Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10130 |
| ensemblid | ENSG00000143870.13 |
| hgncid | 30168 |
| symbol | PDIA6 |
| name | protein disulfide isomerase family A member 6 |
| refseq_nuc | NM_005742.4 |
| refseq_prot | NP_005733.1 |
| ensembl_nuc | ENST00000272227.8 |
| ensembl_prot | ENSP00000272227.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 10783391 |
| end | 10812785 |
| strand | - |
| ver | v1.2 |
| region | chr2:10783391-10812785 |
| region5000 | chr2:10778391-10817785 |
| regionname0 | PDIA6_chr2_10783391_10812785 |
| regionname5000 | PDIA6_chr2_10778391_10817785 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 440 | 255 | 85 | 52 | 81 | 10 | 25 | 63 | PDIA6_chr2_10778391_10817785 | PDIA6 | MALLV others(435): Show |
chr2 | 10778391 | 10817785 |
| a0002 | 0/0 | 440 | 83 | 7 | 19 | 43 | 2 | 12 | 31 | PDIA6_chr2_10778391_10817785 | PDIA6 | MALLV others(435): Show |
chr2 | 10778391 | 10817785 |
| a0003 | 0/0 | 440 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | MALLV others(435): Show |
chr2 | 10778391 | 10817785 |
| a0004 | 0/0 | 440 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | MALLV others(435): Show |
chr2 | 10778391 | 10817785 |
| a0005 | 0/0 | 440 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | MALLV others(435): Show |
chr2 | 10778391 | 10817785 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1320 | 167 | 51 | 31 | 69 | 5 | 9 | PDIA6_chr2_10778391_10817785 | PDIA6 | ATGGC others(1315): Show |
chr2 | 10778391 | 10817785 | ||
| a0001c0003 | 0/0 | 1320 | 34 | 3 | 13 | 11 | 3 | 4 | PDIA6_chr2_10778391_10817785 | PDIA6 | ATGGC others(1315): Show |
chr2 | 10778391 | 10817785 | ||
| a0001c0004 | 0/0 | 1320 | 31 | 28 | 3 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | ATGGC others(1315): Show |
chr2 | 10778391 | 10817785 | ||
| a0001c0005 | 0/0 | 1320 | 21 | 2 | 4 | 1 | 2 | 12 | PDIA6_chr2_10778391_10817785 | PDIA6 | ATGGC others(1315): Show |
chr2 | 10778391 | 10817785 | ||
| a0001c0012 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | ATGGC others(1315): Show |
chr2 | 10778391 | 10817785 | ||
| a0001c0013 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | ATGGC others(1315): Show |
chr2 | 10778391 | 10817785 | ||
| a0002c0002 | 0/0 | 1320 | 79 | 7 | 17 | 41 | 2 | 12 | PDIA6_chr2_10778391_10817785 | PDIA6 | ATGGC others(1315): Show |
chr2 | 10778391 | 10817785 | ||
| a0002c0006 | 0/0 | 1320 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | ATGGC others(1315): Show |
chr2 | 10778391 | 10817785 | ||
| a0002c0009 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | ATGGC others(1315): Show |
chr2 | 10778391 | 10817785 | ||
| a0002c0011 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | ATGGC others(1315): Show |
chr2 | 10778391 | 10817785 | ||
| a0003c0007 | 0/0 | 1320 | 2 | 1 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | ATGGC others(1315): Show |
chr2 | 10778391 | 10817785 | ||
| a0004c0010 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | ATGGC others(1315): Show |
chr2 | 10778391 | 10817785 | ||
| a0005c0008 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | ATGGC others(1315): Show |
chr2 | 10778391 | 10817785 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2279 | 135 | 26 | 25 | 69 | 4 | 9 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0001t0004 | 0/0 | 2278 | 17 | 13 | 4 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2273): Show |
chr2 | 10778391 | 10817785 |
| a0001c0001t0005 | 0/0 | 2279 | 9 | 8 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0001t0009 | 0/0 | 2279 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0001t0011 | 0/0 | 2279 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0001t0012 | 0/0 | 2279 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0001t0013 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0001t0014 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0003t0001 | 0/0 | 2279 | 28 | 3 | 10 | 10 | 3 | 2 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0003t0006 | 0/0 | 2280 | 2 | 0 | 0 | 0 | 0 | 2 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2275): Show |
chr2 | 10778391 | 10817785 |
| a0001c0003t0008 | 0/0 | 2279 | 3 | 0 | 3 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0003t0016 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0004t0001 | 0/0 | 2279 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0004t0002 | 0/0 | 2279 | 27 | 25 | 2 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0004t0010 | 0/0 | 2279 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0004t0015 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2275): Show |
chr2 | 10778391 | 10817785 |
| a0001c0005t0003 | 0/0 | 2279 | 21 | 2 | 4 | 1 | 2 | 12 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0012t0002 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0001c0013t0002 | 0/0 | 2279 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0002c0002t0001 | 0/0 | 2279 | 72 | 7 | 17 | 34 | 2 | 12 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0002c0002t0006 | 0/0 | 2280 | 3 | 0 | 0 | 3 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2275): Show |
chr2 | 10778391 | 10817785 |
| a0002c0002t0007 | 0/0 | 2279 | 4 | 0 | 0 | 4 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0002c0006t0001 | 0/0 | 2279 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0002c0009t0001 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0002c0011t0001 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0003c0007t0005 | 0/0 | 2279 | 2 | 1 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0004c0010t0001 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| a0005c0008t0001 | 0/0 | 2279 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | GGGAC others(2274): Show |
chr2 | 10778391 | 10817785 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 5 | 0 | 1 | 2 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0009 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0004g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0005g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0012g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0013g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0001t0014g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0006g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0006g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0008g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0003t0016g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0010g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0004t0015g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0012 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0005t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0012t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0001c0013t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0002t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0006t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0006t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0009t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0002c0011t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0003c0007t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0003c0007t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0004c0010t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| a0005c0008t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0005 | t0003 | g0012 | EUR | FIN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0232 | EUR | FIN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00323 | hp2 | a0001 | c0001 | t0011 | g0066 | EUR | FIN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00597 | hp2 | a0001 | c0003 | t0001 | g0222 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0221 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00639 | hp1 | a0001 | c0004 | t0002 | g0274 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00639 | hp2 | a0001 | c0013 | t0002 | g0264 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00733 | hp1 | a0001 | c0003 | t0001 | g0236 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00735 | hp1 | a0002 | c0006 | t0001 | g0239 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0187 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01069 | hp2 | a0001 | c0003 | t0008 | g0013 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0190 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01071 | hp1 | a0001 | c0003 | t0008 | g0013 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0164 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01099 | hp1 | a0001 | c0005 | t0003 | g0019 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0223 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0040 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0207 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0265 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0211 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01192 | hp2 | a0001 | c0003 | t0008 | g0013 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0237 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0235 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0020 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0020 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01261 | hp1 | a0001 | c0004 | t0002 | g0270 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01433 | hp1 | a0002 | c0006 | t0001 | g0201 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01433 | hp2 | a0001 | c0005 | t0003 | g0134 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01496 | hp2 | a0003 | c0007 | t0005 | g0063 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0022 | EUR | IBS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0176 | EUR | IBS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0022 | EUR | IBS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01884 | hp1 | a0001 | c0004 | t0002 | g0268 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0243 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01928 | hp2 | a0001 | c0001 | t0012 | g0094 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01934 | hp1 | a0001 | c0005 | t0003 | g0241 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0174 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01943 | hp1 | a0001 | c0005 | t0003 | g0125 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0175 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0224 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0163 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0031 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0230 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02040 | hp1 | a0002 | c0002 | t0007 | g0142 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02055 | hp1 | a0001 | c0004 | t0002 | g0272 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02055 | hp2 | a0001 | c0001 | t0013 | g0275 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02071 | hp2 | a0002 | c0011 | t0001 | g0024 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0226 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | CDX | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | CDX | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02257 | hp2 | a0001 | c0004 | t0002 | g0257 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02258 | hp1 | a0004 | c0010 | t0001 | g0181 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0213 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02451 | hp2 | a0001 | c0004 | t0002 | g0260 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0228 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02622 | hp1 | a0003 | c0007 | t0005 | g0062 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0200 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02630 | hp1 | a0001 | c0004 | t0002 | g0263 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02647 | hp2 | a0001 | c0004 | t0002 | g0255 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0168 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02698 | hp2 | a0001 | c0005 | t0003 | g0133 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02717 | hp1 | a0001 | c0004 | t0002 | g0023 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02717 | hp2 | a0001 | c0004 | t0002 | g0262 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02723 | hp1 | a0001 | c0004 | t0002 | g0247 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02735 | hp1 | a0001 | c0005 | t0003 | g0019 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0167 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02738 | hp1 | a0001 | c0003 | t0006 | g0280 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0220 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02809 | hp1 | a0001 | c0004 | t0015 | g0282 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02818 | hp2 | a0001 | c0004 | t0002 | g0267 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02896 | hp1 | a0001 | c0004 | t0002 | g0258 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02897 | hp2 | a0001 | c0004 | t0002 | g0256 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02922 | hp1 | a0001 | c0004 | t0002 | g0269 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0276 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0189 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03041 | hp2 | a0001 | c0004 | t0002 | g0254 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03098 | hp1 | a0001 | c0012 | t0002 | g0261 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03098 | hp2 | a0001 | c0004 | t0002 | g0245 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03195 | hp1 | a0001 | c0005 | t0003 | g0132 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0242 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03209 | hp2 | a0001 | c0004 | t0002 | g0251 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03225 | hp2 | a0001 | c0004 | t0010 | g0246 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03239 | hp1 | a0001 | c0005 | t0003 | g0128 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0196 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0210 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03490 | hp2 | a0001 | c0005 | t0003 | g0137 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0178 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03491 | hp2 | a0001 | c0005 | t0003 | g0138 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03516 | hp1 | a0001 | c0004 | t0002 | g0273 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03540 | hp2 | a0001 | c0004 | t0002 | g0271 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0216 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03579 | hp2 | a0001 | c0004 | t0002 | g0252 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03654 | hp1 | a0001 | c0005 | t0003 | g0129 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03688 | hp1 | a0001 | c0005 | t0003 | g0135 | SAS | STU | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03688 | hp2 | a0005 | c0008 | t0001 | g0206 | SAS | STU | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03704 | hp1 | a0001 | c0005 | t0003 | g0012 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0188 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03710 | hp1 | a0001 | c0005 | t0003 | g0131 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03831 | hp1 | a0001 | c0005 | t0003 | g0130 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0183 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0238 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0214 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03942 | hp1 | a0001 | c0005 | t0003 | g0136 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0144 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG04184 | hp2 | a0001 | c0003 | t0006 | g0281 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0148 | SAS | STU | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG04228 | hp1 | a0001 | c0005 | t0003 | g0126 | SAS | STU | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | YRI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18943 | hp1 | a0001 | c0003 | t0001 | g0233 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18951 | hp1 | a0002 | c0002 | t0007 | g0139 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18969 | hp1 | a0002 | c0002 | t0007 | g0141 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0225 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18993 | hp2 | a0002 | c0002 | t0007 | g0140 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18999 | hp1 | a0002 | c0009 | t0001 | g0179 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19005 | hp2 | a0001 | c0003 | t0016 | g0283 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19006 | hp1 | a0002 | c0002 | t0006 | g0278 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | LWK | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19030 | hp2 | a0001 | c0005 | t0003 | g0240 | AFR | LWK | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0266 | AFR | LWK | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19064 | hp2 | a0002 | c0002 | t0006 | g0279 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19070 | hp1 | a0001 | c0005 | t0003 | g0127 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19083 | hp2 | a0002 | c0002 | t0006 | g0277 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0208 | AFR | YRI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA19240 | hp2 | a0001 | c0004 | t0002 | g0248 | AFR | YRI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | ASW | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0124 | AFR | ASW | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA20752 | hp2 | a0001 | c0005 | t0003 | g0012 | EUR | TSI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | TSI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0197 | EUR | TSI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0234 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0177 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02486 | hp2 | a0001 | c0004 | t0002 | g0023 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02559 | hp1 | a0001 | c0004 | t0010 | g0253 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG03471 | hp2 | a0001 | c0004 | t0002 | g0250 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0123 | AFR | USA | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| HG06807 | hp2 | a0001 | c0004 | t0002 | g0259 | AFR | USA | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0151 | AFR | USA | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA20300 | hp2 | a0001 | c0004 | t0002 | g0249 | AFR | USA | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0098 | REF | REF | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0009 | REF | REF | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:10784271 | T | C | 1 | a0003 | 2 | HG01496.hp2 HG02622.hp1 |
missense_variant | MODERATE | c.1310A>G | p.Lys437Arg | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 1399/2279 | 1310/1323 | 437/440 | chr2 | 10784271 | |||
| chr2:10784320 | C | T | 1 | a0004 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1261G>A | p.Val421Met | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 1350/2279 | 1261/1323 | 421/440 | chr2 | 10784320 | |||
