Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 240 |
| ensemblid | ENSG00000012779.12 |
| hgncid | 435 |
| symbol | ALOX5 |
| name | arachidonate 5-lipoxygenase |
| refseq_nuc | NM_000698.5 |
| refseq_prot | NP_000689.1 |
| ensembl_nuc | ENST00000374391.7 |
| ensembl_prot | ENSP00000363512.2 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 45374216 |
| end | 45446117 |
| strand | + |
| ver | v1.2 |
| region | chr10:45374216-45446117 |
| region5000 | chr10:45369216-45451117 |
| regionname0 | ALOX5_chr10_45374216_45446117 |
| regionname5000 | ALOX5_chr10_45369216_45451117 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 674 | 321 | 86 | 53 | 136 | 14 | 31 | 111 | ALOX5_chr10_45369216_45451117 | ALOX5 | MPSYT others(669): Show |
chr10 | 45369216 | 45451117 |
| a0002 | 0/0 | 674 | 16 | 5 | 1 | 9 | 0 | 1 | 6 | ALOX5_chr10_45369216_45451117 | ALOX5 | MPSYT others(669): Show |
chr10 | 45369216 | 45451117 |
| a0003 | 0/0 | 674 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | MPSYT others(669): Show |
chr10 | 45369216 | 45451117 |
| a0004 | 0/0 | 370 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | MPSYT others(365): Show |
chr10 | 45369216 | 45451117 |
| a0005 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | MPSYT others(669): Show |
chr10 | 45369216 | 45451117 |
| a0006 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | MPSYT others(669): Show |
chr10 | 45369216 | 45451117 |
| a0007 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | MPSYT others(576): Show |
chr10 | 45369216 | 45451117 |
| a0008 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | MPSYT others(669): Show |
chr10 | 45369216 | 45451117 |
| a0009 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | MPSYT others(669): Show |
chr10 | 45369216 | 45451117 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2022 | 172 | 30 | 33 | 77 | 6 | 25 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0001c0002 | 0/0 | 2022 | 57 | 11 | 9 | 27 | 5 | 5 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0001c0003 | 0/0 | 2022 | 36 | 23 | 5 | 8 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0001c0004 | 0/0 | 2022 | 31 | 11 | 2 | 16 | 2 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0001c0006 | 0/0 | 2022 | 7 | 6 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0001c0007 | 0/0 | 2022 | 6 | 0 | 0 | 6 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0001c0008 | 0/0 | 2022 | 3 | 2 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0001c0009 | 0/0 | 2022 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0001c0011 | 0/0 | 2022 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0001c0015 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0001c0019 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0001c0020 | 0/0 | 2022 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0001c0021 | 0/0 | 2022 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0001c0022 | 0/0 | 2022 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0002c0005 | 0/0 | 2022 | 16 | 5 | 1 | 9 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0003c0010 | 0/0 | 2022 | 2 | 0 | 0 | 0 | 0 | 2 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0004c0013 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0005c0014 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0006c0016 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0007c0017 | 0/0 | 2011 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2006): Show |
chr10 | 45369216 | 45451117 | ||
| a0008c0012 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 | ||
| a0009c0018 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | ATGCC others(2017): Show |
chr10 | 45369216 | 45451117 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2519 | 166 | 28 | 32 | 75 | 6 | 24 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0001t0002 | 0/0 | 2519 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0001t0004 | 0/0 | 2517 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2512): Show |
chr10 | 45369216 | 45451117 |
| a0001c0001t0005 | 0/0 | 2519 | 2 | 0 | 1 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0001t0008 | 0/0 | 2519 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0002t0002 | 0/0 | 2519 | 54 | 11 | 9 | 25 | 5 | 4 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0002t0006 | 0/0 | 2519 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0002t0007 | 0/0 | 2517 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2512): Show |
chr10 | 45369216 | 45451117 |
| a0001c0003t0001 | 0/0 | 2519 | 26 | 21 | 2 | 3 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0003t0002 | 0/0 | 2519 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0003t0003 | 0/0 | 2519 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0003t0004 | 0/0 | 2517 | 8 | 0 | 3 | 5 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2512): Show |
chr10 | 45369216 | 45451117 |
| a0001c0004t0001 | 0/0 | 2519 | 31 | 11 | 2 | 16 | 2 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0006t0001 | 0/0 | 2519 | 6 | 5 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0006t0009 | 0/0 | 2519 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0007t0001 | 0/0 | 2519 | 6 | 0 | 0 | 6 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0008t0002 | 0/0 | 2519 | 3 | 2 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0009t0001 | 0/0 | 2519 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0011t0002 | 0/0 | 2519 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0015t0001 | 0/0 | 2519 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0019t0001 | 0/0 | 2519 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0020t0001 | 0/0 | 2519 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0021t0006 | 0/0 | 2519 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0001c0022t0002 | 0/0 | 2519 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0002c0005t0003 | 0/0 | 2519 | 16 | 5 | 1 | 9 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0003c0010t0001 | 0/0 | 2519 | 2 | 0 | 0 | 0 | 0 | 2 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0004c0013t0001 | 0/0 | 2519 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0005c0014t0001 | 0/0 | 2519 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0006c0016t0001 | 0/0 | 2519 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0007c0017t0001 | 0/0 | 2508 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2503): Show |
chr10 | 45369216 | 45451117 |
| a0008c0012t0001 | 0/0 | 2519 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| a0009c0018t0001 | 0/0 | 2519 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | AGATG others(2514): Show |
chr10 | 45369216 | 45451117 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0001t0008g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0006g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0002t0007g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0003t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0004t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0006t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0006t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0006t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0006t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0006t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0006t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0007t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0007t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0007t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0007t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0007t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0007t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0008t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0008t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0008t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0009t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0009t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0011t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0011t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0015t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0019t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0020t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0021t0006g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0001c0022t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0002c0005t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0003c0010t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0003c0010t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0004c0013t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0005c0014t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0006c0016t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0007c0017t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0008c0012t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| a0009c0018t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0296 | EUR | GBR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0278 | EUR | GBR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | FIN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00280 | hp2 | a0001 | c0004 | t0001 | g0200 | EUR | FIN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0292 | EUR | FIN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00408 | hp1 | a0001 | c0004 | t0001 | g0020 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0312 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00642 | hp2 | a0001 | c0022 | t0002 | g0277 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG00741 | hp2 | a0001 | c0011 | t0002 | g0257 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0266 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0265 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0146 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01109 | hp1 | a0001 | c0008 | t0002 | g0311 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01167 | hp1 | a0001 | c0004 | t0001 | g0014 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01169 | hp1 | a0001 | c0004 | t0001 | g0014 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0293 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01192 | hp2 | a0001 | c0011 | t0002 | g0256 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0310 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01243 | hp2 | a0002 | c0005 | t0003 | g0041 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0175 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01261 | hp2 | a0001 | c0003 | t0004 | g0049 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0096 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0281 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0028 | EUR | IBS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01517 | hp1 | a0001 | c0004 | t0001 | g0169 | EUR | IBS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0028 | EUR | IBS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0287 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01884 | hp2 | a0001 | c0006 | t0001 | g0005 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0286 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01928 | hp2 | a0001 | c0003 | t0004 | g0055 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01993 | hp1 | a0001 | c0003 | t0004 | g0048 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0267 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0294 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0279 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02040 | hp1 | a0002 | c0005 | t0003 | g0157 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02056 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02080 | hp2 | a0002 | c0005 | t0003 | g0125 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0263 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02155 | hp1 | a0002 | c0005 | t0003 | g0124 | EAS | CDX | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02155 | hp2 | a0001 | c0003 | t0001 | g0056 | EAS | CDX | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0007 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02258 | hp2 | a0004 | c0013 | t0001 | g0252 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02451 | hp2 | a0001 | c0006 | t0001 | g0005 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0283 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02572 | hp1 | a0001 | c0009 | t0001 | g0141 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0284 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0142 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0288 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02647 | hp2 | a0002 | c0005 | t0003 | g0159 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02698 | hp1 | a0001 | c0021 | t0006 | g0290 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02717 | hp1 | a0001 | c0009 | t0001 | g0077 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0149 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02723 | hp1 | a0001 | c0003 | t0002 | g0255 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02723 | hp2 | a0001 | c0006 | t0001 | g0143 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0148 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0029 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0153 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0156 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02897 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02922 | hp2 | a0001 | c0008 | t0002 | g0258 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02970 | hp1 | a0001 | c0006 | t0001 | g0145 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0285 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03041 | hp1 | a0001 | c0006 | t0001 | g0035 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0147 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03098 | hp1 | a0002 | c0005 | t0003 | g0040 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0152 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03195 | hp1 | a0002 | c0005 | t0003 | g0160 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0038 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0039 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0069 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0254 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0308 