Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51031 |
| ensemblid | ENSG00000167699.14 |
| hgncid | 14111 |
| symbol | GLOD4 |
| name | glyoxalase domain containing 4 |
| refseq_nuc | NM_016080.4 |
| refseq_prot | NP_057164.3 |
| ensembl_nuc | ENST00000301329.11 |
| ensembl_prot | ENSP00000301329.6 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 759330 |
| end | 782280 |
| strand | - |
| ver | v1.2 |
| region | chr17:759330-782280 |
| region5000 | chr17:754330-787280 |
| regionname0 | GLOD4_chr17_759330_782280 |
| regionname5000 | GLOD4_chr17_754330_787280 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 298 | 403 | 92 | 71 | 176 | 17 | 45 | 138 | GLOD4_chr17_754330_787280 | GLOD4 | MAARR others(293): Show |
chr17 | 754330 | 787280 |
| a0002 | 0/0 | 298 | 12 | 0 | 2 | 9 | 0 | 1 | 7 | GLOD4_chr17_754330_787280 | GLOD4 | MAARR others(293): Show |
chr17 | 754330 | 787280 |
| a0003 | 0/0 | 298 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | MAARR others(293): Show |
chr17 | 754330 | 787280 |
| a0004 | 0/0 | 298 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | MAARR others(293): Show |
chr17 | 754330 | 787280 |
| a0005 | 0/0 | 298 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | MAARR others(293): Show |
chr17 | 754330 | 787280 |
| a0006 | 0/0 | 298 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | MAARR others(293): Show |
chr17 | 754330 | 787280 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 894 | 394 | 92 | 71 | 171 | 15 | 43 | GLOD4_chr17_754330_787280 | GLOD4 | ATGGC others(889): Show |
chr17 | 754330 | 787280 | ||
| a0001c0003 | 0/0 | 894 | 5 | 0 | 0 | 5 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | ATGGC others(889): Show |
chr17 | 754330 | 787280 | ||
| a0001c0005 | 0/0 | 894 | 2 | 0 | 0 | 0 | 2 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | ATGGC others(889): Show |
chr17 | 754330 | 787280 | ||
| a0001c0007 | 0/0 | 894 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | ATGGC others(889): Show |
chr17 | 754330 | 787280 | ||
| a0001c0008 | 0/0 | 894 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | ATGGC others(889): Show |
chr17 | 754330 | 787280 | ||
| a0002c0002 | 0/0 | 894 | 12 | 0 | 2 | 9 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | ATGGC others(889): Show |
chr17 | 754330 | 787280 | ||
| a0003c0004 | 0/0 | 894 | 2 | 0 | 1 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | ATGGC others(889): Show |
chr17 | 754330 | 787280 | ||
| a0004c0006 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | ATGGC others(889): Show |
chr17 | 754330 | 787280 | ||
| a0005c0010 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | ATGGC others(889): Show |
chr17 | 754330 | 787280 | ||
| a0006c0009 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | ATGGC others(889): Show |
chr17 | 754330 | 787280 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1765 | 383 | 88 | 70 | 165 | 15 | 43 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0001c0001t0003 | 0/0 | 1765 | 5 | 0 | 0 | 5 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0001c0001t0004 | 0/0 | 1765 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0001c0001t0005 | 0/0 | 1765 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0001c0001t0006 | 0/0 | 1765 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0001c0001t0007 | 0/0 | 1765 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0001c0003t0001 | 0/0 | 1765 | 5 | 0 | 0 | 5 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0001c0005t0001 | 0/0 | 1765 | 2 | 0 | 0 | 0 | 2 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0001c0007t0001 | 0/0 | 1765 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0001c0008t0001 | 0/0 | 1765 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0002c0002t0002 | 0/0 | 1765 | 11 | 0 | 2 | 8 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0002c0002t0008 | 0/0 | 1765 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0003c0004t0001 | 0/0 | 1765 | 2 | 0 | 1 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0004c0006t0001 | 0/0 | 1765 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0005c0010t0001 | 0/0 | 1765 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| a0006c0009t0001 | 0/0 | 1765 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | GTGAC others(1760): Show |
chr17 | 754330 | 787280 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 24 | 2 | 5 | 14 | 3 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0002 | 0/0 | 22 | 1 | 13 | 4 | 1 | 3 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0003 | 0/0 | 11 | 0 | 2 | 8 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 0 | 4 | 1 | 4 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 1 | 3 | 0 | 3 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0011 | 0/0 | 5 | 2 | 0 | 0 | 0 | 3 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0019 | 1/0 | 3 | 0 | 1 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0004g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0001t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0005t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0007t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0001c0008t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0002c0002t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0002c0002t0008g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0003c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0003c0004t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0004c0006t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0005c0010t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| a0006c0009t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0004 | t0001 | g0203 | EUR | GBR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | GBR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | GBR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00280 | hp2 | a0001 | c0005 | t0001 | g0047 | EUR | FIN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0250 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0062 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01106 | hp2 | a0003 | c0004 | t0001 | g0205 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01515 | hp1 | a0001 | c0005 | t0001 | g0047 | EUR | IBS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CDX | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CDX | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0252 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | ESN | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03669 | hp1 | a0001 | c0008 | t0001 | g0207 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03704 | hp2 | a0001 | c0007 | t0001 | g0094 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0166 | EAS | CHB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | CHB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18947 | hp2 | a0004 | c0006 | t0001 | g0119 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18968 | hp2 | a0002 | c0002 | t0008 | g0253 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18973 | hp1 | a0005 | c0010 | t0001 | g0208 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18979 | hp1 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18993 | hp1 | a0006 | c0009 | t0001 | g0088 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0179 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19083 | hp1 | a0001 | c0001 | t0007 | g0104 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19090 | hp1 | a0001 | c0003 | t0001 | g0186 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ASW | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | GIH | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | GIH | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0255 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | USA | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | USA | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | USA | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0165 | REF | REF | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0019 | REF | REF | GLOD4_chr17_754330_787280 | GLOD4 | chr17 | 754330 | 787280 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:760228 | G | T | 1 | a0002 | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
missense_variant | MODERATE | c.842C>A | p.Ala281Glu | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 867/1765 | 842/897 | 281/298 | chr17 | 760228 | |||
| chr17:760232 | C | A | 1 | a0003 | 2 | HG00099.hp1 HG01106.hp2 |
missense_variant | MODERATE | c.838G>T | p.Ala280Ser | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 863/1765 | 838/897 | 280/298 | chr17 | 760232 | |||
| chr17:760233 | C | T | 1 | a0004 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.837G>A | p.Met279Ile | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 862/1765 | 837/897 | 279/298 | chr17 | 760233 | |||
| chr17:775858 | G | A | 1 | a0006 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.323C>T | p.Thr108Met | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/9 | 348/1765 | 323/897 | 108/298 | chr17 | 775858 | |||
| chr17:776905 | T | C | 1 | a0005 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.224A>G | p.Tyr75Cys | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/9 | 249/1765 | 224/897 | 75/298 | chr17 | 776905 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:760182 | A | C | 1 | a0001c0007 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.888T>G | p.Ala296Ala | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 913/1765 | 888/897 | 296/298 | chr17 | 760182 | |||
| chr17:760188 | G | A | 1 | a0001c0003 | 5 | NA18747.hp1 NA18971.hp1 NA18979.hp1 others(2): Show |
synonymous_variant | LOW | c.882C>T | p.Pro294Pro | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 907/1765 | 882/897 | 294/298 | chr17 | 760188 | |||
| chr17:760227 | T | A | 1 | a0002c0002 | 12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
synonymous_variant | LOW | c.843A>T | p.Ala281Ala | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 868/1765 | 843/897 | 281/298 | chr17 | 760227 | |||
| chr17:769950 | T | A | 1 | a0001c0005 | 2 | HG00280.hp2 HG01515.hp1 |
synonymous_variant | LOW | c.750A>T | p.Gly250Gly | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/9 | 775/1765 | 750/897 | 250/298 | chr17 | 769950 | |||
| chr17:775830 | G | A | 1 | a0001c0008 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.351C>T | p.Thr117Thr | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/9 | 376/1765 | 351/897 | 117/298 | chr17 | 775830 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:759379 | C | T | 1 | a0001c0001t0003 | 5 | HG00558.hp1 HG00597.hp1 NA18961.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*794G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 794 | chr17 | 759379 | ||||||
| chr17:759524 | C | G | 1 | a0001c0001t0007 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 649 | chr17 | 759524 | ||||||
| chr17:759657 | T | C | 1 | a0001c0001t0004 | 2 | HG02451.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*516A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 516 | chr17 | 759657 | ||||||