| chr2:10790777 | T | C | 3 | a0002 a0004 a0005 |
85 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(82): Show |
missense_variant | MODERATE | c.641A>G | p.Lys214Arg | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/13 | 730/2279 | 641/1323 | 214/440 | chr2 | 10790777 | |||
| chr2:10802550 | C | T | 1 | a0005 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.110G>A | p.Arg37Gln | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/13 | 199/2279 | 110/1323 | 37/440 | chr2 | 10802550 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:10785003 | C | T | 1 | a0001c0013 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.1185G>A | p.Thr395Thr | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/13 | 1274/2279 | 1185/1323 | 395/440 | chr2 | 10785003 | |||
| chr2:10789812 | G | A | 2 | a0002c0006 a0005c0008 |
3 | HG00735.hp1 HG01433.hp1 HG03688.hp2 |
synonymous_variant | LOW | c.777C>T | p.Ser259Ser | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/13 | 866/2279 | 777/1323 | 259/440 | chr2 | 10789812 | |||
| chr2:10789857 | C | T | 1 | a0002c0009 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.732G>A | p.Gln244Gln | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/13 | 821/2279 | 732/1323 | 244/440 | chr2 | 10789857 | |||
| chr2:10793123 | C | T | 7 | a0001c0003 a0002c0002 a0002c0006 others(4): Show |
119 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(116): Show |
synonymous_variant | LOW | c.426G>A | p.Arg142Arg | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/13 | 515/2279 | 426/1323 | 142/440 | chr2 | 10793123 | |||
| chr2:10793168 | C | T | 1 | a0001c0012 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.381G>A | p.Ala127Ala | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/13 | 470/2279 | 381/1323 | 127/440 | chr2 | 10793168 | |||
| chr2:10802561 | C | T | 7 | a0001c0003 a0001c0005 a0002c0002 others(4): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
synonymous_variant | LOW | c.99G>A | p.Ser33Ser | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/13 | 188/2279 | 99/1323 | 33/440 | chr2 | 10802561 | |||
| chr2:10802576 | G | A | 3 | a0001c0004 a0001c0012 a0001c0013 |
33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
synonymous_variant | LOW | c.84C>T | p.Ile28Ile | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/13 | 173/2279 | 84/1323 | 28/440 | chr2 | 10802576 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:10783455 | C | T | 8 | a0001c0003t0008 a0001c0003t0016 a0001c0004t0002 others(5): Show |
57 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*803G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 803 | chr2 | 10783455 | ||||||
| chr2:10783540 | G | A | 2 | a0001c0001t0005 a0003c0007t0005 |
11 | HG01496.hp2 HG01978.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*718C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 718 | chr2 | 10783540 | ||||||
| chr2:10783565 | T | C | 1 | a0001c0003t0008 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*693A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 693 | chr2 | 10783565 | ||||||
| chr2:10783574 | T | C | 2 | a0001c0001t0005 a0003c0007t0005 |
11 | HG01496.hp2 HG01978.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*684A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 684 | chr2 | 10783574 | ||||||
| chr2:10783695 | C | T | 5 | a0001c0004t0002 a0001c0004t0010 a0001c0004t0015 others(2): Show |
32 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*563G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 563 | chr2 | 10783695 | ||||||
| chr2:10783843 | T | C | 1 | a0002c0002t0007 | 4 | HG02040.hp1 NA18951.hp1 NA18969.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*415A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 415 | chr2 | 10783843 | ||||||
| chr2:10783865 | T | C | 5 | a0001c0004t0002 a0001c0004t0010 a0001c0004t0015 others(2): Show |
32 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*393A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 393 | chr2 | 10783865 | ||||||
| chr2:10783877 | T | C | 1 | a0001c0004t0010 | 2 | HG02559.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*381A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 381 | chr2 | 10783877 | ||||||
| chr2:10784006 | A | G | 1 | a0001c0001t0012 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*252T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 252 | chr2 | 10784006 | ||||||
| chr2:10784050 | C | T | 1 | a0001c0001t0009 | 2 | HG01884.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*208G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 208 | chr2 | 10784050 | ||||||
| chr2:10784186 | TG | T | 2 | a0001c0001t0004 a0001c0001t0014 |
18 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*71delC | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 71 | chr2 | 10784186 | ||||||
| chr2:10784209 | C | T | 1 | a0001c0001t0011 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*49G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 49 | chr2 | 10784209 | ||||||
| chr2:10812755 | G | A | 1 | a0001c0001t0013 | 1 | HG02055.hp2 | 5_prime_UTR_variant | MODIFIER | c.-59C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/13 | 59 | chr2 | 10812755 | ||||||
| chr2:10812767 | G | A | 1 | a0001c0003t0016 | 1 | NA19005.hp2 | 5_prime_UTR_variant | MODIFIER | c.-71C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/13 | 71 | chr2 | 10812767 | ||||||
| chr2:10812767 | G | GC | 4 | a0001c0001t0014 a0001c0003t0006 a0001c0004t0015 others(1): Show |
7 | HG02738.hp1 HG02809.hp1 HG02970.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-72dupG | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/13 | 72 | chr2 | 10812767 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:10784398 | T | C | 166 | a0001c0001t0001g0115 a0001c0001t0009g0242 a0001c0001t0009g0243 others(163): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1255-72A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784398 | |||||||
| chr2:10784458 | C | A | 2 | a0001c0003t0008g0013 a0001c0003t0016g0283 |
4 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-132G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784458 | |||||||
| chr2:10784487 | C | T | 2 | a0001c0003t0008g0013 a0001c0003t0016g0283 |
4 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-161G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784487 | |||||||
| chr2:10784559 | AC | A | 41 | a0001c0003t0008g0013 a0001c0003t0016g0283 a0001c0004t0002g0023 others(38): Show |
47 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.1255-234delG | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784559 | |||||||
| chr2:10784560 | CT | C | 125 | a0001c0001t0001g0115 a0001c0001t0009g0242 a0001c0001t0009g0243 others(122): Show |
128 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1255-235delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784560 | |||||||
| chr2:10784567 | G | A | 45 | a0001c0003t0008g0013 a0001c0003t0016g0283 a0001c0004t0002g0023 others(42): Show |
51 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1255-241C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784567 | |||||||
| chr2:10784709 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1254+225T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784709 | |||||||
| chr2:10785276 | T | G | 1 | a0001c0004t0002g0257 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1158-246A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785276 | |||||||
| chr2:10785280 | C | T | 53 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0003t0008g0013 others(50): Show |
59 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1158-250G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785280 | |||||||
| chr2:10785435 | C | G | 53 | a0001c0001t0001g0029 a0001c0003t0008g0013 a0001c0003t0016g0283 others(50): Show |
59 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1158-405G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785435 | |||||||
| chr2:10785448 | C | T | 3 | a0001c0001t0004g0004 a0001c0001t0004g0037 a0001c0001t0004g0039 |
7 | HG02572.hp1 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1158-418G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785448 | |||||||
| chr2:10785619 | AT | A | 3 | a0001c0001t0005g0014 a0001c0001t0005g0025 a0001c0001t0005g0028 |
4 | HG03041.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1158-590delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785619 | |||||||
| chr2:10785764 | T | G | 1 | a0001c0001t0004g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1158-734A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785764 | |||||||
| chr2:10785877 | C | T | 1 | a0001c0003t0001g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1158-847G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785877 | |||||||
| chr2:10785975 | A | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0113 |
2 | NA18986.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1158-945T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785975 | |||||||
| chr2:10786005 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1158-975G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786005 | |||||||
| chr2:10786006 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1158-976T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786006 | |||||||
| chr2:10786062 | C | T | 7 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0001t0001g0059 others(4): Show |
7 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1158-1032G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786062 | |||||||
| chr2:10786097 | T | C | 1 | a0002c0002t0001g0168 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1158-1067A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786097 | |||||||
| chr2:10786196 | G | A | 2 | a0001c0001t0009g0242 a0001c0001t0009g0243 |
2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1157+1085C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786196 | |||||||
| chr2:10786248 | G | A | 1 | a0001c0004t0002g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1157+1033C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786248 | |||||||
| chr2:10786271 | C | T | 1 | a0001c0005t0003g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1157+1010G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786271 | |||||||
| chr2:10786280 | G | A | 1 | a0002c0002t0001g0148 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1157+1001C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786280 | |||||||
| chr2:10786291 | C | T | 1 | a0001c0003t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1157+990G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786291 | |||||||
| chr2:10786318 | T | C | 87 | a0001c0001t0001g0029 a0001c0001t0001g0093 a0001c0001t0001g0109 others(84): Show |
100 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1157+963A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786318 | |||||||
| chr2:10786319 | G | C | 3 | a0001c0001t0001g0102 a0002c0002t0001g0158 a0002c0002t0001g0184 |
3 | HG00408.hp1 NA18979.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1157+962C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786319 | |||||||
| chr2:10786325 | G | GA | 117 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0047 others(114): Show |
122 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.1157+955dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786325 | |||||||
| chr2:10786404 | G | A | 26 | a0001c0001t0001g0110 a0001c0001t0004g0039 a0001c0003t0001g0123 others(23): Show |
27 | HG01099.hp1 HG01934.hp1 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.1157+877C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786404 | |||||||
| chr2:10786407 | G | A | 1 | a0001c0003t0016g0283 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1157+874C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786407 | |||||||
| chr2:10786407 | G | C | 8 | a0001c0001t0001g0096 a0001c0001t0001g0100 a0001c0001t0001g0106 others(5): Show |
8 | HG01346.hp2 HG02148.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+874C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786407 | |||||||
| chr2:10786489 | A | G | 30 | a0001c0004t0001g0265 a0001c0004t0002g0023 a0001c0004t0002g0245 others(27): Show |
31 | HG00639.hp1 HG01175.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.1157+792T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786489 | |||||||
| chr2:10786509 | CTCTCCAC others(16): Show |
C | 46 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0056 others(43): Show |
51 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.1157+749_1157+771d others(25): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786509 | |||||||
| chr2:10786641 | A | G | 24 | a0001c0001t0001g0088 a0001c0003t0001g0020 a0001c0003t0001g0021 others(21): Show |
27 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.1157+640T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786641 | |||||||
| chr2:10786693 | C | T | 32 | a0001c0004t0001g0265 a0001c0004t0002g0023 a0001c0004t0002g0245 others(29): Show |
33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1157+588G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786693 | |||||||
| chr2:10786694 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(2): Show |
9 | HG00558.hp2 NA18955.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.1157+587C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786694 | |||||||
| chr2:10786767 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1157+514C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786767 | |||||||
| chr2:10786784 | A | G | 32 | a0001c0004t0001g0265 a0001c0004t0002g0023 a0001c0004t0002g0245 others(29): Show |
33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1157+497T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786784 | |||||||
| chr2:10786876 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1157+405A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786876 | |||||||
| chr2:10786894 | G | T | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0112 |
3 | HG00408.hp1 HG01943.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1157+387C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786894 | |||||||
| chr2:10786912 | C | T | 85 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0001g0145 others(82): Show |
85 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.1157+369G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786912 | |||||||
| chr2:10786918 | C | T | 32 | a0001c0004t0001g0265 a0001c0004t0002g0023 a0001c0004t0002g0245 others(29): Show |
33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1157+363G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786918 | |||||||
| chr2:10786930 | A | T | 1 | a0001c0003t0016g0283 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1157+351T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786930 | |||||||
| chr2:10787077 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1157+204G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10787077 | |||||||
| chr2:10787092 | C | A | 6 | a0001c0003t0001g0223 a0001c0003t0001g0232 a0001c0003t0001g0234 others(3): Show |
6 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.1157+189G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10787092 | |||||||
| chr2:10787219 | T | C | 139 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0001c0003t0008g0013 others(136): Show |
145 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.1157+62A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10787219 | |||||||
| chr2:10787463 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.999-24C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787463 | |||||||
| chr2:10787475 | CTT | C | 6 | a0001c0004t0002g0268 a0001c0004t0002g0269 a0001c0004t0002g0270 others(3): Show |
6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-38_999-37delAA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787475 | |||||||
| chr2:10787526 | C | T | 1 | a0002c0002t0001g0196 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.999-87G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787526 | |||||||
| chr2:10787611 | A | G | 20 | a0001c0003t0008g0013 a0001c0003t0016g0283 a0001c0005t0003g0012 others(17): Show |
25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.999-172T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787611 | |||||||
| chr2:10787792 | C | A | 1 | a0002c0002t0001g0162 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.999-353G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787792 | |||||||
| chr2:10787792 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.999-353G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787792 | |||||||
| chr2:10787865 | G | C | 32 | a0001c0004t0001g0265 a0001c0004t0002g0023 a0001c0004t0002g0245 others(29): Show |
33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.999-426C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787865 | |||||||
| chr2:10787918 | T | A | 1 | a0001c0004t0010g0246 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.999-479A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787918 | |||||||
| chr2:10787922 | C | T | 2 | a0001c0003t0001g0123 a0001c0003t0001g0124 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.999-483G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787922 | |||||||
| chr2:10787939 | G | A | 32 | a0001c0004t0001g0265 a0001c0004t0002g0023 a0001c0004t0002g0245 others(29): Show |
33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.999-500C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787939 | |||||||
| chr2:10787954 | T | A | 1 | a0001c0003t0006g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.999-515A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787954 | |||||||
| chr2:10787956 | C | T | 87 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0002c0002t0001g0143 others(84): Show |
87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.999-517G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787956 | |||||||
| chr2:10788022 | T | C | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.999-583A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788022 | |||||||
| chr2:10788065 | C | CAAAAA | 23 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(20): Show |
26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.998+627_999-627dup others(5): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788065 | |||||||
| chr2:10788065 | C | CAAAAAA | 6 | a0001c0003t0001g0233 a0001c0005t0003g0132 a0002c0002t0001g0155 others(3): Show |
6 | HG00558.hp1 HG03195.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.998+626_999-627dup others(6): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788065 | |||||||
| chr2:10788065 | C | CAAAAAAA | 94 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0001c0005t0003g0012 others(91): Show |
97 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.998+625_999-627dup others(7): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788065 | |||||||
| chr2:10788065 | C | CAAAAAAA others(8): Show |
1 | a0001c0003t0016g0283 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.998+617_999-627dup others(15): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788065 | |||||||
| chr2:10788065 | C | CAAAAAAA others(9): Show |