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0155 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03491 | hp2 | a0003 | c0010 | t0001 | g0245 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03492 | hp2 | a0003 | c0010 | t0001 | g0244 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0065 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0144 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03579 | hp1 | a0002 | c0005 | t0003 | g0062 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0297 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0260 | SAS | BEB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0295 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG04204 | hp1 | a0002 | c0005 | t0003 | g0118 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0280 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG04228 | hp2 | a0001 | c0002 | t0006 | g0289 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18522 | hp1 | a0001 | c0015 | t0001 | g0063 | AFR | YRI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | YRI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18939 | hp2 | a0001 | c0019 | t0001 | g0211 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18941 | hp1 | a0001 | c0004 | t0001 | g0131 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18941 | hp2 | a0005 | c0014 | t0001 | g0097 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18942 | hp2 | a0002 | c0005 | t0003 | g0114 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18945 | hp2 | a0002 | c0005 | t0003 | g0136 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0302 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18948 | hp1 | a0001 | c0003 | t0004 | g0054 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18949 | hp1 | a0001 | c0007 | t0001 | g0126 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0032 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18952 | hp1 | a0001 | c0007 | t0001 | g0132 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0178 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18957 | hp2 | a0001 | c0003 | t0004 | g0053 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0275 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18959 | hp2 | a0002 | c0005 | t0003 | g0240 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18960 | hp1 | a0007 | c0017 | t0001 | g0226 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18961 | hp2 | a0001 | c0002 | t0007 | g0306 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18962 | hp2 | a0001 | c0004 | t0001 | g0177 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18968 | hp2 | a0008 | c0012 | t0001 | g0219 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18971 | hp2 | a0001 | c0004 | t0001 | g0202 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18973 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18974 | hp2 | a0001 | c0002 | t0007 | g0307 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18975 | hp2 | a0001 | c0004 | t0001 | g0086 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18977 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18978 | hp1 | a0001 | c0007 | t0001 | g0109 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18981 | hp1 | a0001 | c0004 | t0001 | g0020 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18998 | hp2 | a0002 | c0005 | t0003 | g0122 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18999 | hp1 | a0001 | c0007 | t0001 | g0015 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19000 | hp1 | a0002 | c0005 | t0003 | g0037 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19002 | hp1 | a0001 | c0003 | t0004 | g0058 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19005 | hp1 | a0009 | c0018 | t0001 | g0024 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19010 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19010 | hp2 | a0001 | c0007 | t0001 | g0129 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19012 | hp2 | a0002 | c0005 | t0003 | g0123 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0033 | AFR | LWK | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0164 | AFR | LWK | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19058 | hp1 | a0001 | c0004 | t0001 | g0087 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19062 | hp1 | a0001 | c0006 | t0001 | g0050 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19063 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19076 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19079 | hp1 | a0001 | c0003 | t0004 | g0052 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19082 | hp1 | a0001 | c0003 | t0004 | g0051 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19086 | hp1 | a0001 | c0004 | t0001 | g0176 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19086 | hp2 | a0001 | c0003 | t0001 | g0059 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19087 | hp1 | a0001 | c0007 | t0001 | g0133 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19090 | hp2 | a0001 | c0004 | t0001 | g0104 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0007 | AFR | YRI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | YRI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0232 | AFR | ASW | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA20129 | hp2 | a0002 | c0005 | t0003 | g0161 | AFR | ASW | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA20752 | hp1 | a0001 | c0020 | t0001 | g0221 | EUR | TSI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | TSI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | GIH | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | GIH | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0291 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02109 | hp2 | a0001 | c0008 | t0002 | g0259 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02486 | hp1 | a0001 | c0006 | t0009 | g0154 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0276 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03471 | hp1 | a0001 | c0003 | t0003 | g0151 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0309 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | USA | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0066 | AFR | USA | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA18955 | hp2 | a0006 | c0016 | t0001 | g0080 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | USA | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | USA | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0262 | AFR | LWK | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0179 | REF | REF | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:45374371 | G | A | 1 | a0008 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.92G>A | p.Gly31Asp | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/14 | 156/2519 | 92/2025 | 31/674 | chr10 | 45374371 | |||
| chr10:45382625 | T | A | 1 | a0005 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.293T>A | p.Phe98Tyr | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/14 | 357/2519 | 293/2025 | 98/674 | chr10 | 45382625 | |||
| chr10:45425058 | G | A | 1 | a0002 | 16 | HG01243.hp2 HG02040.hp1 HG02080.hp2 others(13): Show |
missense_variant | MODERATE | c.760G>A | p.Glu254Lys | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/14 | 824/2519 | 760/2025 | 254/674 | chr10 | 45425058 | |||
| chr10:45440532 | G | A | 1 | a0006 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1084G>A | p.Val362Ile | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/14 | 1148/2519 | 1084/2025 | 362/674 | chr10 | 45440532 | |||
| chr10:45440559 | C | T | 1 | a0004 | 1 | HG02258.hp2 | stop_gained | HIGH | c.1111C>T | p.Arg371* | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/14 | 1175/2519 | 1111/2025 | 371/674 | chr10 | 45440559 | |||
| chr10:45443104 | G | T | 1 | a0009 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.1339G>T | p.Ala447Ser | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 10/14 | 1403/2519 | 1339/2025 | 447/674 | chr10 | 45443104 | |||
| chr10:45443652 | ATCCGGGC others(79): Show |
A | 1 | a0007 | 1 | NA18960.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.1574-73_1586delCGG others(83): Show |
p.Phe526fs | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 12/14 | 1574/2025 | 525/674 | INFO_REALIGN_3_PRIME | chr10 | 45443652 | |||
| chr10:45445628 | A | C | 1 | a0003 | 2 | HG03491.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.1966A>C | p.Lys656Gln | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 14/14 | 2030/2519 | 1966/2025 | 656/674 | chr10 | 45445628 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:45374300 | C | T | 5 | a0001c0002 a0001c0008 a0001c0011 others(2): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
synonymous_variant | LOW | c.21C>T | p.Thr7Thr | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/14 | 85/2519 | 21/2025 | 7/674 | chr10 | 45374300 | |||
| chr10:45382569 | C | T | 1 | a0001c0020 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.237C>T | p.Asp79Asp | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/14 | 301/2519 | 237/2025 | 79/674 | chr10 | 45382569 | |||
| chr10:45382602 | G | A | 4 | a0001c0003 a0001c0006 a0001c0021 others(1): Show |
45 | HG01099.hp1 HG01258.hp1 HG01261.hp2 others(42): Show |
synonymous_variant | LOW | c.270G>A | p.Thr90Thr | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/14 | 334/2519 | 270/2025 | 90/674 | chr10 | 45382602 | |||
| chr10:45382650 | C | T | 1 | a0001c0019 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.318C>T | p.Gly106Gly | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/14 | 382/2519 | 318/2025 | 106/674 | chr10 | 45382650 | |||
| chr10:45425069 | G | A | 1 | a0001c0022 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.771G>A | p.Pro257Pro | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/14 | 835/2519 | 771/2025 | 257/674 | chr10 | 45425069 | |||
| chr10:45425078 | G | A | 1 | a0001c0007 | 6 | NA18949.hp1 NA18952.hp1 NA18978.hp1 others(3): Show |
synonymous_variant | LOW | c.780G>A | p.Thr260Thr | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/14 | 844/2519 | 780/2025 | 260/674 | chr10 | 45425078 | |||
| chr10:45440444 | G | A | 2 | a0001c0011 a0001c0015 |
3 | HG00741.hp2 HG01192.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.996G>A | p.Pro332Pro | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/14 | 1060/2519 | 996/2025 | 332/674 | chr10 | 45440444 | |||
| chr10:45443061 | G | C | 1 | a0001c0009 | 2 | HG02572.hp1 HG02717.hp1 |
synonymous_variant | LOW | c.1296G>C | p.Gly432Gly | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 10/14 | 1360/2519 | 1296/2025 | 432/674 | chr10 | 45443061 | |||
| chr10:45444169 | A | G | 4 | a0001c0004 a0001c0006 a0001c0008 others(1): Show |
43 | HG00280.hp2 HG00408.hp1 HG01109.hp1 others(40): Show |
synonymous_variant | LOW | c.1728A>G | p.Pro576Pro | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/14 | 1792/2519 | 1728/2025 | 576/674 | chr10 | 45444169 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:45374221 | C | T | 9 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0006 others(6): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
5_prime_UTR_variant | MODIFIER | c.-59C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/14 | 59 | chr10 | 45374221 | ||||||
| chr10:45374252 | G | C | 9 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0006 others(6): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
5_prime_UTR_variant | MODIFIER | c.-28G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/14 | 28 | chr10 | 45374252 | ||||||
| chr10:45374265 | C | G | 9 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0006 others(6): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-15C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/14 | chr10 | 45374265 | |||||||
| chr10:45374267 | C | A | 2 | a0001c0002t0006 a0001c0021t0006 |
2 | HG02698.hp1 HG04228.hp2 |
5_prime_UTR_variant | MODIFIER | c.-13C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/14 | 13 | chr10 | 45374267 | ||||||
| chr10:45445702 | TCA | T | 3 | a0001c0001t0004 a0001c0002t0007 a0001c0003t0004 |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*17_*18delAC | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 14/14 | 17 | INFO_REALIGN_3_PRIME | chr10 | 45445702 | |||||
| chr10:45445758 | T | C | 1 | a0001c0001t0008 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*71T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 14/14 | 71 | chr10 | 45445758 | ||||||
| chr10:45445957 | C | T | 1 | a0001c0006t0009 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*270C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 14/14 | 270 | chr10 | 45445957 | ||||||
| chr10:45445963 | C | A | 2 | a0001c0003t0003 a0002c0005t0003 |
17 | HG01243.hp2 HG02040.hp1 HG02080.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*276C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 14/14 | 276 | chr10 | 45445963 | ||||||
| chr10:45446051 | C | A | 1 | a0001c0001t0005 | 2 | HG01346.hp1 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*364C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 14/14 | 364 | chr10 | 45446051 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:45374447 | A | G | 62 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(59): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+18A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374447 | |||||||
| chr10:45374455 | A | G | 62 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(59): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+26A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374455 | |||||||
| chr10:45374470 | G | A | 1 | a0001c0004t0001g0029 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.150+41G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374470 | |||||||
| chr10:45374567 | C | G | 1 | a0001c0002t0002g0312 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.150+138C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374567 | |||||||
| chr10:45374572 | A | C | 61 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(58): Show |
66 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150+143A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374572 | |||||||
| chr10:45374693 | T | G | 61 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(58): Show |