| chr17:759671 | T | G | 1 | a0002c0002t0008 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*502A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 502 | chr17 | 759671 | ||||||
| chr17:759850 | G | A | 2 | a0002c0002t0002 a0002c0002t0008 |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*323C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 323 | chr17 | 759850 | ||||||
| chr17:759942 | C | T | 1 | a0001c0001t0006 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*231G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 231 | chr17 | 759942 | ||||||
| chr17:760099 | T | C | 1 | a0001c0001t0005 | 2 | HG02809.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*74A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 9/9 | 74 | chr17 | 760099 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:760397 | A | T | 1 | a0001c0001t0001g0046 | 2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.832-159T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760397 | |||||||
| chr17:760580 | GA | G | 3 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0096 |
3 | NA18968.hp1 NA18979.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.832-343delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760580 | |||||||
| chr17:760690 | C | T | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-452G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760690 | |||||||
| chr17:760730 | C | T | 1 | a0001c0003t0001g0222 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.832-492G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760730 | |||||||
| chr17:760897 | T | C | 18 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(15): Show |
21 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.832-659A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760897 | |||||||
| chr17:760924 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.832-686A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760924 | |||||||
| chr17:760926 | C | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
367 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.832-688G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 760926 | |||||||
| chr17:761007 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.832-769C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761007 | |||||||
| chr17:761055 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832-817C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761055 | |||||||
| chr17:761355 | A | T | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-1117T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761355 | |||||||
| chr17:761357 | CTGATT | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0247 |
4 | HG00438.hp1 HG02080.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-1124_832-1120d others(7): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761357 | |||||||
| chr17:761384 | A | T | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-1146T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761384 | |||||||
| chr17:761486 | T | G | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-1248A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761486 | |||||||
| chr17:761520 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.832-1282A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761520 | |||||||
| chr17:761617 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0006g0062 |
2 | HG00741.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.832-1379C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761617 | |||||||
| chr17:761689 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.832-1451T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761689 | |||||||
| chr17:761715 | G | A | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-1477C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761715 | |||||||
| chr17:761759 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.832-1521G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761759 | |||||||
| chr17:761760 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.832-1522G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761760 | |||||||
| chr17:761779 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.832-1541G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761779 | |||||||
| chr17:761812 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.832-1574C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761812 | |||||||
| chr17:761889 | C | A | 1 | a0001c0001t0001g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.832-1651G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 761889 | |||||||
| chr17:762029 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.832-1791T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762029 | |||||||
| chr17:762246 | C | T | 2 | a0002c0002t0002g0248 a0002c0002t0002g0255 |
2 | HG01123.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.832-2008G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762246 | |||||||
| chr17:762315 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.832-2077C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762315 | |||||||
| chr17:762364 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(20): Show |
43 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.832-2126G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762364 | |||||||
| chr17:762395 | C | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0114 a0001c0001t0001g0129 |
4 | HG01175.hp2 HG01192.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-2157G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762395 | |||||||
| chr17:762405 | T | A | 12 | a0001c0001t0004g0036 a0002c0002t0002g0053 a0002c0002t0002g0248 others(9): Show |
14 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.832-2167A>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762405 | |||||||
| chr17:762420 | G | GGCCTGCA others(200): Show |
1 | a0001c0001t0001g0117 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.832-2389_832-2183d others(209): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762420 | |||||||
| chr17:762424 | TGCACCTA others(61): Show |
T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0039 others(29): Show |
58 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.832-2254_832-2187d others(70): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762424 | |||||||
| chr17:762487 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.832-2249G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762487 | |||||||
| chr17:762488 | GGCCGGCA others(132): Show |
G | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-2389_832-2251d others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762488 | |||||||
| chr17:762492 | G | T | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2254C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762492 | |||||||
| chr17:762492 | GGCACCTA others(200): Show |
G | 2 | a0001c0001t0005g0057 a0001c0001t0005g0084 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-2461_832-2255d others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762492 | |||||||
| chr17:762507 | CGTGATCT others(132): Show |
C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-2408_832-2270d others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762507 | |||||||
| chr17:762556 | G | T | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2318C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762556 | |||||||
| chr17:762560 | G | T | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2322C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762560 | |||||||
| chr17:762575 | C | T | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2337G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762575 | |||||||
| chr17:762587 | G | A | 3 | a0001c0003t0001g0179 a0001c0003t0001g0186 a0001c0003t0001g0227 |
3 | NA18979.hp1 NA19007.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.832-2349C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762587 | |||||||
| chr17:762604 | T | TTCATCAC others(194): Show |
1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2367_832-2366i others(203): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762604 | |||||||
| chr17:762604 | TATTTCAT others(129): Show |
T | 1 | a0001c0001t0001g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.832-2502_832-2367d others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762604 | |||||||
| chr17:762617 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0063 others(1): Show |
6 | HG00609.hp2 HG02165.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-2379A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762617 | |||||||
| chr17:762627 | T | G | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2389A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762627 | |||||||
| chr17:762646 | T | C | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-2408A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762646 | |||||||
| chr17:762652 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0191 |
3 | NA18959.hp2 NA18977.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.832-2414G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762652 | |||||||
| chr17:762677 | C | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(20): Show |
43 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.832-2439G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762677 | |||||||
| chr17:762695 | G | T | 15 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(12): Show |
17 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.832-2457C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762695 | |||||||
| chr17:762714 | C | CGTGATCT others(61): Show |
1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2477_832-2476i others(70): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762714 | |||||||
| chr17:762714 | C | T | 15 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(12): Show |
17 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.832-2476G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762714 | |||||||
| chr17:762782 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.832-2544C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762782 | |||||||
| chr17:762909 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0023 others(17): Show |
30 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.832-2671C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762909 | |||||||
| chr17:762952 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0058 a0001c0001t0001g0137 others(2): Show |
7 | HG02615.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-2714C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762952 | |||||||
| chr17:762973 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-2735C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 762973 | |||||||
| chr17:763108 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.832-2870C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763108 | |||||||
| chr17:763139 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(40): Show |
76 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.832-2901G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763139 | |||||||