1 | a0001c0003t0008g0013 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.999-627_999-626ins others(16): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788065 | |||||||
| chr2:10788081 | G | A | 87 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0002c0002t0001g0143 others(84): Show |
87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.998+616C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788081 | |||||||
| chr2:10788124 | G | A | 18 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0125 others(15): Show |
21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.998+573C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788124 | |||||||
| chr2:10788149 | A | G | 87 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0002c0002t0001g0143 others(84): Show |
87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.998+548T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788149 | |||||||
| chr2:10788261 | G | T | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.998+436C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788261 | |||||||
| chr2:10788462 | C | G | 1 | a0001c0001t0005g0031 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.998+235G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788462 | |||||||
| chr2:10788484 | T | C | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.998+213A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788484 | |||||||
| chr2:10788541 | A | G | 18 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0125 others(15): Show |
21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.998+156T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788541 | |||||||
| chr2:10788568 | G | A | 1 | a0002c0002t0007g0140 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.998+129C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788568 | |||||||
| chr2:10788568 | G | GA | 97 | a0001c0001t0001g0076 a0001c0001t0001g0086 a0001c0001t0005g0028 others(94): Show |
97 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.998+128dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788568 | |||||||
| chr2:10788568 | G | GAA | 41 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(38): Show |
47 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.998+127_998+128dup others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788568 | |||||||
| chr2:10788568 | GA | G | 8 | a0001c0003t0008g0013 a0001c0004t0002g0257 a0001c0004t0002g0258 others(5): Show |
10 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.998+128delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788568 | |||||||
| chr2:10788584 | A | C | 87 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0002c0002t0001g0143 others(84): Show |
87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.998+113T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788584 | |||||||
| chr2:10788651 | A | C | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.998+46T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788651 | |||||||
| chr2:10788780 | T | C | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.926-11A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 9/12 | chr2 | 10788780 | |||||||
| chr2:10788836 | A | G | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.925+61T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 9/12 | chr2 | 10788836 | |||||||
| chr2:10789007 | A | G | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.841-26T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789007 | |||||||
| chr2:10789066 | C | T | 10 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0047 others(7): Show |
10 | HG01109.hp2 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-85G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789066 | |||||||
| chr2:10789191 | A | G | 76 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0033 others(73): Show |
85 | HG00639.hp2 HG01069.hp1 HG01070.hp2 others(82): Show |
intron_variant | MODIFIER | c.841-210T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789191 | |||||||
| chr2:10789198 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.841-217C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789198 | |||||||
| chr2:10789216 | A | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0093 others(143): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.841-235T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789216 | |||||||
| chr2:10789259 | CACTT | C | 87 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0001c0004t0002g0273 others(84): Show |
87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.841-282_841-279del others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789259 | |||||||
| chr2:10789266 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.841-285A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789266 | |||||||
| chr2:10789267 | T | G | 1 | a0002c0002t0006g0278 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.841-286A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789267 | |||||||
| chr2:10789268 | G | T | 1 | a0002c0002t0006g0278 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.841-287C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789268 | |||||||
| chr2:10789289 | A | G | 18 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0125 others(15): Show |
21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.841-308T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789289 | |||||||
| chr2:10789362 | AT | A | 202 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0046 others(199): Show |
216 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.841-382delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789362 | |||||||
| chr2:10789407 | G | GAAAAC | 113 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(110): Show |
118 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.840+337_840+341dup others(5): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789407 | |||||||
| chr2:10789407 | GAAAAC | G | 18 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0125 others(15): Show |
21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.840+337_840+341del others(5): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789407 | |||||||
| chr2:10789437 | C | T | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.840+312G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789437 | |||||||
| chr2:10789476 | T | C | 164 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(161): Show |
173 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.840+273A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789476 | |||||||
| chr2:10789513 | A | C | 3 | a0002c0002t0001g0177 a0002c0002t0001g0200 a0002c0002t0001g0208 |
3 | HG02109.hp1 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.840+236T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789513 | |||||||
| chr2:10789741 | T | C | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
splice_region_variant&intron_variant | LOW | c.840+8A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789741 | |||||||
| chr2:10789924 | A | T | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.700-35T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10789924 | |||||||
| chr2:10789980 | AT | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0050 others(15): Show |
22 | HG01069.hp1 HG01978.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.700-92delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10789980 | |||||||
| chr2:10789980 | ATTT | A | 68 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(65): Show |
74 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.700-94_700-92delAA others(1): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10789980 | |||||||
| chr2:10789980 | ATTTT | A | 63 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0008g0013 others(60): Show |
65 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.700-95_700-92delAA others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10789980 | |||||||
| chr2:10790025 | C | T | 1 | a0001c0001t0005g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.700-136G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790025 | |||||||
| chr2:10790071 | T | C | 1 | a0001c0005t0003g0132 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.700-182A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790071 | |||||||
| chr2:10790082 | A | G | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.700-193T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790082 | |||||||
| chr2:10790126 | A | G | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.700-237T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790126 | |||||||
| chr2:10790140 | G | A | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.700-251C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790140 | |||||||
| chr2:10790141 | G | A | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.700-252C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790141 | |||||||
| chr2:10790167 | C | T | 2 | a0001c0004t0002g0268 a0001c0004t0002g0269 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.700-278G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790167 | |||||||
| chr2:10790235 | GTGT | G | 10 | a0001c0004t0002g0245 a0001c0004t0002g0247 a0001c0004t0002g0248 others(7): Show |
10 | HG00639.hp1 HG02559.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.700-349_700-347del others(3): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790235 | |||||||
| chr2:10790309 | T | G | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.699+410A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790309 | |||||||
| chr2:10790515 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.699+204G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790515 | |||||||
| chr2:10790645 | A | G | 1 | a0002c0002t0007g0140 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.699+74T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790645 | |||||||
| chr2:10790875 | A | G | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.585-42T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10790875 | |||||||
| chr2:10790920 | G | A | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.585-87C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10790920 | |||||||
| chr2:10790937 | T | C | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.585-104A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10790937 | |||||||
| chr2:10790968 | T | A | 6 | a0001c0004t0002g0268 a0001c0004t0002g0269 a0001c0004t0002g0270 others(3): Show |
6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.585-135A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10790968 | |||||||
| chr2:10790972 | A | G | 2 | a0001c0003t0001g0123 a0001c0003t0001g0124 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.585-139T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10790972 | |||||||
| chr2:10791150 | CT | C | 133 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(130): Show |
141 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.585-318delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10791150 | |||||||
| chr2:10791176 | T | C | 25 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(22): Show |
28 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.585-343A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10791176 | |||||||
| chr2:10791259 | T | A | 1 | a0001c0001t0001g0105 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.585-426A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10791259 | |||||||
| chr2:10791309 | A | C | 23 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(20): Show |
26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.585-476T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10791309 | |||||||
| chr2:10791677 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0083 |
2 | HG02027.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.584+118C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10791677 | |||||||
| chr2:10791956 | T | C | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.454-31A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10791956 | |||||||
| chr2:10792081 | C | A | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.454-156G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792081 | |||||||
| chr2:10792098 | T | C | 6 | a0001c0004t0002g0268 a0001c0004t0002g0269 a0001c0004t0002g0270 others(3): Show |
6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.454-173A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792098 | |||||||
| chr2:10792174 | T | C | 133 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(130): Show |
141 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.454-249A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792174 | |||||||
| chr2:10792314 | C | T | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.454-389G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792314 | |||||||
| chr2:10792431 | C | T | 1 | a0002c0002t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.454-506G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792431 | |||||||
| chr2:10792552 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.453+544G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792552 | |||||||
| chr2:10792622 | T | C | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.453+474A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792622 | |||||||
| chr2:10792639 | C | T | 23 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(20): Show |
26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.453+457G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792639 | |||||||
| chr2:10792735 | A | AAT | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.453+359_453+360dup others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792735 | |||||||
| chr2:10792796 | C | T | 1 | a0001c0004t0002g0260 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.453+300G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792796 | |||||||
| chr2:10792808 | A | G | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.453+288T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792808 | |||||||
| chr2:10792863 | G | A | 87 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0002c0002t0001g0143 others(84): Show |
87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.453+233C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792863 | |||||||
| chr2:10792898 | C | T | 20 | a0001c0003t0008g0013 a0001c0003t0016g0283 a0001c0005t0003g0012 others(17): Show |
25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.453+198G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792898 | |||||||
| chr2:10792913 | G | A | 1 | a0001c0001t0005g0031 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.453+183C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792913 | |||||||
| chr2:10792950 | T | C | 6 | a0001c0004t0002g0268 a0001c0004t0002g0269 a0001c0004t0002g0270 others(3): Show |
6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+146A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792950 | |||||||
| chr2:10793037 | G | A | 32 | a0001c0004t0001g0265 a0001c0004t0002g0023 a0001c0004t0002g0245 others(29): Show |
33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.453+59C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10793037 | |||||||
| chr2:10793069 | T | A | 20 | a0001c0003t0008g0013 a0001c0003t0016g0283 a0001c0005t0003g0012 others(17): Show |
25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.453+27A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10793069 | |||||||
| chr2:10793220 | T | TAGGC | 86 | a0001c0004t0002g0262 a0001c0004t0002g0267 a0002c0002t0001g0143 others(83): Show |
86 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.347-22_347-19dupGC others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793220 | |||||||
| chr2:10793264 | C | T | 2 | a0001c0005t0003g0240 a0001c0005t0003g0241 |
2 | HG01934.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.347-62G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793264 | |||||||
| chr2:10793265 | G | C | 1 | a0002c0002t0001g0148 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.347-63C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793265 | |||||||
| chr2:10793294 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.347-92G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793294 | |||||||
| chr2:10793295 | G | A | 165 | a0001c0001t0001g0089 a0001c0003t0001g0020 a0001c0003t0001g0021 others(162): Show |
174 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.347-93C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793295 | |||||||
| chr2:10793296 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.347-94C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793296 | |||||||
| chr2:10793367 | T | C | 87 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0002c0002t0001g0143 others(84): Show |
87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.347-165A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793367 | |||||||
| chr2:10793375 | A | G | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-173T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793375 | |||||||
| chr2:10793556 | A | G | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-354T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793556 | |||||||
| chr2:10793697 | C | T | 2 | a0001c0003t0001g0221 a0001c0003t0001g0222 |
2 | HG00597.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.347-495G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793697 | |||||||
| chr2:10793698 | G | A | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-496C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793698 | |||||||
| chr2:10793774 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.347-572T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793774 | |||||||
| chr2:10793795 | A | G | 164 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(161): Show |
173 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.347-593T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793795 | |||||||
| chr2:10793886 | A | G | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-684T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793886 | |||||||
| chr2:10793941 | C | T | 1 | a0001c0004t0002g0266 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.347-739G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793941 | |||||||
| chr2:10794075 | GA | G | 11 | a0002c0002t0001g0147 a0002c0002t0001g0149 a0002c0002t0001g0156 others(8): Show |
11 | HG02083.hp2 NA18945.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-874delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794075 | |||||||
| chr2:10794088 | AACATATG others(7): Show |
A | 112 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(109): Show |
115 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.347-900_347-887del others(14): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794088 | |||||||
| chr2:10794211 | A | G | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-1009T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794211 | |||||||
| chr2:10794218 | C | T | 2 | a0001c0001t0004g0034 a0001c0001t0004g0042 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.347-1016G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794218 | |||||||
