | |||||||
| chr9:136222631 | G | T | 1 | a0001c0004t0003g0063 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.676-690C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222631 | |||||||
| chr9:136222689 | C | CCTGCA | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.676-753_676-749dup others(5): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222689 | |||||||
| chr9:136222754 | C | T | 2 | a0001c0020t0003g0171 a0007c0021t0019g0170 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.676-813G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222754 | |||||||
| chr9:136222755 | G | C | 1 | a0001c0004t0003g0108 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.676-814C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222755 | |||||||
| chr9:136222778 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.676-837C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222778 | |||||||
| chr9:136222896 | T | C | 2 | a0001c0001t0002g0296 a0001c0001t0032g0295 |
2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.675+867A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222896 | |||||||
| chr9:136222900 | G | A | 1 | a0001c0002t0050g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.675+863C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222900 | |||||||
| chr9:136222954 | G | A | 8 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(5): Show |
11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.675+809C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136222954 | |||||||
| chr9:136223075 | C | T | 1 | a0001c0004t0003g0062 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.675+688G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136223075 | |||||||
| chr9:136223106 | G | A | 1 | a0001c0002t0001g0069 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.675+657C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136223106 | |||||||
| chr9:136223127 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.675+636T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136223127 | |||||||
| chr9:136223381 | A | C | 2 | a0001c0001t0002g0296 a0001c0001t0032g0295 |
2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.675+382T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136223381 | |||||||
| chr9:136223470 | G | A | 1 | a0002c0003t0002g0241 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.675+293C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 5/11 | chr9 | 136223470 | |||||||
| chr9:136223970 | C | T | 1 | a0001c0023t0030g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.584+37G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 4/11 | chr9 | 136223970 | |||||||
| chr9:136224153 | G | A | 20 | a0001c0001t0002g0264 a0001c0001t0004g0011 a0001c0001t0004g0029 others(17): Show |
24 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.479-41C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224153 | |||||||
| chr9:136224383 | G | A | 1 | a0001c0001t0021g0268 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.479-271C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224383 | |||||||
| chr9:136224406 | C | A | 4 | a0001c0002t0012g0012 a0001c0002t0012g0044 a0001c0002t0012g0045 others(1): Show |
6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-294G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224406 | |||||||
| chr9:136224425 | A | ACAGGC | 3 | a0001c0001t0004g0185 a0001c0001t0004g0188 a0001c0001t0004g0190 |
3 | HG01106.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.479-318_479-314dup others(5): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224425 | |||||||
| chr9:136224447 | G | A | 2 | a0001c0005t0001g0192 a0008c0018t0001g0169 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.479-335C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224447 | |||||||
| chr9:136224449 | G | A | 14 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(11): Show |
17 | HG01074.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.479-337C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224449 | |||||||
| chr9:136224477 | G | A | 2 | a0001c0001t0020g0196 a0001c0001t0020g0282 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.479-365C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224477 | |||||||
| chr9:136224712 | C | T | 1 | a0001c0002t0013g0122 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.478+149G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224712 | |||||||
| chr9:136224820 | G | A | 17 | a0001c0001t0002g0296 a0001c0001t0004g0178 a0001c0001t0004g0179 others(14): Show |
17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.478+41C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 3/11 | chr9 | 136224820 | |||||||
| chr9:136224986 | G | A | 2 | a0002c0003t0015g0205 a0002c0016t0002g0161 |
2 | NA18962.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.430-77C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136224986 | |||||||
| chr9:136225052 | C | T | 8 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(5): Show |
11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-143G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225052 | |||||||
| chr9:136225061 | T | G | 56 | a0001c0001t0002g0264 a0001c0001t0002g0296 a0001c0001t0004g0011 others(53): Show |
63 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.430-152A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225061 | |||||||
| chr9:136225100 | A | G | 1 | a0001c0007t0004g0162 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.430-191T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225100 | |||||||
| chr9:136225255 | G | A | 6 | a0001c0001t0010g0250 a0001c0001t0010g0251 a0001c0001t0010g0252 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-346C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225255 | |||||||
| chr9:136225380 | G | A | 1 | a0001c0002t0001g0167 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.430-471C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225380 | |||||||
| chr9:136225444 | G | C | 1 | a0001c0002t0001g0131 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.430-535C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225444 | |||||||
| chr9:136225511 | G | A | 1 | a0001c0005t0004g0191 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.430-602C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225511 | |||||||
| chr9:136225624 | A | G | 1 | a0002c0003t0002g0235 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.430-715T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225624 | |||||||
| chr9:136225632 | G | A | 1 | a0001c0002t0001g0150 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.430-723C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225632 | |||||||
| chr9:136225699 | G | A | 1 | a0002c0003t0043g0242 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.430-790C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225699 | |||||||
| chr9:136225752 | C | T | 67 | a0001c0001t0002g0264 a0001c0001t0002g0296 a0001c0001t0004g0011 others(64): Show |
78 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.430-843G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225752 | |||||||
| chr9:136225801 | G | A | 4 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0033g0175 others(1): Show |
4 | HG00741.hp2 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-892C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225801 | |||||||
| chr9:136225873 | A | C | 17 | a0001c0001t0002g0296 a0001c0001t0004g0178 a0001c0001t0004g0179 others(14): Show |
17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.429+901T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136225873 | |||||||
| chr9:136226013 | T | C | 3 | a0001c0004t0003g0052 a0001c0004t0003g0053 a0001c0004t0003g0054 |
3 | HG00639.hp1 HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.429+761A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226013 | |||||||
| chr9:136226332 | T | C | 6 | a0001c0002t0001g0151 a0001c0002t0001g0155 a0001c0002t0002g0008 others(3): Show |
9 | NA18954.hp2 NA18964.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.429+442A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226332 | |||||||
| chr9:136226415 | C | T | 1 | a0001c0007t0003g0095 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.429+359G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226415 | |||||||
| chr9:136226424 | C | T | 10 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0010g0250 others(7): Show |
10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.429+350G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226424 | |||||||
| chr9:136226530 | G | A | 1 | a0001c0001t0010g0273 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.429+244C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226530 | |||||||
| chr9:136226552 | TC | T | 21 | a0001c0001t0002g0264 a0001c0001t0004g0011 a0001c0001t0004g0029 others(18): Show |
25 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.429+221delG | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226552 | |||||||
| chr9:136226621 | A | G | 1 | a0001c0001t0007g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429+153T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226621 | |||||||
| chr9:136226669 | C | T | 3 | a0001c0004t0003g0052 a0001c0004t0003g0053 a0001c0004t0003g0054 |
3 | HG00639.hp1 HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.429+105G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226669 | |||||||
| chr9:136226704 | C | T | 5 | a0001c0001t0001g0224 a0001c0001t0005g0004 a0001c0001t0005g0222 others(2): Show |
9 | HG02523.hp2 HG02559.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.429+70G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226704 | |||||||
| chr9:136226760 | C | T | 12 | a0001c0001t0007g0255 a0001c0001t0007g0274 a0001c0001t0007g0299 others(9): Show |
13 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+14G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 2/11 | chr9 | 136226760 | |||||||
| chr9:136226959 | C | T | 1 | a0001c0004t0003g0087 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.329-85G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136226959 | |||||||
| chr9:136226989 | C | A | 1 | a0001c0004t0003g0138 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.329-115G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136226989 | |||||||
| chr9:136227196 | C | A | 67 | a0001c0001t0002g0264 a0001c0001t0002g0296 a0001c0001t0004g0011 others(64): Show |
78 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.329-322G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227196 | |||||||