66 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150+264T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374693 | |||||||
| chr10:45374857 | T | G | 62 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(59): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+428T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374857 | |||||||
| chr10:45374858 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG01361.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.150+429G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374858 | |||||||
| chr10:45374890 | G | A | 2 | a0001c0011t0002g0256 a0001c0011t0002g0257 |
2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.150+461G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374890 | |||||||
| chr10:45374999 | G | A | 1 | a0001c0004t0001g0032 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.150+570G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374999 | |||||||
| chr10:45375077 | C | T | 2 | a0001c0001t0001g0253 a0001c0001t0008g0254 |
2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.150+648C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375077 | |||||||
| chr10:45375095 | C | G | 1 | a0004c0013t0001g0252 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.150+666C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375095 | |||||||
| chr10:45375113 | T | G | 62 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(59): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+684T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375113 | |||||||
| chr10:45375162 | T | C | 62 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(59): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+733T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375162 | |||||||
| chr10:45375240 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(94): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.150+811C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375240 | |||||||
| chr10:45375242 | A | G | 62 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(59): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+813A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375242 | |||||||
| chr10:45375339 | T | A | 6 | a0001c0001t0001g0036 a0001c0003t0001g0006 a0001c0003t0001g0033 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.150+910T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375339 | |||||||
| chr10:45375379 | G | T | 1 | a0001c0003t0002g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+950G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375379 | |||||||
| chr10:45375436 | G | A | 1 | a0001c0003t0002g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+1007G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375436 | |||||||
| chr10:45375537 | G | C | 1 | a0001c0004t0001g0169 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.150+1108G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375537 | |||||||
| chr10:45375541 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.150+1112A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375541 | |||||||
| chr10:45375710 | C | CT | 62 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(59): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+1281_150+1282i others(3): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375710 | |||||||
| chr10:45375731 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.150+1302A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375731 | |||||||
| chr10:45375775 | C | T | 1 | a0001c0008t0002g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150+1346C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375775 | |||||||
| chr10:45375881 | G | A | 62 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(59): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+1452G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375881 | |||||||
| chr10:45375903 | C | T | 1 | a0001c0003t0002g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+1474C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375903 | |||||||
| chr10:45375984 | G | A | 62 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(59): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+1555G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375984 | |||||||
| chr10:45376106 | T | C | 62 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(59): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+1677T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376106 | |||||||
| chr10:45376190 | T | TCTTCCCC others(4): Show |
62 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(59): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+1762_150+1763i others(13): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 45376190 | ||||||
| chr10:45376192 | G | T | 63 | a0001c0001t0001g0250 a0001c0001t0002g0304 a0001c0001t0002g0305 others(60): Show |
68 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.150+1763G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376192 | |||||||
| chr10:45376217 | G | A | 1 | a0001c0003t0002g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+1788G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376217 | |||||||
| chr10:45376263 | G | A | 1 | a0001c0003t0002g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+1834G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376263 | |||||||
| chr10:45376333 | G | A | 1 | a0002c0005t0003g0037 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.150+1904G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376333 | |||||||
| chr10:45376435 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.150+2006A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376435 | |||||||
| chr10:45376469 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.150+2040A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376469 | |||||||
| chr10:45376695 | C | T | 3 | a0001c0002t0002g0308 a0001c0002t0002g0309 a0001c0002t0002g0310 |
3 | HG01243.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.150+2266C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376695 | |||||||
| chr10:45376762 | T | A | 61 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(58): Show |
66 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150+2333T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376762 | |||||||
| chr10:45376768 | G | T | 1 | a0001c0001t0001g0249 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.150+2339G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376768 | |||||||
| chr10:45376833 | G | A | 61 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(58): Show |
66 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150+2404G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376833 | |||||||
| chr10:45376904 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.150+2475C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376904 | |||||||
| chr10:45376907 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.150+2478A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376907 | |||||||
| chr10:45376910 | C | G | 2 | a0001c0002t0007g0306 a0001c0002t0007g0307 |
2 | NA18961.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.150+2481C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376910 | |||||||
| chr10:45377124 | C | T | 6 | a0001c0001t0001g0036 a0001c0003t0001g0006 a0001c0003t0001g0033 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.150+2695C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377124 | |||||||
| chr10:45377185 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.150+2756A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377185 | |||||||
| chr10:45377246 | A | T | 1 | a0001c0003t0001g0164 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.150+2817A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377246 | |||||||
| chr10:45377416 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(94): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.150+2987C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377416 | |||||||
| chr10:45377436 | T | C | 1 | a0001c0004t0001g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.150+3007T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377436 | |||||||
| chr10:45377506 | C | T | 61 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(58): Show |
66 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150+3077C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377506 | |||||||
| chr10:45377519 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.150+3090A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377519 | |||||||
| chr10:45377657 | C | G | 1 | a0001c0001t0001g0163 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.150+3228C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377657 | |||||||
| chr10:45377744 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.150+3315C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377744 | |||||||
| chr10:45377748 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.150+3319C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377748 | |||||||
| chr10:45377830 | A | G | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.150+3401A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377830 | |||||||
| chr10:45377958 | G | C | 1 | a0001c0003t0002g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+3529G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377958 | |||||||
| chr10:45378054 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.150+3625C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45378054 | |||||||
| chr10:45378181 | C | CT | 58 | a0001c0001t0002g0304 a0001c0002t0002g0004 a0001c0002t0002g0026 others(55): Show |
63 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.150+3754dupT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 45378181 | ||||||
| chr10:45378253 | AG | A | 4 | a0001c0004t0001g0038 a0001c0004t0001g0039 a0002c0005t0003g0040 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+3827delG | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 45378253 | ||||||
| chr10:45378673 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.151-3810G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45378673 | |||||||
| chr10:45378881 | G | C | 1 | a0001c0001t0001g0253 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.151-3602G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45378881 | |||||||
| chr10:45378892 | T | C | 59 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(56): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-3591T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45378892 | |||||||
| chr10:45379062 | C | T | 2 | a0001c0008t0002g0258 a0001c0008t0002g0259 |
2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.151-3421C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379062 | |||||||
| chr10:45379120 | G | A | 2 | a0001c0001t0001g0172 a0001c0004t0001g0039 |
2 | HG00280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.151-3363G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379120 | |||||||
| chr10:45379212 | A | G | 59 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(56): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-3271A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379212 | |||||||
| chr10:45379356 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.151-3127G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379356 | |||||||
| chr10:45379369 | G | T | 59 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(56): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-3114G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379369 | |||||||
| chr10:45379370 | C | T | 59 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(56): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-3113C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379370 | |||||||
| chr10:45379385 | C | T | 4 | a0001c0001t0001g0158 a0002c0005t0003g0159 a0002c0005t0003g0160 others(1): Show |
4 | HG02647.hp2 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-3098C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379385 | |||||||
| chr10:45379452 | C | T | 2 | a0001c0008t0002g0258 a0001c0008t0002g0259 |
2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.151-3031C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379452 | |||||||
| chr10:45379614 | G | A | 4 | a0001c0004t0001g0038 a0001c0004t0001g0039 a0002c0005t0003g0040 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-2869G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379614 | |||||||
| chr10:45379618 | T | C | 59 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(56): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-2865T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379618 | |||||||
| chr10:45379643 | T | C | 6 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0003t0001g0175 others(3): Show |
6 | HG01258.hp1 HG01358.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.151-2840T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379643 | |||||||
| chr10:45379647 | T | A | 6 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0003t0001g0175 others(3): Show |
6 | HG01258.hp1 HG01358.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.151-2836T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379647 | |||||||
| chr10:45379684 | C | T | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151-2799C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379684 | |||||||
| chr10:45379685 | G | A | 5 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0034 others(2): Show |
7 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-2798G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379685 | |||||||
| chr10:45379816 | C | G | 7 | a0001c0002t0002g0298 a0001c0002t0002g0299 a0001c0002t0002g0300 others(4): Show |
7 | HG00408.hp2 NA18942.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-2667C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379816 | |||||||
| chr10:45379882 | G | C | 59 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(56): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-2601G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379882 | |||||||
| chr10:45379924 | G | C | 1 | a0001c0001t0005g0043 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.151-2559G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379924 | |||||||
| chr10:45379961 | A | G | 59 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(56): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-2522A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379961 | |||||||
