Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5768 |
| ensemblid | ENSG00000116260.17 |
| hgncid | 9756 |
| symbol | QSOX1 |
| name | quiescin sulfhydryl oxidase 1 |
| refseq_nuc | NM_002826.5 |
| refseq_prot | NP_002817.2 |
| ensembl_nuc | ENST00000367602.8 |
| ensembl_prot | ENSP00000356574.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 180154869 |
| end | 180204030 |
| strand | + |
| ver | v1.2 |
| region | chr1:180154869-180204030 |
| region5000 | chr1:180149869-180209030 |
| regionname0 | QSOX1_chr1_180154869_180204030 |
| regionname5000 | QSOX1_chr1_180149869_180209030 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 747 | 275 | 66 | 46 | 112 | 14 | 35 | 80 | QSOX1_chr1_180149869_180209030 | QSOX1 | MRRCN others(742): Show |
chr1 | 180149869 | 180209030 |
| a0002 | 0/0 | 747 | 47 | 0 | 1 | 44 | 1 | 1 | 35 | QSOX1_chr1_180149869_180209030 | QSOX1 | MRRCN others(742): Show |
chr1 | 180149869 | 180209030 |
| a0003 | 0/0 | 747 | 28 | 6 | 5 | 15 | 0 | 2 | 12 | QSOX1_chr1_180149869_180209030 | QSOX1 | MRRCN others(742): Show |
chr1 | 180149869 | 180209030 |
| a0004 | 0/0 | 747 | 16 | 5 | 6 | 0 | 3 | 2 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | MRRCN others(742): Show |
chr1 | 180149869 | 180209030 |
| a0005 | 0/0 | 747 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | MRRCN others(742): Show |
chr1 | 180149869 | 180209030 |
| a0006 | 0/0 | 747 | 5 | 0 | 4 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | MRRCN others(742): Show |
chr1 | 180149869 | 180209030 |
| a0007 | 0/0 | 693 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | MRRCN others(688): Show |
chr1 | 180149869 | 180209030 |
| a0008 | 0/0 | 747 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | MRRCN others(742): Show |
chr1 | 180149869 | 180209030 |
| a0009 | 0/0 | 747 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | MRRCN others(742): Show |
chr1 | 180149869 | 180209030 |
| a0010 | 0/0 | 747 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | MRRCN others(742): Show |
chr1 | 180149869 | 180209030 |
| a0011 | 0/0 | 747 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | MRRCN others(742): Show |
chr1 | 180149869 | 180209030 |
| a0012 | 0/0 | 747 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | MRRCN others(742): Show |
chr1 | 180149869 | 180209030 |
| a0013 | 0/0 | 747 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | MRRCN others(742): Show |
chr1 | 180149869 | 180209030 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2241 | 159 | 19 | 35 | 74 | 9 | 21 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0001c0002 | 1/0 | 2241 | 62 | 14 | 7 | 29 | 1 | 10 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0001c0004 | 0/0 | 2241 | 35 | 23 | 4 | 0 | 4 | 4 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0001c0007 | 0/0 | 2241 | 9 | 0 | 0 | 9 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0001c0012 | 0/0 | 2241 | 4 | 4 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0001c0013 | 0/0 | 2241 | 4 | 4 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0001c0017 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0001c0021 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0002c0003 | 0/0 | 2241 | 47 | 0 | 1 | 44 | 1 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0003c0005 | 0/0 | 2241 | 22 | 6 | 5 | 9 | 0 | 2 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0003c0009 | 0/0 | 2241 | 6 | 0 | 0 | 6 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0004c0006 | 0/0 | 2241 | 10 | 0 | 5 | 0 | 3 | 2 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0004c0011 | 0/0 | 2241 | 4 | 3 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0004c0018 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0004c0019 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0005c0008 | 0/0 | 2241 | 8 | 7 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0006c0010 | 0/0 | 2241 | 5 | 0 | 4 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0007c0015 | 0/0 | 2241 | 2 | 1 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0008c0014 | 0/0 | 2241 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0009c0016 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0010c0023 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0011c0020 | 0/0 | 2241 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0012c0024 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 | ||
| a0013c0022 | 0/0 | 2241 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATGAG others(2236): Show |
chr1 | 180149869 | 180209030 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 9279 | 88 | 0 | 18 | 49 | 6 | 14 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9274): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0002 | 0/0 | 9276 | 7 | 0 | 0 | 5 | 0 | 2 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0003 | 0/0 | 9278 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0004 | 0/0 | 9276 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0005 | 0/0 | 9276 | 3 | 2 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0006 | 0/0 | 9280 | 14 | 1 | 7 | 3 | 0 | 3 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9275): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0007 | 0/0 | 9276 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0008 | 0/0 | 9278 | 7 | 0 | 1 | 5 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0011 | 0/0 | 9276 | 6 | 0 | 0 | 6 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0013 | 0/0 | 9278 | 5 | 1 | 4 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0014 | 0/0 | 9273 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9268): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0015 | 0/0 | 9278 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0016 | 0/0 | 9278 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0022 | 0/0 | 9278 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0023 | 0/0 | 9279 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9274): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0024 | 0/0 | 9276 | 2 | 0 | 1 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0026 | 0/0 | 9276 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0032 | 0/0 | 9276 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0034 | 0/0 | 9292 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9287): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0036 | 0/0 | 9276 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0037 | 0/0 | 9278 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0042 | 0/0 | 9279 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9274): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0045 | 0/0 | 9279 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9274): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0046 | 0/0 | 9278 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0048 | 0/0 | 9279 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9274): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0049 | 0/0 | 9277 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9272): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0050 | 0/0 | 9278 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0052 | 0/0 | 9277 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9272): Show |
chr1 | 180149869 | 180209030 |
| a0001c0001t0059 | 0/0 | 9280 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9275): Show |
chr1 | 180149869 | 180209030 |
| a0001c0002t0002 | 0/0 | 9276 | 42 | 3 | 6 | 27 | 1 | 5 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0002t0019 | 0/0 | 9277 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9272): Show |
chr1 | 180149869 | 180209030 |
| a0001c0002t0020 | 0/0 | 9276 | 3 | 0 | 0 | 0 | 0 | 3 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0002t0025 | 0/0 | 9275 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9270): Show |
chr1 | 180149869 | 180209030 |
| a0001c0002t0027 | 0/0 | 9274 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9269): Show |
chr1 | 180149869 | 180209030 |
| a0001c0002t0030 | 0/0 | 9276 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0002t0031 | 0/0 | 9276 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0002t0040 | 1/0 | 9276 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0002t0058 | 0/0 | 9276 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0002t0061 | 0/0 | 9276 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0002t0062 | 0/0 | 9276 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0002t0063 | 0/0 | 9277 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9272): Show |
chr1 | 180149869 | 180209030 |
| a0001c0002t0064 | 0/0 | 9274 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9269): Show |
chr1 | 180149869 | 180209030 |
| a0001c0004t0004 | 0/0 | 9276 | 26 | 20 | 2 | 0 | 2 | 2 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0004t0005 | 0/0 | 9276 | 2 | 1 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0004t0012 | 0/0 | 9277 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9272): Show |
chr1 | 180149869 | 180209030 |
| a0001c0004t0028 | 0/0 | 9276 | 2 | 0 | 0 | 0 | 1 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0004t0033 | 0/0 | 9277 | 2 | 1 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9272): Show |
chr1 | 180149869 | 180209030 |
| a0001c0004t0053 | 0/0 | 9276 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0004t0054 | 0/0 | 9275 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9270): Show |
chr1 | 180149869 | 180209030 |
| a0001c0007t0001 | 0/0 | 9279 | 7 | 0 | 0 | 7 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9274): Show |
chr1 | 180149869 | 180209030 |
| a0001c0007t0006 | 0/0 | 9280 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9275): Show |
chr1 | 180149869 | 180209030 |
| a0001c0007t0026 | 0/0 | 9276 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0012t0018 | 0/0 | 9274 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9269): Show |
chr1 | 180149869 | 180209030 |
| a0001c0012t0057 | 0/0 | 9274 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9269): Show |
chr1 | 180149869 | 180209030 |
| a0001c0013t0017 | 0/0 | 9277 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9272): Show |
chr1 | 180149869 | 180209030 |
| a0001c0013t0056 | 0/0 | 9277 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9272): Show |
chr1 | 180149869 | 180209030 |
| a0001c0017t0055 | 0/0 | 9276 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0001c0021t0015 | 0/0 | 9278 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0002c0003t0003 | 0/0 | 9278 | 36 | 0 | 1 | 34 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0002c0003t0010 | 0/0 | 9279 | 6 | 0 | 0 | 6 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9274): Show |
chr1 | 180149869 | 180209030 |
| a0002c0003t0011 | 0/0 | 9276 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0002c0003t0029 | 0/0 | 9279 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9274): Show |
chr1 | 180149869 | 180209030 |
| a0002c0003t0038 | 0/0 | 9278 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0002c0003t0041 | 0/0 | 9279 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9274): Show |
chr1 | 180149869 | 180209030 |
| a0003c0005t0002 | 0/0 | 9276 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0003c0005t0005 | 0/0 | 9276 | 13 | 0 | 5 | 8 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0003c0005t0012 | 0/0 | 9277 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9272): Show |
chr1 | 180149869 | 180209030 |
| a0003c0005t0021 | 0/0 | 9276 | 3 | 1 | 0 | 0 | 0 | 2 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0003c0005t0051 | 0/0 | 9276 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0003c0009t0001 | 0/0 | 9279 | 4 | 0 | 0 | 4 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9274): Show |
chr1 | 180149869 | 180209030 |
| a0003c0009t0006 | 0/0 | 9280 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9275): Show |
chr1 | 180149869 | 180209030 |
| a0003c0009t0043 | 0/0 | 9279 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9274): Show |
chr1 | 180149869 | 180209030 |
| a0004c0006t0007 | 0/0 | 9276 | 9 | 0 | 5 | 0 | 2 | 2 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0004c0006t0039 | 0/0 | 9276 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0004c0011t0008 | 0/0 | 9278 | 2 | 1 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0004c0011t0035 | 0/0 | 9278 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0004c0011t0044 | 0/0 | 9277 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9272): Show |
chr1 | 180149869 | 180209030 |
| a0004c0018t0008 | 0/0 | 9278 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0004c0019t0014 | 0/0 | 9273 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9268): Show |
chr1 | 180149869 | 180209030 |
| a0005c0008t0009 | 0/0 | 9277 | 8 | 7 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9272): Show |
chr1 | 180149869 | 180209030 |
| a0006c0010t0007 | 0/0 | 9276 | 5 | 0 | 4 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0007c0015t0016 | 0/0 | 9278 | 2 | 1 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9273): Show |
chr1 | 180149869 | 180209030 |
| a0008c0014t0012 | 0/0 | 9277 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9272): Show |
chr1 | 180149869 | 180209030 |
| a0009c0016t0004 | 0/0 | 9276 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0010c0023t0047 | 0/0 | 9276 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0011c0020t0002 | 0/0 | 9276 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0012c0024t0060 | 0/0 | 9276 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9271): Show |
chr1 | 180149869 | 180209030 |
| a0013c0022t0010 | 0/0 | 9279 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | ATCCG others(9274): Show |
chr1 | 180149869 | 180209030 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 0 | 0 | 8 | 1 | 3 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0006g0001 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0006g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0006g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0008g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0008g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0008g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0008g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0008g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0008g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0011g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0011g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0011g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0011g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0013g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0013g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0013g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0013g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0014g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0014g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0014g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0015g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0015g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0016g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0022g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0022g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0023g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0024g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0024g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0026g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0032g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0034g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0036g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0037g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0042g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0045g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0046g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0048g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0049g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0050g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0052g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0001t0059g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0002 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0019g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0020g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0020g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0025g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0027g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0027g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0030g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0031g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0031g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0040g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0058g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0061g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0062g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0063g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0002t0064g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0011 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0005g0044 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0012g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0028g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0028g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0033g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0033g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0053g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0004t0054g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0007t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0007t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0007t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0007t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0007t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0007t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0007t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0007t0026g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0012t0018g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0012t0018g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0012t0018g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0012t0057g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0013t0017g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0013t0056g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0017t0055g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0001c0021t0015g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0006 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0010g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0010g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0010g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0010g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0011g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0029g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0029g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0038g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0002c0003t0041g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0005g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0005g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0005g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0012g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0021g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0021g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0005t0051g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0009t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0009t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0009t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0009t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0003c0009t0043g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0006t0007g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0006t0007g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0006t0007g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0006t0007g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0006t0007g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0006t0007g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0006t0007g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0006t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0006t0039g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0011t0008g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0011t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0011t0035g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0011t0044g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0018t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0004c0019t0014g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0005c0008t0009g0003 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0006c0010t0007g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0006c0010t0007g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0006c0010t0007g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0006c0010t0007g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0007c0015t0016g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0008c0014t0012g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0009c0016t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0010c0023t0047g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0011c0020t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0012c0024t0060g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| a0013c0022t0010g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0033 | g0126 | EUR | GBR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | GBR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00140 | hp1 | a0001 | c0001 | t0042 | g0001 | EUR | GBR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00140 | hp2 | a0001 | c0001 | t0048 | g0140 | EUR | GBR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0234 | EUR | FIN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00280 | hp2 | a0002 | c0003 | t0003 | g0078 | EUR | FIN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00323 | hp1 | a0001 | c0004 | t0028 | g0018 | EUR | FIN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00408 | hp1 | a0001 | c0001 | t0023 | g0007 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00423 | hp1 | a0003 | c0005 | t0051 | g0107 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00438 | hp1 | a0001 | c0001 | t0006 | g0240 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00544 | hp1 | a0002 | c0003 | t0003 | g0015 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00544 | hp2 | a0001 | c0001 | t0008 | g0184 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00639 | hp2 | a0001 | c0001 | t0013 | g0142 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0239 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00642 | hp2 | a0001 | c0001 | t0013 | g0046 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00735 | hp1 | a0004 | c0006 | t0007 | g0037 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG00738 | hp2 | a0004 | c0006 | t0007 | g0037 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01069 | hp1 | a0001 | c0001 | t0008 | g0054 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01069 | hp2 | a0004 | c0011 | t0008 | g0248 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01070 | hp2 | a0006 | c0010 | t0007 | g0090 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0152 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01074 | hp2 | a0001 | c0004 | t0012 | g0128 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01099 | hp1 | a0001 | c0001 | t0013 | g0046 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01099 | hp2 | a0001 | c0004 | t0004 | g0129 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01109 | hp1 | a0006 | c0010 | t0007 | g0091 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01109 | hp2 | a0005 | c0008 | t0009 | g0003 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01167 | hp1 | a0001 | c0002 | t0061 | g0163 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01167 | hp2 | a0001 | c0001 | t0013 | g0045 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01168 | hp1 | a0003 | c0005 | t0005 | g0108 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0051 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01169 | hp2 | a0001 | c0001 | t0049 | g0045 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01175 | hp1 | a0001 | c0001 | t0050 | g0141 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0086 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01243 | hp2 | a0007 | c0015 | t0016 | g0035 | AMR | PUR | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01255 | hp1 | a0006 | c0010 | t0007 | g0095 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01256 | hp1 | a0001 | c0001 | t0024 | g0246 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0022 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01258 | hp2 | a0003 | c0005 | t0005 | g0039 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0169 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01346 | hp1 | a0001 | c0004 | t0054 | g0123 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01358 | hp1 | a0003 | c0005 | t0005 | g0039 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01361 | hp1 | a0003 | c0005 | t0005 | g0010 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01433 | hp1 | a0004 | c0006 | t0007 | g0097 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01496 | hp1 | a0002 | c0003 | t0003 | g0006 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01496 | hp2 | a0006 | c0010 | t0007 | g0036 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01515 | hp2 | a0004 | c0006 | t0007 | g0094 | EUR | IBS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01516 | hp1 | a0001 | c0004 | t0004 | g0043 | EUR | IBS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01517 | hp1 | a0001 | c0004 | t0004 | g0043 | EUR | IBS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01884 | hp1 | a0001 | c0001 | t0037 | g0089 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01884 | hp2 | a0001 | c0013 | t0017 | g0019 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01891 | hp1 | a0001 | c0001 | t0036 | g0151 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01891 | hp2 | a0003 | c0005 | t0012 | g0111 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | PEL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02004 | hp2 | a0001 | c0004 | t0004 | g0125 | AMR | PEL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02015 | hp2 | a0002 | c0003 | t0003 | g0079 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02027 | hp1 | a0001 | c0007 | t0001 | g0241 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02055 | hp1 | a0001 | c0004 | t0004 | g0133 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02055 | hp2 | a0001 | c0001 | t0046 | g0087 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02056 | hp1 | a0003 | c0005 | t0005 | g0103 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02071 | hp2 | a0001 | c0001 | t0011 | g0028 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02083 | hp1 | a0002 | c0003 | t0003 | g0058 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02129 | hp1 | a0002 | c0003 | t0003 | g0063 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02132 | hp2 | a0002 | c0003 | t0003 | g0077 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02135 | hp1 | a0003 | c0005 | t0005 | g0105 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02145 | hp1 | a0003 | c0005 | t0021 | g0109 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02145 | hp2 | a0001 | c0004 | t0004 | g0018 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02148 | hp1 | a0003 | c0005 | t0005 | g0115 | AMR | PEL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | PEL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02155 | hp1 | a0002 | c0003 | t0003 | g0072 | EAS | CDX | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02155 | hp2 | a0002 | c0003 | t0029 | g0158 | EAS | CDX | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | CDX | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02165 | hp2 | a0002 | c0003 | t0003 | g0009 | EAS | CDX | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02257 | hp1 | a0001 | c0004 | t0005 | g0044 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02257 | hp2 | a0003 | c0005 | t0002 | g0041 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02258 | hp1 | a0001 | c0012 | t0018 | g0178 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02258 | hp2 | a0004 | c0011 | t0008 | g0249 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02280 | hp1 | a0001 | c0004 | t0004 | g0118 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02280 | hp2 | a0001 | c0004 | t0033 | g0127 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02293 | hp1 | a0004 | c0006 | t0007 | g0099 | AMR | PEL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | PEL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02451 | hp1 | a0001 | c0004 | t0004 | g0130 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02451 | hp2 | a0001 | c0004 | t0004 | g0042 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02572 | hp1 | a0001 | c0002 | t0031 | g0144 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02572 | hp2 | a0001 | c0012 | t0018 | g0180 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02602 | hp2 | a0001 | c0002 | t0020 | g0008 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02615 | hp2 | a0001 | c0001 | t0015 | g0084 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02622 | hp1 | a0001 | c0001 | t0022 | g0033 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02622 | hp2 | a0001 | c0002 | t0063 | g0175 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02647 | hp1 | a0005 | c0008 | t0009 | g0003 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02647 | hp2 | a0001 | c0004 | t0004 | g0042 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0001 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02717 | hp1 | a0001 | c0013 | t0017 | g0019 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02717 | hp2 | a0001 | c0017 | t0055 | g0135 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02723 | hp1 | a0001 | c0004 | t0004 | g0116 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02723 | hp2 | a0004 | c0019 | t0014 | g0155 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02738 | hp1 | a0006 | c0010 | t0007 | g0036 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02809 | hp1 | a0007 | c0015 | t0016 | g0035 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02809 | hp2 | a0001 | c0002 | t0027 | g0161 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02886 | hp1 | a0005 | c0008 | t0009 | g0003 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02886 | hp2 | a0001 | c0004 | t0053 | g0117 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02895 | hp1 | a0005 | c0008 | t0009 | g0003 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02895 | hp2 | a0008 | c0014 | t0012 | g0038 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02896 | hp1 | a0001 | c0004 | t0004 | g0018 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02897 | hp1 | a0008 | c0014 | t0012 | g0038 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02922 | hp1 | a0001 | c0004 | t0004 | g0121 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02922 | hp2 | a0001 | c0001 | t0034 | g0033 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02965 | hp1 | a0001 | c0004 | t0004 | g0011 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02965 | hp2 | a0001 | c0004 | t0004 | g0017 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02970 | hp1 | a0001 | c0002 | t0031 | g0145 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02970 | hp2 | a0004 | c0018 | t0008 | g0252 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02976 | hp1 | a0001 | c0001 | t0032 | g0047 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02976 | hp2 | a0001 | c0001 | t0022 | g0081 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03041 | hp1 | a0001 | c0002 | t0064 | g0088 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03041 | hp2 | a0001 | c0002 | t0019 | g0026 | AFR | GWD | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03098 | hp1 | a0005 | c0008 | t0009 | g0003 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03098 | hp2 | a0001 | c0001 | t0015 | g0034 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03130 | hp1 | a0005 | c0008 | t0009 | g0003 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0082 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03195 | hp1 | a0001 | c0004 | t0004 | g0124 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03195 | hp2 | a0001 | c0004 | t0004 | g0011 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03209 | hp1 | a0001 | c0004 | t0004 | g0131 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03209 | hp2 | a0001 | c0002 | t0019 | g0026 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03225 | hp1 | a0010 | c0023 | t0047 | g0148 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03225 | hp2 | a0001 | c0012 | t0057 | g0156 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03239 | hp1 | a0001 | c0004 | t0005 | g0044 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03239 | hp2 | a0001 | c0001 | t0008 | g0229 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03453 | hp1 | a0001 | c0004 | t0004 | g0132 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03453 | hp2 | a0001 | c0002 | t0027 | g0160 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03486 | hp1 | a0001 | c0021 | t0015 | g0034 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03486 | hp2 | a0001 | c0001 | t0016 | g0154 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0005 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03490 | hp2 | a0001 | c0002 | t0020 | g0002 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03492 | hp2 | a0001 | c0002 | t0020 | g0002 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03516 | hp1 | a0005 | c0008 | t0009 | g0003 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03516 | hp2 | a0001 | c0004 | t0004 | g0119 | AFR | ESN | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03579 | hp1 | a0004 | c0011 | t0044 | g0250 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03579 | hp2 | a0001 | c0002 | t0025 | g0020 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03654 | hp2 | a0001 | c0004 | t0004 | g0011 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03688 | hp1 | a0001 | c0002 | t0062 | g0008 | SAS | STU | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | STU | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03704 | hp2 | a0003 | c0005 | t0021 | g0040 | SAS | PJL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03831 | hp1 | a0001 | c0001 | t0024 | g0247 | SAS | BEB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0181 | SAS | BEB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | BEB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03834 | hp2 | a0003 | c0005 | t0021 | g0040 | SAS | BEB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03942 | hp2 | a0001 | c0004 | t0004 | g0137 | SAS | BEB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG04115 | hp2 | a0004 | c0006 | t0007 | g0092 | SAS | STU | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG04184 | hp1 | a0004 | c0006 | t0007 | g0096 | SAS | BEB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG04184 | hp2 | a0001 | c0001 | t0006 | g0200 | SAS | BEB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG04199 | hp2 | a0011 | c0020 | t0002 | g0008 | SAS | STU | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | STU | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG04204 | hp2 | a0001 | c0002 | t0058 | g0168 | SAS | STU | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG04228 | hp1 | a0002 | c0003 | t0041 | g0061 | SAS | STU | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18522 | hp1 | a0001 | c0004 | t0004 | g0011 | AFR | YRI | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18522 | hp2 | a0005 | c0008 | t0009 | g0003 | AFR | YRI | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18612 | hp1 | a0002 | c0003 | t0010 | g0014 | EAS | CHB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | CHB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | CHB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18906 | hp1 | a0001 | c0004 | t0004 | g0017 | AFR | YRI | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18906 | hp2 | a0003 | c0005 | t0012 | g0114 | AFR | YRI | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18942 | hp1 | a0002 | c0003 | t0010 | g0014 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18942 | hp2 | a0003 | c0005 | t0005 | g0106 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18945 | hp2 | a0002 | c0003 | t0003 | g0076 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18946 | hp1 | a0001 | c0001 | t0008 | g0053 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18949 | hp2 | a0003 | c0009 | t0001 | g0016 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18950 | hp1 | a0001 | c0007 | t0001 | g0211 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18950 | hp2 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18951 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18951 | hp2 | a0003 | c0009 | t0001 | g0112 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18952 | hp1 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18959 | hp1 | a0003 | c0009 | t0001 | g0113 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18959 | hp2 | a0002 | c0003 | t0003 | g0067 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18960 | hp2 | a0002 | c0003 | t0003 | g0031 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18962 | hp2 | a0002 | c0003 | t0003 | g0015 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18964 | hp2 | a0001 | c0001 | t0011 | g0028 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18965 | hp1 | a0002 | c0003 | t0010 | g0032 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18967 | hp2 | a0002 | c0003 | t0003 | g0073 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18969 | hp1 | a0002 | c0003 | t0003 | g0060 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18969 | hp2 | a0001 | c0001 | t0026 | g0206 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18971 | hp1 | a0002 | c0003 | t0003 | g0012 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18972 | hp2 | a0002 | c0003 | t0010 | g0009 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18974 | hp1 | a0003 | c0009 | t0043 | g0101 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18974 | hp2 | a0002 | c0003 | t0003 | g0157 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18975 | hp1 | a0001 | c0001 | t0045 | g0217 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18975 | hp2 | a0002 | c0003 | t0003 | g0069 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18979 | hp2 | a0001 | c0001 | t0011 | g0195 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18980 | hp1 | a0003 | c0009 | t0001 | g0016 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18980 | hp2 | a0002 | c0003 | t0038 | g0064 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18981 | hp1 | a0003 | c0005 | t0005 | g0010 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18983 | hp1 | a0001 | c0001 | t0011 | g0028 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18983 | hp2 | a0001 | c0007 | t0026 | g0056 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18985 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18986 | hp1 | a0001 | c0007 | t0001 | g0199 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18986 | hp2 | a0002 | c0003 | t0003 | g0012 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18988 | hp1 | a0002 | c0003 | t0010 | g0006 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18991 | hp1 | a0002 | c0003 | t0003 | g0075 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18993 | hp2 | a0002 | c0003 | t0003 | g0066 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18994 | hp2 | a0002 | c0003 | t0003 | g0032 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18995 | hp2 | a0002 | c0003 | t0003 | g0071 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18999 | hp1 | a0002 | c0003 | t0003 | g0031 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19000 | hp1 | a0002 | c0003 | t0010 | g0014 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19000 | hp2 | a0001 | c0007 | t0001 | g0055 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19005 | hp2 | a0002 | c0003 | t0003 | g0015 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19006 | hp2 | a0001 | c0001 | t0059 | g0059 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19009 | hp1 | a0002 | c0003 | t0003 | g0065 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19009 | hp2 | a0001 | c0007 | t0001 | g0055 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19010 | hp1 | a0003 | c0009 | t0006 | g0016 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19010 | hp2 | a0001 | c0007 | t0001 | g0197 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19011 | hp1 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19011 | hp2 | a0003 | c0005 | t0005 | g0010 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19012 | hp1 | a0002 | c0003 | t0003 | g0012 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19030 | hp1 | a0001 | c0012 | t0018 | g0179 | AFR | LWK | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0176 | AFR | LWK | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19043 | hp1 | a0001 | c0001 | t0014 | g0085 | AFR | LWK | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19043 | hp2 | a0012 | c0024 | t0060 | g0174 | AFR | LWK | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19054 | hp1 | a0003 | c0005 | t0005 | g0104 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19057 | hp1 | a0001 | c0001 | t0008 | g0186 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19057 | hp2 | a0002 | c0003 | t0003 | g0074 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19058 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19058 | hp2 | a0002 | c0003 | t0011 | g0062 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19060 | hp2 | a0002 | c0003 | t0003 | g0012 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19063 | hp1 | a0002 | c0003 | t0029 | g0192 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19064 | hp2 | a0001 | c0002 | t0030 | g0002 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19065 | hp2 | a0001 | c0001 | t0006 | g0232 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19066 | hp1 | a0001 | c0007 | t0006 | g0056 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19067 | hp2 | a0003 | c0005 | t0005 | g0010 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19074 | hp2 | a0003 | c0005 | t0005 | g0102 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19077 | hp1 | a0002 | c0003 | t0003 | g0068 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19079 | hp1 | a0001 | c0001 | t0011 | g0196 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19081 | hp1 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19086 | hp2 | a0013 | c0022 | t0010 | g0070 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19088 | hp1 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19088 | hp2 | a0001 | c0007 | t0001 | g0219 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19090 | hp1 | a0001 | c0001 | t0011 | g0193 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19090 | hp2 | a0001 | c0001 | t0023 | g0007 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | YRI | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA19240 | hp2 | a0003 | c0005 | t0002 | g0041 | AFR | YRI | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0243 | AFR | ASW | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA20129 | hp2 | a0001 | c0001 | t0032 | g0047 | AFR | ASW | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0022 | EUR | TSI | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA20805 | hp1 | a0004 | c0006 | t0007 | g0093 | EUR | TSI | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA20805 | hp2 | a0004 | c0006 | t0039 | g0100 | EUR | TSI | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0149 | SAS | GIH | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA20905 | hp2 | a0001 | c0004 | t0028 | g0134 | SAS | GIH | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01123 | hp1 | a0004 | c0006 | t0007 | g0098 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02109 | hp1 | a0009 | c0016 | t0004 | g0120 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02109 | hp2 | a0001 | c0013 | t0056 | g0136 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02486 | hp1 | a0001 | c0013 | t0017 | g0019 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02486 | hp2 | a0001 | c0002 | t0019 | g0026 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02559 | hp1 | a0001 | c0002 | t0025 | g0020 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG02559 | hp2 | a0003 | c0005 | t0012 | g0110 | AFR | ACB | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03471 | hp1 | a0001 | c0001 | t0052 | g0153 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG03471 | hp2 | a0001 | c0004 | t0004 | g0017 | AFR | MSL | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG06807 | hp1 | a0001 | c0001 | t0013 | g0143 | AFR | USA | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| HG06807 | hp2 | a0001 | c0004 | t0004 | g0122 | AFR | USA | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA18955 | hp2 | a0001 | c0002 | t0030 | g0002 | EAS | JPT | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA21309 | hp1 | a0001 | c0001 | t0014 | g0083 | AFR | LWK | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| NA21309 | hp2 | a0004 | c0011 | t0035 | g0251 | AFR | LWK | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0201 | REF | REF | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0040 | g0020 | REF | REF | QSOX1_chr1_180149869_180209030 | QSOX1 | chr1 | 180149869 | 180209030 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:180154926 | G | C | 2 | a0003 a0008 |
30 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(27): Show |
missense_variant | MODERATE | c.19G>C | p.Gly7Arg | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/12 | 58/9276 | 19/2244 | 7/747 | chr1 | 180154926 | |||
| chr1:180154960 | T | G | 1 | a0009 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.53T>G | p.Leu18Arg | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/12 | 92/9276 | 53/2244 | 18/747 | chr1 | 180154960 | |||
| chr1:180154993 | C | T | 1 | a0005 | 8 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(5): Show |
missense_variant | MODERATE | c.86C>T | p.Ala29Val | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/12 | 125/9276 | 86/2244 | 29/747 | chr1 | 180154993 | |||
| chr1:180155082 | A | G | 1 | a0012 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.175A>G | p.Ser59Gly | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/12 | 214/9276 | 175/2244 | 59/747 | chr1 | 180155082 | |||
| chr1:180166566 | A | G | 2 | a0005 a0010 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
missense_variant | MODERATE | c.341A>G | p.Asn114Ser | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/12 | 380/9276 | 341/2244 | 114/747 | chr1 | 180166566 | |||
| chr1:180178877 | G | C | 2 | a0004 a0006 |
21 | HG00735.hp1 HG00738.hp2 HG01069.hp2 others(18): Show |
missense_variant | MODERATE | c.599G>C | p.Gly200Ala | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/12 | 638/9276 | 599/2244 | 200/747 | chr1 | 180178877 | |||
| chr1:180186119 | G | C | 1 | a0008 | 2 | HG02895.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.954G>C | p.Arg318Ser | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/12 | 993/9276 | 954/2244 | 318/747 | chr1 | 180186119 | |||
| chr1:180190543 | G | T | 1 | a0013 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.1251G>T | p.Gln417His | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/12 | 1290/9276 | 1251/2244 | 417/747 | chr1 | 180190543 | |||
| chr1:180194255 | A | G | 2 | a0006 a0011 |
6 | HG01070.hp2 HG01109.hp1 HG01255.hp1 others(3): Show |
missense_variant | MODERATE | c.1331A>G | p.His444Arg | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/12 | 1370/9276 | 1331/2244 | 444/747 | chr1 | 180194255 | |||
| chr1:180196564 | A | C | 2 | a0002 a0013 |
48 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(45): Show |
missense_variant | MODERATE | c.1771A>C | p.Asn591His | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1810/9276 | 1771/2244 | 591/747 | chr1 | 180196564 | |||
| chr1:180196607 | G | C | 2 | a0005 a0010 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
missense_variant | MODERATE | c.1814G>C | p.Arg605Pro | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1853/9276 | 1814/2244 | 605/747 | chr1 | 180196607 | |||
| chr1:180196873 | C | T | 1 | a0007 | 2 | HG01243.hp2 HG02809.hp1 |
stop_gained | HIGH | c.2080C>T | p.Arg694* | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2119/9276 | 2080/2244 | 694/747 | chr1 | 180196873 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:180155153 | G | C | 3 | a0001c0004 a0001c0017 a0009c0016 |
37 | HG00099.hp1 HG00323.hp1 HG01074.hp2 others(34): Show |
synonymous_variant | LOW | c.246G>C | p.Ala82Ala | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/12 | 285/9276 | 246/2244 | 82/747 | chr1 | 180155153 | |||
| chr1:180175350 | G | A | 4 | a0004c0006 a0004c0011 a0004c0018 others(1): Show |
20 | HG00735.hp1 HG00738.hp2 HG01069.hp2 others(17): Show |