| chr9:136227351 | G | A | 2 | a0001c0001t0020g0196 a0001c0001t0020g0282 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.329-477C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227351 | |||||||
| chr9:136227369 | A | G | 79 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(76): Show |
113 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.329-495T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227369 | |||||||
| chr9:136227377 | C | A | 2 | a0004c0009t0004g0304 a0004c0009t0004g0305 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.329-503G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227377 | |||||||
| chr9:136227391 | G | C | 1 | a0001c0023t0030g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.329-517C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227391 | |||||||
| chr9:136227593 | A | G | 1 | a0001c0002t0006g0112 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.329-719T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227593 | |||||||
| chr9:136227601 | C | T | 1 | a0001c0001t0004g0266 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.329-727G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227601 | |||||||
| chr9:136227716 | T | C | 2 | a0004c0009t0004g0304 a0004c0009t0004g0305 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.329-842A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227716 | |||||||
| chr9:136227765 | A | C | 5 | a0001c0005t0005g0030 a0001c0005t0005g0181 a0001c0005t0005g0183 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-891T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227765 | |||||||
| chr9:136227847 | C | T | 8 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(5): Show |
11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.329-973G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136227847 | |||||||
| chr9:136228032 | G | T | 1 | a0002c0003t0002g0289 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.329-1158C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228032 | |||||||
| chr9:136228033 | T | G | 1 | a0002c0003t0002g0289 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.329-1159A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228033 | |||||||
| chr9:136228045 | C | T | 1 | a0001c0004t0003g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.329-1171G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228045 | |||||||
| chr9:136228125 | C | G | 1 | a0001c0002t0013g0023 | 2 | NA18998.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.329-1251G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228125 | |||||||
| chr9:136228149 | T | C | 1 | a0001c0002t0018g0128 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.329-1275A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228149 | |||||||
| chr9:136228197 | C | G | 93 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(90): Show |
128 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.329-1323G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228197 | |||||||
| chr9:136228259 | A | G | 21 | a0001c0001t0002g0264 a0001c0001t0004g0011 a0001c0001t0004g0029 others(18): Show |
25 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.329-1385T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228259 | |||||||
| chr9:136228318 | A | G | 25 | a0001c0001t0002g0264 a0001c0001t0004g0011 a0001c0001t0004g0029 others(22): Show |
29 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.329-1444T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228318 | |||||||
| chr9:136228330 | C | T | 7 | a0001c0001t0007g0255 a0001c0001t0007g0274 a0001c0001t0007g0299 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-1456G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228330 | |||||||
| chr9:136228381 | A | G | 4 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 others(1): Show |
5 | HG02165.hp1 HG03831.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.329-1507T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228381 | |||||||
| chr9:136228473 | A | G | 12 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(9): Show |
12 | HG01069.hp2 HG01106.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.329-1599T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228473 | |||||||
| chr9:136228615 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.329-1741G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228615 | |||||||
| chr9:136228771 | G | A | 1 | a0001c0002t0025g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.329-1897C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228771 | |||||||
| chr9:136228835 | C | A | 12 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(9): Show |
12 | HG01069.hp2 HG01106.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.329-1961G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228835 | |||||||
| chr9:136228959 | A | G | 8 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(5): Show |
11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.329-2085T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228959 | |||||||
| chr9:136228982 | T | C | 79 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(76): Show |
113 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.329-2108A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136228982 | |||||||
| chr9:136229012 | C | A | 2 | a0002c0003t0002g0233 a0002c0003t0002g0240 |
2 | NA19004.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.329-2138G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229012 | |||||||
| chr9:136229146 | C | T | 7 | a0001c0001t0007g0255 a0001c0001t0007g0274 a0001c0001t0007g0299 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-2272G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229146 | |||||||
| chr9:136229148 | C | T | 1 | a0001c0001t0010g0253 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.329-2274G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229148 | |||||||
| chr9:136229216 | C | T | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.329-2342G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229216 | |||||||
| chr9:136229227 | C | T | 2 | a0001c0001t0002g0296 a0001c0001t0032g0295 |
2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.329-2353G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229227 | |||||||
| chr9:136229265 | G | A | 2 | a0001c0020t0003g0171 a0007c0021t0019g0170 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.329-2391C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229265 | |||||||
| chr9:136229269 | A | C | 8 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(5): Show |
11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.329-2395T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229269 | |||||||
| chr9:136229312 | C | T | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.329-2438G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229312 | |||||||
| chr9:136229506 | A | G | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.329-2632T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229506 | |||||||
| chr9:136229515 | A | T | 21 | a0001c0001t0002g0264 a0001c0001t0004g0011 a0001c0001t0004g0029 others(18): Show |
25 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.329-2641T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229515 | |||||||
| chr9:136229607 | G | A | 8 | a0001c0001t0004g0039 a0001c0001t0004g0275 a0001c0001t0004g0279 others(5): Show |
10 | HG01884.hp2 HG02280.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-2733C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229607 | |||||||
| chr9:136229751 | C | A | 2 | a0001c0005t0005g0297 a0001c0008t0013g0047 |
2 | HG02083.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.329-2877G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229751 | |||||||
| chr9:136229875 | G | C | 21 | a0001c0001t0002g0264 a0001c0001t0004g0011 a0001c0001t0004g0029 others(18): Show |
25 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.329-3001C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229875 | |||||||
| chr9:136229894 | A | C | 174 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(171): Show |
222 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.329-3020T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136229894 | |||||||
| chr9:136230018 | C | A | 2 | a0001c0001t0020g0196 a0001c0001t0020g0282 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.329-3144G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230018 | |||||||
| chr9:136230075 | T | C | 2 | a0001c0001t0020g0196 a0001c0001t0020g0282 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.329-3201A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230075 | |||||||
| chr9:136230218 | G | A | 12 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(9): Show |
12 | HG01069.hp2 HG01106.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.329-3344C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230218 | |||||||
| chr9:136230257 | G | A | 1 | a0001c0002t0006g0043 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.329-3383C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230257 | |||||||
| chr9:136230265 | G | A | 1 | a0001c0001t0010g0273 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.329-3391C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230265 | |||||||
| chr9:136230306 | T | G | 8 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(5): Show |
11 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.329-3432A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230306 | |||||||
| chr9:136230322 | C | T | 1 | a0001c0007t0003g0126 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.329-3448G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230322 | |||||||
| chr9:136230329 | G | A | 10 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0010g0250 others(7): Show |
10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-3455C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230329 | |||||||
| chr9:136230517 | G | A | 79 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(76): Show |
113 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.329-3643C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230517 | |||||||
| chr9:136230683 | C | T | 1 | a0002c0003t0002g0244 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.329-3809G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230683 | |||||||
| chr9:136230701 | G | A | 17 | a0001c0001t0002g0296 a0001c0001t0004g0178 a0001c0001t0004g0179 others(14): Show |
17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.329-3827C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230701 | |||||||
| chr9:136230863 | G | A | 2 | a0001c0020t0003g0171 a0007c0021t0019g0170 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.329-3989C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230863 | |||||||