| chr2:10794394 | T | C | 32 | a0001c0004t0001g0265 a0001c0004t0002g0023 a0001c0004t0002g0245 others(29): Show |
33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.347-1192A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794394 | |||||||
| chr2:10794400 | C | T | 1 | a0001c0001t0005g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.347-1198G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794400 | |||||||
| chr2:10794405 | C | T | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-1203G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794405 | |||||||
| chr2:10794432 | C | T | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-1230G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794432 | |||||||
| chr2:10794433 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.347-1231C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794433 | |||||||
| chr2:10794448 | G | GA | 25 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0068 others(22): Show |
26 | HG00639.hp1 HG00639.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.347-1247dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794448 | |||||||
| chr2:10794448 | G | GAA | 6 | a0001c0004t0001g0265 a0001c0004t0002g0247 a0001c0004t0002g0249 others(3): Show |
6 | HG01175.hp2 HG02559.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-1248_347-1247d others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794448 | |||||||
| chr2:10794460 | AAAT | A | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-1261_347-1259d others(5): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794460 | |||||||
| chr2:10794462 | AT | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0087 others(1): Show |
4 | HG00323.hp2 HG01106.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-1261delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794462 | |||||||
| chr2:10794468 | C | CT | 17 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0085 others(14): Show |
17 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.347-1267dupA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794468 | |||||||
| chr2:10794468 | C | CTT | 10 | a0001c0001t0004g0040 a0001c0004t0002g0245 a0001c0004t0002g0252 others(7): Show |
10 | HG01169.hp1 HG01261.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.347-1268_347-1267d others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794468 | |||||||
| chr2:10794468 | CTTTTTT | C | 129 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(126): Show |
137 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.347-1272_347-1267d others(8): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794468 | |||||||
| chr2:10794468 | CTTTTTTT others(4): Show |
C | 15 | a0001c0004t0002g0023 a0001c0004t0002g0254 a0001c0004t0002g0255 others(12): Show |
16 | HG00639.hp2 HG02257.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.347-1277_347-1267d others(13): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794468 | |||||||
| chr2:10794472 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.347-1270A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794472 | |||||||
| chr2:10794495 | T | C | 1 | a0001c0001t0013g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.347-1293A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794495 | |||||||
| chr2:10794514 | C | G | 20 | a0001c0003t0008g0013 a0001c0003t0016g0283 a0001c0005t0003g0012 others(17): Show |
25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.347-1312G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794514 | |||||||
| chr2:10794538 | C | A | 2 | a0001c0003t0001g0123 a0001c0003t0001g0124 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-1336G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794538 | |||||||
| chr2:10794625 | C | G | 2 | a0001c0003t0001g0123 a0001c0003t0001g0124 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-1423G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794625 | |||||||
| chr2:10794626 | T | G | 2 | a0001c0003t0001g0123 a0001c0003t0001g0124 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-1424A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794626 | |||||||
| chr2:10794828 | G | T | 2 | a0001c0003t0001g0123 a0001c0003t0001g0124 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-1626C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794828 | |||||||
| chr2:10795013 | G | A | 4 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0001g0145 others(1): Show |
4 | HG01081.hp2 HG01258.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-1811C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795013 | |||||||
| chr2:10795098 | T | C | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-1896A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795098 | |||||||
| chr2:10795119 | C | T | 1 | a0001c0004t0002g0249 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.347-1917G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795119 | |||||||
| chr2:10795187 | G | A | 1 | a0001c0004t0010g0246 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.346+1894C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795187 | |||||||
| chr2:10795402 | C | T | 112 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(109): Show |
115 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.346+1679G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795402 | |||||||
| chr2:10795488 | CAGACGA | C | 130 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(127): Show |
138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.346+1587_346+1592d others(8): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795488 | |||||||
| chr2:10795504 | C | T | 2 | a0001c0003t0008g0013 a0001c0003t0016g0283 |
4 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+1577G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795504 | |||||||
| chr2:10795669 | C | T | 2 | a0001c0004t0002g0258 a0001c0004t0015g0282 |
2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.346+1412G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795669 | |||||||
| chr2:10795735 | C | T | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.346+1346G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795735 | |||||||
| chr2:10795825 | C | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
336 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.346+1256G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795825 | |||||||
| chr2:10795963 | T | C | 2 | a0001c0001t0009g0242 a0001c0001t0009g0243 |
2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.346+1118A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795963 | |||||||
| chr2:10795966 | A | G | 109 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0001g0190 others(106): Show |
114 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.346+1115T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795966 | |||||||
| chr2:10795996 | A | C | 20 | a0001c0003t0008g0013 a0001c0003t0016g0283 a0001c0005t0003g0012 others(17): Show |
25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.346+1085T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795996 | |||||||
| chr2:10796060 | C | CT | 52 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0033 others(49): Show |
60 | HG00639.hp1 HG01069.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.346+1020dupA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796060 | |||||||
| chr2:10796060 | C | CTT | 7 | a0001c0001t0005g0031 a0001c0004t0001g0265 a0001c0004t0002g0247 others(4): Show |
7 | HG01175.hp2 HG01978.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+1019_346+1020d others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796060 | |||||||
| chr2:10796060 | CTTTTTTT others(1): Show |
C | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.346+1013_346+1020d others(10): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796060 | |||||||
| chr2:10796069 | T | G | 2 | a0001c0005t0003g0240 a0001c0005t0003g0241 |
2 | HG01934.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.346+1012A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796069 | |||||||
| chr2:10796072 | T | C | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.346+1009A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796072 | |||||||
| chr2:10796128 | A | G | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.346+953T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796128 | |||||||
| chr2:10796146 | C | T | 28 | a0001c0004t0001g0265 a0001c0004t0002g0023 a0001c0004t0002g0247 others(25): Show |
29 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.346+935G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796146 | |||||||
| chr2:10796156 | C | T | 87 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0002c0002t0001g0143 others(84): Show |
87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.346+925G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796156 | |||||||
| chr2:10796197 | T | G | 132 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.346+884A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796197 | |||||||
| chr2:10796254 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.346+827G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796254 | |||||||
| chr2:10796270 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.346+811C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796270 | |||||||
| chr2:10796300 | G | A | 1 | a0002c0002t0001g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.346+781C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796300 | |||||||
| chr2:10796333 | A | G | 1 | a0002c0002t0001g0154 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.346+748T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796333 | |||||||
| chr2:10796341 | T | C | 136 | a0001c0001t0001g0091 a0001c0001t0001g0109 a0001c0001t0001g0110 others(133): Show |
144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.346+740A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796341 | |||||||
| chr2:10796343 | A | G | 141 | a0001c0001t0001g0091 a0001c0001t0001g0109 a0001c0001t0001g0110 others(138): Show |
149 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.346+738T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796343 | |||||||
| chr2:10796438 | G | A | 136 | a0001c0001t0001g0057 a0001c0001t0001g0109 a0001c0001t0001g0110 others(133): Show |
144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.346+643C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796438 | |||||||
| chr2:10796443 | C | T | 137 | a0001c0001t0001g0057 a0001c0001t0001g0109 a0001c0001t0001g0110 others(134): Show |
145 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.346+638G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796443 | |||||||
| chr2:10796500 | TA | T | 37 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0073 others(34): Show |
46 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.346+580delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796500 | |||||||
| chr2:10796583 | T | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.346+498A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796583 | |||||||
| chr2:10796679 | G | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.346+402C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796679 | |||||||
| chr2:10796698 | C | CAG | 133 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(130): Show |
141 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.346+381_346+382dup others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796698 | |||||||
| chr2:10796853 | C | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.346+228G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796853 | |||||||
| chr2:10796854 | A | T | 1 | a0001c0001t0011g0066 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.346+227T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796854 | |||||||
| chr2:10796863 | T | C | 1 | a0001c0004t0002g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.346+218A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796863 | |||||||
| chr2:10796911 | T | G | 111 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(108): Show |
114 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.346+170A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796911 | |||||||
| chr2:10796939 | T | C | 86 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0002c0002t0001g0143 others(83): Show |
86 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.346+142A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796939 | |||||||
| chr2:10796969 | T | A | 23 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(20): Show |
26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.346+112A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796969 | |||||||
| chr2:10797283 | C | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.220-76G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 3/12 | chr2 | 10797283 | |||||||
| chr2:10797465 | A | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.219+235T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 3/12 | chr2 | 10797465 | |||||||
| chr2:10797500 | A | G | 1 | a0001c0004t0010g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.219+200T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 3/12 | chr2 | 10797500 | |||||||
| chr2:10797561 | G | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.219+139C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 3/12 | chr2 | 10797561 | |||||||
| chr2:10797579 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0005g0014 a0001c0001t0005g0025 others(1): Show |
5 | HG02257.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+121G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 3/12 | chr2 | 10797579 | |||||||
| chr2:10797629 | G | GAATATGG others(24): Show |
1 | a0002c0002t0001g0143 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.219+40_219+70dupTT others(29): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 3/12 | chr2 | 10797629 | |||||||
| chr2:10797854 | T | C | 23 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(20): Show |
26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.162-97A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10797854 | |||||||
| chr2:10797917 | T | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-160A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10797917 | |||||||
| chr2:10797953 | AGGAG | A | 15 | a0001c0001t0001g0052 a0001c0001t0004g0004 a0001c0001t0004g0034 others(12): Show |
19 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.162-200_162-197del others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10797953 | |||||||
| chr2:10798053 | G | A | 1 | a0001c0003t0001g0234 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.162-296C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798053 | |||||||
| chr2:10798054 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-297A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798054 | |||||||
| chr2:10798055 | G | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-298C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798055 | |||||||
| chr2:10798102 | C | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-345G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798102 | |||||||
| chr2:10798136 | G | T | 1 | a0001c0001t0005g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.162-379C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798136 | |||||||
| chr2:10798401 | C | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-644G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798401 | |||||||
| chr2:10798546 | C | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-789G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798546 | |||||||
| chr2:10798568 | CCA | C | 80 | a0001c0003t0001g0190 a0001c0003t0001g0222 a0001c0003t0001g0225 others(77): Show |
80 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.162-813_162-812del others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798568 | |||||||
| chr2:10798569 | CA | C | 6 | a0001c0003t0001g0216 a0002c0002t0001g0152 a0002c0002t0001g0159 others(3): Show |
6 | HG02040.hp2 HG02155.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-813delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798569 | |||||||
| chr2:10798570 | A | C | 45 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(42): Show |
53 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.162-813T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798570 | |||||||
| chr2:10798572 | CCAA | C | 20 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(17): Show |
23 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.162-818_162-816del others(3): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798572 | |||||||
| chr2:10798573 | C | CA | 48 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(45): Show |
67 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.162-817dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798573 | |||||||
| chr2:10798573 | CA | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0056 a0001c0001t0001g0058 others(8): Show |
15 | HG00673.hp1 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.162-817delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798573 | |||||||
| chr2:10798573 | CAAAA | C | 20 | a0001c0003t0008g0013 a0001c0003t0016g0283 a0001c0005t0003g0012 others(17): Show |
25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.162-820_162-817del others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798573 | |||||||
| chr2:10798574 | A | C | 80 | a0001c0003t0001g0190 a0001c0003t0001g0222 a0001c0003t0001g0225 others(77): Show |
80 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.162-817T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798574 | |||||||
| chr2:10798578 | A | C | 1 | a0001c0005t0003g0133 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.162-821T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798578 | |||||||
| chr2:10798850 | A | G | 163 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(160): Show |
172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.162-1093T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798850 | |||||||
| chr2:10798890 | T | C | 163 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(160): Show |
172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.162-1133A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798890 | |||||||
| chr2:10798991 | C | T | 25 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(22): Show |
28 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.162-1234G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798991 | |||||||
| chr2:10799035 | AAG | A | 112 | a0001c0001t0005g0030 a0001c0003t0001g0020 a0001c0003t0001g0021 others(109): Show |
115 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.162-1280_162-1279d others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799035 | |||||||
| chr2:10799115 | A | G | 25 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(22): Show |
28 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.162-1358T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799115 | |||||||
| chr2:10799187 | G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.162-1430C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799187 | |||||||