synonymous_variant | LOW | c.396G>A | p.Ser132Ser | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 3/12 | 435/9276 | 396/2244 | 132/747 | chr1 | 180175350 | |||
| chr1:180175953 | A | G | 18 | a0001c0001 a0001c0004 a0001c0007 others(15): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
synonymous_variant | LOW | c.435A>G | p.Thr145Thr | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/12 | 474/9276 | 435/2244 | 145/747 | chr1 | 180175953 | |||
| chr1:180190486 | G | A | 1 | a0004c0018 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.1194G>A | p.Pro398Pro | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/12 | 1233/9276 | 1194/2244 | 398/747 | chr1 | 180190486 | |||
| chr1:180190519 | C | T | 5 | a0001c0017 a0003c0005 a0004c0006 others(2): Show |
40 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(37): Show |
synonymous_variant | LOW | c.1227C>T | p.Val409Val | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/12 | 1266/9276 | 1227/2244 | 409/747 | chr1 | 180190519 | |||
| chr1:180190522 | C | T | 5 | a0001c0017 a0003c0005 a0004c0006 others(2): Show |
40 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(37): Show |
synonymous_variant | LOW | c.1230C>T | p.Leu410Leu | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/12 | 1269/9276 | 1230/2244 | 410/747 | chr1 | 180190522 | |||
| chr1:180196323 | T | C | 1 | a0001c0017 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.1530T>C | p.Ser510Ser | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1569/9276 | 1530/2244 | 510/747 | chr1 | 180196323 | |||
| chr1:180196473 | C | A | 3 | a0001c0012 a0001c0013 a0001c0017 |
9 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
synonymous_variant | LOW | c.1680C>A | p.Ala560Ala | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1719/9276 | 1680/2244 | 560/747 | chr1 | 180196473 | |||
| chr1:180196785 | C | T | 1 | a0001c0013 | 4 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
synonymous_variant | LOW | c.1992C>T | p.Gly664Gly | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2031/9276 | 1992/2244 | 664/747 | chr1 | 180196785 | |||
| chr1:180196812 | C | A | 1 | a0001c0007 | 9 | HG02027.hp1 NA18950.hp1 NA18983.hp2 others(6): Show |
synonymous_variant | LOW | c.2019C>A | p.Arg673Arg | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2058/9276 | 2019/2244 | 673/747 | chr1 | 180196812 | |||
| chr1:180196872 | C | A | 1 | a0001c0021 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.2079C>A | p.Gly693Gly | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2118/9276 | 2079/2244 | 693/747 | chr1 | 180196872 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:180154900 | C | A | 2 | a0001c0001t0022 a0001c0001t0034 |
3 | HG02622.hp1 HG02922.hp2 HG02976.hp2 |
5_prime_UTR_variant | MODIFIER | c.-8C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/12 | 8 | chr1 | 180154900 | ||||||
| chr1:180197092 | C | T | 1 | a0001c0002t0064 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*55C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 55 | chr1 | 180197092 | ||||||
| chr1:180197336 | A | G | 1 | a0001c0002t0063 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*299A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 299 | chr1 | 180197336 | ||||||
| chr1:180197429 | C | T | 6 | a0001c0001t0032 a0001c0004t0012 a0001c0004t0033 others(3): Show |
13 | HG00099.hp1 HG01074.hp2 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*392C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 392 | chr1 | 180197429 | ||||||
| chr1:180197515 | G | C | 1 | a0001c0001t0023 | 2 | HG00408.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*478G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 478 | chr1 | 180197515 | ||||||
| chr1:180197925 | T | G | 1 | a0004c0011t0035 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*888T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 888 | chr1 | 180197925 | ||||||
| chr1:180197955 | C | T | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(20): Show |
125 | HG00280.hp2 HG00544.hp1 HG00609.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*918C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 918 | chr1 | 180197955 | ||||||
| chr1:180198213 | C | T | 5 | a0001c0012t0018 a0001c0012t0057 a0001c0013t0017 others(2): Show |
9 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1176C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1176 | chr1 | 180198213 | ||||||
| chr1:180198222 | G | C | 1 | a0001c0001t0036 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1185G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1185 | chr1 | 180198222 | ||||||
| chr1:180198274 | C | A | 1 | a0001c0002t0058 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1237C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1237 | chr1 | 180198274 | ||||||
| chr1:180198279 | C | G | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(20): Show |
125 | HG00280.hp2 HG00544.hp1 HG00609.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1242C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1242 | chr1 | 180198279 | ||||||
| chr1:180198305 | A | G | 23 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0032 others(20): Show |
75 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1268A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1268 | chr1 | 180198305 | ||||||
| chr1:180198509 | T | C | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(23): Show |
128 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1472T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1472 | chr1 | 180198509 | ||||||
| chr1:180198639 | C | T | 4 | a0001c0001t0013 a0001c0001t0048 a0001c0001t0049 others(1): Show |
8 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1602C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1602 | chr1 | 180198639 | ||||||
| chr1:180198714 | T | C | 1 | a0001c0017t0055 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1677T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1677 | chr1 | 180198714 | ||||||
| chr1:180198753 | C | A | 1 | a0001c0001t0024 | 2 | HG01256.hp1 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1716C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1716 | chr1 | 180198753 | ||||||
| chr1:180198842 | C | T | 2 | a0001c0002t0027 a0001c0002t0064 |
3 | HG02809.hp2 HG03041.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1805C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 1805 | chr1 | 180198842 | ||||||
| chr1:180199071 | A | G | 14 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0019 others(11): Show |
70 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*2034A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2034 | chr1 | 180199071 | ||||||
| chr1:180199103 | A | C | 13 | a0001c0001t0004 a0001c0001t0014 a0001c0002t0031 others(10): Show |
43 | HG00099.hp1 HG00323.hp1 HG01099.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2066A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2066 | chr1 | 180199103 | ||||||
| chr1:180199133 | C | T | 1 | a0001c0001t0046 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2096C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2096 | chr1 | 180199133 | ||||||
| chr1:180199302 | G | A | 1 | a0001c0001t0046 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2265G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2265 | chr1 | 180199302 | ||||||
| chr1:180199525 | G | A | 1 | a0001c0002t0030 | 2 | NA18955.hp2 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2488G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2488 | chr1 | 180199525 | ||||||
| chr1:180199591 | T | A | 2 | a0001c0001t0015 a0001c0021t0015 |
3 | HG02615.hp2 HG03098.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2554T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2554 | chr1 | 180199591 | ||||||
| chr1:180199655 | A | T | 2 | a0001c0001t0032 a0001c0004t0033 |
4 | HG00099.hp1 HG02280.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2618A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2618 | chr1 | 180199655 | ||||||
| chr1:180199657 | G | A | 2 | a0001c0012t0018 a0001c0012t0057 |
4 | HG02258.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2620G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2620 | chr1 | 180199657 | ||||||
| chr1:180199682 | C | T | 2 | a0005c0008t0009 a0010c0023t0047 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2645C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2645 | chr1 | 180199682 | ||||||
| chr1:180199792 | G | A | 2 | a0001c0012t0018 a0001c0012t0057 |
4 | HG02258.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2755G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2755 | chr1 | 180199792 | ||||||
| chr1:180199795 | A | AG | 4 | a0001c0001t0007 a0004c0006t0007 a0004c0006t0039 others(1): Show |
16 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2762dupG | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2763 | INFO_REALIGN_3_PRIME | chr1 | 180199795 | |||||
| chr1:180199893 | G | T | 1 | a0001c0001t0045 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2856G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2856 | chr1 | 180199893 | ||||||
| chr1:180199973 | C | T | 12 | a0001c0001t0002 a0001c0001t0011 a0001c0002t0002 others(9): Show |
69 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2936C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2936 | chr1 | 180199973 | ||||||
| chr1:180200025 | C | A | 6 | a0001c0001t0032 a0001c0004t0012 a0001c0004t0033 others(3): Show |
13 | HG00099.hp1 HG01074.hp2 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2988C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 2988 | chr1 | 180200025 | ||||||
| chr1:180200195 | C | T | 40 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(37): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*3158C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 3158 | chr1 | 180200195 | ||||||
| chr1:180200213 | T | C | 1 | a0001c0004t0053 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3176T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 3176 | chr1 | 180200213 | ||||||
| chr1:180200232 | C | T | 5 | a0001c0001t0005 a0001c0001t0052 a0001c0004t0005 others(2): Show |
20 | HG00423.hp1 HG01074.hp1 HG01168.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3195C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 3195 | chr1 | 180200232 | ||||||
| chr1:180200270 | G | A | 14 | a0001c0001t0004 a0001c0001t0032 a0001c0004t0004 others(11): Show |
54 | HG00099.hp1 HG00323.hp1 HG01074.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3233G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 3233 | chr1 | 180200270 | ||||||
| chr1:180200357 | G | T | 2 | a0001c0001t0014 a0004c0019t0014 |
4 | HG02723.hp2 HG03130.hp2 NA19043.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3320G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 3320 | chr1 | 180200357 | ||||||
| chr1:180200434 | C | T | 2 | a0001c0002t0020 a0001c0012t0057 |
4 | HG02602.hp2 HG03225.hp2 HG03490.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3397C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 3397 | chr1 | 180200434 | ||||||
| chr1:180200680 | C | T | 3 | a0001c0001t0016 a0001c0001t0046 a0007c0015t0016 |
4 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3643C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 3643 | chr1 | 180200680 | ||||||
| chr1:180200719 | T | C | 3 | a0001c0001t0007 a0004c0006t0007 a0006c0010t0007 |
15 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3682T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 3682 | chr1 | 180200719 | ||||||
| chr1:180200814 | C | T | 12 | a0001c0001t0002 a0001c0001t0011 a0001c0002t0002 others(9): Show |
69 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*3777C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 3777 | chr1 | 180200814 | ||||||
| chr1:180200879 | C | T | 2 | a0001c0013t0017 a0001c0013t0056 |
4 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3842C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 3842 | chr1 | 180200879 | ||||||
| chr1:180200914 | G | A | 14 | a0001c0001t0004 a0001c0001t0032 a0001c0004t0004 others(11): Show |
54 | HG00099.hp1 HG00323.hp1 HG01074.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3877G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 3877 | chr1 | 180200914 | ||||||
| chr1:180201023 | G | A | 5 | a0001c0001t0032 a0001c0004t0012 a0003c0005t0012 others(2): Show |
11 | HG01074.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3986G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 3986 | chr1 | 180201023 | ||||||
| chr1:180201097 | G | A | 2 | a0001c0001t0014 a0004c0019t0014 |
4 | HG02723.hp2 HG03130.hp2 NA19043.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4060G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 4060 | chr1 | 180201097 | ||||||
| chr1:180201106 | A | G | 10 | a0001c0001t0003 a0001c0001t0059 a0001c0002t0019 others(7): Show |
52 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*4069A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 4069 | chr1 | 180201106 | ||||||
| chr1:180201129 | C | T | 1 | a0001c0001t0050 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4092C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 4092 | chr1 | 180201129 | ||||||
| chr1:180201226 | C | T | 48 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(45): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*4189C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 4189 | chr1 | 180201226 | ||||||
| chr1:180201308 | A | G | 10 | a0001c0001t0003 a0001c0001t0059 a0001c0002t0019 others(7): Show |
52 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*4271A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 4271 | chr1 | 180201308 | ||||||
| chr1:180201937 | A | G | 45 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(42): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*4900A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 4900 | chr1 | 180201937 | ||||||
| chr1:180202119 | T | C | 59 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(56): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*5082T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5082 | chr1 | 180202119 | ||||||
| chr1:180202290 | G | A | 1 | a0001c0001t0042 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5253G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5253 | chr1 | 180202290 | ||||||
| chr1:180202351 | C | G | 10 | a0001c0001t0003 a0001c0001t0059 a0001c0002t0019 others(7): Show |
52 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*5314C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5314 | chr1 | 180202351 | ||||||
| chr1:180202531 | A | G | 42 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(39): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*5494A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5494 | chr1 | 180202531 | ||||||
| chr1:180202556 | AG | A | 2 | a0001c0001t0014 a0004c0019t0014 |
4 | HG02723.hp2 HG03130.hp2 NA19043.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5522delG | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5522 | INFO_REALIGN_3_PRIME | chr1 | 180202556 | |||||
| chr1:180202606 | A | G | 2 | a0001c0002t0027 a0001c0002t0064 |
3 | HG02809.hp2 HG03041.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5569A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5569 | chr1 | 180202606 | ||||||
| chr1:180202675 | C | CA | 12 | a0001c0001t0049 a0001c0001t0052 a0001c0002t0019 others(9): Show |
27 | HG00099.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5654dupA | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5655 | INFO_REALIGN_3_PRIME | chr1 | 180202675 | |||||
| chr1:180202675 | C | CAA | 17 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0013 others(14): Show |
66 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*5653_*5654dupAA | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5655 | INFO_REALIGN_3_PRIME | chr1 | 180202675 | |||||
| chr1:180202675 | C | CAAA | 12 | a0001c0001t0001 a0001c0001t0023 a0001c0001t0042 others(9): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*5652_*5654dupAAA | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5655 | INFO_REALIGN_3_PRIME | chr1 | 180202675 | |||||
| chr1:180202675 | C | CAAAA | 4 | a0001c0001t0006 a0001c0001t0059 a0001c0007t0006 others(1): Show |
17 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5651_*5654dupAAAA | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5655 | INFO_REALIGN_3_PRIME | chr1 | 180202675 | |||||
| chr1:180202675 | CA | C | 6 | a0001c0001t0007 a0001c0002t0025 a0001c0004t0054 others(3): Show |
19 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5654delA | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5654 | INFO_REALIGN_3_PRIME | chr1 | 180202675 | |||||
| chr1:180202675 | CAA | C | 6 | a0001c0001t0014 a0001c0002t0027 a0001c0002t0064 others(3): Show |
11 | HG02258.hp1 HG02572.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5653_*5654delAA | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5653 | INFO_REALIGN_3_PRIME | chr1 | 180202675 | |||||
| chr1:180202691 | A | G | 1 | a0001c0002t0062 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5654 | chr1 | 180202691 | ||||||
| chr1:180202796 | A | G | 2 | a0001c0002t0019 a0001c0002t0063 |
4 | HG02486.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5759A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5759 | chr1 | 180202796 | ||||||
| chr1:180202846 | A | T | 1 | a0001c0004t0028 | 2 | HG00323.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5809A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 5809 | chr1 | 180202846 | ||||||
| chr1:180203360 | G | T | 14 | a0001c0001t0002 a0001c0001t0011 a0001c0002t0002 others(11): Show |
73 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*6323G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 6323 | chr1 | 180203360 | ||||||
| chr1:180203361 | A | G | 58 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(55): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*6324A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 6324 | chr1 | 180203361 | ||||||
| chr1:180203365 | T | TAAGTCAG others(7): Show |
1 | a0001c0001t0034 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6339_*6340insCGGA others(10): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 6340 | INFO_REALIGN_3_PRIME | chr1 | 180203365 | |||||
| chr1:180203377 | T | C | 70 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(67): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*6340T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 6340 | chr1 | 180203377 | ||||||
| chr1:180203380 | A | G | 1 | a0003c0009t0043 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6343A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 6343 | chr1 | 180203380 | ||||||
| chr1:180203486 | G | A | 1 | a0001c0002t0061 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6449G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 6449 | chr1 | 180203486 | ||||||
| chr1:180203604 | A | G | 12 | a0001c0001t0004 a0001c0001t0032 a0001c0004t0004 others(9): Show |
45 | HG00099.hp1 HG00323.hp1 HG01074.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*6567A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 6567 | chr1 | 180203604 | ||||||
| chr1:180203829 | G | A | 2 | a0001c0012t0018 a0001c0012t0057 |
4 | HG02258.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6792G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 6792 | chr1 | 180203829 | ||||||
| chr1:180203840 | C | G | 2 | a0001c0013t0017 a0001c0013t0056 |
4 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6803C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 6803 | chr1 | 180203840 | ||||||
| chr1:180203966 | C | T | 4 | a0001c0001t0013 a0001c0001t0048 a0001c0001t0049 others(1): Show |
8 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6929C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 6929 | chr1 | 180203966 | ||||||
| chr1:180203984 | A | T | 1 | a0001c0001t0034 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6947A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 6947 | chr1 | 180203984 | ||||||
| chr1:180203985 | T | A | 1 | a0001c0001t0034 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6948T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 12/12 | 6948 | chr1 | 180203985 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:180155196 | C | T | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+24C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155196 | |||||||
| chr1:180155212 | C | G | 1 | a0001c0001t0024g0247 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.265+40C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155212 | |||||||
| chr1:180155244 | T | C | 140 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(137): Show |
187 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.265+72T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155244 | |||||||
| chr1:180155315 | A | C | 140 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(137): Show |
187 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.265+143A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155315 | |||||||
| chr1:180155499 | C | T | 54 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(51): Show |
79 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.265+327C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155499 | |||||||
| chr1:180155532 | G | T | 90 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(87): Show |
125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.265+360G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155532 | |||||||
| chr1:180155672 | C | T | 24 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(21): Show |
38 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.265+500C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155672 | |||||||
| chr1:180155697 | A | G | 22 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(19): Show |
30 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.265+525A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155697 | |||||||
| chr1:180155705 | C | T | 2 | a0001c0001t0024g0246 a0001c0001t0024g0247 |
2 | HG01256.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.265+533C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155705 | |||||||
| chr1:180155737 | T | C | 140 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(137): Show |
187 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.265+565T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155737 | |||||||
| chr1:180155753 | C | A | 2 | a0001c0001t0013g0045 a0001c0001t0049g0045 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.265+581C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155753 | |||||||
| chr1:180155781 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.265+609C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155781 | |||||||
| chr1:180155809 | G | T | 1 | a0001c0002t0064g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.265+637G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155809 | |||||||
| chr1:180155834 | G | A | 23 | a0001c0001t0037g0089 a0003c0005t0002g0041 a0003c0005t0005g0010 others(20): Show |
31 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.265+662G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155834 | |||||||
| chr1:180155856 | C | A | 33 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(30): Show |
47 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.265+684C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155856 | |||||||
| chr1:180155967 | A | G | 12 | a0001c0001t0004g0086 a0001c0001t0014g0082 a0001c0001t0014g0083 others(9): Show |
13 | HG01192.hp2 HG01243.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.265+795A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155967 | |||||||
| chr1:180155998 | G | T | 3 | a0001c0004t0004g0043 a0001c0004t0004g0137 a0001c0004t0005g0044 |
5 | HG01516.hp1 HG01517.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+826G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180155998 | |||||||
| chr1:180156029 | T | C | 12 | a0001c0001t0004g0086 a0001c0001t0014g0082 a0001c0001t0014g0083 others(9): Show |
13 | HG01192.hp2 HG01243.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.265+857T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180156029 | |||||||
| chr1:180156231 | A | G | 34 | a0001c0001t0002g0138 a0001c0001t0003g0080 a0001c0001t0059g0059 others(31): Show |
48 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.265+1059A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180156231 | |||||||
| chr1:180156237 | T | C | 139 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(136): Show |
186 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.265+1065T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180156237 | |||||||