| chr9:136230892 | C | G | 2 | a0001c0001t0002g0296 a0001c0001t0032g0295 |
2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.329-4018G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230892 | |||||||
| chr9:136230936 | T | C | 2 | a0001c0001t0020g0196 a0001c0001t0020g0282 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.329-4062A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230936 | |||||||
| chr9:136230966 | G | A | 1 | a0001c0002t0006g0051 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.329-4092C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136230966 | |||||||
| chr9:136231113 | C | G | 10 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0010g0250 others(7): Show |
10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-4239G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231113 | |||||||
| chr9:136231135 | G | T | 1 | a0001c0002t0050g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.329-4261C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231135 | |||||||
| chr9:136231150 | C | T | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.329-4276G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231150 | |||||||
| chr9:136231178 | G | C | 1 | a0002c0003t0002g0241 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.329-4304C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231178 | |||||||
| chr9:136231195 | G | A | 1 | a0001c0001t0004g0266 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.329-4321C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231195 | |||||||
| chr9:136231219 | C | T | 1 | a0001c0002t0050g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.329-4345G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231219 | |||||||
| chr9:136231225 | T | C | 1 | a0001c0002t0001g0118 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.329-4351A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231225 | |||||||
| chr9:136231316 | C | T | 10 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0010g0250 others(7): Show |
10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-4442G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231316 | |||||||
| chr9:136231585 | T | C | 12 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(9): Show |
12 | HG01069.hp2 HG01106.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.329-4711A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231585 | |||||||
| chr9:136231629 | C | A | 2 | a0001c0001t0002g0296 a0001c0001t0032g0295 |
2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.329-4755G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231629 | |||||||
| chr9:136231794 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.329-4920G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231794 | |||||||
| chr9:136231853 | C | T | 5 | a0001c0001t0002g0296 a0001c0001t0026g0307 a0001c0001t0026g0308 others(2): Show |
5 | HG02027.hp2 HG02129.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.329-4979G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231853 | |||||||
| chr9:136231868 | GC | G | 7 | a0001c0001t0007g0255 a0001c0001t0007g0274 a0001c0001t0007g0299 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-4995delG | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231868 | |||||||
| chr9:136231870 | AATCCGCC others(20): Show |
A | 2 | a0001c0001t0004g0262 a0001c0001t0004g0263 |
2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.329-5023_329-4997d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231870 | |||||||
| chr9:136231871 | A | C | 58 | a0001c0001t0002g0264 a0001c0001t0002g0296 a0001c0001t0004g0011 others(55): Show |
65 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.329-4997T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231871 | |||||||
| chr9:136231883 | C | T | 1 | a0001c0002t0006g0149 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.329-5009G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231883 | |||||||
| chr9:136231888 | C | T | 1 | a0001c0001t0007g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.329-5014G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231888 | |||||||
| chr9:136231902 | A | G | 2 | a0001c0001t0004g0262 a0001c0001t0004g0263 |
2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.329-5028T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231902 | |||||||
| chr9:136231915 | C | A | 1 | a0002c0003t0002g0241 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.329-5041G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231915 | |||||||
| chr9:136231924 | TCTCCGCC others(2): Show |
T | 4 | a0001c0001t0011g0003 a0001c0001t0011g0173 a0001c0001t0011g0197 others(1): Show |
8 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.329-5059_329-5051d others(11): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231924 | |||||||
| chr9:136231931 | CTCCTCCG others(2): Show |
C | 3 | a0001c0001t0007g0193 a0001c0001t0007g0194 a0001c0001t0007g0195 |
3 | HG02258.hp2 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.329-5066_329-5058d others(11): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231931 | |||||||
| chr9:136231940 | A | T | 4 | a0001c0001t0011g0003 a0001c0001t0011g0173 a0001c0001t0011g0197 others(1): Show |
8 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.329-5066T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136231940 | |||||||
| chr9:136232057 | C | T | 1 | a0001c0002t0006g0111 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.329-5183G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232057 | |||||||
| chr9:136232068 | C | T | 10 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0010g0250 others(7): Show |
10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-5194G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232068 | |||||||
| chr9:136232187 | G | A | 3 | a0001c0001t0005g0219 a0001c0001t0020g0196 a0001c0001t0020g0282 |
3 | HG01943.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.329-5313C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232187 | |||||||
| chr9:136232244 | G | A | 7 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0006g0057 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-5370C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232244 | |||||||
| chr9:136232260 | A | G | 60 | a0001c0001t0002g0264 a0001c0001t0002g0296 a0001c0001t0004g0011 others(57): Show |
67 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.329-5386T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232260 | |||||||
| chr9:136232286 | C | T | 3 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 |
3 | HG01069.hp2 HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.329-5412G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232286 | |||||||
| chr9:136232302 | A | C | 17 | a0001c0001t0002g0296 a0001c0001t0004g0178 a0001c0001t0004g0179 others(14): Show |
17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.329-5428T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232302 | |||||||
| chr9:136232338 | C | T | 1 | a0002c0003t0002g0233 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.329-5464G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232338 | |||||||
| chr9:136232533 | T | C | 1 | a0002c0003t0002g0231 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.329-5659A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232533 | |||||||
| chr9:136232706 | G | A | 10 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(7): Show |
10 | HG01069.hp2 HG01106.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-5832C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232706 | |||||||
| chr9:136232917 | C | CA | 43 | a0001c0001t0004g0178 a0001c0001t0007g0255 a0001c0001t0007g0274 others(40): Show |
50 | HG00140.hp2 HG00741.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.329-6044dupT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232917 | |||||||
| chr9:136232917 | CA | C | 20 | a0001c0001t0002g0264 a0001c0001t0004g0029 a0001c0001t0004g0257 others(17): Show |
21 | HG00323.hp1 HG00408.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.329-6044delT | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232917 | |||||||
| chr9:136232934 | A | G | 2 | a0001c0020t0003g0171 a0007c0021t0019g0170 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.329-6060T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232934 | |||||||
| chr9:136232935 | A | AG | 75 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(72): Show |
109 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.329-6062_329-6061i others(3): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232935 | |||||||
| chr9:136232935 | A | G | 1 | a0002c0003t0002g0232 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.329-6061T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232935 | |||||||
| chr9:136232943 | A | C | 10 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0010g0250 others(7): Show |
10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-6069T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232943 | |||||||
| chr9:136232960 | A | G | 3 | a0001c0001t0002g0247 a0001c0001t0015g0203 a0001c0001t0051g0202 |
3 | HG01261.hp2 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.329-6086T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232960 | |||||||
| chr9:136232963 | A | G | 1 | a0001c0023t0030g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.329-6089T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232963 | |||||||
| chr9:136232968 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.329-6094C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232968 | |||||||
| chr9:136232975 | G | C | 1 | a0001c0001t0007g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.329-6101C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136232975 | |||||||
| chr9:136233010 | C | A | 52 | a0001c0001t0002g0264 a0001c0001t0002g0296 a0001c0001t0004g0011 others(49): Show |
56 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.329-6136G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233010 | |||||||
| chr9:136233284 | G | A | 1 | a0001c0004t0028g0092 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.329-6410C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233284 | |||||||
| chr9:136233320 | G | T | 7 | a0001c0001t0007g0255 a0001c0001t0007g0274 a0001c0001t0007g0299 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-6446C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233320 | |||||||
| chr9:136233355 | G | T | 1 | a0001c0001t0007g0220 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.329-6481C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233355 | |||||||