| chr2:10799199 | G | GTTTATT | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-1448_162-1443d others(8): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799199 | |||||||
| chr2:10799264 | A | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-1507T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799264 | |||||||
| chr2:10799313 | A | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-1556T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799313 | |||||||
| chr2:10799433 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-1676A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799433 | |||||||
| chr2:10799534 | G | A | 2 | a0001c0005t0003g0019 a0001c0005t0003g0133 |
3 | HG01099.hp1 HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.162-1777C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799534 | |||||||
| chr2:10799601 | G | C | 2 | a0001c0001t0004g0045 a0001c0001t0014g0276 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.162-1844C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799601 | |||||||
| chr2:10799642 | G | A | 1 | a0001c0001t0013g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162-1885C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799642 | |||||||
| chr2:10799659 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.162-1902C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799659 | |||||||
| chr2:10799785 | A | G | 163 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(160): Show |
172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.162-2028T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799785 | |||||||
| chr2:10799912 | GA | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(58): Show |
91 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.162-2156delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799912 | |||||||
| chr2:10799919 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.162-2162T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799919 | |||||||
| chr2:10799994 | GA | G | 16 | a0001c0004t0002g0023 a0001c0004t0002g0254 a0001c0004t0002g0255 others(13): Show |
17 | HG00639.hp2 HG02257.hp2 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.162-2238delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799994 | |||||||
| chr2:10799995 | A | G | 130 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(127): Show |
138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.162-2238T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799995 | |||||||
| chr2:10799996 | A | G | 1 | a0002c0002t0001g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.162-2239T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799996 | |||||||
| chr2:10800152 | C | A | 15 | a0001c0004t0002g0023 a0001c0004t0002g0254 a0001c0004t0002g0255 others(12): Show |
16 | HG00639.hp2 HG02257.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.161+2347G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800152 | |||||||
| chr2:10800218 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.161+2281G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800218 | |||||||
| chr2:10800283 | C | T | 1 | a0001c0004t0001g0265 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.161+2216G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800283 | |||||||
| chr2:10800354 | C | T | 1 | a0001c0003t0016g0283 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.161+2145G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800354 | |||||||
| chr2:10800355 | T | C | 1 | a0001c0004t0002g0249 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161+2144A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800355 | |||||||
| chr2:10800356 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.161+2143T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800356 | |||||||
| chr2:10800370 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.161+2129A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800370 | |||||||
| chr2:10800475 | C | G | 23 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(20): Show |
26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.161+2024G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800475 | |||||||
| chr2:10800512 | T | C | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0100 others(2): Show |
5 | HG01346.hp2 HG02148.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+1987A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800512 | |||||||
| chr2:10800528 | GT | G | 129 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(126): Show |
137 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.161+1970delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800528 | |||||||
| chr2:10800539 | C | T | 2 | a0001c0001t0004g0040 a0001c0001t0004g0041 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.161+1960G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800539 | |||||||
| chr2:10800574 | ATTTTGAT | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1918_161+1924d others(9): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800574 | |||||||
| chr2:10800592 | A | T | 1 | a0002c0002t0001g0192 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.161+1907T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800592 | |||||||
| chr2:10800731 | G | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1768C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800731 | |||||||
| chr2:10800830 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0083 |
2 | HG02027.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.161+1669G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800830 | |||||||
| chr2:10800853 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1646A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800853 | |||||||
| chr2:10801017 | A | G | 7 | a0001c0004t0002g0023 a0001c0004t0002g0254 a0001c0004t0002g0255 others(4): Show |
8 | HG02451.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.161+1482T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801017 | |||||||
| chr2:10801046 | A | G | 1 | a0001c0005t0003g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.161+1453T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801046 | |||||||
| chr2:10801123 | A | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1376T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801123 | |||||||
| chr2:10801139 | C | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1360G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801139 | |||||||
| chr2:10801143 | G | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1356C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801143 | |||||||
| chr2:10801175 | G | A | 23 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(20): Show |
26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.161+1324C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801175 | |||||||
| chr2:10801186 | G | A | 1 | a0001c0004t0001g0265 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.161+1313C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801186 | |||||||
| chr2:10801262 | T | G | 2 | a0001c0001t0004g0040 a0001c0001t0004g0041 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.161+1237A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801262 | |||||||
| chr2:10801272 | T | TCTCTCAA others(5): Show |
1 | a0002c0002t0001g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.161+1215_161+1226d others(14): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801272 | |||||||
| chr2:10801359 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.161+1140A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801359 | |||||||
| chr2:10801394 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.161+1105A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801394 | |||||||
| chr2:10801412 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1087A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801412 | |||||||
| chr2:10801495 | A | C | 2 | a0001c0004t0002g0245 a0001c0004t0002g0252 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.161+1004T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801495 | |||||||
| chr2:10801551 | C | T | 32 | a0001c0004t0001g0265 a0001c0004t0002g0023 a0001c0004t0002g0245 others(29): Show |
33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+948G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801551 | |||||||
| chr2:10801574 | T | C | 1 | a0001c0003t0008g0013 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.161+925A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801574 | |||||||
| chr2:10801597 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+902A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801597 | |||||||
| chr2:10801618 | A | G | 199 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0046 others(196): Show |
213 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.161+881T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801618 | |||||||
| chr2:10802011 | T | C | 7 | a0001c0004t0002g0023 a0001c0004t0002g0254 a0001c0004t0002g0255 others(4): Show |
8 | HG02451.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.161+488A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802011 | |||||||
| chr2:10802012 | G | GT | 5 | a0001c0003t0001g0216 a0001c0003t0001g0222 a0002c0002t0001g0204 others(2): Show |
5 | HG00597.hp2 HG03579.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+486dupA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802012 | |||||||
| chr2:10802207 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+292A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802207 | |||||||
| chr2:10802228 | G | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+271C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802228 | |||||||
| chr2:10802266 | A | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+233T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802266 | |||||||
| chr2:10802285 | G | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+214C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802285 | |||||||
| chr2:10802310 | C | T | 1 | a0002c0002t0001g0146 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.161+189G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802310 | |||||||
| chr2:10802394 | C | T | 25 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(22): Show |
28 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.161+105G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802394 | |||||||
| chr2:10802441 | G | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+58C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802441 | |||||||
| chr2:10802445 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.161+54A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802445 | |||||||
| chr2:10802689 | G | C | 6 | a0001c0004t0002g0268 a0001c0004t0002g0269 a0001c0004t0002g0270 others(3): Show |
6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-49C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10802689 | |||||||
| chr2:10802864 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-224A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10802864 | |||||||
| chr2:10802874 | C | T | 32 | a0001c0004t0001g0265 a0001c0004t0002g0023 a0001c0004t0002g0245 others(29): Show |
33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.20-234G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10802874 | |||||||
| chr2:10802937 | A | G | 1 | a0001c0004t0002g0252 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.20-297T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10802937 | |||||||
| chr2:10803005 | G | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.20-365C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803005 | |||||||
| chr2:10803029 | G | A | 3 | a0001c0004t0002g0262 a0001c0004t0002g0267 a0002c0002t0001g0176 |
3 | HG01515.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.20-389C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803029 | |||||||
| chr2:10803100 | G | A | 1 | a0002c0002t0001g0156 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.20-460C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803100 | |||||||
| chr2:10803130 | T | C | 23 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(20): Show |
26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.20-490A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803130 | |||||||
| chr2:10803237 | A | C | 23 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(20): Show |
26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.20-597T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803237 | |||||||
| chr2:10803291 | G | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-651C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803291 | |||||||
| chr2:10803298 | C | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-658G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803298 | |||||||
| chr2:10803505 | C | CACATTAT others(2): Show |
131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-874_20-866dupTG others(7): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803505 | |||||||
| chr2:10803536 | A | G | 18 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0125 others(15): Show |
21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-896T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803536 | |||||||
| chr2:10803589 | C | A | 2 | a0003c0007t0005g0062 a0003c0007t0005g0063 |
2 | HG01496.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.20-949G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803589 | |||||||
| chr2:10803675 | A | AACTG | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1036_20-1035ins others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803675 | |||||||
| chr2:10803689 | T | C | 1 | a0002c0002t0001g0209 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.20-1049A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803689 | |||||||
| chr2:10803756 | A | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1116T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803756 | |||||||
| chr2:10803789 | A | G | 3 | a0002c0002t0001g0155 a0002c0002t0001g0157 a0002c0002t0001g0205 |
3 | HG00558.hp1 NA18960.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.20-1149T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803789 | |||||||
| chr2:10803823 | T | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
332 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.20-1183A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803823 | |||||||
| chr2:10803824 | A | G | 1 | a0002c0002t0006g0278 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-1184T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803824 | |||||||
| chr2:10803878 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.20-1238C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803878 | |||||||
| chr2:10803889 | G | A | 1 | a0002c0002t0001g0205 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.20-1249C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803889 | |||||||
| chr2:10803909 | G | T | 1 | a0002c0002t0006g0278 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-1269C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803909 | |||||||
| chr2:10803911 | G | GT | 10 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0071 others(7): Show |
11 | HG01261.hp2 HG02071.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-1272dupA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | |||||||
| chr2:10803911 | G | GTTTTTTT others(1): Show |
21 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0001g0146 others(18): Show |
21 | HG01081.hp2 HG01192.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.20-1279_20-1272dup others(8): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | |||||||
| chr2:10803911 | G | GTTTTTTT others(2): Show |
64 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(61): Show |
67 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.20-1280_20-1272dup others(9): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | |||||||
| chr2:10803911 | G | GTTTTTTT others(3): Show |
18 | a0001c0003t0001g0226 a0001c0003t0001g0230 a0001c0003t0006g0280 others(15): Show |
18 | HG01981.hp2 HG02074.hp1 HG02738.hp1 others(15): Show |
intron_variant | MODIFIER | c.20-1281_20-1272dup others(10): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | |||||||
| chr2:10803911 | G | GTTTTTTT others(4): Show |
4 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0001g0225 others(1): Show |
4 | HG06807.hp1 NA18945.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-1282_20-1272dup others(11): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | |||||||
| chr2:10803911 | G | GTTTTTTT others(5): Show |
9 | a0001c0003t0016g0283 a0001c0005t0003g0019 a0001c0005t0003g0125 others(6): Show |
10 | HG01099.hp1 HG01943.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-1283_20-1272dup others(12): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | |||||||
| chr2:10803911 | G | GTTTTTTT others(6): Show |
8 | a0001c0003t0008g0013 a0001c0005t0003g0012 a0001c0005t0003g0128 others(5): Show |
12 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.20-1284_20-1272dup others(13): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | |||||||
| chr2:10803911 | G | GTTTTTTT others(7): Show |
2 | a0001c0005t0003g0126 a0001c0005t0003g0130 |
2 | HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.20-1285_20-1272dup others(14): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | |||||||
| chr2:10803911 | G | T | 1 | a0002c0002t0006g0278 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-1271C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | |||||||
| chr2:10803965 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.20-1325A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803965 | |||||||
| chr2:10804027 | A | G | 1 | a0001c0003t0001g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.20-1387T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804027 | |||||||
| chr2:10804028 | C | G | 1 | a0001c0003t0001g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.20-1388G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804028 | |||||||
| chr2:10804076 | T | G | 31 | a0001c0004t0002g0023 a0001c0004t0002g0245 a0001c0004t0002g0247 others(28): Show |
32 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.20-1436A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804076 | |||||||
| chr2:10804098 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.20-1458A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804098 | |||||||
| chr2:10804159 | C | T | 2 | a0001c0003t0008g0013 a0001c0003t0016g0283 |
4 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-1519G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804159 | |||||||
| chr2:10804199 | T | C | 1 | a0001c0003t0008g0013 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.20-1559A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804199 | |||||||
| chr2:10804223 | T | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1583A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804223 | |||||||
| chr2:10804275 | C | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1635G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804275 | |||||||
| chr2:10804285 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1645A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804285 | |||||||