| chr17:763162 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0071 others(1): Show |
6 | HG00408.hp1 NA18968.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-2924C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763162 | |||||||
| chr17:763172 | G | C | 1 | a0001c0001t0001g0101 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.832-2934C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763172 | |||||||
| chr17:763178 | G | A | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-2940C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763178 | |||||||
| chr17:763181 | T | TA | 54 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0034 others(51): Show |
86 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.832-2944dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763181 | |||||||
| chr17:763323 | A | C | 18 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(15): Show |
21 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.832-3085T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763323 | |||||||
| chr17:763419 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.832-3181G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763419 | |||||||
| chr17:763421 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.832-3183A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763421 | |||||||
| chr17:763520 | C | T | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-3282G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763520 | |||||||
| chr17:763756 | A | G | 2 | a0001c0001t0005g0057 a0001c0001t0005g0084 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-3518T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763756 | |||||||
| chr17:763803 | T | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0109 others(4): Show |
12 | HG01952.hp2 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-3565A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763803 | |||||||
| chr17:763988 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.832-3750C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763988 | |||||||
| chr17:763994 | C | T | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-3756G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763994 | |||||||
| chr17:763995 | G | A | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.832-3757C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 763995 | |||||||
| chr17:764008 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.832-3770C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764008 | |||||||
| chr17:764137 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0041 others(13): Show |
25 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.832-3899C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764137 | |||||||
| chr17:764270 | T | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0075 others(2): Show |
7 | HG00609.hp1 HG02132.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-4032A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764270 | |||||||
| chr17:764403 | C | G | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-4165G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764403 | |||||||
| chr17:764418 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.832-4180C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764418 | |||||||
| chr17:764516 | AAC | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-4280_832-4279d others(4): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764516 | |||||||
| chr17:764735 | G | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0120 a0001c0001t0001g0123 others(1): Show |
4 | HG00438.hp2 NA18947.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-4497C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764735 | |||||||
| chr17:764736 | C | G | 8 | a0001c0001t0001g0028 a0001c0001t0001g0156 a0001c0001t0001g0193 others(5): Show |
11 | HG00280.hp2 HG00733.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.832-4498G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764736 | |||||||
| chr17:764742 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.832-4504G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764742 | |||||||
| chr17:764747 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.832-4509T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764747 | |||||||
| chr17:764751 | GTAATCCC others(814): Show |
G | 25 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(22): Show |
44 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.831+4297_832-4514d others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764751 | |||||||
| chr17:764755 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.832-4517A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764755 | |||||||
| chr17:764762 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.832-4524G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764762 | |||||||
| chr17:764773 | C | T | 6 | a0002c0002t0002g0249 a0002c0002t0002g0250 a0002c0002t0002g0251 others(3): Show |
6 | HG00733.hp2 HG02602.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-4535G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764773 | |||||||
| chr17:764775 | A | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0044 others(22): Show |
36 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.832-4537T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764775 | |||||||
| chr17:764779 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.832-4541A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764779 | |||||||
| chr17:764781 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.832-4543C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764781 | |||||||
| chr17:764783 | T | C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0099 a0001c0001t0001g0107 |
3 | HG00621.hp1 NA18941.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.832-4545A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764783 | |||||||
| chr17:764791 | A | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0099 a0001c0001t0001g0107 |
4 | HG00621.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-4553T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764791 | |||||||
| chr17:764810 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.832-4572G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764810 | |||||||
| chr17:764811 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.832-4573T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764811 | |||||||
| chr17:764811 | A | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0154 a0001c0001t0001g0193 others(6): Show |
12 | HG00280.hp2 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-4573T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764811 | |||||||
| chr17:764812 | T | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0145 |
4 | HG01109.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-4574A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764812 | |||||||
| chr17:764815 | T | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0054 a0001c0001t0001g0243 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-4577A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764815 | |||||||
| chr17:764822 | C | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0025 others(57): Show |
97 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.832-4584G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764822 | |||||||
| chr17:764824 | C | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0051 a0001c0001t0001g0172 |
4 | HG01243.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-4586G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764824 | |||||||
| chr17:764824 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.832-4586G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764824 | |||||||
| chr17:764831 | A | AC | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(35): Show |
67 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.832-4594dupG | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764831 | |||||||
| chr17:764831 | A | AT | 23 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(20): Show |
39 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.832-4594_832-4593i others(3): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764831 | |||||||
| chr17:764834 | C | T | 37 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(34): Show |
53 | HG00423.hp2 HG00609.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.832-4596G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764834 | |||||||
| chr17:764876 | A | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(21): Show |
43 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.832-4638T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764876 | |||||||
| chr17:764879 | T | C | 40 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(37): Show |
68 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.832-4641A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764879 | |||||||
| chr17:764902 | T | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0027 others(2): Show |
7 | HG00423.hp2 HG02717.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-4664A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764902 | |||||||
| chr17:764983 | G | A | 2 | a0001c0001t0005g0057 a0001c0001t0005g0084 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-4745C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764983 | |||||||
| chr17:764985 | T | C | 22 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(19): Show |
41 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.832-4747A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764985 | |||||||
| chr17:764986 | G | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(19): Show |
41 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.832-4748C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764986 | |||||||
| chr17:764986 | G | C | 1 | a0001c0001t0001g0002 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.832-4748C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764986 | |||||||
| chr17:764993 | C | G | 1 | a0001c0001t0001g0002 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.832-4755G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 764993 | |||||||
| chr17:765398 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0061 |
2 | NA19007.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.831+4471C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765398 | |||||||
| chr17:765457 | G | C | 1 | a0001c0001t0001g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.831+4412C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765457 | |||||||
| chr17:765469 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.831+4400T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765469 | |||||||
| chr17:765542 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.831+4327A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765542 | |||||||
| chr17:765689 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.831+4180G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765689 | |||||||
| chr17:765715 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.831+4154C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765715 | |||||||