| chr9:136233433 | T | C | 1 | a0002c0003t0043g0242 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.329-6559A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233433 | |||||||
| chr9:136233503 | T | C | 2 | a0001c0001t0007g0255 a0001c0001t0007g0274 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.329-6629A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233503 | |||||||
| chr9:136233570 | C | T | 5 | a0001c0005t0005g0030 a0001c0005t0005g0181 a0001c0005t0005g0183 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-6696G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233570 | |||||||
| chr9:136233703 | C | T | 10 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0010g0250 others(7): Show |
10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-6829G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233703 | |||||||
| chr9:136233780 | C | T | 1 | a0008c0018t0001g0169 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.329-6906G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233780 | |||||||
| chr9:136233819 | T | C | 17 | a0001c0001t0002g0296 a0001c0001t0004g0178 a0001c0001t0004g0179 others(14): Show |
17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.329-6945A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233819 | |||||||
| chr9:136233850 | T | G | 5 | a0001c0001t0004g0029 a0001c0001t0004g0259 a0001c0001t0004g0260 others(2): Show |
6 | HG02135.hp2 NA18961.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-6976A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233850 | |||||||
| chr9:136233983 | G | A | 4 | a0001c0001t0020g0196 a0001c0001t0020g0282 a0001c0020t0003g0171 others(1): Show |
4 | HG02723.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.329-7109C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136233983 | |||||||
| chr9:136234034 | AGGACAAA others(36): Show |
A | 6 | a0001c0001t0020g0196 a0001c0001t0020g0282 a0001c0002t0012g0012 others(3): Show |
8 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.329-7203_329-7161d others(45): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234034 | |||||||
| chr9:136234044 | T | C | 297 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(294): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.329-7170A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234044 | |||||||
| chr9:136234094 | G | C | 1 | a0001c0002t0006g0135 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.329-7220C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234094 | |||||||
| chr9:136234095 | A | T | 2 | a0001c0020t0003g0171 a0007c0021t0019g0170 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.329-7221T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234095 | |||||||
| chr9:136234136 | C | T | 1 | a0001c0002t0001g0121 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.329-7262G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234136 | |||||||
| chr9:136234214 | T | C | 2 | a0004c0009t0004g0304 a0004c0009t0004g0305 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.329-7340A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234214 | |||||||
| chr9:136234215 | G | A | 1 | a0001c0001t0008g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.329-7341C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234215 | |||||||
| chr9:136234219 | G | A | 7 | a0001c0001t0007g0255 a0001c0001t0007g0274 a0001c0001t0007g0299 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-7345C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234219 | |||||||
| chr9:136234231 | G | A | 1 | a0001c0001t0005g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.329-7357C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234231 | |||||||
| chr9:136234247 | C | G | 17 | a0001c0001t0002g0296 a0001c0001t0004g0178 a0001c0001t0004g0179 others(14): Show |
17 | HG01069.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.329-7373G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234247 | |||||||
| chr9:136234265 | A | T | 21 | a0001c0001t0002g0264 a0001c0001t0004g0011 a0001c0001t0004g0029 others(18): Show |
25 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.329-7391T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234265 | |||||||
| chr9:136234274 | C | T | 160 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(157): Show |
206 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.329-7400G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234274 | |||||||
| chr9:136234297 | G | A | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.329-7423C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234297 | |||||||
| chr9:136234327 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0005g0209 a0001c0001t0005g0211 |
3 | HG02602.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.329-7453G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234327 | |||||||
| chr9:136234349 | G | T | 2 | a0001c0002t0001g0017 a0001c0002t0001g0065 |
3 | HG01258.hp1 HG01993.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.329-7475C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234349 | |||||||
| chr9:136234448 | G | A | 2 | a0001c0001t0007g0255 a0001c0001t0007g0274 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.329-7574C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234448 | |||||||
| chr9:136234451 | C | A | 2 | a0001c0002t0014g0124 a0001c0002t0050g0083 |
2 | HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.329-7577G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234451 | |||||||
| chr9:136234587 | C | A | 1 | a0001c0002t0001g0121 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.329-7713G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234587 | |||||||
| chr9:136234723 | G | GGCTTGGG others(70): Show |
1 | a0001c0004t0003g0127 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(147): Show |
1 | a0004c0009t0004g0304 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(301): Show |
1 | a0004c0009t0004g0305 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(310): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(70): Show |
1 | a0001c0002t0012g0045 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(147): Show |
1 | a0001c0008t0013g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(148): Show |
1 | a0001c0002t0006g0153 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(157): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(70): Show |
66 | a0001c0001t0001g0034 a0001c0001t0001g0210 a0001c0001t0001g0224 others(63): Show |
90 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(147): Show |
24 | a0001c0002t0001g0016 a0001c0002t0001g0055 a0001c0002t0001g0068 others(21): Show |
33 | HG00140.hp2 HG00642.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(224): Show |
7 | a0001c0002t0001g0015 a0001c0002t0001g0072 a0001c0002t0001g0073 others(4): Show |
9 | HG02698.hp2 HG03492.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(609): Show |
1 | a0001c0002t0001g0065 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(618): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(686): Show |
1 | a0001c0002t0001g0017 | 2 | HG01993.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(695): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(224): Show |
4 | a0001c0002t0001g0027 a0001c0002t0001g0064 a0001c0002t0001g0167 others(1): Show |
5 | HG00099.hp2 HG02723.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(302): Show |
1 | a0001c0002t0006g0154 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(311): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(301): Show |
2 | a0001c0002t0002g0165 a0001c0002t0002g0166 |
2 | NA18954.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(310): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(378): Show |
3 | a0001c0002t0001g0143 a0001c0002t0002g0164 a0001c0002t0006g0142 |
3 | HG00408.hp1 NA18964.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(387): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(302): Show |
1 | a0001c0002t0001g0077 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(311): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(301): Show |
1 | a0001c0001t0020g0196 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(310): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(840): Show |
1 | a0001c0001t0020g0282 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(849): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(147): Show |
14 | a0001c0001t0007g0038 a0001c0001t0007g0220 a0001c0001t0007g0221 others(11): Show |
17 | HG00280.hp1 HG00558.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(224): Show |
2 | a0001c0002t0001g0018 a0001c0002t0001g0125 |
3 | HG01943.hp2 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(224): Show |
2 | a0001c0001t0001g0208 a0001c0004t0003g0108 |
2 | HG03225.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(455): Show |
2 | a0001c0001t0026g0307 a0001c0001t0054g0309 |
2 | HG02165.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(464): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(456): Show |
1 | a0001c0001t0026g0308 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(465): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(147): Show |
1 | a0001c0001t0007g0302 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(70): Show |
1 | a0001c0001t0004g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(147): Show |
1 | a0006c0022t0005g0276 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(71): Show |
1 | a0001c0001t0005g0222 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(80): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(73): Show |
3 | a0001c0002t0001g0019 a0001c0002t0006g0093 a0001c0002t0023g0061 |
4 | HG00423.hp1 NA18940.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(82): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(150): Show |
5 | a0001c0002t0001g0121 a0001c0002t0013g0023 a0001c0002t0013g0120 others(2): Show |
6 | HG00621.hp1 HG00673.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(159): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(150): Show |
1 | a0001c0001t0004g0269 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(159): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(227): Show |
2 | a0001c0001t0004g0261 a0001c0002t0049g0110 |
2 | HG02135.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(236): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(304): Show |
6 | a0001c0001t0004g0011 a0001c0001t0004g0256 a0001c0001t0004g0258 others(3): Show |
9 | HG00408.hp2 HG00609.hp1 HG04199.hp2 others(6): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(313): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(381): Show |
5 | a0001c0001t0004g0260 a0001c0001t0004g0266 a0001c0001t0004g0267 others(2): Show |