| chr10:45380106 | C | T | 8 | a0001c0002t0002g0028 a0001c0002t0002g0291 a0001c0002t0002g0292 others(5): Show |
9 | HG00099.hp1 HG00323.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.151-2377C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380106 | |||||||
| chr10:45380180 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.151-2303G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380180 | |||||||
| chr10:45380345 | T | C | 59 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(56): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-2138T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380345 | |||||||
| chr10:45380370 | G | A | 1 | a0001c0002t0002g0260 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.151-2113G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380370 | |||||||
| chr10:45380387 | G | A | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.151-2096G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380387 | |||||||
| chr10:45380485 | C | T | 2 | a0003c0010t0001g0244 a0003c0010t0001g0245 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.151-1998C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380485 | |||||||
| chr10:45380532 | C | T | 59 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(56): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-1951C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380532 | |||||||
| chr10:45380553 | A | T | 1 | a0001c0001t0001g0243 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.151-1930A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380553 | |||||||
| chr10:45380561 | C | T | 2 | a0001c0008t0002g0258 a0001c0008t0002g0259 |
2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.151-1922C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380561 | |||||||
| chr10:45380901 | C | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.151-1582C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380901 | |||||||
| chr10:45380933 | C | T | 1 | a0002c0005t0003g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.151-1550C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380933 | |||||||
| chr10:45380937 | A | G | 7 | a0001c0002t0002g0028 a0001c0002t0002g0292 a0001c0002t0002g0293 others(4): Show |
8 | HG00099.hp1 HG00323.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-1546A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380937 | |||||||
| chr10:45380974 | G | A | 1 | a0001c0002t0002g0261 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.151-1509G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380974 | |||||||
| chr10:45381159 | C | T | 57 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(54): Show |
62 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.151-1324C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381159 | |||||||
| chr10:45381225 | T | C | 65 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0002g0304 others(62): Show |
70 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.151-1258T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381225 | |||||||
| chr10:45381329 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0002g0304 |
2 | HG01175.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.151-1154C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381329 | |||||||
| chr10:45381335 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.151-1148G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381335 | |||||||
| chr10:45381468 | C | T | 59 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(56): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-1015C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381468 | |||||||
| chr10:45381492 | G | T | 1 | a0001c0001t0001g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.151-991G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381492 | |||||||
| chr10:45381558 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.151-925G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381558 | |||||||
| chr10:45381669 | A | G | 1 | a0002c0005t0003g0240 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.151-814A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381669 | |||||||
| chr10:45381709 | G | A | 59 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(56): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-774G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381709 | |||||||
| chr10:45381711 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.151-772G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381711 | |||||||
| chr10:45381993 | C | A | 58 | a0001c0001t0002g0304 a0001c0002t0002g0004 a0001c0002t0002g0026 others(55): Show |
63 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.151-490C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381993 | |||||||
| chr10:45382035 | C | T | 2 | a0001c0008t0002g0258 a0001c0008t0002g0259 |
2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.151-448C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382035 | |||||||
| chr10:45382112 | G | A | 58 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(55): Show |
63 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.151-371G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382112 | |||||||
| chr10:45382170 | G | A | 1 | a0001c0002t0002g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.151-313G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382170 | |||||||
| chr10:45382195 | A | T | 25 | a0001c0003t0001g0006 a0001c0003t0001g0016 a0001c0003t0001g0017 others(22): Show |
30 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.151-288A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382195 | |||||||
| chr10:45382217 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.151-266T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382217 | |||||||
| chr10:45382392 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151-91G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382392 | |||||||
| chr10:45382451 | C | T | 57 | a0001c0001t0002g0304 a0001c0002t0002g0004 a0001c0002t0002g0026 others(54): Show |
62 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.151-32C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382451 | |||||||
| chr10:45382725 | G | A | 13 | a0001c0003t0001g0056 a0001c0003t0001g0057 a0001c0003t0001g0059 others(10): Show |
13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.349+44G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382725 | |||||||
| chr10:45382810 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.349+129T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382810 | |||||||
| chr10:45382818 | G | A | 14 | a0001c0001t0001g0061 a0001c0003t0001g0056 a0001c0003t0001g0057 others(11): Show |
14 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.349+137G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382818 | |||||||
| chr10:45382865 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+184C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382865 | |||||||
| chr10:45382933 | G | A | 1 | a0001c0008t0002g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.349+252G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382933 | |||||||
| chr10:45382934 | G | A | 93 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0068 others(90): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.349+253G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382934 | |||||||
| chr10:45382935 | G | T | 1 | a0001c0002t0002g0303 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.349+254G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382935 | |||||||
| chr10:45382938 | G | T | 1 | a0001c0002t0002g0303 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.349+257G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382938 | |||||||
| chr10:45383015 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.349+334G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383015 | |||||||
| chr10:45383023 | C | G | 1 | a0001c0001t0001g0239 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.349+342C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383023 | |||||||
| chr10:45383229 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0165 a0001c0001t0001g0166 others(6): Show |
12 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+548G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383229 | |||||||
| chr10:45383351 | C | T | 5 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0034 others(2): Show |
7 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.349+670C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383351 | |||||||
| chr10:45383352 | G | A | 11 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(8): Show |
12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+671G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383352 | |||||||
| chr10:45383444 | C | G | 3 | a0001c0001t0002g0305 a0001c0008t0002g0258 a0001c0008t0002g0259 |
3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.349+763C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383444 | |||||||
| chr10:45383450 | A | G | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349+769A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383450 | |||||||
| chr10:45383460 | A | G | 60 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(57): Show |
65 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.349+779A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383460 | |||||||
| chr10:45383610 | G | T | 2 | a0001c0004t0001g0008 a0001c0004t0001g0069 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.349+929G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383610 | |||||||
| chr10:45383612 | G | A | 4 | a0001c0004t0001g0038 a0001c0004t0001g0039 a0002c0005t0003g0040 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+931G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383612 | |||||||
| chr10:45383614 | G | A | 35 | a0001c0002t0002g0026 a0001c0002t0002g0027 a0001c0002t0002g0260 others(32): Show |
37 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.349+933G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383614 | |||||||
| chr10:45383636 | T | C | 1 | a0001c0008t0002g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.349+955T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383636 | |||||||
| chr10:45383841 | C | T | 1 | a0001c0003t0004g0058 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.349+1160C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383841 | |||||||
| chr10:45384018 | A | G | 1 | a0001c0002t0002g0283 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.349+1337A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384018 | |||||||
| chr10:45384143 | G | C | 1 | a0001c0002t0002g0263 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.349+1462G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384143 | |||||||
| chr10:45384158 | C | T | 14 | a0001c0001t0001g0140 a0001c0003t0001g0056 a0001c0003t0001g0057 others(11): Show |
14 | HG01255.hp1 HG01261.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.349+1477C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384158 | |||||||
| chr10:45384540 | C | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG01361.hp1 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.349+1859C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384540 | |||||||
| chr10:45384571 | C | A | 1 | a0001c0003t0004g0048 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.349+1890C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384571 | |||||||
| chr10:45384608 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(253): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.349+1927C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384608 | |||||||
| chr10:45384616 | C | G | 3 | a0001c0001t0002g0305 a0001c0008t0002g0258 a0001c0008t0002g0259 |
3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.349+1935C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384616 | |||||||
| chr10:45384776 | G | A | 1 | a0001c0002t0006g0289 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.349+2095G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384776 | |||||||
| chr10:45384833 | C | CTAT | 6 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0107 others(3): Show |
7 | HG01069.hp1 HG02109.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+2175_349+2177d others(5): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45384833 | ||||||
| chr10:45384833 | C | CTATTAT | 5 | a0001c0001t0001g0070 a0001c0004t0001g0038 a0001c0004t0001g0039 others(2): Show |
5 | HG01243.hp2 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+2172_349+2177d others(8): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45384833 | ||||||
| chr10:45384833 | C | CTATTATT others(5): Show |
13 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(10): Show |
14 | HG00099.hp1 HG00642.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.349+2166_349+2177d others(14): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45384833 | ||||||
| chr10:45384833 | C | CTATTATT others(8): Show |
2 | a0001c0001t0001g0183 a0001c0002t0002g0292 |
2 | HG00323.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.349+2163_349+2177d others(17): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45384833 | ||||||
| chr10:45384833 | C | CTATTATT others(14): Show |
1 | a0001c0008t0002g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.349+2157_349+2177d others(23): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45384833 | ||||||
| chr10:45384912 | A | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+2231A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384912 | |||||||
| chr10:45384918 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG00438.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.349+2237C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384918 | |||||||
| chr10:45385176 | A | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+2495A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385176 | |||||||
| chr10:45385210 | G | A | 15 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0142 others(12): Show |
17 | HG01099.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.349+2529G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385210 | |||||||
| chr10:45385220 | C | G | 15 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0142 others(12): Show |