| chr17:765778 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.831+4091T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765778 | |||||||
| chr17:765780 | C | T | 3 | a0002c0002t0002g0249 a0002c0002t0002g0251 a0002c0002t0002g0257 |
3 | NA18943.hp2 NA19010.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.831+4089G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765780 | |||||||
| chr17:765912 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.831+3957G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 765912 | |||||||
| chr17:766067 | T | C | 2 | a0001c0001t0004g0036 a0001c0001t0005g0057 |
3 | HG02451.hp2 HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.831+3802A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766067 | |||||||
| chr17:766068 | G | A | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+3801C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766068 | |||||||
| chr17:766126 | C | T | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+3743G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766126 | |||||||
| chr17:766134 | G | C | 17 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(14): Show |
20 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.831+3735C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766134 | |||||||
| chr17:766167 | G | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0039 others(37): Show |
69 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.831+3702C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766167 | |||||||
| chr17:766306 | A | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
366 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(363): Show |
intron_variant | MODIFIER | c.831+3563T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766306 | |||||||
| chr17:766322 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.831+3547C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766322 | |||||||
| chr17:766371 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.831+3498C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766371 | |||||||
| chr17:766473 | G | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+3396C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766473 | |||||||
| chr17:766520 | C | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0070 a0001c0001t0001g0081 others(1): Show |
4 | HG00140.hp1 HG00621.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+3349G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766520 | |||||||
| chr17:766831 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0078 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.831+3038C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 766831 | |||||||
| chr17:767106 | T | A | 37 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(34): Show |
66 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.831+2763A>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767106 | |||||||
| chr17:767156 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.831+2713T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767156 | |||||||
| chr17:767314 | T | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0114 others(5): Show |
11 | HG01175.hp2 HG01192.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+2555A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767314 | |||||||
| chr17:767441 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.831+2428G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767441 | |||||||
| chr17:767476 | AAGAAGAA others(49): Show |
A | 9 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0180 others(6): Show |
10 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.831+2337_831+2392d others(58): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767476 | |||||||
| chr17:767517 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.831+2352C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767517 | |||||||
| chr17:767555 | A | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+2314T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767555 | |||||||
| chr17:767673 | G | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(19): Show |
41 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.831+2196C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767673 | |||||||
| chr17:767685 | G | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0004g0036 |
4 | HG02145.hp2 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+2184C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767685 | |||||||
| chr17:767687 | G | A | 1 | a0001c0001t0001g0048 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.831+2182C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767687 | |||||||
| chr17:767690 | TTCAGATT others(50): Show |
T | 1 | a0001c0001t0001g0100 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.831+2122_831+2178d others(59): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767690 | |||||||
| chr17:767724 | G | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0052 |
3 | HG01891.hp2 HG01928.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.831+2145C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767724 | |||||||
| chr17:767782 | G | A | 1 | a0001c0003t0001g0166 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.831+2087C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767782 | |||||||
| chr17:767795 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.831+2074G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767795 | |||||||
| chr17:767906 | C | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0041 others(11): Show |
23 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.831+1963G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767906 | |||||||
| chr17:767943 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0131 a0001c0001t0001g0134 |
3 | NA18944.hp1 NA18954.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.831+1926T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767943 | |||||||
| chr17:767943 | AAG | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1924_831+1925d others(4): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767943 | |||||||
| chr17:767961 | G | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0152 others(5): Show |
11 | HG00673.hp1 HG01993.hp1 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+1908C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767961 | |||||||
| chr17:767976 | G | C | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+1893C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767976 | |||||||
| chr17:767996 | TGA | T | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+1871_831+1872d others(4): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 767996 | |||||||
| chr17:768015 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.831+1854C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768015 | |||||||
| chr17:768031 | A | AAGAAGAA others(437): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0092 |
3 | HG02080.hp2 HG02083.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.831+1394_831+1837d others(446): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768031 | |||||||
| chr17:768041 | C | G | 1 | a0001c0001t0005g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.831+1828G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768041 | |||||||
| chr17:768093 | GA | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1775delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768093 | |||||||
| chr17:768103 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.831+1766C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768103 | |||||||
| chr17:768128 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1741A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768128 | |||||||
| chr17:768162 | C | T | 6 | a0001c0001t0001g0054 a0001c0001t0001g0111 a0001c0001t0001g0193 others(3): Show |
7 | HG01070.hp1 HG02145.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+1707G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768162 | |||||||
| chr17:768178 | G | A | 16 | a0001c0001t0001g0054 a0001c0001t0001g0193 a0001c0001t0001g0243 others(13): Show |
18 | HG00733.hp2 HG01070.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.831+1691C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768178 | |||||||
| chr17:768180 | C | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1689G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768180 | |||||||
| chr17:768181 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.831+1688C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768181 | |||||||
| chr17:768183 | A | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1686T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768183 | |||||||
| chr17:768199 | AAGAAGAA others(47): Show |
A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1616_831+1669d others(56): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768199 | |||||||
| chr17:768215 | A | G | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+1654T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768215 | |||||||
| chr17:768266 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1603C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768266 | |||||||
| chr17:768273 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1596A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768273 | |||||||
| chr17:768291 | G | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1578C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768291 | |||||||
| chr17:768323 | A | AAGAGGAC others(47): Show |
11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+1545_831+1546i others(56): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768323 | |||||||
| chr17:768323 | A | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1546T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768323 | |||||||
| chr17:768333 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1536C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768333 | |||||||
| chr17:768338 | AGAGAAAC others(104): Show |
A | 1 | a0001c0001t0001g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.831+1420_831+1530d others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768338 | |||||||
| chr17:768350 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.831+1519G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768350 | |||||||
| chr17:768353 | A | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1516T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768353 | |||||||
| chr17:768364 | TAGA | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1502_831+1504d others(5): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768364 | |||||||
| chr17:768388 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1481C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768388 | |||||||
| chr17:768390 | A | G | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.831+1479T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768390 | |||||||
| chr17:768395 | A | G | 5 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(2): Show |