5 | HG00323.hp1 HG02965.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(390): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(458): Show |
1 | a0001c0001t0004g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(467): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(535): Show |
1 | a0001c0001t0004g0259 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(544): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(150): Show |
3 | a0001c0001t0004g0262 a0001c0002t0001g0021 a0001c0002t0006g0043 |
4 | HG02135.hp1 HG03710.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.329-7850_329-7849i others(159): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(227): Show |
1 | a0001c0001t0004g0029 | 2 | NA18998.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(236): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(304): Show |
2 | a0001c0001t0002g0264 a0001c0001t0004g0263 |
2 | HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.329-7850_329-7849i others(313): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(612): Show |
1 | a0001c0001t0004g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.329-7850_329-7849i others(621): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | G | GGCTTGGG others(228): Show |
1 | a0001c0001t0021g0177 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.329-7850_329-7849i others(237): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234723 | GGCTTGGG others(70): Show |
G | 24 | a0001c0001t0002g0247 a0001c0001t0002g0296 a0001c0001t0004g0178 others(21): Show |
28 | HG00741.hp2 HG01261.hp2 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.329-7926_329-7850d others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234723 | |||||||
| chr9:136234734 | A | AAGGCTGG others(70): Show |
1 | a0001c0002t0001g0086 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.329-7861_329-7860i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234734 | |||||||
| chr9:136234734 | A | AAGGCTGG others(70): Show |
4 | a0001c0002t0012g0044 a0001c0005t0005g0297 a0001c0020t0003g0171 others(1): Show |
4 | HG02083.hp1 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.329-7861_329-7860i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234734 | |||||||
| chr9:136234749 | A | AAGGCCCC others(70): Show |
12 | a0001c0002t0001g0013 a0001c0002t0001g0117 a0001c0002t0001g0118 others(9): Show |
14 | HG00621.hp2 HG01168.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.329-7952_329-7876d others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234749 | |||||||
| chr9:136234749 | A | AAGGCCCC others(301): Show |
1 | a0001c0002t0006g0050 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.329-7876_329-7875i others(310): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234749 | |||||||
| chr9:136234749 | A | G | 248 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(245): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.329-7875T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234749 | |||||||
| chr9:136234752 | G | GCCCCCCA others(148): Show |
1 | a0001c0002t0001g0156 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.329-7879_329-7878i others(157): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234752 | |||||||
| chr9:136234769 | C | T | 4 | a0001c0001t0004g0039 a0001c0001t0004g0275 a0001c0001t0005g0040 others(1): Show |
6 | HG01884.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.329-7895G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234769 | |||||||
| chr9:136234770 | G | A | 5 | a0001c0001t0004g0179 a0001c0001t0004g0180 a0001c0002t0012g0012 others(2): Show |
7 | HG01069.hp2 HG01109.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.329-7896C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234770 | |||||||
| chr9:136234770 | G | GCCCGCCC others(148): Show |
1 | a0001c0006t0009g0157 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.329-7897_329-7896i others(157): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234770 | |||||||
| chr9:136234770 | G | GCCCGCCC others(70): Show |
1 | a0002c0003t0002g0231 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.329-7897_329-7896i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234770 | |||||||
| chr9:136234770 | G | GCCCGCCC others(70): Show |
1 | a0001c0023t0030g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.329-7897_329-7896i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234770 | |||||||
| chr9:136234773 | C | T | 1 | a0001c0002t0038g0084 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.329-7899G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234773 | |||||||
| chr9:136234792 | C | CACACCCC others(70): Show |
1 | a0002c0003t0002g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.329-7919_329-7918i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234792 | |||||||
| chr9:136234811 | A | AAGGCTGG others(224): Show |
1 | a0001c0019t0036g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.329-7938_329-7937i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234811 | |||||||
| chr9:136234811 | A | AAGGCTGG others(224): Show |
5 | a0001c0001t0008g0032 a0001c0001t0008g0198 a0001c0001t0008g0200 others(2): Show |
6 | HG02055.hp2 HG02257.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.329-7938_329-7937i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234811 | |||||||
| chr9:136234811 | A | AAGGCTGG others(378): Show |
1 | a0001c0001t0008g0031 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.329-7938_329-7937i others(387): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234811 | |||||||
| chr9:136234811 | A | AAGGCTGG others(455): Show |
1 | a0001c0001t0008g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.329-7938_329-7937i others(464): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234811 | |||||||
| chr9:136234811 | A | AAGGCTGG others(378): Show |
1 | a0001c0001t0008g0033 | 2 | HG01074.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.329-7938_329-7937i others(387): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234811 | |||||||
| chr9:136234811 | A | G | 3 | a0001c0001t0011g0173 a0004c0009t0004g0305 a0006c0022t0005g0276 |
3 | HG01884.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.329-7937T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234811 | |||||||
| chr9:136234812 | A | G | 1 | a0001c0002t0050g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.329-7938T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234812 | |||||||
| chr9:136234826 | G | A | 3 | a0001c0002t0001g0082 a0001c0002t0001g0158 a0001c0006t0009g0028 |
4 | HG01106.hp2 HG02015.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-7952C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234826 | |||||||
| chr9:136234826 | G | GAGGCCCC others(147): Show |
1 | a0001c0005t0005g0030 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.329-7953_329-7952i others(156): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234826 | |||||||
| chr9:136234826 | G | GAGGCCCC others(224): Show |
3 | a0001c0005t0005g0183 a0001c0005t0005g0184 a0001c0005t0017g0182 |
3 | HG02486.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.329-7953_329-7952i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234826 | |||||||
| chr9:136234847 | G | GCCCGCCC others(70): Show |
2 | a0001c0001t0014g0248 a0001c0001t0014g0249 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.329-7974_329-7973i others(79): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234847 | |||||||
| chr9:136234847 | G | GCCCGCCC others(224): Show |
1 | a0001c0001t0007g0255 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.329-7974_329-7973i others(233): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234847 | |||||||
| chr9:136234847 | G | GCCCGCCC others(301): Show |
1 | a0001c0001t0007g0274 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.329-7974_329-7973i others(310): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234847 | |||||||
| chr9:136234907 | T | C | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.329-8033A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234907 | |||||||
| chr9:136234926 | C | T | 2 | a0001c0001t0007g0193 a0001c0001t0007g0194 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.329-8052G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234926 | |||||||
| chr9:136234927 | C | T | 16 | a0001c0001t0002g0296 a0001c0001t0007g0255 a0001c0001t0007g0274 others(13): Show |
16 | HG00741.hp2 HG01243.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.329-8053G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234927 | |||||||
| chr9:136234943 | C | T | 30 | a0001c0002t0001g0015 a0001c0002t0001g0017 a0001c0002t0001g0018 others(27): Show |
36 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.329-8069G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136234943 | |||||||
| chr9:136235038 | T | C | 2 | a0001c0001t0007g0194 a0001c0001t0007g0195 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.329-8164A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235038 | |||||||
| chr9:136235057 | G | A | 1 | a0001c0019t0036g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.329-8183C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235057 | |||||||
| chr9:136235201 | C | T | 1 | a0002c0003t0002g0231 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.329-8327G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235201 | |||||||
| chr9:136235289 | G | C | 10 | a0001c0001t0007g0193 a0001c0001t0007g0274 a0001c0002t0006g0057 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.329-8415C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235289 | |||||||
| chr9:136235474 | G | A | 1 | a0001c0001t0002g0296 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.329-8600C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235474 | |||||||
| chr9:136235598 | A | T | 1 | a0002c0003t0002g0231 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.329-8724T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235598 | |||||||
| chr9:136235628 | G | A | 1 | a0001c0001t0054g0309 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.329-8754C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235628 | |||||||
| chr9:136235643 | G | T | 12 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0010g0250 others(9): Show |
12 | HG00741.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.329-8769C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235643 | |||||||
| chr9:136235649 | T | G | 1 | a0001c0008t0013g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.329-8775A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235649 | |||||||
| chr9:136235719 | G | A | 1 | a0001c0001t0020g0196 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.329-8845C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235719 | |||||||