17 | HG01099.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.349+2539C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385220 | |||||||
| chr10:45385306 | G | A | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349+2625G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385306 | |||||||
| chr10:45385530 | G | A | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+2849G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385530 | |||||||
| chr10:45385966 | G | T | 1 | a0001c0002t0002g0028 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.349+3285G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385966 | |||||||
| chr10:45385991 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.349+3310C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385991 | |||||||
| chr10:45386066 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.349+3385C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386066 | |||||||
| chr10:45386073 | G | A | 4 | a0001c0001t0002g0304 a0001c0003t0001g0155 a0001c0003t0001g0164 others(1): Show |
4 | HG02486.hp1 HG02615.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+3392G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386073 | |||||||
| chr10:45386097 | C | G | 1 | a0001c0002t0002g0292 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.349+3416C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386097 | |||||||
| chr10:45386230 | A | G | 69 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(66): Show |
74 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.349+3549A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386230 | |||||||
| chr10:45386300 | CA | C | 28 | a0001c0001t0001g0044 a0001c0002t0002g0302 a0001c0003t0001g0006 others(25): Show |
33 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.349+3635delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45386300 | ||||||
| chr10:45386467 | TA | T | 7 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(4): Show |
7 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+3794delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45386467 | ||||||
| chr10:45386582 | G | GA | 8 | a0001c0001t0001g0071 a0001c0001t0001g0165 a0001c0001t0001g0166 others(5): Show |
8 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+3910dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45386582 | ||||||
| chr10:45386626 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.349+3945T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386626 | |||||||
| chr10:45386670 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.349+3989A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386670 | |||||||
| chr10:45386710 | C | T | 5 | a0001c0001t0001g0061 a0002c0005t0003g0062 a0002c0005t0003g0159 others(2): Show |
5 | HG02647.hp2 HG03195.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+4029C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386710 | |||||||
| chr10:45387055 | G | A | 2 | a0001c0004t0001g0038 a0001c0004t0001g0039 |
2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.349+4374G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387055 | |||||||
| chr10:45387115 | G | A | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349+4434G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387115 | |||||||
| chr10:45387144 | A | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+4463A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387144 | |||||||
| chr10:45387293 | A | G | 69 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(66): Show |
74 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.349+4612A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387293 | |||||||
| chr10:45387374 | G | A | 1 | a0001c0002t0007g0306 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.349+4693G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387374 | |||||||
| chr10:45387412 | G | A | 3 | a0001c0003t0001g0155 a0001c0003t0001g0164 a0001c0006t0009g0154 |
3 | HG02486.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.349+4731G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387412 | |||||||
| chr10:45387498 | C | CTTTCTCC others(67): Show |
1 | a0001c0001t0001g0106 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.349+4818_349+4891d others(76): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45387498 | ||||||
| chr10:45387516 | A | C | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.349+4835A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387516 | |||||||
| chr10:45387568 | A | G | 1 | a0001c0003t0002g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.349+4887A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387568 | |||||||
| chr10:45387618 | G | C | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.349+4937G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387618 | |||||||
| chr10:45387630 | C | T | 1 | a0002c0005t0003g0136 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.349+4949C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387630 | |||||||
| chr10:45387643 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.349+4962G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387643 | |||||||
| chr10:45387858 | A | G | 2 | a0001c0011t0002g0256 a0001c0011t0002g0257 |
2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.349+5177A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387858 | |||||||
| chr10:45387958 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(253): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.349+5277A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387958 | |||||||
| chr10:45387972 | C | G | 1 | a0001c0001t0001g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.349+5291C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387972 | |||||||
| chr10:45388023 | T | A | 16 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
17 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.349+5342T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388023 | |||||||
| chr10:45388088 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.349+5407A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388088 | |||||||
| chr10:45388144 | T | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+5463T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388144 | |||||||
| chr10:45388277 | G | A | 7 | a0001c0001t0001g0137 a0001c0001t0001g0165 a0001c0001t0001g0166 others(4): Show |
7 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+5596G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388277 | |||||||
| chr10:45388326 | AG | A | 16 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
17 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.349+5646delG | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388326 | |||||||
| chr10:45388570 | G | A | 4 | a0001c0004t0001g0038 a0001c0004t0001g0039 a0002c0005t0003g0040 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+5889G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388570 | |||||||
| chr10:45388671 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.349+5990A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388671 | |||||||
| chr10:45388687 | A | G | 4 | a0001c0004t0001g0038 a0001c0004t0001g0039 a0002c0005t0003g0040 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+6006A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388687 | |||||||
| chr10:45388777 | C | A | 13 | a0001c0003t0001g0056 a0001c0003t0001g0057 a0001c0003t0001g0059 others(10): Show |
13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.349+6096C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388777 | |||||||
| chr10:45388814 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.349+6133C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388814 | |||||||
| chr10:45388835 | G | A | 1 | a0002c0005t0003g0159 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.349+6154G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388835 | |||||||
| chr10:45388885 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0107 a0001c0001t0001g0108 |
4 | HG01069.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+6204A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388885 | |||||||
| chr10:45388923 | C | CA | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+6249dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45388923 | ||||||
| chr10:45389034 | T | C | 1 | a0004c0013t0001g0252 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.349+6353T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389034 | |||||||
| chr10:45389063 | C | T | 1 | a0002c0005t0003g0136 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.349+6382C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389063 | |||||||
| chr10:45389069 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0073 |
2 | HG01123.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.349+6388G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389069 | |||||||
| chr10:45389123 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+6442C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389123 | |||||||
| chr10:45389158 | A | T | 7 | a0001c0002t0002g0004 a0001c0002t0002g0262 a0001c0002t0002g0284 others(4): Show |
9 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.349+6477A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389158 | |||||||
| chr10:45389283 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.350-6572A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389283 | |||||||
| chr10:45389443 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.350-6412G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389443 | |||||||
| chr10:45389458 | C | G | 7 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(4): Show |
7 | HG00099.hp1 HG00642.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-6397C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389458 | |||||||
| chr10:45389506 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-6349C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389506 | |||||||
| chr10:45389546 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.350-6309C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389546 | |||||||
| chr10:45389721 | ACCAG | A | 43 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(40): Show |
47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-6130_350-6127d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45389721 | ||||||
| chr10:45389793 | C | T | 1 | a0001c0004t0001g0104 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.350-6062C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389793 | |||||||
| chr10:45389807 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.350-6048A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389807 | |||||||
| chr10:45389813 | G | A | 1 | a0001c0002t0002g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.350-6042G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389813 | |||||||
| chr10:45389872 | T | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0044 |
3 | HG01070.hp1 HG01071.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.350-5983T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389872 | |||||||
| chr10:45389873 | GCTCCAAT others(29): Show |
G | 1 | a0001c0001t0001g0235 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.350-5981_350-5946d others(38): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389873 | |||||||
| chr10:45389878 | A | T | 1 | a0001c0002t0002g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.350-5977A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389878 | |||||||
| chr10:45389959 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.350-5896C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389959 | |||||||
| chr10:45389960 | G | A | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.350-5895G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389960 | |||||||
| chr10:45389973 | A | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-5882A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389973 | |||||||
| chr10:45390029 | G | C | 16 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
17 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.350-5826G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390029 | |||||||
| chr10:45390151 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0102 others(1): Show |
6 | HG00621.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-5704C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390151 | |||||||
| chr10:45390226 | C | T | 1 | a0001c0008t0002g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.350-5629C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390226 | |||||||
| chr10:45390364 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-5491C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390364 | |||||||
| chr10:45390418 | T | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-5437T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390418 | |||||||
| chr10:45390483 | C | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0107 others(4): Show |
8 | HG01069.hp1 HG02109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-5372C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390483 | |||||||
| chr10:45390581 | C | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-5274C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390581 | |||||||
| chr10:45390602 | A | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-5253A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390602 | |||||||
| chr10:45390605 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.350-5250G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390605 | |||||||
| chr10:45390834 | T | C | 10 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(7): Show |
12 | HG02258.hp1 HG02809.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.350-5021T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390834 | |||||||
| chr10:45390846 | C | G | 7 | a0001c0002t0002g0004 a0001c0002t0002g0262 a0001c0002t0002g0284 others(4): Show |
9 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-5009C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390846 | |||||||
| chr10:45390847 | A | G | 43 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(40): Show |
47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-5008A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390847 | |||||||