| chr2:10804354 | T | G | 1 | a0002c0002t0006g0278 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-1714A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804354 | |||||||
| chr2:10804355 | G | T | 1 | a0002c0002t0006g0278 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-1715C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804355 | |||||||
| chr2:10804356 | T | G | 1 | a0002c0002t0006g0278 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-1716A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804356 | |||||||
| chr2:10804369 | C | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1729G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804369 | |||||||
| chr2:10804370 | A | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1730T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804370 | |||||||
| chr2:10804396 | G | C | 163 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(160): Show |
172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.20-1756C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804396 | |||||||
| chr2:10804429 | T | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1789A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804429 | |||||||
| chr2:10804440 | ATTGCTT | A | 129 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(126): Show |
137 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.20-1806_20-1801del others(6): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804440 | |||||||
| chr2:10804441 | T | G | 2 | a0002c0002t0001g0204 a0002c0002t0006g0277 |
2 | NA19060.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.20-1801A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804441 | |||||||
| chr2:10804452 | T | C | 1 | a0002c0002t0006g0277 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.20-1812A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804452 | |||||||
| chr2:10804484 | A | ATATGCGG others(51): Show |
1 | a0002c0002t0006g0277 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.20-1845_20-1844ins others(58): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804484 | |||||||
| chr2:10804485 | C | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1845G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804485 | |||||||
| chr2:10804487 | G | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1847C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804487 | |||||||
| chr2:10804490 | A | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1850T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804490 | |||||||
| chr2:10804555 | T | A | 1 | a0002c0002t0001g0171 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.20-1915A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804555 | |||||||
| chr2:10804651 | G | A | 20 | a0001c0003t0008g0013 a0001c0003t0016g0283 a0001c0005t0003g0012 others(17): Show |
25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.20-2011C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804651 | |||||||
| chr2:10804713 | T | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-2073A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804713 | |||||||
| chr2:10804726 | T | G | 1 | a0001c0004t0001g0265 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.20-2086A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804726 | |||||||
| chr2:10804780 | G | A | 8 | a0001c0004t0002g0257 a0001c0004t0002g0258 a0001c0004t0002g0259 others(5): Show |
8 | HG00639.hp2 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.20-2140C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804780 | |||||||
| chr2:10804784 | T | C | 108 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0001g0190 others(105): Show |
113 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.20-2144A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804784 | |||||||
| chr2:10804881 | C | A | 10 | a0001c0004t0002g0245 a0001c0004t0002g0247 a0001c0004t0002g0248 others(7): Show |
10 | HG00639.hp1 HG02559.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.20-2241G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804881 | |||||||
| chr2:10804968 | C | CTGTT | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-2329_20-2328ins others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804968 | |||||||
| chr2:10805040 | A | G | 6 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0127 others(3): Show |
9 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-2400T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805040 | |||||||
| chr2:10805083 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-2443A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805083 | |||||||
| chr2:10805156 | C | G | 1 | a0001c0001t0001g0070 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.20-2516G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805156 | |||||||
| chr2:10805246 | G | A | 33 | a0001c0004t0002g0023 a0001c0004t0002g0254 a0001c0004t0002g0255 others(30): Show |
37 | HG00280.hp1 HG00639.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.20-2606C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805246 | |||||||
| chr2:10805321 | A | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-2681T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805321 | |||||||
| chr2:10805363 | C | T | 1 | a0001c0003t0008g0013 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.20-2723G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805363 | |||||||
| chr2:10805387 | A | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0051 |
2 | HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.20-2747T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805387 | |||||||
| chr2:10805429 | TGGAGAAA others(17): Show |
T | 1 | a0002c0002t0001g0173 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.20-2813_20-2790del others(24): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805429 | |||||||
| chr2:10805435 | A | C | 130 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(127): Show |
138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.20-2795T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805435 | |||||||
| chr2:10805453 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.20-2813G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805453 | |||||||
| chr2:10805502 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0069 a0001c0001t0001g0080 |
5 | HG02027.hp1 HG02071.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-2862G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805502 | |||||||
| chr2:10805544 | A | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-2904T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805544 | |||||||
| chr2:10805580 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.20-2940T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805580 | |||||||
| chr2:10805610 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-2970A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805610 | |||||||
| chr2:10805688 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.20-3048T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805688 | |||||||
| chr2:10805695 | T | C | 2 | a0001c0001t0009g0242 a0001c0001t0009g0243 |
2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.20-3055A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805695 | |||||||
| chr2:10805792 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.20-3152G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805792 | |||||||
| chr2:10805803 | T | C | 132 | a0001c0001t0001g0067 a0001c0003t0001g0020 a0001c0003t0001g0021 others(129): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.20-3163A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805803 | |||||||
| chr2:10805826 | C | T | 20 | a0001c0003t0008g0013 a0001c0003t0016g0283 a0001c0005t0003g0012 others(17): Show |
25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.20-3186G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805826 | |||||||
| chr2:10805867 | A | C | 1 | a0002c0002t0001g0211 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.20-3227T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805867 | |||||||
| chr2:10805868 | C | A | 1 | a0002c0002t0001g0211 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.20-3228G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805868 | |||||||
| chr2:10805915 | T | TG | 7 | a0001c0001t0005g0031 a0001c0004t0001g0265 a0001c0005t0003g0136 others(4): Show |
7 | HG00735.hp2 HG01175.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.20-3276dupC | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805915 | |||||||
| chr2:10805915 | TGGGGGGA | T | 25 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(22): Show |
28 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.20-3282_20-3276del others(7): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805915 | |||||||
| chr2:10805922 | A | AG | 8 | a0001c0001t0001g0002 a0001c0003t0008g0013 a0001c0005t0003g0240 others(5): Show |
8 | HG01192.hp2 HG01517.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.20-3283dupC | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805922 | |||||||
| chr2:10805929 | A | G | 1 | a0002c0002t0001g0218 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.20-3289T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805929 | |||||||
| chr2:10805994 | G | GGCACATG others(29): Show |
131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-3355_20-3354ins others(36): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805994 | |||||||
| chr2:10806025 | T | TA | 26 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(23): Show |
33 | HG00408.hp1 HG00597.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.20-3386dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806025 | |||||||
| chr2:10806025 | TA | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0046 others(6): Show |
9 | HG00733.hp2 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-3386delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806025 | |||||||
| chr2:10806025 | TAA | T | 7 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0053 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-3387_20-3386del others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806025 | |||||||
| chr2:10806025 | TAAA | T | 13 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0002c0002t0001g0149 others(10): Show |
13 | HG00408.hp2 HG02040.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.20-3388_20-3386del others(3): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806025 | |||||||
| chr2:10806025 | TAAAA | T | 65 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0002c0002t0001g0143 others(62): Show |
65 | HG00558.hp1 HG00642.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.20-3389_20-3386del others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806025 | |||||||
| chr2:10806025 | TAAAAAA | T | 19 | a0001c0003t0008g0013 a0001c0003t0016g0283 a0001c0005t0003g0012 others(16): Show |
24 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.20-3391_20-3386del others(6): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806025 | |||||||
| chr2:10806040 | A | C | 1 | a0002c0002t0006g0277 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.20-3400T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806040 | |||||||
| chr2:10806041 | AAAAC | A | 22 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(19): Show |
25 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.20-3405_20-3402del others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806041 | |||||||
| chr2:10806042 | A | C | 11 | a0001c0004t0002g0245 a0001c0004t0002g0247 a0001c0004t0002g0248 others(8): Show |
11 | HG00639.hp1 HG02559.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.20-3402T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806042 | |||||||
| chr2:10806046 | G | A | 105 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0001g0190 others(102): Show |
110 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.20-3406C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806046 | |||||||
| chr2:10806046 | G | C | 25 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(22): Show |
28 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.20-3406C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806046 | |||||||
| chr2:10806179 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0097 |
4 | NA18960.hp1 NA18972.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-3539C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806179 | |||||||
| chr2:10806288 | G | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-3648C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806288 | |||||||
| chr2:10806330 | A | C | 1 | a0002c0002t0001g0143 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.20-3690T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806330 | |||||||
| chr2:10806330 | A | G | 129 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(126): Show |
137 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.20-3690T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806330 | |||||||
| chr2:10806367 | C | CA | 5 | a0001c0001t0001g0015 a0001c0001t0001g0061 a0001c0001t0001g0108 others(2): Show |
6 | HG06807.hp1 NA18973.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-3728dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806367 | |||||||
| chr2:10806367 | CA | C | 93 | a0001c0001t0001g0050 a0001c0001t0001g0097 a0001c0003t0001g0190 others(90): Show |
94 | HG00558.hp1 HG00639.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.20-3728delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806367 | |||||||
| chr2:10806400 | G | C | 16 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0125 others(13): Show |
19 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-3760C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806400 | |||||||
| chr2:10806421 | C | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-3781G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806421 | |||||||
| chr2:10806458 | T | TA | 100 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(97): Show |
105 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.20-3819dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806458 | |||||||
| chr2:10806458 | TA | T | 16 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0004g0004 others(13): Show |
20 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.20-3819delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806458 | |||||||
| chr2:10806477 | T | TTAGAAAG others(2980): Show |
1 | a0001c0003t0006g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.20-3838_20-3837ins others(2987): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806477 | |||||||
| chr2:10806505 | A | G | 9 | a0001c0001t0001g0029 a0001c0001t0005g0014 a0001c0001t0005g0025 others(6): Show |
10 | HG01978.hp2 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-3865T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806505 | |||||||
| chr2:10806563 | C | A | 6 | a0001c0004t0002g0268 a0001c0004t0002g0269 a0001c0004t0002g0270 others(3): Show |
6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-3923G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806563 | |||||||
| chr2:10806567 | C | G | 20 | a0001c0003t0008g0013 a0001c0003t0016g0283 a0001c0005t0003g0012 others(17): Show |
25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.20-3927G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806567 | |||||||
| chr2:10806622 | T | TAAAGAGA others(238): Show |
1 | a0001c0003t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.20-3983_20-3982ins others(245): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806622 | |||||||
| chr2:10806622 | T | TAAAGAGA others(221): Show |
1 | a0002c0002t0001g0169 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.20-3983_20-3982ins others(228): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806622 | |||||||
| chr2:10806622 | T | TAAAGAGA others(222): Show |
1 | a0001c0003t0001g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.20-3983_20-3982ins others(229): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806622 | |||||||
| chr2:10806628 | C | A | 4 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0002c0002t0001g0169 others(1): Show |
4 | HG01070.hp2 HG01192.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-3988G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAA | 26 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(23): Show |
29 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAAGAA others(192): Show |
1 | a0002c0002t0001g0215 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(199): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(184): Show |
1 | a0002c0006t0001g0239 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(191): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(180): Show |
1 | a0002c0006t0001g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(187): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(163): Show |
1 | a0005c0008t0001g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(170): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(248): Show |
1 | a0002c0002t0007g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(255): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(199): Show |
1 | a0004c0010t0001g0181 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(206): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(179): Show |
1 | a0002c0002t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(186): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(179): Show |
1 | a0002c0002t0001g0189 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(186): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(155): Show |
1 | a0002c0002t0001g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(162): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(163): Show |
1 | a0002c0002t0001g0146 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(170): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(580): Show |
1 | a0002c0002t0001g0213 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(587): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(464): Show |
1 | a0002c0002t0001g0147 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(471): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(526): Show |
1 | a0002c0002t0001g0173 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(533): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(438): Show |
1 | a0002c0002t0001g0203 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(445): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(449): Show |
1 | a0002c0002t0001g0145 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(456): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(298): Show |
1 | a0002c0002t0001g0197 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(305): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(322): Show |
1 | a0002c0002t0001g0149 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(329): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(254): Show |
1 | a0002c0002t0001g0209 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(261): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(246): Show |