| chr9:136235720 | C | A | 76 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0224 others(73): Show |
109 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.329-8846G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235720 | |||||||
| chr9:136235721 | G | A | 3 | a0001c0001t0007g0301 a0001c0001t0007g0302 a0001c0001t0053g0303 |
3 | HG02258.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.329-8847C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235721 | |||||||
| chr9:136235750 | C | T | 5 | a0001c0001t0004g0029 a0001c0001t0004g0259 a0001c0001t0004g0260 others(2): Show |
6 | HG02135.hp2 NA18961.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-8876G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235750 | |||||||
| chr9:136235761 | A | G | 4 | a0001c0002t0012g0012 a0001c0002t0012g0044 a0001c0002t0012g0045 others(1): Show |
6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.329-8887T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235761 | |||||||
| chr9:136235763 | A | C | 1 | a0001c0001t0007g0301 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.329-8889T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235763 | |||||||
| chr9:136235832 | G | A | 2 | a0001c0020t0003g0171 a0007c0021t0019g0170 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.329-8958C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235832 | |||||||
| chr9:136235876 | A | G | 1 | a0001c0008t0041g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.329-9002T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235876 | |||||||
| chr9:136235912 | T | G | 1 | a0001c0001t0053g0303 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.329-9038A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136235912 | |||||||
| chr9:136236150 | G | C | 1 | a0001c0005t0005g0297 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.329-9276C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236150 | |||||||
| chr9:136236195 | T | C | 2 | a0001c0005t0005g0297 a0001c0008t0013g0047 |
2 | HG02083.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328+9281A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236195 | |||||||
| chr9:136236221 | A | G | 19 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(16): Show |
19 | HG00741.hp2 HG01069.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.328+9255T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236221 | |||||||
| chr9:136236236 | G | A | 2 | a0001c0001t0001g0224 a0001c0001t0005g0225 |
2 | NA18975.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.328+9240C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236236 | |||||||
| chr9:136236243 | G | A | 12 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0010g0250 others(9): Show |
12 | HG00741.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.328+9233C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236243 | |||||||
| chr9:136236268 | G | T | 1 | a0001c0005t0004g0191 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.328+9208C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236268 | |||||||
| chr9:136236345 | A | ATGT | 35 | a0001c0001t0002g0296 a0001c0001t0004g0178 a0001c0001t0004g0179 others(32): Show |
42 | HG01069.hp2 HG01106.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.328+9130_328+9131i others(5): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236345 | |||||||
| chr9:136236358 | C | T | 3 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0006g0057 |
3 | HG01891.hp1 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.328+9118G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236358 | |||||||
| chr9:136236468 | G | A | 17 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(14): Show |
18 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.328+9008C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236468 | |||||||
| chr9:136236495 | C | T | 4 | a0001c0002t0012g0012 a0001c0002t0012g0044 a0001c0002t0012g0045 others(1): Show |
6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.328+8981G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236495 | |||||||
| chr9:136236647 | G | A | 1 | a0001c0001t0007g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.328+8829C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236647 | |||||||
| chr9:136236711 | G | A | 1 | a0001c0007t0003g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.328+8765C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236711 | |||||||
| chr9:136236723 | T | C | 66 | a0001c0001t0002g0264 a0001c0001t0002g0296 a0001c0001t0004g0011 others(63): Show |
77 | HG00323.hp1 HG00609.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.328+8753A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236723 | |||||||
| chr9:136236738 | G | A | 1 | a0001c0004t0003g0138 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.328+8738C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236738 | |||||||
| chr9:136236785 | G | A | 30 | a0001c0002t0001g0016 a0001c0002t0001g0026 a0001c0002t0001g0027 others(27): Show |
41 | HG00408.hp1 HG00558.hp1 HG02015.hp1 others(38): Show |
intron_variant | MODIFIER | c.328+8691C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236785 | |||||||
| chr9:136236789 | G | A | 2 | a0001c0005t0005g0183 a0001c0005t0005g0184 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.328+8687C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236789 | |||||||
| chr9:136236833 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0008g0207 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.328+8643T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236833 | |||||||
| chr9:136236901 | AGCCCGTC others(43): Show |
A | 1 | a0001c0004t0003g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.328+8525_328+8574d others(52): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236901 | |||||||
| chr9:136236905 | C | T | 20 | a0001c0001t0002g0264 a0001c0001t0004g0011 a0001c0001t0004g0029 others(17): Show |
24 | HG00323.hp1 HG00609.hp1 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.328+8571G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236905 | |||||||
| chr9:136236966 | ACACCTGG others(20): Show |
A | 1 | a0001c0005t0005g0297 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.328+8483_328+8509d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236966 | |||||||
| chr9:136236978 | TGTCCTGG others(20): Show |
T | 1 | a0001c0002t0001g0013 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.328+8471_328+8497d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136236978 | |||||||
| chr9:136237016 | G | A | 2 | a0001c0005t0001g0192 a0008c0018t0001g0169 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.328+8460C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237016 | |||||||
| chr9:136237032 | T | TGTCCTGG others(20): Show |
1 | a0002c0003t0002g0246 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.328+8443_328+8444i others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237032 | |||||||
| chr9:136237032 | T | TGTCCTGT others(16): Show |
1 | a0001c0026t0005g0306 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.328+8421_328+8443d others(25): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237032 | |||||||
| chr9:136237032 | TGTCCTGT others(16): Show |
T | 1 | a0002c0003t0002g0291 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.328+8421_328+8443d others(25): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237032 | |||||||
| chr9:136237125 | A | ATCCTGGG others(20): Show |
2 | a0001c0001t0004g0257 a0001c0001t0004g0258 |
2 | HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.328+8324_328+8350d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237125 | |||||||
| chr9:136237138 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.328+8338C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237138 | |||||||
| chr9:136237278 | C | T | 2 | a0001c0001t0007g0038 a0001c0001t0007g0226 |
3 | HG01074.hp1 HG01167.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.328+8198G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237278 | |||||||
| chr9:136237293 | TCACCTGG others(170): Show |
T | 2 | a0001c0001t0007g0038 a0001c0001t0007g0226 |
3 | HG01074.hp1 HG01167.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.328+8006_328+8182d others(2): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237293 | |||||||
| chr9:136237405 | T | C | 2 | a0001c0001t0020g0196 a0001c0004t0003g0127 |
2 | HG02004.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.328+8071A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237405 | |||||||
| chr9:136237433 | GTCCTGTG others(16): Show |
G | 1 | a0001c0004t0027g0089 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.328+8020_328+8042d others(25): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237433 | |||||||
| chr9:136237456 | A | ATCCTGTG others(20): Show |
1 | a0001c0002t0001g0015 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.328+8019_328+8020i others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | |||||||
| chr9:136237456 | A | ATCCTGTG others(20): Show |
83 | a0001c0001t0004g0185 a0001c0001t0004g0188 a0001c0001t0004g0190 others(80): Show |
96 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.328+7993_328+8019d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | |||||||
| chr9:136237456 | A | ATCCTGTG others(47): Show |
7 | a0001c0001t0007g0193 a0001c0001t0007g0194 a0001c0001t0007g0195 others(4): Show |
11 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.328+7966_328+8019d others(56): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | |||||||
| chr9:136237456 | A | ATCCTGTG others(74): Show |
3 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 |
3 | HG01069.hp2 HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.328+7939_328+8019d others(83): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | |||||||
| chr9:136237456 | A | G | 1 | a0001c0002t0001g0069 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.328+8020T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | |||||||
| chr9:136237456 | ATCCTGTG others(20): Show |
A | 63 | a0001c0001t0001g0208 a0001c0001t0001g0290 a0001c0001t0002g0247 others(60): Show |
89 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.328+7993_328+8019d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | |||||||
| chr9:136237456 | ATCCTGTG others(47): Show |
A | 23 | a0001c0001t0001g0034 a0001c0001t0001g0210 a0001c0001t0001g0224 others(20): Show |
32 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.328+7966_328+8019d others(56): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237456 | |||||||