| chr10:45390988 | CCCCTCT | C | 4 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0234 others(1): Show |
4 | HG01106.hp1 HG03669.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-4863_350-4858d others(8): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45390988 | ||||||
| chr10:45390998 | CTCTCCCC others(35): Show |
C | 2 | a0001c0002t0002g0265 a0001c0002t0002g0266 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.350-4845_350-4804d others(44): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45390998 | ||||||
| chr10:45391002 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.350-4853C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391002 | |||||||
| chr10:45391003 | CCCTCTCT | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(178): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.350-4845_350-4839d others(9): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391003 | ||||||
| chr10:45391009 | CT | C | 9 | a0001c0001t0002g0305 a0001c0002t0002g0273 a0001c0002t0002g0274 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-4845delT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391009 | |||||||
| chr10:45391010 | T | C | 78 | a0001c0001t0001g0042 a0001c0001t0001g0060 a0001c0001t0001g0061 others(75): Show |
83 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.350-4845T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391010 | |||||||
| chr10:45391012 | C | A | 18 | a0001c0001t0001g0216 a0001c0003t0001g0056 a0001c0003t0001g0057 others(15): Show |
18 | HG01243.hp2 HG01256.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.350-4843C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391012 | |||||||
| chr10:45391015 | TCCCATCT others(8): Show |
T | 1 | a0001c0009t0001g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.350-4836_350-4822d others(17): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391015 | ||||||
| chr10:45391018 | CA | C | 44 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0002t0002g0004 others(41): Show |
48 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.350-4836delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391018 | |||||||
| chr10:45391019 | A | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0216 a0001c0002t0002g0308 others(6): Show |
10 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-4836A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391019 | |||||||
| chr10:45391022 | TC | T | 35 | a0001c0001t0002g0304 a0001c0002t0002g0004 a0001c0002t0002g0026 others(32): Show |
39 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.350-4829delC | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391022 | ||||||
| chr10:45391025 | CCTCTCCC others(23): Show |
C | 9 | a0001c0001t0002g0305 a0001c0002t0002g0273 a0001c0002t0002g0274 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-4826_350-4797d others(32): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391025 | ||||||
| chr10:45391026 | C | A | 4 | a0001c0004t0001g0007 a0001c0004t0001g0065 a0001c0004t0001g0066 others(1): Show |
5 | HG02258.hp1 HG03516.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-4829C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391026 | |||||||
| chr10:45391030 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.350-4825C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391030 | |||||||
| chr10:45391032 | CCTCTCCC others(16): Show |
C | 35 | a0001c0001t0002g0304 a0001c0002t0002g0004 a0001c0002t0002g0026 others(32): Show |
39 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.350-4819_350-4797d others(25): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391032 | ||||||
| chr10:45391039 | CA | C | 8 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(5): Show |
9 | HG02572.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-4815delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391039 | |||||||
| chr10:45391040 | A | C | 4 | a0001c0004t0001g0007 a0001c0004t0001g0065 a0001c0004t0001g0066 others(1): Show |
5 | HG02258.hp1 HG03516.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-4815A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391040 | |||||||
| chr10:45391043 | TC | T | 12 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(9): Show |
14 | HG02258.hp1 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-4808delC | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391043 | ||||||
| chr10:45391046 | C | G | 22 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0036 others(19): Show |
23 | HG01069.hp1 HG02071.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.350-4809C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391046 | |||||||
| chr10:45391050 | TC | T | 4 | a0001c0004t0001g0007 a0001c0004t0001g0065 a0001c0004t0001g0066 others(1): Show |
5 | HG02258.hp1 HG03516.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-4801delC | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391050 | ||||||
| chr10:45391053 | CCT | C | 8 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(5): Show |
9 | HG02572.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-4798_350-4797d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391053 | ||||||
| chr10:45391057 | T | A | 52 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(49): Show |
57 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.350-4798T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391057 | |||||||
| chr10:45391059 | C | G | 52 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(49): Show |
57 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.350-4796C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391059 | |||||||
| chr10:45391060 | C | CCACGG | 4 | a0001c0004t0001g0007 a0001c0004t0001g0065 a0001c0004t0001g0066 others(1): Show |
5 | HG02258.hp1 HG03516.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-4795_350-4794i others(7): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391060 | |||||||
| chr10:45391060 | C | G | 52 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(49): Show |
57 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.350-4795C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391060 | |||||||
| chr10:45391072 | CCACGG | C | 56 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(53): Show |
62 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.350-4782_350-4778d others(7): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391072 | |||||||
| chr10:45391077 | G | GTCTCCC | 7 | a0001c0001t0001g0174 a0001c0001t0001g0180 a0001c0001t0001g0215 others(4): Show |
7 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-4765_350-4760d others(8): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391077 | ||||||
| chr10:45391077 | G | GTCTCCCT others(5): Show |
185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(182): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.350-4771_350-4760d others(14): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391077 | ||||||
| chr10:45391077 | G | GTCTCCCT others(40): Show |
1 | a0001c0001t0001g0235 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.350-4760_350-4759i others(49): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391077 | ||||||
| chr10:45391081 | C | CCCTCTCC others(5): Show |
6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-4763_350-4762i others(14): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391081 | ||||||
| chr10:45391092 | T | TCCCTCTC others(6): Show |
1 | a0001c0007t0001g0109 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.350-4760_350-4759i others(15): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391092 | ||||||
| chr10:45391106 | C | A | 1 | a0002c0005t0003g0240 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.350-4749C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391106 | |||||||
| chr10:45391218 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.350-4637G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391218 | |||||||
| chr10:45391240 | G | A | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.350-4615G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391240 | |||||||
| chr10:45391245 | G | A | 1 | a0001c0003t0001g0164 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.350-4610G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391245 | |||||||
| chr10:45391256 | CTG | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0181 a0001c0001t0001g0182 |
6 | NA18944.hp2 NA18947.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-4597_350-4596d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391256 | ||||||
| chr10:45391326 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.350-4529C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391326 | |||||||
| chr10:45391329 | G | A | 43 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(40): Show |
47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-4526G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391329 | |||||||
| chr10:45391425 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.350-4430C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391425 | |||||||
| chr10:45391438 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.350-4417C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391438 | |||||||
| chr10:45391508 | C | T | 12 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(9): Show |
13 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.350-4347C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391508 | |||||||
| chr10:45391513 | A | AC | 21 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0075 others(18): Show |
21 | HG00621.hp1 HG00642.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.350-4338dupC | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391513 | ||||||
| chr10:45391538 | C | T | 1 | a0001c0003t0001g0018 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.350-4317C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391538 | |||||||
| chr10:45391550 | A | G | 7 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(4): Show |
7 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-4305A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391550 | |||||||
| chr10:45391557 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0008g0254 |
2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.350-4298G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391557 | |||||||
| chr10:45391568 | A | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-4287A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391568 | |||||||
| chr10:45391580 | T | C | 2 | a0001c0008t0002g0258 a0001c0008t0002g0259 |
2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.350-4275T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391580 | |||||||
| chr10:45391587 | C | A | 43 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(40): Show |
47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-4268C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391587 | |||||||
| chr10:45391612 | G | A | 2 | a0001c0001t0001g0192 a0001c0003t0004g0048 |
2 | HG00140.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.350-4243G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391612 | |||||||
| chr10:45391622 | G | A | 43 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(40): Show |
47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-4233G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391622 | |||||||
| chr10:45391667 | C | T | 16 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
17 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.350-4188C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391667 | |||||||
| chr10:45391670 | A | G | 16 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
17 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.350-4185A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391670 | |||||||
| chr10:45391671 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.350-4184T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391671 | |||||||
| chr10:45391673 | G | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0165 a0001c0001t0001g0172 others(6): Show |
10 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-4182G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391673 | |||||||
| chr10:45391770 | G | A | 1 | a0001c0007t0001g0126 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.350-4085G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391770 | |||||||
| chr10:45391783 | C | G | 1 | a0004c0013t0001g0252 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.350-4072C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391783 | |||||||
| chr10:45391783 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(131): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.350-4072C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391783 | |||||||
| chr10:45391806 | ACCCTCCG others(57): Show |
A | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.350-4026_350-3963d others(66): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391806 | ||||||
| chr10:45391808 | C | T | 1 | a0002c0005t0003g0040 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.350-4047C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391808 | |||||||
| chr10:45391817 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.350-4038G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391817 | |||||||
| chr10:45391824 | G | A | 16 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
17 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.350-4031G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391824 | |||||||
| chr10:45391829 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(248): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.350-4026A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391829 | |||||||
| chr10:45391853 | ATCTGAGA others(33): Show |
A | 18 | a0001c0001t0001g0079 a0001c0001t0001g0135 a0001c0001t0001g0183 others(15): Show |
19 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.350-3962_350-3923d others(42): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391853 | ||||||
| chr10:45391877 | G | A | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3978G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391877 | |||||||
| chr10:45391893 | T | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(236): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.350-3962T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391893 | |||||||