| chr1:180156239 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.265+1067C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180156239 | |||||||
| chr1:180156241 | G | A | 1 | a0001c0012t0057g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.265+1069G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180156241 | |||||||
| chr1:180156387 | G | C | 1 | a0001c0002t0002g0050 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.265+1215G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180156387 | |||||||
| chr1:180156444 | A | C | 2 | a0001c0001t0046g0087 a0007c0015t0016g0035 |
3 | HG01243.hp2 HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.265+1272A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180156444 | |||||||
| chr1:180156470 | A | G | 1 | a0004c0006t0039g0100 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.265+1298A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180156470 | |||||||
| chr1:180156618 | T | C | 28 | a0001c0004t0004g0011 a0001c0004t0004g0017 a0001c0004t0004g0018 others(25): Show |
37 | HG00099.hp1 HG00323.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.265+1446T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180156618 | |||||||
| chr1:180156871 | G | T | 1 | a0001c0002t0002g0245 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.265+1699G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180156871 | |||||||
| chr1:180156888 | T | A | 1 | a0002c0003t0003g0157 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.265+1716T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180156888 | |||||||
| chr1:180157006 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.265+1834A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180157006 | |||||||
| chr1:180157026 | G | A | 1 | a0002c0003t0029g0158 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.265+1854G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180157026 | |||||||
| chr1:180157119 | A | C | 1 | a0001c0001t0004g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.265+1947A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180157119 | |||||||
| chr1:180157325 | C | T | 33 | a0001c0001t0002g0138 a0001c0001t0003g0080 a0001c0001t0059g0059 others(30): Show |
47 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.265+2153C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180157325 | |||||||
| chr1:180157431 | G | A | 1 | a0001c0001t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.265+2259G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180157431 | |||||||
| chr1:180157533 | G | A | 1 | a0001c0002t0064g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.265+2361G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180157533 | |||||||
| chr1:180157799 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.265+2627A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180157799 | |||||||
| chr1:180157901 | C | T | 11 | a0001c0001t0014g0082 a0001c0001t0014g0083 a0001c0001t0014g0085 others(8): Show |
12 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.265+2729C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180157901 | |||||||
| chr1:180157915 | C | T | 1 | a0001c0001t0006g0243 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.265+2743C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180157915 | |||||||
| chr1:180157922 | T | A | 2 | a0001c0004t0004g0017 a0001c0004t0004g0042 |
5 | HG02451.hp2 HG02647.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+2750T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180157922 | |||||||
| chr1:180157972 | A | C | 59 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(56): Show |
81 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.265+2800A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180157972 | |||||||
| chr1:180157990 | A | C | 1 | a0001c0007t0001g0241 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.265+2818A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180157990 | |||||||
| chr1:180158216 | G | A | 3 | a0006c0010t0007g0036 a0006c0010t0007g0090 a0006c0010t0007g0091 |
4 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+3044G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180158216 | |||||||
| chr1:180158245 | A | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.265+3073A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180158245 | |||||||
| chr1:180158323 | C | G | 1 | a0001c0002t0002g0050 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.265+3151C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180158323 | |||||||
| chr1:180158459 | G | A | 22 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(19): Show |
30 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.265+3287G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180158459 | |||||||
| chr1:180158562 | G | A | 22 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(19): Show |
30 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.265+3390G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180158562 | |||||||
| chr1:180158613 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.265+3441C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180158613 | |||||||
| chr1:180158799 | C | G | 1 | a0001c0002t0002g0181 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.265+3627C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180158799 | |||||||
| chr1:180158809 | G | A | 1 | a0001c0004t0004g0116 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.265+3637G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180158809 | |||||||
| chr1:180158855 | C | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.265+3683C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180158855 | |||||||
| chr1:180158872 | A | G | 2 | a0001c0001t0013g0045 a0001c0001t0049g0045 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.265+3700A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180158872 | |||||||
| chr1:180158909 | T | G | 17 | a0001c0001t0001g0242 a0001c0001t0013g0045 a0001c0001t0013g0046 others(14): Show |
18 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.265+3737T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180158909 | |||||||
| chr1:180158954 | G | A | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+3782G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180158954 | |||||||
| chr1:180159046 | A | G | 1 | a0001c0001t0006g0240 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.265+3874A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180159046 | |||||||
| chr1:180159216 | G | A | 33 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(30): Show |
47 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.265+4044G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180159216 | |||||||
| chr1:180159220 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0182 others(8): Show |
18 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.265+4048T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180159220 | |||||||
| chr1:180159326 | A | G | 22 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(19): Show |
30 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.265+4154A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180159326 | |||||||
| chr1:180159356 | G | A | 1 | a0001c0001t0006g0240 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.265+4184G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180159356 | |||||||
| chr1:180159564 | T | C | 1 | a0004c0006t0039g0100 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.265+4392T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180159564 | |||||||
| chr1:180159595 | G | C | 5 | a0001c0001t0059g0059 a0002c0003t0003g0060 a0002c0003t0010g0014 others(2): Show |
7 | HG04228.hp1 NA18612.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.265+4423G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180159595 | |||||||
| chr1:180159607 | C | A | 32 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(29): Show |
46 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(43): Show |
intron_variant | MODIFIER | c.265+4435C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180159607 | |||||||
| chr1:180159628 | C | T | 32 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(29): Show |
46 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(43): Show |
intron_variant | MODIFIER | c.265+4456C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180159628 | |||||||
| chr1:180159879 | T | C | 3 | a0001c0001t0032g0047 a0001c0002t0031g0144 a0001c0002t0031g0145 |
4 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+4707T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180159879 | |||||||
| chr1:180160070 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.265+4898T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180160070 | |||||||
| chr1:180160345 | T | C | 1 | a0008c0014t0012g0038 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.265+5173T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180160345 | |||||||
| chr1:180160363 | T | C | 1 | a0001c0013t0056g0136 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.265+5191T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180160363 | |||||||
| chr1:180160506 | G | A | 10 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(7): Show |
20 | HG01109.hp2 HG02572.hp1 HG02647.hp1 others(17): Show |
intron_variant | MODIFIER | c.265+5334G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180160506 | |||||||
| chr1:180160531 | A | G | 1 | a0001c0001t0013g0143 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.265+5359A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180160531 | |||||||
| chr1:180160798 | C | T | 1 | a0002c0003t0003g0079 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.265+5626C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180160798 | |||||||
| chr1:180160829 | A | G | 3 | a0001c0012t0018g0178 a0001c0012t0018g0179 a0001c0012t0018g0180 |
3 | HG02258.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.265+5657A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180160829 | |||||||
| chr1:180160899 | T | G | 4 | a0001c0004t0004g0118 a0001c0004t0004g0119 a0001c0004t0053g0117 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-5592T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180160899 | |||||||
| chr1:180160917 | G | C | 1 | a0001c0002t0064g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.266-5574G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180160917 | |||||||
| chr1:180160927 | G | A | 13 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(10): Show |
15 | HG00735.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.266-5564G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180160927 | |||||||
| chr1:180161137 | G | T | 13 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(10): Show |
15 | HG00735.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.266-5354G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180161137 | |||||||
| chr1:180161208 | T | A | 1 | a0001c0001t0037g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.266-5283T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180161208 | |||||||
| chr1:180161253 | A | AT | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-5237dupT | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 180161253 | ||||||
| chr1:180161530 | A | G | 1 | a0001c0001t0006g0239 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.266-4961A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180161530 | |||||||
| chr1:180161574 | A | G | 3 | a0001c0001t0004g0086 a0001c0001t0046g0087 a0007c0015t0016g0035 |
4 | HG01192.hp2 HG01243.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-4917A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180161574 | |||||||
| chr1:180161578 | C | T | 22 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(19): Show |
30 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.266-4913C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180161578 | |||||||
| chr1:180161588 | C | T | 7 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0142 others(4): Show |
8 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.266-4903C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180161588 | |||||||
| chr1:180161638 | A | C | 3 | a0001c0012t0018g0178 a0001c0012t0018g0179 a0001c0012t0018g0180 |
3 | HG02258.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.266-4853A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180161638 | |||||||
| chr1:180161883 | C | T | 2 | a0001c0001t0005g0139 a0001c0001t0052g0153 |
2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.266-4608C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180161883 | |||||||
| chr1:180161884 | G | A | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-4607G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180161884 | |||||||
| chr1:180161909 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.266-4582A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180161909 | |||||||
| chr1:180161914 | C | T | 1 | a0001c0001t0013g0143 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.266-4577C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180161914 | |||||||
| chr1:180161948 | C | T | 33 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(30): Show |
47 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.266-4543C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180161948 | |||||||
| chr1:180161997 | A | G | 5 | a0001c0001t0005g0139 a0001c0001t0005g0150 a0001c0001t0005g0152 others(2): Show |
5 | HG01074.hp1 HG01891.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-4494A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180161997 | |||||||
| chr1:180162407 | G | A | 1 | a0004c0019t0014g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.266-4084G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180162407 | |||||||
| chr1:180162489 | ACT | A | 33 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(30): Show |
47 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.266-4001_266-4000d others(4): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180162489 | |||||||
| chr1:180162505 | G | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.266-3986G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180162505 | |||||||
| chr1:180162564 | C | T | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-3927C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180162564 | |||||||
| chr1:180162583 | T | A | 33 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(30): Show |
47 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.266-3908T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180162583 | |||||||
| chr1:180162662 | C | T | 22 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(19): Show |
30 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.266-3829C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180162662 | |||||||
| chr1:180162806 | G | C | 43 | a0001c0001t0002g0021 a0001c0001t0003g0080 a0001c0001t0037g0089 others(40): Show |
66 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.266-3685G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180162806 | |||||||
| chr1:180162850 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0002t0002g0149 |
5 | HG03491.hp2 HG03492.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-3641A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180162850 | |||||||
| chr1:180162883 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.266-3608A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180162883 | |||||||
| chr1:180163116 | T | C | 1 | a0004c0019t0014g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.266-3375T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163116 | |||||||
| chr1:180163133 | C | CA | 21 | a0001c0001t0001g0188 a0001c0001t0005g0150 a0001c0001t0046g0087 others(18): Show |
23 | HG00735.hp1 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.266-3345dupA | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 180163133 | ||||||
| chr1:180163133 | CA | C | 32 | a0001c0001t0002g0138 a0002c0003t0003g0006 a0002c0003t0003g0009 others(29): Show |
46 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(43): Show |
intron_variant | MODIFIER | c.266-3345delA | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 180163133 | ||||||
| chr1:180163144 | A | C | 2 | a0005c0008t0009g0003 a0010c0023t0047g0148 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.266-3347A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163144 | |||||||
| chr1:180163157 | A | G | 1 | a0003c0005t0005g0115 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.266-3334A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163157 | |||||||
| chr1:180163206 | T | C | 1 | a0003c0009t0043g0101 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.266-3285T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163206 | |||||||
| chr1:180163378 | C | T | 22 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(19): Show |
30 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.266-3113C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163378 | |||||||
| chr1:180163524 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.266-2967C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163524 | |||||||
| chr1:180163530 | A | G | 33 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(30): Show |
47 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.266-2961A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163530 | |||||||
| chr1:180163553 | A | G | 42 | a0001c0001t0003g0080 a0001c0001t0037g0089 a0001c0002t0002g0002 others(39): Show |
63 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.266-2938A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163553 | |||||||
| chr1:180163568 | C | A | 1 | a0002c0003t0003g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.266-2923C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163568 | |||||||
| chr1:180163667 | A | G | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-2824A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163667 | |||||||
| chr1:180163716 | A | G | 22 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(19): Show |
30 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.266-2775A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163716 | |||||||
| chr1:180163775 | G | A | 22 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(19): Show |
30 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.266-2716G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163775 | |||||||
| chr1:180163825 | A | G | 21 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(18): Show |
25 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.266-2666A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163825 | |||||||
| chr1:180163851 | G | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.266-2640G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180163851 | |||||||
| chr1:180164030 | A | G | 8 | a0002c0003t0003g0031 a0002c0003t0003g0032 a0002c0003t0003g0074 others(5): Show |
9 | HG00280.hp2 HG02132.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.266-2461A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164030 | |||||||
| chr1:180164304 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.266-2187G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164304 | |||||||
| chr1:180164438 | T | C | 10 | a0003c0005t0005g0010 a0003c0005t0005g0039 a0003c0005t0005g0102 others(7): Show |
14 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.266-2053T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164438 | |||||||
| chr1:180164453 | G | A | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-2038G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164453 | |||||||
| chr1:180164468 | G | A | 3 | a0001c0001t0004g0086 a0001c0001t0046g0087 a0007c0015t0016g0035 |
4 | HG01192.hp2 HG01243.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-2023G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164468 | |||||||
| chr1:180164523 | T | C | 1 | a0001c0001t0037g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.266-1968T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164523 | |||||||
| chr1:180164533 | C | T | 1 | a0001c0001t0046g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.266-1958C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164533 | |||||||
| chr1:180164649 | G | C | 33 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(30): Show |
47 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.266-1842G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164649 | |||||||
| chr1:180164676 | G | A | 1 | a0004c0011t0008g0248 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.266-1815G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164676 | |||||||
| chr1:180164721 | C | T | 4 | a0001c0001t0006g0053 a0001c0001t0008g0053 a0005c0008t0009g0003 others(1): Show |
11 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.266-1770C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164721 | |||||||
| chr1:180164747 | G | A | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-1744G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164747 | |||||||
| chr1:180164840 | G | A | 5 | a0001c0001t0005g0139 a0001c0001t0005g0150 a0001c0001t0005g0152 others(2): Show |
5 | HG01074.hp1 HG01891.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-1651G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164840 | |||||||
| chr1:180164934 | G | T | 1 | a0001c0001t0001g0235 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.266-1557G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164934 | |||||||
| chr1:180164940 | G | A | 42 | a0001c0001t0003g0080 a0001c0001t0037g0089 a0001c0002t0002g0002 others(39): Show |
63 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.266-1551G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164940 | |||||||
| chr1:180164982 | T | C | 1 | a0004c0006t0007g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.266-1509T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164982 | |||||||
| chr1:180164999 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(205): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.266-1492T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180164999 | |||||||
| chr1:180165005 | G | T | 1 | a0001c0001t0013g0142 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.266-1486G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165005 | |||||||
| chr1:180165015 | G | T | 2 | a0001c0002t0002g0052 a0001c0002t0002g0177 |
3 | HG00609.hp1 HG00621.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.266-1476G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165015 | |||||||
| chr1:180165074 | C | A | 33 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(30): Show |
47 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.266-1417C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165074 | |||||||
| chr1:180165084 | C | T | 33 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(30): Show |
47 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.266-1407C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165084 | |||||||
| chr1:180165085 | G | A | 42 | a0001c0001t0003g0080 a0001c0001t0037g0089 a0001c0002t0002g0002 others(39): Show |
63 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.266-1406G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165085 | |||||||
| chr1:180165205 | G | A | 2 | a0005c0008t0009g0003 a0010c0023t0047g0148 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.266-1286G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165205 | |||||||
| chr1:180165301 | C | G | 34 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(31): Show |
48 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.266-1190C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165301 | |||||||
| chr1:180165475 | C | T | 1 | a0001c0001t0007g0234 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.266-1016C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165475 | |||||||
| chr1:180165507 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.266-984G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165507 | |||||||
| chr1:180165553 | C | T | 22 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(19): Show |
30 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.266-938C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165553 | |||||||
| chr1:180165604 | TGAGAGTT others(7): Show |
T | 1 | a0001c0002t0002g0159 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.266-886_266-873del others(14): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165604 | |||||||
| chr1:180165663 | T | G | 1 | a0001c0002t0002g0159 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.266-828T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165663 | |||||||
| chr1:180165664 | T | G | 1 | a0001c0002t0002g0159 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.266-827T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165664 | |||||||