1 | a0002c0002t0001g0192 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(253): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(337): Show |
1 | a0002c0002t0001g0152 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(344): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(210): Show |
2 | a0002c0002t0001g0217 a0002c0009t0001g0179 |
2 | NA18999.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(217): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(373): Show |
1 | a0002c0002t0001g0158 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(380): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(229): Show |
1 | a0002c0002t0001g0168 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(236): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(202): Show |
1 | a0002c0002t0001g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(209): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(198): Show |
1 | a0002c0002t0001g0218 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(205): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(288): Show |
1 | a0002c0002t0001g0156 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(295): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(209): Show |
1 | a0002c0002t0001g0195 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(216): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(366): Show |
1 | a0002c0002t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(373): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(206): Show |
1 | a0002c0002t0001g0160 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(213): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(186): Show |
1 | a0002c0002t0001g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(193): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(254): Show |
1 | a0002c0002t0001g0193 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(261): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(190): Show |
1 | a0002c0002t0001g0176 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(197): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(628): Show |
1 | a0002c0002t0001g0143 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(635): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(228): Show |
1 | a0002c0002t0001g0186 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(235): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(453): Show |
1 | a0002c0002t0001g0202 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(460): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(222): Show |
1 | a0002c0002t0001g0154 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(229): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(533): Show |
1 | a0002c0002t0001g0204 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(540): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(154): Show |
1 | a0002c0002t0001g0219 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(161): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(142): Show |
1 | a0002c0002t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(149): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(233): Show |
1 | a0002c0002t0001g0188 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(240): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(204): Show |
1 | a0002c0002t0001g0210 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(211): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(238): Show |
1 | a0002c0002t0001g0157 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(245): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(309): Show |
1 | a0002c0002t0001g0153 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(316): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(175): Show |
1 | a0002c0002t0001g0171 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(182): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(555): Show |
1 | a0002c0002t0001g0196 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(562): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(464): Show |
1 | a0002c0002t0001g0172 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(471): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(413): Show |
1 | a0002c0002t0001g0144 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(420): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(178): Show |
1 | a0002c0002t0001g0183 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(185): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(236): Show |
1 | a0002c0002t0001g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(243): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(186): Show |
1 | a0002c0002t0001g0163 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(193): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(182): Show |
1 | a0002c0002t0001g0159 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(189): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(166): Show |
1 | a0002c0002t0001g0165 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(173): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(186): Show |
1 | a0002c0002t0001g0191 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(193): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(201): Show |
1 | a0002c0002t0001g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(208): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(194): Show |
1 | a0002c0002t0001g0150 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(201): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAA others(414): Show |
1 | a0002c0002t0006g0277 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(421): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGAAG others(508): Show |
1 | a0002c0002t0001g0170 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(515): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGACA others(194): Show |
1 | a0002c0002t0001g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(201): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAAGACA others(430): Show |
1 | a0002c0002t0001g0162 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(437): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAGAAAA others(441): Show |
1 | a0002c0002t0001g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(448): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAGAAAG others(174): Show |
1 | a0002c0002t0001g0205 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(181): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAGAAAG others(600): Show |
1 | a0002c0002t0001g0178 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(607): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAAGAAAG others(367): Show |
1 | a0002c0002t0001g0184 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(374): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAGAAAGA others(340): Show |
1 | a0002c0002t0006g0279 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(347): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAGACAGA others(33): Show |
1 | a0001c0005t0003g0132 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(40): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAGACAGA others(33): Show |
2 | a0001c0005t0003g0125 a0001c0005t0003g0240 |
2 | HG01943.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(40): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAGACAGA others(37): Show |
8 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0127 others(5): Show |
11 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(44): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAGACAGA others(41): Show |
4 | a0001c0003t0016g0283 a0001c0005t0003g0128 a0001c0005t0003g0129 others(1): Show |
4 | HG03239.hp1 HG03490.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(48): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAGACAGA others(45): Show |
3 | a0001c0005t0003g0130 a0001c0005t0003g0131 a0001c0005t0003g0241 |
3 | HG01934.hp1 HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(52): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAGACAGA others(29): Show |
1 | a0001c0003t0008g0013 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(36): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAGACAGA others(41): Show |
1 | a0001c0005t0003g0126 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(48): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CAGACAGA others(144): Show |
1 | a0002c0002t0001g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(151): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAAGAA others(224): Show |
1 | a0002c0002t0001g0199 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(231): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAAGAA others(298): Show |
1 | a0002c0002t0006g0278 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(305): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAAGAA others(484): Show |
1 | a0002c0002t0007g0142 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(491): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAAGAA others(387): Show |
1 | a0002c0002t0001g0174 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(394): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAAGAA others(255): Show |
1 | a0002c0002t0001g0161 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(262): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAAGAA others(212): Show |
1 | a0002c0002t0001g0200 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(219): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAAGAA others(211): Show |
1 | a0002c0002t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(218): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAAGAA others(215): Show |
1 | a0002c0002t0001g0194 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(222): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAAGAA others(203): Show |
1 | a0002c0002t0001g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(210): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAAGAA others(204): Show |
1 | a0002c0002t0001g0167 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(211): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAAGAA others(231): Show |
1 | a0002c0002t0007g0141 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(238): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAAGAA others(227): Show |
1 | a0002c0002t0007g0140 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(234): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAAGAA others(113): Show |
2 | a0001c0003t0001g0123 a0001c0003t0001g0124 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(120): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806628 | C | CGAAGGAA others(190): Show |
1 | a0002c0002t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(197): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | |||||||
| chr2:10806648 | A | AAGAAAGA others(289): Show |
1 | a0002c0002t0001g0212 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(296): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | |||||||
| chr2:10806648 | A | AAGAAAGA others(255): Show |
1 | a0002c0002t0001g0211 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(262): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | |||||||
| chr2:10806648 | A | AAGAAAGA others(461): Show |
1 | a0002c0002t0001g0220 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(468): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | |||||||
| chr2:10806648 | A | AAGAAGGA others(86): Show |
1 | a0001c0003t0006g0280 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(93): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | |||||||
| chr2:10806648 | A | AAGAAGGA others(98): Show |
5 | a0001c0003t0001g0020 a0001c0003t0001g0223 a0001c0003t0001g0224 others(2): Show |
6 | HG01099.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-4009_20-4008ins others(105): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | |||||||
| chr2:10806648 | A | AAGAAGGA others(94): Show |
6 | a0001c0003t0001g0225 a0001c0003t0001g0226 a0001c0003t0001g0227 others(3): Show |
6 | HG01123.hp2 HG02074.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-4009_20-4008ins others(101): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | |||||||
| chr2:10806648 | A | AAGAAGGA others(90): Show |
5 | a0001c0003t0001g0022 a0001c0003t0001g0229 a0001c0003t0001g0235 others(2): Show |
6 | HG00733.hp1 HG01255.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-4009_20-4008ins others(97): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | |||||||
| chr2:10806648 | A | AAGAAGGA others(86): Show |
1 | a0001c0003t0006g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(93): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | |||||||
| chr2:10806648 | A | AAGAAGGA others(98): Show |
2 | a0001c0003t0001g0021 a0001c0003t0001g0232 |
3 | HG00323.hp1 NA18945.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.20-4009_20-4008ins others(105): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | |||||||
| chr2:10806648 | A | AAGAAGGA others(90): Show |
1 | a0001c0003t0001g0237 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(97): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | |||||||
| chr2:10806648 | A | AAGAAGGA others(82): Show |
1 | a0001c0003t0001g0222 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(89): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | |||||||
| chr2:10806648 | A | AAGAAGGA others(102): Show |
1 | a0001c0003t0001g0221 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(109): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | |||||||
| chr2:10806648 | A | C | 84 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0001g0190 others(81): Show |
84 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.20-4008T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | |||||||
| chr2:10806650 | A | AGAAAGAA others(586): Show |
1 | a0002c0002t0001g0148 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.20-4011_20-4010ins others(593): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806650 | |||||||
| chr2:10806650 | A | G | 130 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(127): Show |
138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.20-4010T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806650 | |||||||
| chr2:10806695 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-4055A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806695 | |||||||
| chr2:10806758 | A | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-4118T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806758 | |||||||
| chr2:10806860 | C | T | 23 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(20): Show |
26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.20-4220G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806860 | |||||||
| chr2:10806863 | G | C | 1 | a0002c0002t0001g0213 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.20-4223C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806863 | |||||||
| chr2:10806865 | C | A | 1 | a0002c0002t0001g0143 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.20-4225G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806865 | |||||||
| chr2:10806866 | G | A | 9 | a0001c0001t0001g0029 a0001c0001t0005g0014 a0001c0001t0005g0025 others(6): Show |
10 | HG01978.hp2 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-4226C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806866 | |||||||
| chr2:10806876 | A | G | 163 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(160): Show |
172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.20-4236T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806876 | |||||||
| chr2:10806909 | C | T | 1 | a0001c0001t0005g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.20-4269G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806909 | |||||||
| chr2:10806920 | G | A | 1 | a0002c0002t0001g0189 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.20-4280C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806920 | |||||||
| chr2:10806993 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-4353A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806993 | |||||||
| chr2:10807044 | T | G | 1 | a0001c0001t0001g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.20-4404A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807044 | |||||||
| chr2:10807046 | A | G | 1 | a0002c0002t0001g0144 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.20-4406T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807046 | |||||||
| chr2:10807134 | A | G | 2 | a0001c0001t0009g0242 a0001c0001t0009g0243 |
2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.20-4494T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807134 | |||||||
| chr2:10807250 | C | T | 1 | a0001c0004t0002g0257 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.20-4610G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807250 | |||||||
| chr2:10807258 | G | T | 1 | a0001c0003t0001g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.20-4618C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807258 | |||||||
| chr2:10807393 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.20-4753T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807393 | |||||||
| chr2:10807675 | A | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+5003T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807675 | |||||||
| chr2:10807731 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+4947A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807731 | |||||||
| chr2:10807799 | A | G | 2 | a0001c0003t0001g0190 a0001c0003t0001g0216 |
2 | HG01070.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19+4879T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807799 | |||||||
| chr2:10807814 | A | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+4864T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807814 | |||||||
| chr2:10807867 | C | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+4811G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807867 | |||||||
| chr2:10807926 | T | A | 11 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0047 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+4752A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807926 | |||||||
| chr2:10807964 | A | G | 23 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(20): Show |
26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.19+4714T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807964 | |||||||
| chr2:10808015 | A | G | 18 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0125 others(15): Show |
21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.19+4663T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808015 | |||||||
| chr2:10808157 | A | C | 2 | a0003c0007t0005g0062 a0003c0007t0005g0063 |
2 | HG01496.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.19+4521T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808157 | |||||||
| chr2:10808283 | G | A | 130 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(127): Show |
138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.19+4395C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808283 | |||||||
| chr2:10808283 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.19+4395C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808283 | |||||||