| chr10:45391912 | CCTCCGCC others(33): Show |
C | 1 | a0001c0001t0001g0241 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.350-3927_350-3888d others(42): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391912 | ||||||
| chr10:45391920 | C | G | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.350-3935C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391920 | |||||||
| chr10:45391926 | C | A | 15 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(12): Show |
16 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.350-3929C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391926 | |||||||
| chr10:45391927 | C | T | 1 | a0001c0008t0002g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.350-3928C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391927 | |||||||
| chr10:45391928 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-3927G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391928 | |||||||
| chr10:45391933 | G | A | 1 | a0001c0002t0002g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.350-3922G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391933 | |||||||
| chr10:45391948 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.350-3907A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391948 | |||||||
| chr10:45391951 | G | A | 1 | a0001c0003t0001g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.350-3904G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391951 | |||||||
| chr10:45391957 | G | A | 7 | a0001c0002t0002g0004 a0001c0002t0002g0262 a0001c0002t0002g0284 others(4): Show |
9 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-3898G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391957 | |||||||
| chr10:45391996 | GTCAGCCC others(38): Show |
G | 1 | a0001c0002t0002g0298 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.350-3826_350-3782d others(47): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391996 | ||||||
| chr10:45392024 | G | A | 1 | a0001c0004t0001g0014 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.350-3831G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392024 | |||||||
| chr10:45392026 | C | T | 1 | a0001c0004t0001g0032 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.350-3829C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392026 | |||||||
| chr10:45392027 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(145): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.350-3828C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392027 | |||||||
| chr10:45392040 | G | C | 26 | a0001c0003t0001g0006 a0001c0003t0001g0016 a0001c0003t0001g0017 others(23): Show |
31 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.350-3815G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392040 | |||||||
| chr10:45392051 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3804C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392051 | |||||||
| chr10:45392064 | G | A | 68 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(65): Show |
73 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.350-3791G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392064 | |||||||
| chr10:45392064 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.350-3791G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392064 | |||||||
| chr10:45392069 | G | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0107 others(4): Show |
8 | HG01069.hp1 HG02109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-3786G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392069 | |||||||
| chr10:45392074 | A | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3781A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392074 | |||||||
| chr10:45392083 | T | A | 17 | a0001c0002t0002g0026 a0001c0002t0002g0261 a0001c0002t0002g0263 others(14): Show |
18 | HG00408.hp2 HG02132.hp2 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.350-3772T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392083 | |||||||
| chr10:45392112 | T | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3743T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392112 | |||||||
| chr10:45392122 | G | A | 26 | a0001c0003t0001g0006 a0001c0003t0001g0016 a0001c0003t0001g0017 others(23): Show |
31 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.350-3733G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392122 | |||||||
| chr10:45392145 | T | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3710T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392145 | |||||||
| chr10:45392182 | T | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3673T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392182 | |||||||
| chr10:45392247 | T | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3608T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392247 | |||||||
| chr10:45392352 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.350-3503G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392352 | |||||||
| chr10:45392416 | C | G | 1 | a0001c0011t0002g0257 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.350-3439C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392416 | |||||||
| chr10:45392470 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(253): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.350-3385A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392470 | |||||||
| chr10:45392513 | G | A | 10 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(7): Show |
12 | HG02258.hp1 HG02809.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.350-3342G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392513 | |||||||
| chr10:45392517 | C | G | 22 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(19): Show |
23 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.350-3338C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392517 | |||||||
| chr10:45392571 | G | A | 43 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(40): Show |
47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-3284G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392571 | |||||||
| chr10:45392574 | T | A | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.350-3281T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392574 | |||||||
| chr10:45392578 | C | T | 2 | a0001c0001t0001g0236 a0001c0001t0002g0305 |
2 | HG00621.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.350-3277C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392578 | |||||||
| chr10:45392617 | G | C | 5 | a0001c0001t0001g0166 a0001c0004t0001g0038 a0001c0004t0001g0039 others(2): Show |
5 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-3238G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392617 | |||||||
| chr10:45392660 | C | T | 44 | a0001c0001t0002g0304 a0001c0002t0002g0004 a0001c0002t0002g0026 others(41): Show |
48 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.350-3195C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392660 | |||||||
| chr10:45392720 | AAAAAAGA others(4): Show |
A | 1 | a0002c0005t0003g0240 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.350-3132_350-3122d others(13): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45392720 | ||||||
| chr10:45392746 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(145): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.350-3109C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392746 | |||||||
| chr10:45392818 | T | C | 1 | a0001c0002t0002g0291 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.350-3037T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392818 | |||||||
| chr10:45392903 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.350-2952G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392903 | |||||||
| chr10:45392955 | T | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-2900T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392955 | |||||||
| chr10:45393008 | G | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(184): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.350-2847G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393008 | |||||||
| chr10:45393015 | A | C | 2 | a0001c0011t0002g0256 a0001c0011t0002g0257 |
2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.350-2840A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393015 | |||||||
| chr10:45393055 | A | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-2800A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393055 | |||||||
| chr10:45393145 | AC | A | 2 | a0001c0003t0001g0016 a0001c0006t0001g0143 |
3 | HG02572.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.350-2709delC | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393145 | |||||||
| chr10:45393148 | C | CA | 5 | a0001c0001t0001g0075 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | HG01109.hp1 HG01261.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-2699dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45393148 | ||||||
| chr10:45393150 | A | C | 34 | a0001c0002t0002g0026 a0001c0002t0002g0027 a0001c0002t0002g0261 others(31): Show |
36 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.350-2705A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393150 | |||||||
| chr10:45393151 | A | AC | 2 | a0001c0003t0001g0016 a0001c0006t0001g0143 |
3 | HG02572.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.350-2704_350-2703i others(3): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393151 | |||||||
| chr10:45393155 | A | G | 2 | a0001c0003t0001g0016 a0001c0006t0001g0143 |
3 | HG02572.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.350-2700A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393155 | |||||||
| chr10:45393157 | C | G | 2 | a0001c0003t0001g0016 a0001c0006t0001g0143 |
3 | HG02572.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.350-2698C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393157 | |||||||
| chr10:45393188 | G | A | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.350-2667G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393188 | |||||||
| chr10:45393279 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.350-2576G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393279 | |||||||
| chr10:45393296 | A | C | 3 | a0001c0001t0002g0305 a0001c0008t0002g0258 a0001c0008t0002g0259 |
3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.350-2559A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393296 | |||||||
| chr10:45393321 | T | C | 3 | a0001c0002t0002g0308 a0001c0002t0002g0309 a0001c0002t0002g0310 |
3 | HG01243.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.350-2534T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393321 | |||||||
| chr10:45393343 | A | T | 1 | a0001c0003t0001g0153 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350-2512A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393343 | |||||||
| chr10:45393352 | C | A | 1 | a0001c0003t0001g0153 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350-2503C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393352 | |||||||
| chr10:45393447 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.350-2408C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393447 | |||||||
| chr10:45393480 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.350-2375A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393480 | |||||||
| chr10:45393488 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.350-2367A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393488 | |||||||
| chr10:45393497 | A | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-2358A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393497 | |||||||
| chr10:45393505 | T | G | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.350-2350T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393505 | |||||||
| chr10:45393507 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.350-2348G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393507 | |||||||
| chr10:45393572 | C | G | 3 | a0001c0002t0002g0308 a0001c0002t0002g0309 a0001c0002t0002g0310 |
3 | HG01243.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.350-2283C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393572 | |||||||
| chr10:45393599 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.350-2256G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393599 | |||||||
| chr10:45393725 | C | T | 20 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(17): Show |
23 | HG01099.hp1 HG02145.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.350-2130C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393725 | |||||||
| chr10:45393794 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.350-2061A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393794 | |||||||
| chr10:45393835 | G | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-2020G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393835 | |||||||
| chr10:45393861 | A | T | 1 | a0002c0005t0003g0240 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.350-1994A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393861 | |||||||
| chr10:45393882 | A | G | 1 | a0001c0002t0002g0282 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.350-1973A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393882 | |||||||
| chr10:45393894 | A | G | 3 | a0001c0001t0002g0305 a0001c0008t0002g0258 a0001c0008t0002g0259 |
3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.350-1961A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393894 | |||||||
| chr10:45393944 | C | T | 43 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(40): Show |
47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-1911C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393944 | |||||||
| chr10:45393980 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1875C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393980 | |||||||
| chr10:45393997 | G | C | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.350-1858G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393997 | |||||||
| chr10:45394091 | T | A | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1764T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394091 | |||||||
| chr10:45394136 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.350-1719C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394136 | |||||||
| chr10:45394137 | G | A | 3 | a0001c0001t0002g0305 a0001c0008t0002g0258 a0001c0008t0002g0259 |