7 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+1474T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768395 | |||||||
| chr17:768397 | A | G | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+1472T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768397 | |||||||
| chr17:768410 | G | A | 5 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(2): Show |
7 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+1459C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768410 | |||||||
| chr17:768434 | G | T | 1 | a0001c0001t0005g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.831+1435C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768434 | |||||||
| chr17:768442 | A | G | 5 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(2): Show |
7 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+1427T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768442 | |||||||
| chr17:768444 | A | AAGAGGGA others(545): Show |
5 | a0001c0001t0001g0050 a0001c0001t0001g0231 a0001c0001t0001g0234 others(2): Show |
6 | HG02074.hp1 HG02132.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+1424_831+1425i others(554): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768444 | |||||||
| chr17:768444 | A | AAGAGGGA others(548): Show |
1 | a0001c0001t0001g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.831+1424_831+1425i others(557): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768444 | |||||||
| chr17:768444 | A | AAGAGGGA others(548): Show |
23 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0046 others(20): Show |
46 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.831+1424_831+1425i others(557): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768444 | |||||||
| chr17:768444 | A | AAGAGGGA others(1707): Show |
1 | a0001c0001t0001g0049 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.831+1424_831+1425i others(1716): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768444 | |||||||
| chr17:768444 | A | G | 5 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(2): Show |
7 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+1425T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768444 | |||||||
| chr17:768449 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1420C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768449 | |||||||
| chr17:768449 | G | GGAGAAAC others(162): Show |
1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.831+1419_831+1420i others(171): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768449 | |||||||
| chr17:768497 | TGA | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1370_831+1371d others(4): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768497 | |||||||
| chr17:768529 | T | TAGA | 12 | a0001c0001t0001g0059 a0002c0002t0002g0053 a0002c0002t0002g0248 others(9): Show |
13 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.831+1337_831+1339d others(5): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768529 | |||||||
| chr17:768537 | A | G | 16 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0243 others(13): Show |
18 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.831+1332T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768537 | |||||||
| chr17:768549 | C | T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0154 a0001c0001t0001g0193 others(8): Show |
14 | HG00280.hp2 HG00621.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.831+1320G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768549 | |||||||
| chr17:768594 | G | A | 16 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0243 others(13): Show |
18 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.831+1275C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768594 | |||||||
| chr17:768614 | A | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(60): Show |
98 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.831+1255T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768614 | |||||||
| chr17:768627 | G | A | 5 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(2): Show |
7 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+1242C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768627 | |||||||
| chr17:768644 | A | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(60): Show |
98 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.831+1225T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768644 | |||||||
| chr17:768651 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0236 |
2 | HG00621.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.831+1218T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768651 | |||||||
| chr17:768664 | G | A | 3 | a0001c0001t0001g0060 a0001c0001t0001g0070 a0001c0001t0001g0081 |
3 | HG00140.hp1 HG01981.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.831+1205C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768664 | |||||||
| chr17:768669 | AGG | A | 63 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(60): Show |
98 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.831+1198_831+1199d others(4): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768669 | |||||||
| chr17:768671 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0236 |
2 | HG00621.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.831+1198C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768671 | |||||||
| chr17:768698 | AGAG | A | 63 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(60): Show |
98 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.831+1168_831+1170d others(5): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768698 | |||||||
| chr17:768700 | A | AAGAAGAA others(102): Show |
1 | a0001c0001t0001g0138 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.831+1168_831+1169i others(111): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768700 | |||||||
| chr17:768701 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0236 |
2 | HG00621.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.831+1168C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768701 | |||||||
| chr17:768701 | G | GGAAGAAA others(45): Show |
149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.831+1167_831+1168i others(54): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768701 | |||||||
| chr17:768701 | G | GGAAGAAA others(486): Show |
1 | a0001c0001t0001g0232 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.831+1167_831+1168i others(495): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768701 | |||||||
| chr17:768701 | G | GGAAGAAA others(216): Show |
1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.831+1167_831+1168i others(225): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768701 | |||||||
| chr17:768703 | A | AAGAAATC others(597): Show |
1 | a0003c0004t0001g0205 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.831+1165_831+1166i others(606): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | |||||||
| chr17:768703 | A | AAGAAATC others(654): Show |
1 | a0001c0001t0001g0200 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | |||||||
| chr17:768703 | A | AAGAAATC others(654): Show |
1 | a0001c0001t0001g0155 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | |||||||
| chr17:768703 | A | AAGAAATC others(654): Show |
24 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0046 others(21): Show |
50 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | |||||||
| chr17:768703 | A | AAGAAATC others(654): Show |
1 | a0001c0001t0001g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | |||||||
| chr17:768703 | A | AAGAAATC others(654): Show |
8 | a0001c0001t0001g0028 a0001c0001t0001g0154 a0001c0001t0001g0193 others(5): Show |
11 | HG00280.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | |||||||
| chr17:768703 | A | AAGAAATC others(654): Show |
1 | a0001c0001t0001g0194 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | |||||||
| chr17:768703 | A | AAGAAATC others(654): Show |
1 | a0001c0001t0001g0195 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.831+1165_831+1166i others(663): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | |||||||
| chr17:768703 | A | AAGAAATC others(1212): Show |
1 | a0001c0001t0001g0236 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.831+1165_831+1166i others(1221): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768703 | |||||||
| chr17:768741 | G | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.831+1128C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768741 | |||||||
| chr17:768750 | T | TTTTTAGA others(46): Show |
1 | a0001c0001t0001g0170 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.831+1118_831+1119i others(55): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768750 | |||||||
| chr17:768774 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.831+1095A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768774 | |||||||
| chr17:768792 | C | G | 17 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(14): Show |
29 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.831+1077G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768792 | |||||||
| chr17:768831 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.831+1038G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768831 | |||||||
| chr17:768848 | G | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0046 others(26): Show |
55 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.831+1021C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768848 | |||||||
| chr17:768849 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.831+1020G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768849 | |||||||
| chr17:768865 | TAGAAGAA others(50): Show |
T | 1 | a0001c0001t0001g0247 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.831+947_831+1003de others(58): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768865 | |||||||
| chr17:768887 | TGA | T | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+980_831+981del others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768887 | |||||||
| chr17:768907 | C | T | 1 | a0001c0005t0001g0047 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.831+962G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768907 | |||||||
| chr17:768922 | A | AAGAAGAA others(99): Show |
11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+946_831+947ins others(106): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 768922 | |||||||
| chr17:769014 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.831+855T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769014 | |||||||
| chr17:769044 | G | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(38): Show |
71 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.831+825C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769044 | |||||||
| chr17:769300 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.831+569C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769300 | |||||||
| chr17:769322 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.831+547C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769322 | |||||||
| chr17:769349 | GGAGAGCT others(67): Show |
G | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.831+446_831+519del others(74): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769349 | |||||||