| chr1:180165674 | G | C | 1 | a0001c0002t0002g0159 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.266-817G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165674 | |||||||
| chr1:180165675 | C | A | 1 | a0001c0002t0002g0159 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.266-816C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165675 | |||||||
| chr1:180165707 | T | G | 1 | a0001c0002t0002g0159 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.266-784T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165707 | |||||||
| chr1:180165708 | G | A | 1 | a0001c0002t0002g0159 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.266-783G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165708 | |||||||
| chr1:180165732 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.266-759C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165732 | |||||||
| chr1:180165737 | C | T | 4 | a0001c0001t0005g0139 a0001c0001t0005g0150 a0001c0001t0005g0152 others(1): Show |
4 | HG01074.hp1 HG02615.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-754C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165737 | |||||||
| chr1:180165788 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0182 |
4 | HG00558.hp2 HG02523.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-703T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165788 | |||||||
| chr1:180165813 | C | T | 1 | a0001c0001t0001g0027 | 3 | HG02523.hp1 NA18964.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.266-678C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165813 | |||||||
| chr1:180165832 | C | T | 1 | a0001c0002t0002g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.266-659C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165832 | |||||||
| chr1:180165851 | C | T | 1 | a0003c0005t0012g0114 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.266-640C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165851 | |||||||
| chr1:180165868 | G | T | 1 | a0002c0003t0003g0073 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.266-623G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165868 | |||||||
| chr1:180165871 | C | CGGCTCTG others(10): Show |
1 | a0001c0004t0054g0123 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.266-618_266-617ins others(17): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 180165871 | ||||||
| chr1:180165878 | T | A | 1 | a0001c0004t0054g0123 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.266-613T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165878 | |||||||
| chr1:180165880 | A | C | 1 | a0001c0004t0054g0123 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.266-611A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165880 | |||||||
| chr1:180165881 | T | A | 1 | a0001c0004t0054g0123 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.266-610T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165881 | |||||||
| chr1:180165884 | A | G | 2 | a0001c0002t0019g0026 a0001c0002t0063g0175 |
4 | HG02486.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-607A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180165884 | |||||||
| chr1:180166151 | G | A | 33 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(30): Show |
47 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.266-340G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180166151 | |||||||
| chr1:180166303 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.266-188C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180166303 | |||||||
| chr1:180166391 | C | A | 3 | a0001c0002t0002g0050 a0001c0002t0031g0144 a0001c0002t0031g0145 |
4 | HG02572.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-100C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 1/11 | chr1 | 180166391 | |||||||
| chr1:180166622 | TG | T | 37 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(34): Show |
49 | HG00099.hp1 HG00323.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.366+34delG | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 180166622 | ||||||
| chr1:180166737 | G | C | 1 | a0001c0001t0001g0235 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.366+146G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180166737 | |||||||
| chr1:180166745 | A | G | 1 | a0001c0001t0014g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.366+154A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180166745 | |||||||
| chr1:180166964 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.366+373C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180166964 | |||||||
| chr1:180167014 | A | C | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.366+423A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167014 | |||||||
| chr1:180167023 | C | T | 2 | a0001c0001t0006g0232 a0001c0001t0006g0240 |
2 | HG00438.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.366+432C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167023 | |||||||
| chr1:180167267 | A | G | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.366+676A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167267 | |||||||
| chr1:180167369 | C | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.366+778C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167369 | |||||||
| chr1:180167384 | G | C | 1 | a0001c0002t0002g0162 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.366+793G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167384 | |||||||
| chr1:180167429 | A | G | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(1): Show |
6 | HG02698.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+838A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167429 | |||||||
| chr1:180167549 | C | T | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.366+958C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167549 | |||||||
| chr1:180167571 | A | C | 34 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(31): Show |
48 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.366+980A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167571 | |||||||
| chr1:180167576 | T | C | 32 | a0001c0001t0002g0021 a0001c0001t0003g0080 a0001c0002t0002g0002 others(29): Show |
52 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.366+985T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167576 | |||||||
| chr1:180167602 | C | T | 2 | a0001c0001t0001g0231 a0001c0002t0002g0176 |
2 | NA18941.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.366+1011C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167602 | |||||||
| chr1:180167631 | G | C | 1 | a0001c0004t0004g0124 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.366+1040G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167631 | |||||||
| chr1:180167675 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.366+1084A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167675 | |||||||
| chr1:180167840 | T | C | 18 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(15): Show |
20 | HG00735.hp1 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.366+1249T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167840 | |||||||
| chr1:180167852 | G | A | 18 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(15): Show |
20 | HG00735.hp1 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.366+1261G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167852 | |||||||
| chr1:180167906 | G | T | 34 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(31): Show |
48 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.366+1315G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167906 | |||||||
| chr1:180167977 | T | C | 1 | a0001c0002t0061g0163 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.366+1386T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180167977 | |||||||
| chr1:180168001 | G | A | 18 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(15): Show |
20 | HG00735.hp1 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.366+1410G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180168001 | |||||||
| chr1:180168152 | G | T | 34 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(31): Show |
48 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.366+1561G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180168152 | |||||||
| chr1:180168164 | C | T | 34 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(31): Show |
48 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.366+1573C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180168164 | |||||||
| chr1:180168202 | G | A | 2 | a0001c0001t0016g0154 a0007c0015t0016g0035 |
3 | HG01243.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.366+1611G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180168202 | |||||||
| chr1:180168320 | A | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0244 |
2 | NA18945.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.366+1729A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180168320 | |||||||
| chr1:180168351 | G | GTCATCTG others(11): Show |
34 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(31): Show |
48 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.366+1761_366+1778d others(20): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 180168351 | ||||||
| chr1:180168644 | A | T | 4 | a0001c0004t0004g0118 a0001c0004t0004g0119 a0001c0004t0053g0117 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+2053A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180168644 | |||||||
| chr1:180168670 | AT | A | 11 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(8): Show |
14 | HG01074.hp1 HG01891.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.366+2090delT | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 180168670 | ||||||
| chr1:180168875 | C | A | 17 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(14): Show |
24 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.366+2284C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180168875 | |||||||
| chr1:180168910 | C | G | 1 | a0001c0012t0057g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.366+2319C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180168910 | |||||||
| chr1:180168964 | T | C | 13 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(10): Show |
15 | HG00735.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.366+2373T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180168964 | |||||||
| chr1:180169013 | G | T | 1 | a0001c0001t0008g0229 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.366+2422G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169013 | |||||||
| chr1:180169033 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0235 |
3 | HG01070.hp1 HG01071.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.366+2442C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169033 | |||||||
| chr1:180169039 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.366+2448T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169039 | |||||||
| chr1:180169058 | A | G | 4 | a0001c0002t0027g0160 a0001c0002t0027g0161 a0001c0002t0064g0088 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.366+2467A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169058 | |||||||
| chr1:180169079 | A | G | 18 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(15): Show |
20 | HG00735.hp1 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.366+2488A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169079 | |||||||
| chr1:180169152 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.366+2561G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169152 | |||||||
| chr1:180169179 | A | G | 17 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(14): Show |
24 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.366+2588A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169179 | |||||||
| chr1:180169183 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.366+2592C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169183 | |||||||
| chr1:180169254 | G | A | 10 | a0001c0001t0002g0138 a0002c0003t0003g0006 a0002c0003t0003g0012 others(7): Show |
17 | HG01496.hp1 NA18952.hp1 NA18959.hp2 others(14): Show |
intron_variant | MODIFIER | c.366+2663G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169254 | |||||||
| chr1:180169336 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.366+2745G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169336 | |||||||
| chr1:180169339 | G | A | 17 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(14): Show |
24 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.366+2748G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169339 | |||||||
| chr1:180169341 | A | T | 5 | a0001c0001t0005g0139 a0001c0001t0005g0150 a0001c0001t0005g0152 others(2): Show |
5 | HG01074.hp1 HG01891.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.366+2750A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169341 | |||||||
| chr1:180169342 | AG | A | 5 | a0001c0001t0005g0139 a0001c0001t0005g0150 a0001c0001t0005g0152 others(2): Show |
5 | HG01074.hp1 HG01891.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.366+2755delG | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 180169342 | ||||||
| chr1:180169344 | G | T | 5 | a0001c0001t0005g0139 a0001c0001t0005g0150 a0001c0001t0005g0152 others(2): Show |
5 | HG01074.hp1 HG01891.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.366+2753G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169344 | |||||||
| chr1:180169539 | G | C | 1 | a0001c0001t0036g0151 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.366+2948G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169539 | |||||||
| chr1:180169583 | G | A | 13 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(10): Show |
15 | HG00735.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.366+2992G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169583 | |||||||
| chr1:180169649 | C | T | 2 | a0005c0008t0009g0003 a0010c0023t0047g0148 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.366+3058C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169649 | |||||||
| chr1:180169665 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(144): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.366+3074G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169665 | |||||||
| chr1:180169704 | T | G | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.366+3113T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169704 | |||||||
| chr1:180169755 | G | A | 45 | a0001c0001t0002g0021 a0001c0001t0003g0080 a0001c0001t0037g0089 others(42): Show |
68 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.366+3164G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169755 | |||||||
| chr1:180169853 | T | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.366+3262T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169853 | |||||||
| chr1:180169869 | G | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0236 |
3 | HG01081.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.366+3278G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169869 | |||||||
| chr1:180169908 | G | A | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.366+3317G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169908 | |||||||
| chr1:180169919 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(144): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.366+3328G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169919 | |||||||
| chr1:180169982 | G | A | 1 | a0001c0004t0004g0137 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.366+3391G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180169982 | |||||||
| chr1:180170058 | G | A | 3 | a0001c0001t0022g0033 a0001c0001t0022g0081 a0001c0001t0034g0033 |
3 | HG02622.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.366+3467G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170058 | |||||||
| chr1:180170074 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.366+3483G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170074 | |||||||
| chr1:180170173 | C | T | 1 | a0001c0001t0005g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.366+3582C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170173 | |||||||
| chr1:180170242 | C | G | 4 | a0001c0004t0004g0118 a0001c0004t0004g0119 a0001c0004t0053g0117 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+3651C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170242 | |||||||
| chr1:180170416 | C | T | 33 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(30): Show |
47 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.366+3825C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170416 | |||||||
| chr1:180170417 | G | A | 6 | a0001c0002t0002g0164 a0004c0011t0008g0248 a0004c0011t0008g0249 others(3): Show |
6 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.366+3826G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170417 | |||||||
| chr1:180170491 | C | T | 16 | a0002c0003t0003g0032 a0002c0003t0003g0078 a0002c0003t0010g0032 others(13): Show |
18 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.366+3900C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170491 | |||||||
| chr1:180170492 | A | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.366+3901A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170492 | |||||||
| chr1:180170496 | T | A | 37 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(34): Show |
53 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.366+3905T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170496 | |||||||
| chr1:180170516 | C | T | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.366+3925C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170516 | |||||||
| chr1:180170652 | G | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.366+4061G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170652 | |||||||
| chr1:180170785 | C | T | 2 | a0001c0001t0005g0150 a0001c0001t0005g0152 |
2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.366+4194C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170785 | |||||||
| chr1:180170809 | G | A | 17 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(14): Show |
24 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.366+4218G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170809 | |||||||
| chr1:180170837 | A | G | 4 | a0001c0002t0027g0160 a0001c0002t0027g0161 a0001c0002t0064g0088 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.366+4246A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170837 | |||||||
| chr1:180170961 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.367-4360C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170961 | |||||||
| chr1:180170966 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
253 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.367-4355G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180170966 | |||||||
| chr1:180171110 | A | C | 1 | a0012c0024t0060g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.367-4211A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171110 | |||||||
| chr1:180171257 | G | A | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.367-4064G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171257 | |||||||
| chr1:180171373 | T | C | 66 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(63): Show |
89 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.367-3948T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171373 | |||||||
| chr1:180171375 | G | GT | 39 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(36): Show |
53 | HG00099.hp1 HG00323.hp1 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.367-3944dupT | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 180171375 | ||||||
| chr1:180171397 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(169): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.367-3924A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171397 | |||||||
| chr1:180171413 | G | A | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.367-3908G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171413 | |||||||
| chr1:180171455 | A | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.367-3866A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171455 | |||||||
| chr1:180171458 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.367-3863A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171458 | |||||||
| chr1:180171482 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.367-3839T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171482 | |||||||
| chr1:180171584 | A | G | 3 | a0001c0002t0002g0024 a0001c0002t0002g0025 a0001c0002t0002g0173 |
7 | HG02129.hp2 NA18962.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-3737A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171584 | |||||||
| chr1:180171588 | G | C | 17 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(14): Show |
24 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.367-3733G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171588 | |||||||
| chr1:180171680 | A | C | 34 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(31): Show |
48 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.367-3641A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171680 | |||||||
| chr1:180171785 | A | G | 3 | a0001c0012t0018g0178 a0001c0012t0018g0179 a0001c0012t0018g0180 |
3 | HG02258.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.367-3536A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171785 | |||||||
| chr1:180171895 | G | A | 34 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(31): Show |
48 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.367-3426G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171895 | |||||||
| chr1:180171989 | A | G | 2 | a0001c0001t0005g0150 a0001c0001t0005g0152 |
2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.367-3332A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180171989 | |||||||
| chr1:180172082 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.367-3239A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180172082 | |||||||
| chr1:180172156 | T | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0194 a0001c0001t0011g0028 others(3): Show |
11 | HG01952.hp2 HG02071.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.367-3165T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180172156 | |||||||
| chr1:180172172 | CT | C | 5 | a0001c0001t0005g0139 a0001c0001t0005g0150 a0001c0001t0005g0152 others(2): Show |
5 | HG01074.hp1 HG01891.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.367-3146delT | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 180172172 | ||||||
| chr1:180172206 | G | A | 1 | a0010c0023t0047g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.367-3115G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180172206 | |||||||
| chr1:180172232 | G | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.367-3089G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180172232 | |||||||
| chr1:180172240 | T | C | 1 | a0001c0002t0064g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.367-3081T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180172240 | |||||||
| chr1:180172250 | G | T | 17 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(14): Show |
24 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.367-3071G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180172250 | |||||||
| chr1:180172495 | A | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.367-2826A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180172495 | |||||||
| chr1:180172707 | C | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.367-2614C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180172707 | |||||||
| chr1:180172710 | G | A | 1 | a0001c0002t0027g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.367-2611G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180172710 | |||||||
| chr1:180172761 | C | T | 27 | a0001c0004t0004g0011 a0001c0004t0004g0017 a0001c0004t0004g0018 others(24): Show |
36 | HG00099.hp1 HG00323.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.367-2560C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180172761 | |||||||
| chr1:180172796 | G | A | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.367-2525G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180172796 | |||||||
| chr1:180172815 | G | A | 3 | a0001c0001t0022g0033 a0001c0001t0022g0081 a0001c0001t0034g0033 |
3 | HG02622.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.367-2506G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180172815 | |||||||
| chr1:180172897 | G | C | 3 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0044g0250 |
3 | HG01069.hp2 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.367-2424G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180172897 | |||||||