| chr9:136237492 | CGGCG | C | 2 | a0001c0001t0007g0038 a0001c0001t0007g0226 |
3 | HG01074.hp1 HG01167.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.328+7980_328+7983d others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237492 | |||||||
| chr9:136237495 | C | T | 1 | a0001c0001t0004g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.328+7981G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237495 | |||||||
| chr9:136237510 | G | A | 2 | a0001c0001t0007g0038 a0001c0001t0007g0226 |
3 | HG01074.hp1 HG01167.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.328+7966C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237510 | |||||||
| chr9:136237519 | C | T | 1 | a0001c0005t0005g0297 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.328+7957G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237519 | |||||||
| chr9:136237524 | A | ACACCTGG others(97): Show |
1 | a0001c0017t0011g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.328+7951_328+7952i others(106): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237524 | |||||||
| chr9:136237524 | ACACCTGG others(43): Show |
A | 1 | a0001c0002t0037g0160 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.328+7902_328+7951d others(52): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237524 | |||||||
| chr9:136237545 | CCACACCT others(16): Show |
C | 10 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0010g0250 others(7): Show |
10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.328+7908_328+7930d others(25): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237545 | |||||||
| chr9:136237568 | G | C | 57 | a0001c0001t0002g0264 a0001c0001t0002g0296 a0001c0001t0004g0011 others(54): Show |
68 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.328+7908C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237568 | |||||||
| chr9:136237569 | C | T | 23 | a0001c0001t0002g0296 a0001c0001t0004g0178 a0001c0001t0004g0179 others(20): Show |
24 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.328+7907G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237569 | |||||||
| chr9:136237610 | A | G | 1 | a0001c0017t0011g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.328+7866T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237610 | |||||||
| chr9:136237695 | C | T | 6 | a0001c0002t0012g0012 a0001c0002t0012g0044 a0001c0002t0012g0045 others(3): Show |
8 | HG01109.hp2 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.328+7781G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237695 | |||||||
| chr9:136237698 | C | T | 7 | a0001c0001t0007g0193 a0001c0001t0007g0194 a0001c0001t0007g0195 others(4): Show |
11 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.328+7778G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237698 | |||||||
| chr9:136237720 | G | A | 1 | a0001c0001t0020g0196 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.328+7756C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237720 | |||||||
| chr9:136237795 | C | T | 3 | a0001c0004t0003g0052 a0001c0004t0003g0053 a0001c0004t0003g0054 |
3 | HG00639.hp1 HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.328+7681G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237795 | |||||||
| chr9:136237914 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0008g0207 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.328+7562C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237914 | |||||||
| chr9:136237973 | A | G | 1 | a0001c0001t0007g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.328+7503T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237973 | |||||||
| chr9:136237974 | T | C | 1 | a0001c0001t0004g0180 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.328+7502A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136237974 | |||||||
| chr9:136238129 | G | A | 1 | a0001c0023t0030g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.328+7347C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238129 | |||||||
| chr9:136238244 | C | T | 1 | a0001c0001t0004g0256 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.328+7232G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238244 | |||||||
| chr9:136238252 | C | G | 5 | a0001c0001t0002g0247 a0001c0001t0015g0203 a0001c0001t0051g0202 others(2): Show |
5 | HG01261.hp2 HG02622.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.328+7224G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238252 | |||||||
| chr9:136238380 | G | A | 1 | a0001c0001t0020g0196 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.328+7096C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238380 | |||||||
| chr9:136238392 | CCAAA | C | 5 | a0001c0005t0005g0030 a0001c0005t0005g0181 a0001c0005t0005g0183 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.328+7080_328+7083d others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238392 | |||||||
| chr9:136238489 | G | C | 10 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0010g0250 others(7): Show |
10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.328+6987C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238489 | |||||||
| chr9:136238518 | G | A | 79 | a0001c0001t0001g0034 a0001c0001t0001g0210 a0001c0001t0001g0224 others(76): Show |
113 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.328+6958C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238518 | |||||||
| chr9:136238536 | G | A | 24 | a0001c0001t0001g0034 a0001c0001t0001g0210 a0001c0001t0001g0224 others(21): Show |
34 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.328+6940C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238536 | |||||||
| chr9:136238613 | C | G | 7 | a0001c0001t0007g0193 a0001c0001t0007g0194 a0001c0001t0007g0195 others(4): Show |
11 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.328+6863G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238613 | |||||||
| chr9:136238663 | C | T | 1 | a0001c0001t0007g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.328+6813G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238663 | |||||||
| chr9:136238664 | G | A | 1 | a0001c0023t0030g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.328+6812C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238664 | |||||||
| chr9:136238693 | A | G | 2 | a0002c0003t0002g0227 a0002c0003t0002g0228 |
2 | HG03831.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.328+6783T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238693 | |||||||
| chr9:136238771 | G | A | 4 | a0001c0001t0011g0003 a0001c0001t0011g0173 a0001c0001t0011g0197 others(1): Show |
8 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.328+6705C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238771 | |||||||
| chr9:136238901 | C | T | 1 | a0001c0002t0006g0051 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.328+6575G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136238901 | |||||||
| chr9:136239096 | C | A | 1 | a0001c0023t0030g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.328+6380G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239096 | |||||||
| chr9:136239145 | T | G | 2 | a0001c0001t0007g0301 a0001c0001t0007g0302 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.328+6331A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239145 | |||||||
| chr9:136239431 | G | C | 3 | a0002c0003t0001g0292 a0002c0003t0002g0293 a0002c0003t0002g0294 |
3 | NA18941.hp1 NA18955.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.328+6045C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239431 | |||||||
| chr9:136239469 | C | T | 24 | a0001c0001t0001g0034 a0001c0001t0001g0210 a0001c0001t0001g0224 others(21): Show |
34 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.328+6007G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239469 | |||||||
| chr9:136239791 | C | CCGAG | 2 | a0001c0002t0001g0013 a0001c0002t0006g0050 |
4 | HG00438.hp1 HG02132.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.328+5681_328+5684d others(6): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239791 | |||||||
| chr9:136239799 | A | G | 10 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0010g0250 others(7): Show |
10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.328+5677T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239799 | |||||||
| chr9:136239847 | C | T | 1 | a0001c0005t0005g0297 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.328+5629G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136239847 | |||||||
| chr9:136240100 | T | TG | 167 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(164): Show |
215 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.328+5375dupC | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240100 | |||||||
| chr9:136240166 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.328+5310C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240166 | |||||||
| chr9:136240216 | G | C | 1 | a0001c0001t0053g0303 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.328+5260C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240216 | |||||||
| chr9:136240394 | C | A | 78 | a0001c0001t0001g0034 a0001c0001t0001g0210 a0001c0001t0001g0224 others(75): Show |
112 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.328+5082G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240394 | |||||||
| chr9:136240449 | G | A | 24 | a0001c0001t0007g0193 a0001c0001t0007g0194 a0001c0001t0007g0195 others(21): Show |
30 | HG00741.hp2 HG01109.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.328+5027C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240449 | |||||||
| chr9:136240454 | T | C | 25 | a0001c0001t0007g0193 a0001c0001t0007g0194 a0001c0001t0007g0195 others(22): Show |
32 | HG00741.hp2 HG01074.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.328+5022A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240454 | |||||||
| chr9:136240454 | T | G | 1 | a0001c0001t0004g0271 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.328+5022A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240454 | |||||||
| chr9:136240744 | T | C | 1 | a0001c0007t0004g0162 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.328+4732A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240744 | |||||||
| chr9:136240762 | G | A | 3 | a0001c0001t0002g0247 a0001c0001t0015g0203 a0001c0001t0051g0202 |
3 | HG01261.hp2 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.328+4714C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240762 | |||||||
| chr9:136240910 | C | T | 1 | a0001c0001t0010g0273 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328+4566G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240910 | |||||||
| chr9:136240933 | G | GCAGTGCT others(20): Show |
1 | a0002c0003t0015g0205 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.328+4516_328+4542d others(29): Show |
QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136240933 | |||||||
| chr9:136241187 | A | G | 73 | a0001c0001t0002g0264 a0001c0001t0002g0296 a0001c0001t0004g0011 others(70): Show |
87 | HG00323.hp1 HG00609.hp1 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.328+4289T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241187 | |||||||
| chr9:136241256 | C | A | 7 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(4): Show |
10 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.328+4220G>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241256 | |||||||
| chr9:136241299 | G | T | 1 | a0001c0001t0007g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.328+4177C>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241299 | |||||||
| chr9:136241391 | C | T | 1 | a0002c0003t0002g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.328+4085G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241391 | |||||||
| chr9:136241521 | A | G | 3 | a0001c0001t0007g0193 a0001c0001t0007g0194 a0001c0001t0007g0195 |
3 | HG02258.hp2 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.328+3955T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241521 | |||||||
| chr9:136241691 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.328+3785C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241691 | |||||||
| chr9:136241772 | G | A | 4 | a0001c0002t0002g0008 a0001c0002t0002g0164 a0001c0002t0002g0165 others(1): Show |
7 | NA18954.hp2 NA18964.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+3704C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241772 | |||||||
| chr9:136241897 | G | A | 1 | a0001c0001t0010g0273 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328+3579C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241897 | |||||||
| chr9:136241901 | G | C | 10 | a0001c0001t0004g0039 a0001c0001t0004g0275 a0001c0001t0004g0279 others(7): Show |
12 | HG01884.hp2 HG02280.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.328+3575C>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136241901 | |||||||
| chr9:136242038 | A | C | 2 | a0001c0001t0002g0296 a0001c0001t0032g0295 |
2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.328+3438T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242038 | |||||||
| chr9:136242043 | T | C | 3 | a0001c0001t0026g0307 a0001c0001t0026g0308 a0001c0001t0054g0309 |
3 | HG02165.hp1 HG03831.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.328+3433A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242043 | |||||||
| chr9:136242086 | T | G | 7 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(4): Show |
10 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.328+3390A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242086 | |||||||
| chr9:136242095 | C | G | 17 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(14): Show |
18 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.328+3381G>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242095 | |||||||
| chr9:136242291 | T | C | 5 | a0001c0001t0002g0296 a0001c0001t0026g0307 a0001c0001t0026g0308 others(2): Show |
5 | HG02027.hp2 HG02129.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.328+3185A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242291 | |||||||
| chr9:136242303 | C | T | 3 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 |
3 | HG01069.hp2 HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.328+3173G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242303 | |||||||
| chr9:136242369 | C | T | 4 | a0001c0002t0012g0012 a0001c0002t0012g0044 a0001c0002t0012g0045 others(1): Show |
6 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.328+3107G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242369 | |||||||
| chr9:136242382 | G | A | 7 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0033 others(4): Show |
10 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.328+3094C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242382 | |||||||
| chr9:136242599 | C | T | 1 | a0001c0008t0041g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.328+2877G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242599 | |||||||
| chr9:136242613 | G | A | 2 | a0004c0009t0004g0304 a0004c0009t0004g0305 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.328+2863C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242613 | |||||||
| chr9:136242623 | C | T | 2 | a0001c0001t0015g0203 a0001c0001t0051g0202 |
2 | HG01261.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.328+2853G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242623 | |||||||
| chr9:136242628 | T | C | 90 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(87): Show |
124 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.328+2848A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242628 | |||||||
| chr9:136242673 | A | G | 1 | a0001c0001t0007g0255 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.328+2803T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242673 | |||||||
| chr9:136242702 | A | C | 17 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(14): Show |
18 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.328+2774T>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242702 | |||||||
| chr9:136242832 | C | T | 1 | a0001c0001t0004g0039 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.328+2644G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242832 | |||||||
| chr9:136242833 | G | A | 10 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0010g0250 others(7): Show |
10 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.328+2643C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242833 | |||||||
| chr9:136242839 | T | C | 18 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(15): Show |
19 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.328+2637A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136242839 | |||||||
| chr9:136243005 | C | T | 1 | a0001c0004t0003g0048 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.328+2471G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243005 | |||||||
| chr9:136243006 | G | A | 1 | a0001c0019t0036g0254 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328+2470C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243006 | |||||||
| chr9:136243135 | A | G | 135 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0210 others(132): Show |
179 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.328+2341T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243135 | |||||||
| chr9:136243307 | C | T | 1 | a0001c0002t0006g0043 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.328+2169G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243307 | |||||||
| chr9:136243308 | G | A | 1 | a0001c0001t0007g0038 | 2 | HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.328+2168C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243308 | |||||||
| chr9:136243470 | T | C | 2 | a0001c0005t0001g0192 a0008c0018t0001g0169 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.328+2006A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243470 | |||||||
| chr9:136243920 | C | T | 1 | a0001c0002t0018g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.328+1556G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243920 | |||||||
| chr9:136243949 | T | C | 17 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(14): Show |
18 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.328+1527A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136243949 | |||||||
| chr9:136244008 | T | C | 10 | a0001c0001t0004g0039 a0001c0001t0004g0275 a0001c0001t0004g0279 others(7): Show |
12 | HG01884.hp2 HG02280.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.328+1468A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244008 | |||||||
| chr9:136244118 | T | G | 8 | a0001c0001t0001g0290 a0002c0003t0002g0283 a0002c0003t0002g0284 others(5): Show |
8 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.328+1358A>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244118 | |||||||
| chr9:136244133 | A | T | 2 | a0001c0001t0002g0296 a0001c0001t0032g0295 |
2 | HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.328+1343T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244133 | |||||||
| chr9:136244551 | A | T | 17 | a0001c0001t0004g0178 a0001c0001t0004g0179 a0001c0001t0004g0180 others(14): Show |
18 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.328+925T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244551 | |||||||
| chr9:136244694 | C | T | 2 | a0001c0001t0004g0029 a0001c0001t0021g0177 |
3 | NA18998.hp2 NA19058.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.328+782G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244694 | |||||||
| chr9:136244884 | A | T | 4 | a0001c0001t0010g0174 a0001c0001t0010g0176 a0001c0001t0033g0175 others(1): Show |
4 | HG00741.hp2 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.328+592T>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244884 | |||||||
| chr9:136244895 | G | A | 5 | a0002c0003t0001g0292 a0002c0003t0002g0005 a0002c0003t0002g0291 others(2): Show |
9 | HG00673.hp2 HG02040.hp2 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.328+581C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244895 | |||||||
| chr9:136244982 | A | G | 3 | a0001c0001t0011g0003 a0001c0001t0011g0173 a0001c0017t0011g0168 |
7 | HG01496.hp2 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+494T>C | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244982 | |||||||
| chr9:136244997 | C | T | 1 | a0005c0025t0002g0172 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.328+479G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136244997 | |||||||
| chr9:136245132 | T | C | 5 | a0001c0001t0002g0296 a0001c0001t0026g0307 a0001c0001t0026g0308 others(2): Show |
5 | HG02027.hp2 HG02129.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.328+344A>G | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136245132 | |||||||
| chr9:136245324 | C | T | 2 | a0001c0020t0003g0171 a0007c0021t0019g0170 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.328+152G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136245324 | |||||||
| chr9:136245331 | C | T | 2 | a0001c0020t0003g0171 a0007c0021t0019g0170 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.328+145G>A | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136245331 | |||||||
| chr9:136245358 | G | A | 155 | a0001c0001t0007g0299 a0001c0001t0007g0300 a0001c0001t0007g0301 others(152): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.328+118C>T | QSOX2 | ENSG00000165661.18 | transcript | ENST00000358701.10 | protein_coding | 1/11 | chr9 | 136245358 |