| chr17:769371 | G | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0168 others(4): Show |
15 | HG01123.hp2 HG01358.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.831+498C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769371 | |||||||
| chr17:769497 | A | AGAGAGCT others(30): Show |
2 | a0001c0001t0001g0054 a0001c0001t0001g0245 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.831+335_831+371dup others(37): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769497 | |||||||
| chr17:769527 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0120 a0004c0006t0001g0119 |
3 | NA18947.hp2 NA18992.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.831+342A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769527 | |||||||
| chr17:769588 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0245 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.831+281C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769588 | |||||||
| chr17:769588 | G | GGATGGAG others(30): Show |
16 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(13): Show |
18 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.831+280_831+281ins others(37): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769588 | |||||||
| chr17:769613 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.831+256C>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769613 | |||||||
| chr17:769748 | C | T | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.831+121G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 8/8 | chr17 | 769748 | |||||||
| chr17:770556 | A | G | 1 | a0001c0001t0005g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.544-49T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 770556 | |||||||
| chr17:770655 | C | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
367 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.544-148G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 770655 | |||||||
| chr17:770694 | T | C | 64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
109 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.544-187A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 770694 | |||||||
| chr17:770695 | G | GT | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(82): Show |
147 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.544-189dupA | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 770695 | |||||||
| chr17:770695 | GT | G | 18 | a0001c0001t0001g0054 a0001c0001t0001g0181 a0001c0001t0001g0243 others(15): Show |
21 | HG00733.hp2 HG01123.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.544-189delA | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 770695 | |||||||
| chr17:771117 | T | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0159 |
4 | HG00280.hp1 HG00323.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+208A>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 771117 | |||||||
| chr17:771135 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.543+190T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 771135 | |||||||
| chr17:771153 | A | G | 17 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(14): Show |
20 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.543+172T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 771153 | |||||||
| chr17:771311 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0138 a0001c0001t0001g0145 |
5 | HG01109.hp1 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+14G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 5/8 | chr17 | 771311 | |||||||
| chr17:771580 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.407-119C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 771580 | |||||||
| chr17:771885 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.407-424G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 771885 | |||||||
| chr17:771961 | C | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0041 others(10): Show |
22 | HG00280.hp1 HG00323.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.407-500G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 771961 | |||||||
| chr17:771973 | G | A | 6 | a0002c0002t0002g0249 a0002c0002t0002g0250 a0002c0002t0002g0251 others(3): Show |
6 | HG00733.hp2 HG02602.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.407-512C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 771973 | |||||||
| chr17:772001 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.407-540T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772001 | |||||||
| chr17:772013 | C | CA | 15 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0054 others(12): Show |
22 | HG00438.hp2 HG01952.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.407-553dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772013 | |||||||
| chr17:772013 | CA | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
209 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.407-553delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772013 | |||||||
| chr17:772013 | CAA | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0024 others(45): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.407-554_407-553del others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772013 | |||||||
| chr17:772056 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.407-595C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772056 | |||||||
| chr17:772113 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0245 |
2 | HG03041.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.407-652G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772113 | |||||||
| chr17:772155 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.407-694G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772155 | |||||||
| chr17:772187 | G | GA | 8 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0113 others(5): Show |
9 | HG00438.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.407-727dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772187 | |||||||
| chr17:772187 | G | GAAA | 8 | a0002c0002t0002g0053 a0002c0002t0002g0250 a0002c0002t0002g0251 others(5): Show |
9 | HG00733.hp2 HG02135.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.407-729_407-727dup others(3): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772187 | |||||||
| chr17:772187 | GA | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
313 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.407-727delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772187 | |||||||
| chr17:772187 | GAA | G | 6 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0099 others(3): Show |
7 | HG01070.hp1 HG01258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.407-728_407-727del others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772187 | |||||||
| chr17:772189 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0163 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.407-728T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772189 | |||||||
| chr17:772202 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.407-741T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772202 | |||||||
| chr17:772247 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.407-786C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772247 | |||||||
| chr17:772248 | C | T | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.407-787G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772248 | |||||||
| chr17:772323 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.407-862C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772323 | |||||||
| chr17:772508 | A | G | 2 | a0001c0001t0001g0231 a0001c0001t0001g0241 |
2 | HG02074.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.407-1047T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772508 | |||||||
| chr17:772554 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0220 |
2 | NA18941.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.407-1093G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772554 | |||||||
| chr17:772800 | C | T | 1 | a0001c0001t0005g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.407-1339G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772800 | |||||||
| chr17:772806 | T | C | 1 | a0001c0001t0003g0185 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.407-1345A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772806 | |||||||
| chr17:772851 | C | T | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.407-1390G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772851 | |||||||
| chr17:772926 | C | T | 1 | a0001c0001t0005g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.407-1465G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772926 | |||||||
| chr17:772938 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.407-1477A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772938 | |||||||
| chr17:772964 | T | C | 1 | a0001c0001t0001g0014 | 4 | HG02258.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.407-1503A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772964 | |||||||
| chr17:772994 | C | CA | 6 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0102 others(3): Show |
6 | HG02738.hp2 NA18961.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.407-1534dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772994 | |||||||
| chr17:772994 | CA | C | 7 | a0001c0001t0001g0058 a0001c0001t0001g0128 a0001c0001t0001g0141 others(4): Show |
7 | HG01069.hp2 HG02976.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.407-1534delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 772994 | |||||||
| chr17:773091 | A | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0046 others(36): Show |
67 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.407-1630T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773091 | |||||||
| chr17:773216 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.407-1755A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773216 | |||||||
| chr17:773312 | A | G | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.407-1851T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773312 | |||||||
| chr17:773509 | G | GGTGTGT | 17 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(14): Show |
20 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.407-2054_407-2049d others(8): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773509 | |||||||
| chr17:773526 | T | C | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.407-2065A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773526 | |||||||
| chr17:773619 | A | G | 1 | a0001c0001t0005g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.406+2156T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773619 | |||||||
| chr17:773634 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.406+2141A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773634 | |||||||
| chr17:773777 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.406+1998C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773777 | |||||||
| chr17:773818 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.406+1957G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773818 | |||||||