| chr1:180173007 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.367-2314A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173007 | |||||||
| chr1:180173057 | A | G | 1 | a0003c0005t0002g0041 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.367-2264A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173057 | |||||||
| chr1:180173128 | A | C | 18 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(15): Show |
20 | HG00735.hp1 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.367-2193A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173128 | |||||||
| chr1:180173261 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.367-2060C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173261 | |||||||
| chr1:180173277 | C | T | 35 | a0001c0001t0002g0138 a0001c0001t0003g0080 a0001c0001t0059g0059 others(32): Show |
49 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.367-2044C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173277 | |||||||
| chr1:180173310 | A | ATGAAAAT others(7): Show |
3 | a0001c0002t0027g0160 a0001c0002t0027g0161 a0001c0002t0064g0088 |
3 | HG02809.hp2 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.367-2010_367-2009i others(16): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 180173310 | ||||||
| chr1:180173313 | T | TCA | 3 | a0001c0002t0027g0160 a0001c0002t0027g0161 a0001c0002t0064g0088 |
3 | HG02809.hp2 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.367-2008_367-2007i others(4): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173313 | |||||||
| chr1:180173424 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0008g0054 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.367-1897T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173424 | |||||||
| chr1:180173510 | A | G | 1 | a0012c0024t0060g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.367-1811A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173510 | |||||||
| chr1:180173647 | G | T | 18 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(15): Show |
20 | HG00735.hp1 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.367-1674G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173647 | |||||||
| chr1:180173682 | A | G | 4 | a0001c0002t0027g0160 a0001c0002t0027g0161 a0001c0002t0064g0088 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-1639A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173682 | |||||||
| chr1:180173691 | T | G | 1 | a0001c0004t0004g0124 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.367-1630T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173691 | |||||||
| chr1:180173762 | G | C | 1 | a0001c0012t0057g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.367-1559G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173762 | |||||||
| chr1:180173929 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.367-1392T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173929 | |||||||
| chr1:180173977 | A | G | 2 | a0004c0006t0007g0098 a0004c0006t0007g0099 |
2 | HG01123.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.367-1344A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180173977 | |||||||
| chr1:180173987 | G | GC | 4 | a0001c0001t0004g0086 a0001c0001t0016g0154 a0001c0001t0046g0087 others(1): Show |
5 | HG01192.hp2 HG01243.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.367-1332dupC | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 180173987 | ||||||
| chr1:180174000 | G | A | 2 | a0005c0008t0009g0003 a0010c0023t0047g0148 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.367-1321G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180174000 | |||||||
| chr1:180174009 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.367-1312C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180174009 | |||||||
| chr1:180174013 | T | C | 2 | a0001c0013t0017g0019 a0001c0013t0056g0136 |
4 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-1308T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180174013 | |||||||
| chr1:180174116 | G | A | 3 | a0001c0002t0027g0160 a0001c0002t0027g0161 a0001c0002t0064g0088 |
3 | HG02809.hp2 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.367-1205G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180174116 | |||||||
| chr1:180174185 | G | A | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.367-1136G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180174185 | |||||||
| chr1:180174273 | G | A | 18 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(15): Show |
20 | HG00735.hp1 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.367-1048G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180174273 | |||||||
| chr1:180174472 | C | T | 5 | a0001c0001t0005g0139 a0001c0001t0005g0150 a0001c0001t0005g0152 others(2): Show |
5 | HG01074.hp1 HG01891.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.367-849C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180174472 | |||||||
| chr1:180174633 | A | G | 18 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(15): Show |
20 | HG00735.hp1 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.367-688A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180174633 | |||||||
| chr1:180174728 | G | A | 17 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(14): Show |
24 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.367-593G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180174728 | |||||||
| chr1:180174797 | A | G | 5 | a0003c0005t0005g0010 a0003c0005t0005g0039 a0003c0005t0005g0108 others(2): Show |
9 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.367-524A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180174797 | |||||||
| chr1:180174867 | A | T | 1 | a0004c0006t0039g0100 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.367-454A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180174867 | |||||||
| chr1:180174999 | CA | C | 34 | a0001c0001t0002g0138 a0001c0001t0003g0080 a0001c0001t0059g0059 others(31): Show |
48 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.367-314delA | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 180174999 | ||||||
| chr1:180175001 | A | C | 19 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(16): Show |
33 | HG00423.hp1 HG01109.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.367-320A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180175001 | |||||||
| chr1:180175105 | C | T | 31 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0022 others(28): Show |
49 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.367-216C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180175105 | |||||||
| chr1:180175114 | G | A | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.367-207G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180175114 | |||||||
| chr1:180175156 | C | CA | 145 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.367-152dupA | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 180175156 | ||||||
| chr1:180175156 | C | CAA | 7 | a0001c0001t0001g0198 a0001c0007t0001g0197 a0003c0009t0001g0016 others(4): Show |
8 | NA18949.hp2 NA18951.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.367-153_367-152dup others(2): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 180175156 | ||||||
| chr1:180175204 | T | G | 1 | a0001c0001t0008g0229 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.367-117T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 2/11 | chr1 | 180175204 | |||||||
| chr1:180175459 | A | G | 10 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(7): Show |
13 | HG01074.hp1 HG01891.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.412+93A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 3/11 | chr1 | 180175459 | |||||||
| chr1:180175720 | C | G | 3 | a0001c0012t0018g0178 a0001c0012t0018g0179 a0001c0012t0018g0180 |
3 | HG02258.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.413-211C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 3/11 | chr1 | 180175720 | |||||||
| chr1:180175876 | T | C | 5 | a0001c0004t0004g0017 a0001c0004t0004g0042 a0001c0004t0004g0125 others(2): Show |
8 | HG00099.hp1 HG02004.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.413-55T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 3/11 | chr1 | 180175876 | |||||||
| chr1:180175894 | C | A | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0146 others(2): Show |
8 | HG02698.hp1 HG02976.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.413-37C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 3/11 | chr1 | 180175894 | |||||||
| chr1:180176050 | C | A | 1 | a0001c0001t0037g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.515+17C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176050 | |||||||
| chr1:180176072 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | NA18971.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.515+39A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176072 | |||||||
| chr1:180176143 | G | A | 1 | a0003c0009t0001g0112 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.515+110G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176143 | |||||||
| chr1:180176159 | C | T | 1 | a0002c0003t0029g0192 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.515+126C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176159 | |||||||
| chr1:180176306 | G | C | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.515+273G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176306 | |||||||
| chr1:180176385 | G | A | 2 | a0001c0002t0002g0162 a0001c0002t0002g0165 |
2 | HG02165.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.515+352G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176385 | |||||||
| chr1:180176410 | G | A | 46 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0022 others(43): Show |
67 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.515+377G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176410 | |||||||
| chr1:180176457 | C | T | 1 | a0004c0019t0014g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.515+424C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176457 | |||||||
| chr1:180176474 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.515+441A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176474 | |||||||
| chr1:180176475 | T | C | 80 | a0001c0001t0002g0138 a0001c0001t0003g0080 a0001c0001t0059g0059 others(77): Show |
115 | HG00280.hp2 HG00544.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.515+442T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176475 | |||||||
| chr1:180176476 | T | G | 1 | a0001c0002t0002g0159 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.515+443T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176476 | |||||||
| chr1:180176553 | G | T | 1 | a0002c0003t0003g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.515+520G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176553 | |||||||
| chr1:180176564 | G | A | 1 | a0001c0002t0002g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.515+531G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176564 | |||||||
| chr1:180176634 | G | T | 80 | a0001c0001t0002g0138 a0001c0001t0003g0080 a0001c0001t0059g0059 others(77): Show |
115 | HG00280.hp2 HG00544.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.515+601G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176634 | |||||||
| chr1:180176758 | G | A | 35 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(32): Show |
44 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.515+725G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176758 | |||||||
| chr1:180176833 | A | G | 1 | a0001c0001t0001g0030 | 3 | HG01081.hp1 HG01123.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.515+800A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176833 | |||||||
| chr1:180176843 | A | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.515+810A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176843 | |||||||
| chr1:180176848 | C | T | 2 | a0001c0013t0017g0019 a0001c0013t0056g0136 |
4 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.515+815C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176848 | |||||||
| chr1:180176868 | T | G | 2 | a0005c0008t0009g0003 a0010c0023t0047g0148 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.515+835T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176868 | |||||||
| chr1:180176906 | G | A | 7 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0142 others(4): Show |
8 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.515+873G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176906 | |||||||
| chr1:180176927 | T | G | 2 | a0001c0002t0027g0160 a0001c0002t0027g0161 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.515+894T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180176927 | |||||||
| chr1:180177045 | T | C | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.515+1012T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177045 | |||||||
| chr1:180177064 | A | T | 1 | a0001c0001t0008g0186 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.515+1031A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177064 | |||||||
| chr1:180177071 | C | A | 13 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(10): Show |
15 | HG00735.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.515+1038C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177071 | |||||||
| chr1:180177072 | T | G | 1 | a0004c0006t0039g0100 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.515+1039T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177072 | |||||||
| chr1:180177088 | A | AGTCTCCT others(4): Show |
1 | a0001c0001t0008g0186 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.515+1055_515+1056i others(13): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177088 | |||||||
| chr1:180177094 | G | A | 1 | a0001c0001t0008g0186 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.515+1061G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177094 | |||||||
| chr1:180177095 | C | G | 1 | a0001c0001t0008g0186 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.515+1062C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177095 | |||||||
| chr1:180177100 | G | C | 1 | a0001c0001t0008g0186 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.515+1067G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177100 | |||||||
| chr1:180177103 | C | A | 1 | a0001c0001t0008g0186 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.515+1070C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177103 | |||||||
| chr1:180177115 | G | C | 1 | a0001c0001t0008g0186 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.515+1082G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177115 | |||||||
| chr1:180177120 | T | C | 1 | a0001c0001t0008g0186 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.515+1087T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177120 | |||||||
| chr1:180177121 | A | T | 1 | a0001c0001t0008g0186 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.515+1088A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177121 | |||||||
| chr1:180177123 | T | A | 1 | a0001c0001t0008g0186 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.515+1090T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177123 | |||||||
| chr1:180177156 | C | T | 1 | a0001c0001t0008g0186 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.515+1123C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177156 | |||||||
| chr1:180177187 | C | G | 5 | a0001c0001t0059g0059 a0002c0003t0003g0060 a0002c0003t0010g0014 others(2): Show |
7 | HG04228.hp1 NA18612.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.515+1154C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177187 | |||||||
| chr1:180177193 | T | G | 1 | a0004c0019t0014g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.515+1160T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177193 | |||||||
| chr1:180177248 | TC | T | 25 | a0003c0005t0002g0041 a0003c0005t0012g0110 a0003c0005t0012g0111 others(22): Show |
30 | HG00735.hp1 HG00738.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.515+1217delC | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 180177248 | ||||||
| chr1:180177250 | C | T | 10 | a0003c0005t0005g0010 a0003c0005t0005g0039 a0003c0005t0005g0102 others(7): Show |
14 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.515+1217C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177250 | |||||||
| chr1:180177250 | CT | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.515+1235delT | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 180177250 | ||||||
| chr1:180177250 | CTTTTTT | C | 1 | a0005c0008t0009g0003 | 8 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.515+1230_515+1235d others(8): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 180177250 | ||||||
| chr1:180177284 | G | A | 6 | a0001c0001t0007g0234 a0001c0007t0001g0055 a0001c0007t0001g0197 others(3): Show |
7 | HG00280.hp1 NA18983.hp2 NA18986.hp1 others(4): Show |
intron_variant | MODIFIER | c.515+1251G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177284 | |||||||
| chr1:180177293 | C | A | 1 | a0012c0024t0060g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.515+1260C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177293 | |||||||
| chr1:180177349 | G | A | 12 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(9): Show |
14 | HG00735.hp1 HG00738.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.515+1316G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177349 | |||||||
| chr1:180177412 | C | A | 2 | a0001c0013t0017g0019 a0001c0013t0056g0136 |
4 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.515+1379C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177412 | |||||||
| chr1:180177479 | A | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.516-1315A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177479 | |||||||
| chr1:180177497 | G | C | 37 | a0001c0017t0055g0135 a0003c0005t0002g0041 a0003c0005t0005g0010 others(34): Show |
46 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.516-1297G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177497 | |||||||
| chr1:180177565 | C | A | 3 | a0001c0001t0016g0154 a0001c0001t0046g0087 a0007c0015t0016g0035 |
4 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.516-1229C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177565 | |||||||
| chr1:180177654 | G | C | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.516-1140G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177654 | |||||||
| chr1:180177686 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.516-1108C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177686 | |||||||
| chr1:180177794 | T | A | 2 | a0005c0008t0009g0003 a0010c0023t0047g0148 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.516-1000T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177794 | |||||||
| chr1:180177882 | ATGTTT | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.516-899_516-895del others(5): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 180177882 | ||||||
| chr1:180177887 | T | G | 1 | a0001c0001t0006g0200 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.516-907T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180177887 | |||||||
| chr1:180178137 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.516-657C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178137 | |||||||
| chr1:180178144 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.516-650G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178144 | |||||||
| chr1:180178221 | A | C | 6 | a0001c0001t0005g0139 a0001c0001t0005g0150 a0001c0001t0005g0152 others(3): Show |
6 | HG01074.hp1 HG01884.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.516-573A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178221 | |||||||
| chr1:180178233 | T | G | 1 | a0001c0001t0006g0239 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.516-561T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178233 | |||||||
| chr1:180178373 | G | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.516-421G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178373 | |||||||
| chr1:180178416 | C | T | 1 | a0004c0006t0007g0097 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.516-378C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178416 | |||||||
| chr1:180178428 | A | G | 1 | a0001c0002t0002g0050 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.516-366A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178428 | |||||||
| chr1:180178447 | C | A | 1 | a0004c0019t0014g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.516-347C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178447 | |||||||
| chr1:180178503 | C | T | 1 | a0001c0001t0004g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.516-291C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178503 | |||||||
| chr1:180178557 | G | A | 1 | a0002c0003t0003g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.516-237G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178557 | |||||||
| chr1:180178579 | A | G | 1 | a0001c0001t0004g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.516-215A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178579 | |||||||
| chr1:180178615 | A | C | 1 | a0001c0001t0001g0238 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.516-179A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178615 | |||||||
| chr1:180178736 | C | A | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.516-58C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178736 | |||||||
| chr1:180178777 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.516-17A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 4/11 | chr1 | 180178777 | |||||||
| chr1:180178941 | G | C | 2 | a0001c0012t0018g0178 a0001c0012t0018g0179 |
2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.606+57G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180178941 | |||||||
| chr1:180178998 | G | A | 2 | a0001c0002t0002g0166 a0001c0002t0002g0167 |
2 | NA19067.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.606+114G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180178998 | |||||||
| chr1:180179068 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0002g0147 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.606+184C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179068 | |||||||
| chr1:180179191 | G | A | 4 | a0002c0003t0003g0015 a0002c0003t0003g0058 a0002c0003t0003g0069 others(1): Show |
6 | HG00544.hp1 HG02083.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+307G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179191 | |||||||
| chr1:180179193 | A | G | 1 | a0001c0007t0001g0199 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.606+309A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179193 | |||||||
| chr1:180179195 | G | A | 1 | a0004c0019t0014g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.606+311G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179195 | |||||||
| chr1:180179229 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.606+345A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179229 | |||||||
| chr1:180179245 | T | A | 1 | a0001c0001t0001g0203 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.606+361T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179245 | |||||||
| chr1:180179403 | G | A | 2 | a0005c0008t0009g0003 a0010c0023t0047g0148 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.606+519G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179403 | |||||||
| chr1:180179433 | A | G | 3 | a0001c0001t0015g0034 a0001c0001t0015g0084 a0001c0021t0015g0034 |
3 | HG02615.hp2 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.606+549A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179433 | |||||||
| chr1:180179434 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.606+550G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179434 | |||||||
| chr1:180179549 | A | C | 1 | a0001c0001t0001g0188 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.606+665A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179549 | |||||||
| chr1:180179568 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.606+684G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179568 | |||||||
| chr1:180179590 | T | C | 37 | a0001c0017t0055g0135 a0003c0005t0002g0041 a0003c0005t0005g0010 others(34): Show |
46 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.606+706T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179590 | |||||||
| chr1:180179597 | A | G | 37 | a0001c0017t0055g0135 a0003c0005t0002g0041 a0003c0005t0005g0010 others(34): Show |
46 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.606+713A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179597 | |||||||
| chr1:180179889 | T | G | 1 | a0002c0003t0003g0074 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.606+1005T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179889 | |||||||