| chr2:10808284 | A | C | 1 | a0001c0001t0001g0079 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.19+4394T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808284 | |||||||
| chr2:10808422 | C | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+4256G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808422 | |||||||
| chr2:10808446 | AC | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+4231delG | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808446 | |||||||
| chr2:10808460 | A | T | 15 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0125 others(12): Show |
18 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.19+4218T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808460 | |||||||
| chr2:10808488 | G | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+4190C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808488 | |||||||
| chr2:10808600 | G | A | 1 | a0001c0004t0002g0250 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19+4078C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808600 | |||||||
| chr2:10808705 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3973A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808705 | |||||||
| chr2:10808736 | A | G | 10 | a0001c0004t0002g0245 a0001c0004t0002g0247 a0001c0004t0002g0248 others(7): Show |
10 | HG00639.hp1 HG02559.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+3942T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808736 | |||||||
| chr2:10808848 | C | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3830G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808848 | |||||||
| chr2:10808870 | G | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3808C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808870 | |||||||
| chr2:10808882 | G | C | 1 | a0001c0004t0001g0265 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.19+3796C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808882 | |||||||
| chr2:10809052 | G | A | 1 | a0001c0004t0002g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19+3626C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809052 | |||||||
| chr2:10809053 | C | A | 6 | a0001c0004t0002g0257 a0001c0004t0002g0258 a0001c0004t0002g0259 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+3625G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809053 | |||||||
| chr2:10809054 | C | G | 6 | a0001c0004t0002g0257 a0001c0004t0002g0258 a0001c0004t0002g0259 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+3624G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809054 | |||||||
| chr2:10809075 | C | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3603G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809075 | |||||||
| chr2:10809088 | C | T | 6 | a0001c0004t0002g0268 a0001c0004t0002g0269 a0001c0004t0002g0270 others(3): Show |
6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+3590G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809088 | |||||||
| chr2:10809105 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.19+3573C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809105 | |||||||
| chr2:10809165 | T | C | 10 | a0001c0004t0002g0245 a0001c0004t0002g0247 a0001c0004t0002g0248 others(7): Show |
10 | HG00639.hp1 HG02559.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+3513A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809165 | |||||||
| chr2:10809206 | T | G | 1 | a0001c0005t0003g0133 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.19+3472A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809206 | |||||||
| chr2:10809241 | T | C | 1 | a0002c0002t0001g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.19+3437A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809241 | |||||||
| chr2:10809304 | A | G | 130 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(127): Show |
138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.19+3374T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809304 | |||||||
| chr2:10809393 | A | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3285T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809393 | |||||||
| chr2:10809447 | C | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0034 a0001c0001t0004g0035 others(11): Show |
18 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.19+3231G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809447 | |||||||
| chr2:10809463 | G | A | 1 | a0001c0003t0008g0013 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.19+3215C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809463 | |||||||
| chr2:10809488 | C | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3190G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809488 | |||||||
| chr2:10809494 | G | A | 1 | a0002c0002t0001g0189 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.19+3184C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809494 | |||||||
| chr2:10809495 | G | A | 86 | a0001c0003t0001g0190 a0001c0003t0001g0216 a0002c0002t0001g0143 others(83): Show |
86 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.19+3183C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809495 | |||||||
| chr2:10809510 | T | C | 130 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(127): Show |
138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.19+3168A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809510 | |||||||
| chr2:10809554 | G | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3124C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809554 | |||||||
| chr2:10809556 | T | C | 111 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(108): Show |
114 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.19+3122A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809556 | |||||||
| chr2:10809645 | C | CA | 14 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0065 others(11): Show |
14 | HG00323.hp2 HG01261.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.19+3032dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | |||||||
| chr2:10809645 | C | CAA | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(32): Show |
46 | HG00280.hp2 HG00609.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.19+3031_19+3032dup others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | |||||||
| chr2:10809645 | C | CAAA | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(31): Show |
55 | HG00558.hp2 HG00642.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.19+3030_19+3032dup others(3): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | |||||||
| chr2:10809645 | C | CAAAA | 31 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0058 others(28): Show |
46 | HG00408.hp1 HG00597.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.19+3029_19+3032dup others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | |||||||
| chr2:10809645 | C | CAAAAA | 20 | a0001c0001t0001g0060 a0001c0001t0001g0109 a0001c0001t0001g0110 others(17): Show |
20 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.19+3028_19+3032dup others(5): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | |||||||
| chr2:10809645 | C | CAAAAAA | 6 | a0001c0001t0001g0117 a0001c0001t0005g0025 a0001c0001t0005g0026 others(3): Show |
6 | HG00733.hp1 HG01243.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+3027_19+3032dup others(6): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | |||||||
| chr2:10809645 | C | CAAAAAAA | 6 | a0001c0001t0001g0029 a0001c0001t0005g0014 a0001c0001t0005g0027 others(3): Show |
7 | HG01978.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+3026_19+3032dup others(7): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | |||||||
| chr2:10809645 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0005g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19+3023_19+3032dup others(10): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | |||||||
| chr2:10809645 | C | CAAAAAAA others(4): Show |
1 | a0001c0004t0002g0266 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.19+3022_19+3032dup others(11): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | |||||||
| chr2:10809645 | CAAA | C | 14 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0125 others(11): Show |
17 | HG00280.hp1 HG01099.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.19+3030_19+3032del others(3): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | |||||||
| chr2:10809645 | CAAAAAAA | C | 12 | a0001c0001t0004g0004 a0001c0001t0004g0034 a0001c0001t0004g0035 others(9): Show |
16 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.19+3026_19+3032del others(7): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | |||||||
| chr2:10809645 | CAAAAAAA others(1): Show |
C | 8 | a0001c0004t0002g0245 a0001c0004t0002g0247 a0001c0004t0002g0248 others(5): Show |
8 | HG00639.hp1 HG02723.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+3025_19+3032del others(8): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | |||||||
| chr2:10809668 | A | AAC | 27 | a0001c0003t0001g0190 a0002c0002t0001g0191 a0002c0002t0001g0192 others(24): Show |
27 | HG01070.hp2 HG01175.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.19+3009_19+3010ins others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809668 | |||||||
| chr2:10809668 | A | AC | 49 | a0002c0002t0001g0144 a0002c0002t0001g0145 a0002c0002t0001g0146 others(46): Show |
49 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.19+3009_19+3010ins others(1): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809668 | |||||||
| chr2:10809668 | A | C | 4 | a0002c0002t0001g0143 a0002c0002t0001g0148 a0002c0002t0006g0277 others(1): Show |
4 | HG01081.hp2 HG04204.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+3010T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809668 | |||||||
| chr2:10809672 | A | T | 1 | a0002c0002t0001g0147 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.19+3006T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809672 | |||||||
| chr2:10809761 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19+2917G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809761 | |||||||
| chr2:10809788 | T | C | 1 | a0001c0004t0002g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.19+2890A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809788 | |||||||
| chr2:10809889 | T | A | 1 | a0002c0002t0001g0220 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.19+2789A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809889 | |||||||
| chr2:10809985 | ATGAC | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+2689_19+2692del others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809985 | |||||||
| chr2:10809990 | T | A | 2 | a0001c0003t0001g0123 a0001c0003t0001g0124 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19+2688A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809990 | |||||||
| chr2:10810010 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+2668A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810010 | |||||||
| chr2:10810111 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
5 | NA18950.hp1 NA18975.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+2567C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810111 | |||||||
| chr2:10810158 | G | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+2520C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810158 | |||||||
| chr2:10810404 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0061 |
3 | NA18973.hp1 NA19002.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.19+2274T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810404 | |||||||
| chr2:10810489 | T | C | 9 | a0001c0001t0001g0029 a0001c0001t0005g0014 a0001c0001t0005g0025 others(6): Show |
10 | HG01978.hp2 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.19+2189A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810489 | |||||||
| chr2:10810510 | T | C | 1 | a0001c0005t0003g0138 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.19+2168A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810510 | |||||||
| chr2:10810539 | T | C | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+2139A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810539 | |||||||
| chr2:10810542 | T | G | 1 | a0001c0003t0008g0013 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.19+2136A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810542 | |||||||
| chr2:10810809 | A | G | 2 | a0001c0003t0001g0221 a0001c0003t0001g0222 |
2 | HG00597.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.19+1869T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810809 | |||||||
| chr2:10810878 | G | C | 1 | a0001c0003t0001g0238 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.19+1800C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810878 | |||||||
| chr2:10810992 | T | A | 18 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0125 others(15): Show |
21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.19+1686A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810992 | |||||||
| chr2:10811035 | G | T | 95 | a0001c0001t0001g0029 a0001c0001t0005g0014 a0001c0001t0005g0025 others(92): Show |
96 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.19+1643C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811035 | |||||||
| chr2:10811036 | A | C | 95 | a0001c0001t0001g0029 a0001c0001t0005g0014 a0001c0001t0005g0025 others(92): Show |
96 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.19+1642T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811036 | |||||||
| chr2:10811042 | C | T | 4 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0001g0145 others(1): Show |
4 | HG01081.hp2 HG01258.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+1636G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811042 | |||||||
| chr2:10811043 | A | G | 206 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0033 others(203): Show |
223 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.19+1635T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811043 | |||||||
| chr2:10811070 | T | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+1608A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811070 | |||||||
| chr2:10811123 | A | C | 4 | a0002c0002t0007g0139 a0002c0002t0007g0140 a0002c0002t0007g0141 others(1): Show |
4 | HG02040.hp1 NA18951.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+1555T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811123 | |||||||
| chr2:10811361 | C | A | 2 | a0001c0003t0001g0123 a0001c0003t0001g0124 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19+1317G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811361 | |||||||
| chr2:10811476 | G | A | 1 | a0001c0003t0016g0283 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.19+1202C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811476 | |||||||
| chr2:10811501 | AACAGAAA others(7): Show |
A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+1163_19+1176del others(14): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811501 | |||||||
| chr2:10811577 | G | C | 6 | a0001c0004t0002g0268 a0001c0004t0002g0269 a0001c0004t0002g0270 others(3): Show |
6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+1101C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811577 | |||||||
| chr2:10811669 | G | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+1009C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811669 | |||||||
| chr2:10811687 | G | C | 1 | a0001c0004t0002g0274 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.19+991C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811687 | |||||||
| chr2:10811785 | C | G | 129 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(126): Show |
137 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.19+893G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811785 | |||||||
| chr2:10812099 | G | C | 1 | a0001c0003t0001g0022 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.19+579C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812099 | |||||||
| chr2:10812100 | G | C | 1 | a0001c0003t0001g0022 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.19+578C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812100 | |||||||
| chr2:10812124 | G | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+554C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812124 | |||||||
| chr2:10812147 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+531A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812147 | |||||||
| chr2:10812167 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.19+511A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812167 | |||||||
| chr2:10812231 | T | G | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+447A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812231 | |||||||
| chr2:10812238 | T | C | 1 | a0001c0003t0008g0013 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.19+440A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812238 | |||||||
| chr2:10812246 | G | A | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+432C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812246 | |||||||
| chr2:10812265 | A | T | 206 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0033 others(203): Show |
223 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.19+413T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812265 | |||||||
| chr2:10812309 | C | A | 1 | a0002c0006t0001g0239 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.19+369G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812309 | |||||||
| chr2:10812321 | G | A | 163 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(160): Show |
172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.19+357C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812321 | |||||||
| chr2:10812343 | T | TCCGGGAA others(14): Show |
18 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0125 others(15): Show |
21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.19+334_19+335insGG others(19): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812343 | |||||||
| chr2:10812354 | A | T | 131 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(128): Show |
139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+324T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812354 | |||||||
| chr2:10812522 | C | G | 1 | a0002c0011t0001g0024 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.19+156G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812522 | |||||||
| chr2:10812522 | C | T | 16 | a0001c0005t0003g0012 a0001c0005t0003g0019 a0001c0005t0003g0125 others(13): Show |
19 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+156G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812522 | |||||||
| chr2:10812589 | G | A | 32 | a0001c0004t0001g0265 a0001c0004t0002g0023 a0001c0004t0002g0245 others(29): Show |
33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.19+89C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812589 | |||||||
| chr2:10812653 | C | G | 2 | a0001c0003t0001g0123 a0001c0003t0001g0124 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19+25G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812653 | |||||||
| chr2:10812664 | T | C | 166 | a0001c0001t0001g0244 a0001c0001t0009g0242 a0001c0001t0009g0243 others(163): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.19+14A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812664 |