| chr17:773823 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0111 |
2 | HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.406+1952A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773823 | |||||||
| chr17:773986 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(39): Show |
73 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.406+1789G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 773986 | |||||||
| chr17:774180 | G | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0014 others(18): Show |
38 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.406+1595C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774180 | |||||||
| chr17:774195 | A | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(39): Show |
73 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.406+1580T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774195 | |||||||
| chr17:774219 | A | G | 17 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(14): Show |
20 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.406+1556T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774219 | |||||||
| chr17:774226 | T | C | 2 | a0001c0001t0004g0036 a0001c0001t0005g0057 |
3 | HG02451.hp2 HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.406+1549A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774226 | |||||||
| chr17:774365 | C | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0216 |
2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.406+1410G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774365 | |||||||
| chr17:774399 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0216 |
2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.406+1376C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774399 | |||||||
| chr17:774406 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.406+1369G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774406 | |||||||
| chr17:774412 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.406+1363C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774412 | |||||||
| chr17:774565 | G | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0148 others(5): Show |
16 | HG00280.hp1 HG00323.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.406+1210C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774565 | |||||||
| chr17:774790 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.406+985G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774790 | |||||||
| chr17:774807 | G | A | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.406+968C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 774807 | |||||||
| chr17:775033 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.406+742C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775033 | |||||||
| chr17:775065 | G | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0175 others(4): Show |
10 | HG01993.hp1 NA18612.hp1 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.406+710C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775065 | |||||||
| chr17:775106 | T | TA | 29 | a0001c0001t0001g0041 a0001c0001t0001g0052 a0001c0001t0001g0058 others(26): Show |
32 | HG00733.hp2 HG00735.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.406+668dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775106 | |||||||
| chr17:775106 | TA | T | 7 | a0001c0001t0001g0054 a0001c0001t0001g0170 a0001c0001t0001g0175 others(4): Show |
8 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.406+668delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775106 | |||||||
| chr17:775124 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.406+651T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775124 | |||||||
| chr17:775140 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
367 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.406+635T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775140 | |||||||
| chr17:775260 | C | CA | 18 | a0001c0001t0001g0054 a0001c0001t0001g0173 a0001c0001t0001g0243 others(15): Show |
21 | HG00733.hp2 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.406+514dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775260 | |||||||
| chr17:775548 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0111 |
2 | HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.406+227T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775548 | |||||||
| chr17:775636 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0127 |
2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.406+139G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 4/8 | chr17 | 775636 | |||||||
| chr17:776236 | T | A | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(60): Show |
108 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.262-317A>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/8 | chr17 | 776236 | |||||||
| chr17:776514 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0137 |
4 | HG02622.hp1 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+354C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/8 | chr17 | 776514 | |||||||
| chr17:776602 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.261+266G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/8 | chr17 | 776602 | |||||||
| chr17:776602 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0197 |
3 | HG01256.hp1 HG01258.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.261+266G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/8 | chr17 | 776602 | |||||||
| chr17:776698 | T | C | 1 | a0001c0001t0005g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.261+170A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/8 | chr17 | 776698 | |||||||
| chr17:776823 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.261+45G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 3/8 | chr17 | 776823 | |||||||
| chr17:777021 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.141-33T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777021 | |||||||
| chr17:777043 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.141-55T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777043 | |||||||
| chr17:777059 | T | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(26): Show |
53 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.141-71A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777059 | |||||||
| chr17:777072 | A | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0022 others(13): Show |
29 | HG01109.hp1 HG01346.hp1 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.141-84T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777072 | |||||||
| chr17:777300 | A | G | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.141-312T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777300 | |||||||
| chr17:777333 | C | G | 2 | a0001c0001t0003g0042 a0001c0001t0003g0174 |
3 | HG00558.hp1 NA18989.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.141-345G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777333 | |||||||
| chr17:777344 | A | G | 1 | a0001c0001t0003g0160 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.141-356T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777344 | |||||||
| chr17:777578 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0025 others(48): Show |
85 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.141-590C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777578 | |||||||
| chr17:777612 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.141-624G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777612 | |||||||
| chr17:777857 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.140+838A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 777857 | |||||||
| chr17:778045 | T | A | 1 | a0001c0001t0001g0063 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+650A>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778045 | |||||||
| chr17:778047 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+648G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778047 | |||||||
| chr17:778048 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+647G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778048 | |||||||
| chr17:778049 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+646G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778049 | |||||||
| chr17:778054 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+641C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778054 | |||||||
| chr17:778055 | A | ATAAAAAA others(126): Show |
1 | a0001c0001t0001g0063 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+639_140+640ins others(133): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778055 | |||||||
| chr17:778172 | G | A | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.140+523C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778172 | |||||||
| chr17:778210 | A | C | 1 | a0001c0001t0001g0063 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.140+485T>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778210 | |||||||
| chr17:778230 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.140+465C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778230 | |||||||
| chr17:778272 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.140+423G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778272 | |||||||
| chr17:778278 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.140+417A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778278 | |||||||
| chr17:778285 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0163 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.140+410C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778285 | |||||||
| chr17:778299 | C | T | 3 | a0001c0001t0001g0162 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | NA18949.hp1 NA19060.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.140+396G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778299 | |||||||
| chr17:778300 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.140+395C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778300 | |||||||
| chr17:778387 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.140+308G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778387 | |||||||
| chr17:778390 | CT | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0046 others(36): Show |
67 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.140+304delA | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778390 | |||||||
| chr17:778498 | TCTTAATT others(87): Show |
T | 1 | a0001c0001t0001g0090 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.140+103_140+196del others(94): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778498 | |||||||
| chr17:778607 | C | G | 2 | a0002c0002t0002g0248 a0002c0002t0002g0255 |
2 | HG01123.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.140+88G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778607 | |||||||
| chr17:778687 | T | G | 1 | a0001c0001t0001g0050 | 2 | NA18969.hp2 NA19012.hp2 |
splice_region_variant&intron_variant | LOW | c.140+8A>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 2/8 | chr17 | 778687 | |||||||
| chr17:778785 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.91-41T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 778785 | |||||||