| chr1:180179917 | G | T | 1 | a0002c0003t0003g0072 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.606+1033G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180179917 | |||||||
| chr1:180180148 | G | C | 1 | a0001c0001t0008g0184 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.606+1264G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180180148 | |||||||
| chr1:180180329 | G | C | 36 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(33): Show |
45 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.606+1445G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180180329 | |||||||
| chr1:180180359 | C | T | 5 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0035g0251 others(2): Show |
5 | HG01069.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.606+1475C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180180359 | |||||||
| chr1:180180399 | G | A | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.606+1515G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180180399 | |||||||
| chr1:180180452 | C | T | 36 | a0001c0017t0055g0135 a0003c0005t0002g0041 a0003c0005t0005g0010 others(33): Show |
45 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.606+1568C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180180452 | |||||||
| chr1:180180485 | C | T | 1 | a0003c0005t0005g0106 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.606+1601C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180180485 | |||||||
| chr1:180180559 | G | A | 1 | a0002c0003t0003g0075 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.607-1615G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180180559 | |||||||
| chr1:180180615 | T | C | 1 | a0001c0002t0002g0245 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.607-1559T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180180615 | |||||||
| chr1:180180699 | T | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(234): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.607-1475T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180180699 | |||||||
| chr1:180180717 | A | G | 1 | a0004c0006t0039g0100 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.607-1457A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180180717 | |||||||
| chr1:180180724 | T | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(194): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.607-1450T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180180724 | |||||||
| chr1:180180844 | T | C | 17 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(14): Show |
24 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.607-1330T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180180844 | |||||||
| chr1:180180929 | G | A | 1 | a0004c0019t0014g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.607-1245G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180180929 | |||||||
| chr1:180181016 | A | C | 31 | a0001c0017t0055g0135 a0003c0005t0002g0041 a0003c0005t0005g0010 others(28): Show |
40 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.607-1158A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181016 | |||||||
| chr1:180181016 | A | T | 34 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(31): Show |
48 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.607-1158A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181016 | |||||||
| chr1:180181043 | G | A | 2 | a0005c0008t0009g0003 a0010c0023t0047g0148 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.607-1131G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181043 | |||||||
| chr1:180181120 | A | G | 30 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(27): Show |
39 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.607-1054A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181120 | |||||||
| chr1:180181194 | T | C | 34 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(31): Show |
48 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.607-980T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181194 | |||||||
| chr1:180181240 | T | C | 2 | a0001c0002t0031g0144 a0001c0002t0031g0145 |
2 | HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.607-934T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181240 | |||||||
| chr1:180181290 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.607-884G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181290 | |||||||
| chr1:180181306 | C | T | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.607-868C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181306 | |||||||
| chr1:180181329 | C | G | 1 | a0002c0003t0003g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.607-845C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181329 | |||||||
| chr1:180181347 | A | C | 2 | a0005c0008t0009g0003 a0010c0023t0047g0148 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.607-827A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181347 | |||||||
| chr1:180181440 | A | G | 2 | a0001c0001t0001g0218 a0001c0001t0045g0217 |
2 | HG00558.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.607-734A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181440 | |||||||
| chr1:180181465 | C | T | 2 | a0001c0013t0017g0019 a0001c0013t0056g0136 |
4 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-709C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181465 | |||||||
| chr1:180181584 | T | G | 30 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(27): Show |
39 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.607-590T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181584 | |||||||
| chr1:180181743 | C | G | 1 | a0001c0001t0036g0151 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.607-431C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181743 | |||||||
| chr1:180181767 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.607-407A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181767 | |||||||
| chr1:180181857 | T | C | 1 | a0004c0019t0014g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.607-317T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181857 | |||||||
| chr1:180181965 | G | T | 1 | a0002c0003t0003g0074 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.607-209G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180181965 | |||||||
| chr1:180182005 | T | G | 1 | a0002c0003t0003g0074 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.607-169T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180182005 | |||||||
| chr1:180182042 | C | T | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.607-132C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180182042 | |||||||
| chr1:180182137 | G | A | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.607-37G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 5/11 | chr1 | 180182137 | |||||||
| chr1:180182531 | A | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.752+212A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180182531 | |||||||
| chr1:180182552 | C | T | 2 | a0001c0007t0006g0056 a0001c0007t0026g0056 |
2 | NA18983.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.752+233C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180182552 | |||||||
| chr1:180182574 | C | T | 7 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0142 others(4): Show |
8 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.752+255C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180182574 | |||||||
| chr1:180182582 | G | A | 3 | a0001c0012t0018g0178 a0001c0012t0018g0179 a0001c0012t0018g0180 |
3 | HG02258.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.752+263G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180182582 | |||||||
| chr1:180182609 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.752+290T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180182609 | |||||||
| chr1:180182625 | C | T | 30 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(27): Show |
39 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.752+306C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180182625 | |||||||
| chr1:180182668 | G | A | 30 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(27): Show |
39 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.752+349G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180182668 | |||||||
| chr1:180182812 | C | T | 1 | a0001c0001t0036g0151 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.752+493C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180182812 | |||||||
| chr1:180182813 | G | A | 1 | a0001c0004t0004g0121 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.752+494G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180182813 | |||||||
| chr1:180182877 | C | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG00099.hp2 NA18971.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.752+558C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180182877 | |||||||
| chr1:180183020 | G | A | 1 | a0002c0003t0003g0078 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.752+701G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183020 | |||||||
| chr1:180183060 | C | T | 2 | a0001c0017t0055g0135 a0004c0019t0014g0155 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.752+741C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183060 | |||||||
| chr1:180183067 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.752+748C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183067 | |||||||
| chr1:180183107 | G | A | 42 | a0001c0001t0002g0021 a0001c0002t0002g0002 a0001c0002t0002g0008 others(39): Show |
65 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.752+788G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183107 | |||||||
| chr1:180183121 | T | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0205 a0001c0001t0001g0207 others(5): Show |
11 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.753-795T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183121 | |||||||
| chr1:180183125 | C | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.753-791C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183125 | |||||||
| chr1:180183168 | C | A | 1 | a0001c0001t0046g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.753-748C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183168 | |||||||
| chr1:180183177 | T | C | 1 | a0001c0002t0002g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.753-739T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183177 | |||||||
| chr1:180183249 | C | T | 1 | a0004c0019t0014g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.753-667C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183249 | |||||||
| chr1:180183374 | A | AC | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.753-540dupC | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 180183374 | ||||||
| chr1:180183385 | C | T | 2 | a0005c0008t0009g0003 a0010c0023t0047g0148 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.753-531C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183385 | |||||||
| chr1:180183541 | C | A | 1 | a0004c0019t0014g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.753-375C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183541 | |||||||
| chr1:180183602 | C | T | 4 | a0001c0001t0004g0086 a0001c0001t0016g0154 a0001c0001t0046g0087 others(1): Show |
5 | HG01192.hp2 HG01243.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.753-314C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183602 | |||||||
| chr1:180183652 | T | C | 30 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(27): Show |
39 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.753-264T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183652 | |||||||
| chr1:180183660 | A | G | 3 | a0004c0011t0008g0248 a0004c0011t0008g0249 a0004c0011t0044g0250 |
3 | HG01069.hp2 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.753-256A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183660 | |||||||
| chr1:180183743 | C | T | 35 | a0001c0001t0002g0138 a0001c0001t0003g0080 a0001c0001t0059g0059 others(32): Show |
49 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.753-173C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 6/11 | chr1 | 180183743 | |||||||
| chr1:180184061 | G | A | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.887+11G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184061 | |||||||
| chr1:180184119 | C | T | 2 | a0005c0008t0009g0003 a0010c0023t0047g0148 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.887+69C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184119 | |||||||
| chr1:180184244 | C | T | 1 | a0002c0003t0003g0068 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.887+194C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184244 | |||||||
| chr1:180184248 | G | A | 1 | a0001c0004t0053g0117 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.887+198G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184248 | |||||||
| chr1:180184286 | G | A | 1 | a0004c0019t0014g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.887+236G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184286 | |||||||
| chr1:180184310 | C | T | 3 | a0001c0001t0013g0142 a0001c0001t0048g0140 a0001c0001t0050g0141 |
3 | HG00140.hp2 HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.887+260C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184310 | |||||||
| chr1:180184428 | C | T | 27 | a0001c0004t0004g0011 a0001c0004t0004g0017 a0001c0004t0004g0018 others(24): Show |
36 | HG00099.hp1 HG00323.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.887+378C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184428 | |||||||
| chr1:180184494 | C | CTACAGCA | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.887+446_887+452dup others(7): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 180184494 | ||||||
| chr1:180184498 | A | G | 31 | a0001c0017t0055g0135 a0003c0005t0002g0041 a0003c0005t0005g0010 others(28): Show |
40 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.887+448A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184498 | |||||||
| chr1:180184650 | T | C | 1 | a0001c0004t0004g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.887+600T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184650 | |||||||
| chr1:180184724 | G | T | 1 | a0001c0012t0057g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.887+674G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184724 | |||||||
| chr1:180184792 | G | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0221 a0001c0001t0001g0225 others(2): Show |
8 | HG00408.hp1 NA18947.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.887+742G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184792 | |||||||
| chr1:180184801 | A | G | 4 | a0001c0002t0002g0023 a0001c0002t0002g0162 a0001c0002t0002g0165 others(1): Show |
6 | HG01928.hp2 HG02135.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.887+751A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184801 | |||||||
| chr1:180184858 | T | C | 1 | a0001c0001t0001g0029 | 3 | HG01175.hp2 HG01261.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.887+808T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184858 | |||||||
| chr1:180184926 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.887+876A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184926 | |||||||
| chr1:180184963 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.887+913T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180184963 | |||||||
| chr1:180185035 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.887+985G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180185035 | |||||||
| chr1:180185075 | G | A | 2 | a0005c0008t0009g0003 a0010c0023t0047g0148 |
9 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.888-978G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180185075 | |||||||
| chr1:180185113 | G | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.888-940G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180185113 | |||||||
| chr1:180185155 | T | C | 1 | a0003c0005t0012g0110 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.888-898T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180185155 | |||||||
| chr1:180185222 | TGGAGGGG others(3): Show |
T | 2 | a0001c0013t0017g0019 a0001c0013t0056g0136 |
4 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-826_888-817del others(10): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 180185222 | ||||||
| chr1:180185299 | C | A | 3 | a0001c0001t0001g0030 a0001c0001t0024g0246 a0001c0001t0024g0247 |
5 | HG01081.hp1 HG01123.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.888-754C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180185299 | |||||||
| chr1:180185365 | C | T | 7 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0142 others(4): Show |
8 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.888-688C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180185365 | |||||||
| chr1:180185405 | G | A | 35 | a0001c0001t0002g0138 a0001c0001t0003g0080 a0001c0001t0059g0059 others(32): Show |
49 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.888-648G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180185405 | |||||||
| chr1:180185410 | C | T | 2 | a0001c0004t0004g0132 a0001c0004t0004g0133 |
2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.888-643C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180185410 | |||||||
| chr1:180185580 | A | C | 31 | a0001c0017t0055g0135 a0003c0005t0002g0041 a0003c0005t0005g0010 others(28): Show |
40 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.888-473A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180185580 | |||||||
| chr1:180185637 | T | C | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.888-416T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180185637 | |||||||
| chr1:180185641 | G | A | 30 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(27): Show |
39 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.888-412G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 7/11 | chr1 | 180185641 | |||||||
| chr1:180186188 | C | A | 3 | a0001c0001t0022g0033 a0001c0001t0022g0081 a0001c0001t0034g0033 |
3 | HG02622.hp1 HG02922.hp2 HG02976.hp2 |
splice_region_variant&intron_variant | LOW | c.1017+6C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180186188 | |||||||
| chr1:180186216 | A | G | 1 | a0001c0001t0011g0196 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1017+34A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180186216 | |||||||
| chr1:180186241 | C | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1017+59C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180186241 | |||||||
| chr1:180186247 | AG | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1017+67delG | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 180186247 | ||||||
| chr1:180186348 | C | G | 1 | a0001c0001t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1017+166C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180186348 | |||||||
| chr1:180186427 | C | T | 1 | a0001c0001t0037g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1017+245C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180186427 | |||||||
| chr1:180186552 | CT | C | 17 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(14): Show |
24 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1017+371delT | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180186552 | |||||||
| chr1:180186560 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1017+378C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180186560 | |||||||
| chr1:180186921 | T | A | 17 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(14): Show |
24 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1017+739T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180186921 | |||||||
| chr1:180187048 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1017+866C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187048 | |||||||
| chr1:180187051 | A | T | 1 | a0002c0003t0011g0062 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1017+869A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187051 | |||||||
| chr1:180187061 | A | G | 31 | a0001c0017t0055g0135 a0003c0005t0002g0041 a0003c0005t0005g0010 others(28): Show |
40 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1017+879A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187061 | |||||||
| chr1:180187103 | G | A | 1 | a0004c0006t0039g0100 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1017+921G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187103 | |||||||
| chr1:180187111 | T | A | 1 | a0001c0001t0006g0243 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1017+929T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187111 | |||||||
| chr1:180187116 | C | T | 31 | a0001c0001t0002g0021 a0001c0002t0002g0002 a0001c0002t0002g0008 others(28): Show |
51 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.1017+934C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187116 | |||||||
| chr1:180187146 | C | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1017+964C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187146 | |||||||
| chr1:180187214 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1017+1032G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187214 | |||||||
| chr1:180187335 | A | G | 1 | a0001c0001t0011g0195 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1017+1153A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187335 | |||||||
| chr1:180187409 | T | G | 31 | a0001c0017t0055g0135 a0003c0005t0002g0041 a0003c0005t0005g0010 others(28): Show |
40 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1017+1227T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187409 | |||||||
| chr1:180187467 | C | T | 1 | a0003c0005t0021g0109 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1017+1285C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187467 | |||||||
| chr1:180187532 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1017+1350C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187532 | |||||||
| chr1:180187565 | A | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.1017+1383A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187565 | |||||||
| chr1:180187649 | A | C | 1 | a0001c0001t0001g0242 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1017+1467A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187649 | |||||||
| chr1:180187670 | C | G | 22 | a0001c0001t0059g0059 a0002c0003t0003g0060 a0002c0003t0010g0014 others(19): Show |
31 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.1017+1488C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187670 | |||||||
| chr1:180187843 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1017+1661G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187843 | |||||||
| chr1:180187953 | T | C | 31 | a0001c0017t0055g0135 a0003c0005t0002g0041 a0003c0005t0005g0010 others(28): Show |
40 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1018-1599T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180187953 | |||||||
| chr1:180188081 | C | A | 3 | a0001c0002t0027g0160 a0001c0002t0027g0161 a0001c0002t0064g0088 |
3 | HG02809.hp2 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1018-1471C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188081 | |||||||
| chr1:180188095 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1018-1457C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188095 | |||||||
| chr1:180188123 | G | A | 1 | a0001c0001t0014g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1018-1429G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188123 | |||||||
| chr1:180188151 | G | T | 1 | a0004c0019t0014g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1018-1401G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188151 | |||||||
| chr1:180188199 | C | T | 1 | a0001c0001t0001g0049 | 2 | NA18954.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1018-1353C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188199 | |||||||
| chr1:180188204 | C | G | 31 | a0001c0017t0055g0135 a0003c0005t0002g0041 a0003c0005t0005g0010 others(28): Show |
40 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1018-1348C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188204 | |||||||
| chr1:180188298 | C | T | 2 | a0001c0001t0016g0154 a0007c0015t0016g0035 |
3 | HG01243.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1018-1254C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188298 | |||||||
| chr1:180188314 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1018-1238G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188314 | |||||||
| chr1:180188342 | T | A | 1 | a0001c0001t0006g0239 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1018-1210T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188342 | |||||||
| chr1:180188375 | T | A | 1 | a0004c0006t0007g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1018-1177T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188375 | |||||||
| chr1:180188432 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1018-1120C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188432 | |||||||
| chr1:180188452 | G | A | 2 | a0004c0011t0008g0248 a0004c0011t0008g0249 |
2 | HG01069.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1018-1100G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188452 | |||||||
| chr1:180188458 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1018-1094G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188458 | |||||||
| chr1:180188588 | C | T | 36 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0002c0003t0003g0006 others(33): Show |
50 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(47): Show |
intron_variant | MODIFIER | c.1018-964C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188588 | |||||||
| chr1:180188626 | C | T | 1 | a0002c0003t0003g0069 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1018-926C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188626 | |||||||
| chr1:180188756 | T | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1018-796T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188756 | |||||||
| chr1:180188807 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1018-745T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188807 | |||||||
| chr1:180188823 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1018-729T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188823 | |||||||
| chr1:180188952 | A | T | 4 | a0001c0004t0004g0130 a0001c0004t0004g0131 a0001c0004t0004g0132 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1018-600A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180188952 | |||||||
| chr1:180189034 | G | T | 4 | a0001c0001t0004g0086 a0001c0001t0016g0154 a0001c0001t0046g0087 others(1): Show |
5 | HG01192.hp2 HG01243.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-518G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180189034 | |||||||
| chr1:180189179 | C | A | 1 | a0001c0001t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1018-373C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180189179 | |||||||
| chr1:180189358 | G | A | 34 | a0001c0002t0027g0160 a0001c0002t0027g0161 a0001c0002t0064g0088 others(31): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1018-194G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180189358 | |||||||
| chr1:180189452 | C | T | 38 | a0001c0001t0002g0138 a0001c0001t0059g0059 a0001c0013t0017g0019 others(35): Show |
54 | HG00280.hp2 HG00544.hp1 HG01496.hp1 others(51): Show |
intron_variant | MODIFIER | c.1018-100C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180189452 | |||||||
| chr1:180189533 | C | T | 31 | a0001c0017t0055g0135 a0003c0005t0002g0041 a0003c0005t0005g0010 others(28): Show |
40 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1018-19C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 8/11 | chr1 | 180189533 | |||||||
| chr1:180189745 | C | T | 3 | a0002c0003t0003g0066 a0002c0003t0003g0067 a0002c0003t0003g0068 |
3 | NA18959.hp2 NA18993.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1140+71C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 9/11 | chr1 | 180189745 | |||||||
| chr1:180189754 | CCTT | C | 3 | a0001c0001t0014g0082 a0001c0001t0014g0083 a0001c0001t0014g0085 |
3 | HG03130.hp2 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1140+85_1140+87del others(3): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 180189754 | ||||||
| chr1:180189759 | T | G | 2 | a0001c0001t0013g0045 a0001c0001t0049g0045 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1140+85T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 9/11 | chr1 | 180189759 | |||||||
| chr1:180189792 | C | G | 13 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(10): Show |
15 | HG00735.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1140+118C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 9/11 | chr1 | 180189792 | |||||||
| chr1:180189836 | C | G | 1 | a0004c0019t0014g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1140+162C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 9/11 | chr1 | 180189836 | |||||||
| chr1:180189838 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1140+164C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 9/11 | chr1 | 180189838 | |||||||
| chr1:180190085 | G | A | 2 | a0001c0002t0027g0160 a0001c0002t0027g0161 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1141-348G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 9/11 | chr1 | 180190085 | |||||||
| chr1:180190197 | C | G | 1 | a0001c0001t0005g0152 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1141-236C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 9/11 | chr1 | 180190197 | |||||||
| chr1:180190335 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1141-98C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 9/11 | chr1 | 180190335 | |||||||
| chr1:180190593 | C | G | 17 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(14): Show |
24 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1288+13C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180190593 | |||||||
| chr1:180190653 | C | T | 1 | a0001c0001t0022g0081 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1288+73C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180190653 | |||||||
| chr1:180190662 | TC | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1288+85delC | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 180190662 | ||||||
| chr1:180190773 | C | T | 30 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(27): Show |
39 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1288+193C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180190773 | |||||||
| chr1:180190779 | C | T | 5 | a0003c0005t0005g0010 a0003c0005t0005g0039 a0003c0005t0005g0108 others(2): Show |
9 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1288+199C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180190779 | |||||||
| chr1:180190865 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1288+285C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180190865 | |||||||
| chr1:180190866 | G | A | 1 | a0001c0004t0004g0124 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1288+286G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180190866 | |||||||
| chr1:180190947 | G | A | 1 | a0001c0002t0002g0165 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1288+367G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180190947 | |||||||
| chr1:180191099 | C | T | 17 | a0003c0005t0002g0041 a0003c0005t0005g0010 a0003c0005t0005g0039 others(14): Show |
24 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1288+519C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191099 | |||||||
| chr1:180191105 | C | T | 1 | a0001c0002t0002g0171 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1288+525C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191105 | |||||||
| chr1:180191193 | C | T | 3 | a0001c0001t0022g0033 a0001c0001t0022g0081 a0001c0001t0034g0033 |
3 | HG02622.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1288+613C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191193 | |||||||
| chr1:180191349 | C | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1288+769C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191349 | |||||||
| chr1:180191368 | C | T | 31 | a0001c0001t0008g0229 a0003c0005t0002g0041 a0003c0005t0005g0010 others(28): Show |
40 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1288+788C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191368 | |||||||
| chr1:180191370 | C | T | 13 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(10): Show |
15 | HG00735.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1288+790C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191370 | |||||||
| chr1:180191417 | C | T | 18 | a0001c0001t0008g0229 a0003c0005t0002g0041 a0003c0005t0005g0010 others(15): Show |
25 | HG00423.hp1 HG01168.hp1 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.1288+837C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191417 | |||||||
| chr1:180191464 | C | A | 1 | a0013c0022t0010g0070 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1288+884C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191464 | |||||||
| chr1:180191540 | G | A | 1 | a0001c0001t0005g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1288+960G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191540 | |||||||
| chr1:180191554 | G | T | 1 | a0013c0022t0010g0070 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1288+974G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191554 | |||||||
| chr1:180191654 | G | A | 4 | a0002c0003t0003g0009 a0002c0003t0003g0079 a0002c0003t0010g0009 others(1): Show |
6 | HG02015.hp2 HG02165.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288+1074G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191654 | |||||||
| chr1:180191743 | G | T | 1 | a0013c0022t0010g0070 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1288+1163G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191743 | |||||||
| chr1:180191776 | C | T | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1288+1196C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191776 | |||||||
| chr1:180191858 | C | T | 27 | a0001c0004t0004g0011 a0001c0004t0004g0017 a0001c0004t0004g0018 others(24): Show |
36 | HG00099.hp1 HG00323.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.1288+1278C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191858 | |||||||
| chr1:180191905 | T | G | 75 | a0001c0001t0002g0021 a0001c0001t0003g0080 a0001c0001t0008g0229 others(72): Show |
107 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.1288+1325T>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191905 | |||||||
| chr1:180191940 | G | A | 1 | a0003c0005t0005g0115 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1288+1360G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180191940 | |||||||
| chr1:180192084 | C | T | 2 | a0001c0013t0017g0019 a0001c0013t0056g0136 |
4 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+1504C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192084 | |||||||
| chr1:180192177 | C | A | 3 | a0001c0002t0019g0026 a0001c0002t0063g0175 a0012c0024t0060g0174 |
5 | HG02486.hp2 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288+1597C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192177 | |||||||
| chr1:180192255 | A | G | 1 | a0013c0022t0010g0070 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1288+1675A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192255 | |||||||
| chr1:180192298 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1288+1718A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192298 | |||||||
| chr1:180192309 | G | A | 32 | a0001c0001t0002g0021 a0001c0002t0002g0002 a0001c0002t0002g0008 others(29): Show |
52 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.1288+1729G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192309 | |||||||
| chr1:180192318 | G | C | 1 | a0013c0022t0010g0070 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1288+1738G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192318 | |||||||
| chr1:180192319 | A | G | 1 | a0013c0022t0010g0070 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1288+1739A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192319 | |||||||
| chr1:180192320 | G | C | 1 | a0013c0022t0010g0070 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1288+1740G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192320 | |||||||
| chr1:180192484 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.1289-1729T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192484 | |||||||
| chr1:180192485 | G | A | 1 | a0003c0005t0005g0102 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1289-1728G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192485 | |||||||
| chr1:180192680 | G | A | 1 | a0001c0001t0008g0229 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1289-1533G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192680 | |||||||
| chr1:180192707 | G | A | 1 | a0001c0001t0016g0154 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1289-1506G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192707 | |||||||
| chr1:180192752 | C | A | 1 | a0001c0001t0015g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1289-1461C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192752 | |||||||
| chr1:180192914 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1289-1299C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192914 | |||||||
| chr1:180192915 | G | C | 1 | a0001c0001t0001g0209 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1289-1298G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192915 | |||||||
| chr1:180192928 | G | A | 5 | a0001c0001t0014g0082 a0001c0001t0014g0083 a0001c0001t0014g0085 others(2): Show |
12 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1289-1285G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192928 | |||||||
| chr1:180192942 | G | C | 1 | a0002c0003t0003g0157 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1289-1271G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192942 | |||||||
| chr1:180192954 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1289-1259A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180192954 | |||||||
| chr1:180193158 | G | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1289-1055G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193158 | |||||||
| chr1:180193184 | A | G | 1 | a0003c0005t0005g0108 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1289-1029A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193184 | |||||||
| chr1:180193229 | C | T | 73 | a0001c0001t0001g0049 a0001c0001t0002g0021 a0001c0001t0002g0147 others(70): Show |
103 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.1289-984C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193229 | |||||||
| chr1:180193261 | G | C | 1 | a0001c0002t0061g0163 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1289-952G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193261 | |||||||
| chr1:180193343 | C | A | 1 | a0013c0022t0010g0070 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1289-870C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193343 | |||||||
| chr1:180193345 | T | C | 1 | a0001c0001t0004g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1289-868T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193345 | |||||||
| chr1:180193406 | C | T | 1 | a0001c0004t0004g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1289-807C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193406 | |||||||
| chr1:180193420 | A | G | 111 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0027 others(108): Show |
169 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.1289-793A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193420 | |||||||
| chr1:180193540 | A | T | 1 | a0002c0003t0003g0157 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1289-673A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193540 | |||||||
| chr1:180193692 | TGGGTGGG others(3): Show |
T | 1 | a0001c0002t0064g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1289-513_1289-504d others(12): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 180193692 | ||||||
| chr1:180193702 | G | C | 1 | a0005c0008t0009g0003 | 2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1289-511G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193702 | |||||||
| chr1:180193707 | G | A | 1 | a0001c0004t0004g0132 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1289-506G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193707 | |||||||
| chr1:180193793 | C | G | 6 | a0001c0001t0032g0047 a0001c0004t0004g0130 a0001c0004t0004g0131 others(3): Show |
7 | HG02055.hp1 HG02451.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1289-420C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193793 | |||||||
| chr1:180193862 | T | A | 1 | a0002c0003t0003g0157 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1289-351T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193862 | |||||||
| chr1:180193957 | G | A | 13 | a0004c0006t0007g0037 a0004c0006t0007g0092 a0004c0006t0007g0093 others(10): Show |
15 | HG00735.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1289-256G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193957 | |||||||
| chr1:180193964 | A | G | 1 | a0004c0011t0035g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1289-249A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 10/11 | chr1 | 180193964 | |||||||
| chr1:180194443 | G | T | 24 | a0001c0001t0005g0139 a0001c0001t0005g0150 a0001c0001t0005g0152 others(21): Show |
32 | HG00423.hp1 HG01074.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1468+51G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180194443 | |||||||
| chr1:180194472 | A | C | 1 | a0002c0003t0029g0192 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1468+80A>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180194472 | |||||||
| chr1:180194537 | C | T | 4 | a0001c0001t0014g0082 a0001c0001t0014g0083 a0001c0001t0014g0085 others(1): Show |
4 | HG02723.hp2 HG03130.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+145C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180194537 | |||||||
| chr1:180194604 | C | T | 4 | a0001c0004t0004g0130 a0001c0004t0004g0131 a0001c0004t0004g0132 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+212C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180194604 | |||||||
| chr1:180194784 | G | A | 24 | a0001c0001t0004g0086 a0001c0004t0004g0011 a0001c0004t0004g0017 others(21): Show |
32 | HG00323.hp1 HG01099.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.1468+392G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180194784 | |||||||
| chr1:180194995 | C | CCGG | 1 | a0005c0008t0009g0003 | 8 | HG01109.hp2 HG02647.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1468+604_1468+606d others(5): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 180194995 | ||||||
| chr1:180194995 | C | CG | 39 | a0001c0001t0059g0059 a0002c0003t0003g0006 a0002c0003t0003g0009 others(36): Show |
55 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1468+603_1468+604i others(3): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180194995 | |||||||
| chr1:180194995 | C | CGG | 6 | a0002c0003t0003g0067 a0002c0003t0038g0064 a0002c0003t0041g0061 others(3): Show |
6 | HG02293.hp1 HG04184.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.1468+603_1468+604i others(4): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180194995 | |||||||
| chr1:180194995 | C | G | 1 | a0013c0022t0010g0070 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1468+603C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180194995 | |||||||
| chr1:180194996 | C | CGGG | 23 | a0001c0001t0002g0138 a0001c0001t0002g0185 a0001c0001t0003g0080 others(20): Show |
39 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468+611_1468+613d others(5): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 180194996 | ||||||
| chr1:180194996 | C | CGGGG | 17 | a0001c0001t0002g0147 a0001c0001t0002g0210 a0001c0001t0011g0193 others(14): Show |
24 | HG00609.hp1 HG00673.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1468+610_1468+613d others(6): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 180194996 | ||||||
| chr1:180194996 | C | G | 50 | a0001c0001t0007g0234 a0001c0001t0059g0059 a0002c0003t0003g0006 others(47): Show |
66 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1468+604C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180194996 | |||||||
| chr1:180194999 | G | C | 1 | a0001c0017t0055g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1468+607G>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180194999 | |||||||
| chr1:180194999 | G | T | 50 | a0001c0001t0004g0086 a0001c0001t0005g0139 a0001c0001t0005g0150 others(47): Show |
66 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1468+607G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180194999 | |||||||
| chr1:180195001 | G | GT | 3 | a0001c0002t0027g0160 a0001c0002t0027g0161 a0001c0002t0064g0088 |
3 | HG02809.hp2 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1468+609_1468+610i others(3): Show |
QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195001 | |||||||
| chr1:180195001 | G | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1468+609G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195001 | |||||||
| chr1:180195022 | G | A | 1 | a0003c0005t0021g0040 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1468+630G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195022 | |||||||
| chr1:180195056 | G | T | 4 | a0001c0001t0014g0082 a0001c0001t0014g0083 a0001c0001t0014g0085 others(1): Show |
4 | HG02723.hp2 HG03130.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+664G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195056 | |||||||
| chr1:180195075 | C | A | 7 | a0001c0007t0001g0055 a0001c0007t0001g0197 a0001c0007t0001g0199 others(4): Show |
8 | NA18950.hp1 NA18983.hp2 NA18986.hp1 others(5): Show |
intron_variant | MODIFIER | c.1468+683C>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195075 | |||||||
| chr1:180195076 | G | A | 2 | a0001c0004t0004g0017 a0001c0004t0004g0042 |
5 | HG02451.hp2 HG02647.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1468+684G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195076 | |||||||
| chr1:180195098 | C | G | 1 | a0001c0001t0001g0222 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1468+706C>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195098 | |||||||
| chr1:180195104 | T | A | 1 | a0001c0001t0001g0222 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1468+712T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195104 | |||||||
| chr1:180195119 | G | T | 1 | a0001c0001t0059g0059 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1468+727G>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195119 | |||||||
| chr1:180195244 | G | A | 1 | a0001c0001t0037g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1468+852G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195244 | |||||||
| chr1:180195272 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1468+880C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195272 | |||||||
| chr1:180195275 | T | C | 3 | a0001c0001t0014g0082 a0001c0001t0014g0083 a0001c0001t0014g0085 |
3 | HG03130.hp2 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1468+883T>C | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195275 | |||||||
| chr1:180195400 | G | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.1469-862G>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195400 | |||||||
| chr1:180195480 | C | T | 47 | a0001c0001t0002g0021 a0001c0001t0002g0138 a0001c0001t0002g0147 others(44): Show |
73 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1469-782C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195480 | |||||||
| chr1:180195632 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1469-630C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195632 | |||||||
| chr1:180195648 | T | A | 1 | a0001c0012t0018g0178 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1469-614T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195648 | |||||||
| chr1:180195771 | T | A | 1 | a0001c0002t0027g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1469-491T>A | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195771 | |||||||
| chr1:180195956 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1469-306A>G | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195956 | |||||||
| chr1:180195998 | C | T | 3 | a0001c0012t0018g0178 a0001c0012t0018g0179 a0001c0012t0018g0180 |
3 | HG02258.hp1 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1469-264C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180195998 | |||||||
| chr1:180196025 | C | T | 14 | a0001c0001t0007g0234 a0004c0006t0007g0037 a0004c0006t0007g0092 others(11): Show |
16 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1469-237C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180196025 | |||||||
| chr1:180196033 | C | T | 14 | a0001c0001t0007g0234 a0001c0001t0011g0195 a0004c0006t0007g0037 others(11): Show |
16 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1469-229C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180196033 | |||||||
| chr1:180196069 | A | T | 50 | a0001c0001t0004g0086 a0001c0001t0005g0139 a0001c0001t0005g0150 others(47): Show |
66 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1469-193A>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180196069 | |||||||
| chr1:180196252 | C | T | 2 | a0001c0002t0019g0026 a0001c0002t0063g0175 |
4 | HG02486.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469-10C>T | QSOX1 | ENSG00000116260.17 | transcript | ENST00000367602.8 | protein_coding | 11/11 | chr1 | 180196252 |