| chr17:778915 | G | T | 1 | a0001c0003t0001g0166 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.91-171C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 778915 | |||||||
| chr17:779039 | G | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0085 others(1): Show |
9 | HG01099.hp1 HG01952.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.91-295C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779039 | |||||||
| chr17:779144 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-400C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779144 | |||||||
| chr17:779267 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0005g0057 |
2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.91-523A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779267 | |||||||
| chr17:779270 | T | C | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-526A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779270 | |||||||
| chr17:779317 | ATT | A | 10 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(7): Show |
11 | HG00733.hp2 HG02135.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.91-575_91-574delAA | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779317 | |||||||
| chr17:779318 | T | A | 1 | a0002c0002t0002g0255 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.91-574A>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779318 | |||||||
| chr17:779319 | T | TAAA | 3 | a0001c0001t0001g0002 a0001c0001t0001g0202 a0003c0004t0001g0205 |
7 | HG00738.hp2 HG01081.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.91-578_91-576dupTT others(1): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779319 | |||||||
| chr17:779319 | TA | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(69): Show |
102 | HG00140.hp2 HG00609.hp1 HG01070.hp1 others(99): Show |
intron_variant | MODIFIER | c.91-576delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779319 | |||||||
| chr17:779319 | TAA | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.91-577_91-576delTT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779319 | |||||||
| chr17:779319 | TAAA | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(20): Show |
26 | HG00323.hp2 HG01069.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.91-578_91-576delTT others(1): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779319 | |||||||
| chr17:779319 | TAAAAAAA others(1): Show |
T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0003g0042 others(4): Show |
8 | HG00558.hp1 NA18949.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.91-583_91-576delTT others(6): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779319 | |||||||
| chr17:779321 | A | T | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-577T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779321 | |||||||
| chr17:779322 | A | T | 10 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(7): Show |
11 | HG00733.hp2 HG02135.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.91-578T>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779322 | |||||||
| chr17:779417 | G | T | 3 | a0001c0001t0001g0058 a0001c0001t0004g0036 a0001c0001t0005g0057 |
4 | HG02451.hp2 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-673C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779417 | |||||||
| chr17:779420 | G | A | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.91-676C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779420 | |||||||
| chr17:779781 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.91-1037C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779781 | |||||||
| chr17:779854 | C | T | 1 | a0001c0001t0001g0054 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.91-1110G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779854 | |||||||
| chr17:779900 | C | G | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-1156G>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779900 | |||||||
| chr17:779907 | G | T | 1 | a0001c0001t0001g0063 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.91-1163C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 779907 | |||||||
| chr17:780096 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.91-1352C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780096 | |||||||
| chr17:780140 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.91-1396C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780140 | |||||||
| chr17:780151 | G | A | 6 | a0001c0001t0001g0162 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | NA18945.hp2 NA18949.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-1407C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780151 | |||||||
| chr17:780400 | T | C | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.91-1656A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780400 | |||||||
| chr17:780464 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.90+1702G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780464 | |||||||
| chr17:780485 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.90+1681G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780485 | |||||||
| chr17:780509 | C | T | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.90+1657G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780509 | |||||||
| chr17:780600 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.90+1566C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780600 | |||||||
| chr17:780648 | C | A | 1 | a0001c0001t0004g0036 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.90+1518G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780648 | |||||||
| chr17:780658 | G | T | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.90+1508C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780658 | |||||||
| chr17:780672 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.90+1494C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780672 | |||||||
| chr17:780741 | C | CA | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): Show |
151 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.90+1424dupT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780741 | |||||||
| chr17:780741 | C | CAA | 20 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0060 others(17): Show |
27 | HG00140.hp1 HG00558.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.90+1423_90+1424dup others(2): Show |
GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780741 | |||||||
| chr17:780741 | CA | C | 15 | a0001c0001t0001g0025 a0001c0001t0001g0054 a0001c0001t0001g0059 others(12): Show |
19 | HG00733.hp2 HG01123.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.90+1424delT | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780741 | |||||||
| chr17:780761 | A | G | 1 | a0001c0001t0005g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.90+1405T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780761 | |||||||
| chr17:780862 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.90+1304A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780862 | |||||||
| chr17:780868 | C | A | 1 | a0001c0001t0001g0147 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.90+1298G>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780868 | |||||||
| chr17:780917 | C | CT | 29 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0032 others(26): Show |
41 | HG00280.hp1 HG00323.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.90+1248dupA | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780917 | |||||||
| chr17:780917 | CT | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
88 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.90+1248delA | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780917 | |||||||
| chr17:780942 | C | T | 1 | a0001c0001t0006g0062 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.90+1224G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780942 | |||||||
| chr17:780957 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+1209C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780957 | |||||||
| chr17:780965 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.90+1201C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780965 | |||||||
| chr17:780980 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.90+1186C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780980 | |||||||
| chr17:780990 | G | T | 20 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0022 others(17): Show |
34 | HG01109.hp1 HG01346.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.90+1176C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 780990 | |||||||
| chr17:781021 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.90+1145C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781021 | |||||||
| chr17:781123 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.90+1043C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781123 | |||||||
| chr17:781234 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.90+932C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781234 | |||||||
| chr17:781235 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.90+931G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781235 | |||||||
| chr17:781257 | G | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.90+909C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781257 | |||||||
| chr17:781294 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0246 |
3 | HG01891.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.90+872A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781294 | |||||||
| chr17:781469 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+697T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781469 | |||||||
| chr17:781489 | C | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(60): Show |
108 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.90+677G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781489 | |||||||
| chr17:781553 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.90+613G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781553 | |||||||
| chr17:781598 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.90+568C>T | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781598 | |||||||
| chr17:781783 | G | T | 2 | a0001c0001t0001g0058 a0001c0001t0005g0057 |
2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.90+383C>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781783 | |||||||
| chr17:781846 | T | C | 11 | a0002c0002t0002g0053 a0002c0002t0002g0248 a0002c0002t0002g0249 others(8): Show |
12 | HG00733.hp2 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.90+320A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781846 | |||||||
| chr17:781992 | T | C | 1 | a0001c0001t0001g0054 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.90+174A>G | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 781992 | |||||||
| chr17:782056 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.90+110T>C | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 782056 | |||||||
| chr17:782133 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.90+33G>A | GLOD4 | ENSG00000167699.14 | transcript | ENST00000301329.11 | protein_coding | 1/8 | chr17 | 782133 |