3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.350-1718G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394137 | |||||||
| chr10:45394346 | C | A | 5 | a0001c0001t0001g0166 a0001c0004t0001g0038 a0001c0004t0001g0039 others(2): Show |
5 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-1509C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394346 | |||||||
| chr10:45394403 | G | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1452G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394403 | |||||||
| chr10:45394434 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1421C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394434 | |||||||
| chr10:45394538 | A | G | 69 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(66): Show |
74 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.350-1317A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394538 | |||||||
| chr10:45394635 | C | T | 5 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0034 others(2): Show |
7 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-1220C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394635 | |||||||
| chr10:45394674 | C | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1181C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394674 | |||||||
| chr10:45394736 | A | G | 1 | a0001c0011t0002g0257 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.350-1119A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394736 | |||||||
| chr10:45394763 | AAAAC | A | 7 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(4): Show |
8 | HG02809.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-1085_350-1082d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45394763 | ||||||
| chr10:45394826 | G | A | 69 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(66): Show |
74 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.350-1029G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394826 | |||||||
| chr10:45394846 | C | A | 20 | a0001c0001t0001g0192 a0001c0001t0001g0195 a0001c0001t0001g0197 others(17): Show |
23 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.350-1009C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394846 | |||||||
| chr10:45394909 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-946C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394909 | |||||||
| chr10:45394928 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.350-927A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394928 | |||||||
| chr10:45394984 | G | A | 69 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(66): Show |
74 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.350-871G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394984 | |||||||
| chr10:45394997 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(253): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.350-858T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394997 | |||||||
| chr10:45395211 | G | A | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.350-644G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395211 | |||||||
| chr10:45395314 | G | T | 44 | a0001c0001t0002g0304 a0001c0002t0002g0004 a0001c0002t0002g0026 others(41): Show |
48 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.350-541G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395314 | |||||||
| chr10:45395350 | G | T | 42 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(39): Show |
46 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.350-505G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395350 | |||||||
| chr10:45395373 | A | G | 43 | a0001c0001t0002g0304 a0001c0002t0002g0004 a0001c0002t0002g0026 others(40): Show |
47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-482A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395373 | |||||||
| chr10:45395389 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.350-466A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395389 | |||||||
| chr10:45395476 | G | C | 2 | a0002c0005t0003g0037 a0002c0005t0003g0114 |
2 | NA18942.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.350-379G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395476 | |||||||
| chr10:45395490 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.350-365A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395490 | |||||||
| chr10:45395492 | A | C | 1 | a0001c0009t0001g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.350-363A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395492 | |||||||
| chr10:45395540 | A | G | 69 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(66): Show |
74 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.350-315A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395540 | |||||||
| chr10:45395546 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0181 a0001c0001t0001g0182 |
6 | NA18944.hp2 NA18947.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-309G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395546 | |||||||
| chr10:45395606 | TA | T | 255 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(252): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.350-236delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45395606 | ||||||
| chr10:45395669 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.350-186G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395669 | |||||||
| chr10:45395713 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0190 a0001c0001t0001g0206 others(2): Show |
6 | HG02132.hp1 NA18945.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-142G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395713 | |||||||
| chr10:45395741 | A | G | 25 | a0001c0003t0001g0006 a0001c0003t0001g0016 a0001c0003t0001g0017 others(22): Show |
30 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.350-114A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395741 | |||||||
| chr10:45395767 | A | G | 12 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(9): Show |
13 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.350-88A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395767 | |||||||
| chr10:45395778 | G | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | NA19070.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.350-77G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395778 | |||||||
| chr10:45395805 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.350-50A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395805 | |||||||
| chr10:45395973 | A | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+37A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45395973 | |||||||
| chr10:45396018 | C | T | 1 | a0001c0002t0002g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.431+82C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396018 | |||||||
| chr10:45396036 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(144): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.431+100A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396036 | |||||||
| chr10:45396087 | CA | C | 3 | a0001c0001t0002g0305 a0001c0008t0002g0258 a0001c0008t0002g0259 |
3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.431+154delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45396087 | ||||||
| chr10:45396115 | CAA | C | 3 | a0001c0001t0001g0098 a0001c0001t0001g0167 a0005c0014t0001g0097 |
3 | NA18941.hp2 NA18978.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.431+180_431+181del others(2): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396115 | |||||||
| chr10:45396154 | C | G | 1 | a0001c0004t0001g0029 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.431+218C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396154 | |||||||
| chr10:45396162 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.431+226T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396162 | |||||||
| chr10:45396252 | T | C | 11 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(8): Show |
12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.431+316T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396252 | |||||||
| chr10:45396289 | T | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+353T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396289 | |||||||
| chr10:45396352 | G | GA | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(253): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.431+420dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45396352 | ||||||
| chr10:45396386 | G | A | 42 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(39): Show |
46 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.431+450G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396386 | |||||||
| chr10:45396396 | G | C | 13 | a0001c0003t0001g0056 a0001c0003t0001g0057 a0001c0003t0001g0059 others(10): Show |
13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.431+460G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396396 | |||||||
| chr10:45396397 | A | T | 13 | a0001c0003t0001g0056 a0001c0003t0001g0057 a0001c0003t0001g0059 others(10): Show |
13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.431+461A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396397 | |||||||
| chr10:45396441 | A | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0102 others(1): Show |
6 | HG00621.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+505A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396441 | |||||||
| chr10:45396492 | C | T | 1 | a0001c0008t0002g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.431+556C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396492 | |||||||
| chr10:45396572 | A | G | 13 | a0001c0003t0001g0056 a0001c0003t0001g0057 a0001c0003t0001g0059 others(10): Show |
13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.431+636A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396572 | |||||||
| chr10:45396711 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.431+775C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396711 | |||||||
| chr10:45396812 | C | T | 44 | a0001c0001t0001g0101 a0001c0001t0002g0304 a0001c0002t0002g0004 others(41): Show |
48 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.431+876C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396812 | |||||||
| chr10:45396950 | T | G | 7 | a0001c0001t0001g0115 a0001c0001t0001g0165 a0001c0001t0001g0166 others(4): Show |
7 | HG01192.hp1 HG01243.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+1014T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396950 | |||||||
| chr10:45396983 | A | G | 1 | a0001c0003t0001g0152 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.431+1047A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396983 | |||||||
| chr10:45396984 | T | C | 8 | a0001c0002t0002g0004 a0001c0002t0002g0262 a0001c0002t0002g0284 others(5): Show |
10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.431+1048T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396984 | |||||||
| chr10:45397109 | G | A | 16 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
17 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.431+1173G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397109 | |||||||
| chr10:45397210 | G | A | 2 | a0001c0001t0001g0116 a0001c0015t0001g0063 |
2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.431+1274G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397210 | |||||||
| chr10:45397295 | A | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+1359A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397295 | |||||||
| chr10:45397344 | C | G | 1 | a0001c0004t0001g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.431+1408C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397344 | |||||||
| chr10:45397369 | C | T | 1 | a0001c0007t0001g0109 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.431+1433C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397369 | |||||||
| chr10:45397413 | A | C | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431+1477A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397413 | |||||||
| chr10:45397516 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.431+1580G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397516 | |||||||
| chr10:45397528 | A | G | 8 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0142 others(5): Show |
10 | HG02145.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.431+1592A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397528 | |||||||
| chr10:45397929 | A | C | 44 | a0001c0001t0002g0304 a0001c0002t0002g0004 a0001c0002t0002g0026 others(41): Show |
48 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.431+1993A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397929 | |||||||
| chr10:45397931 | G | A | 4 | a0001c0004t0001g0038 a0001c0004t0001g0039 a0002c0005t0003g0040 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+1995G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397931 | |||||||
| chr10:45397960 | C | G | 42 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(39): Show |
46 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.431+2024C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397960 | |||||||
| chr10:45398068 | AG | A | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+2134delG | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45398068 | ||||||
| chr10:45398114 | T | G | 6 | a0001c0002t0002g0273 a0001c0002t0002g0274 a0001c0002t0002g0275 others(3): Show |
6 | NA18949.hp2 NA18959.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+2178T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398114 | |||||||
| chr10:45398151 | A | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+2215A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398151 | |||||||
| chr10:45398172 | G | A | 16 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
17 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.431+2236G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398172 | |||||||
| chr10:45398353 | G | A | 8 | a0001c0002t0002g0004 a0001c0002t0002g0262 a0001c0002t0002g0284 others(5): Show |
10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.431+2417G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398353 | |||||||
| chr10:45398410 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.431+2474A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398410 | |||||||
| chr10:45398558 | T | G | 44 | a0001c0001t0002g0304 a0001c0002t0002g0004 a0001c0002t0002g0026 others(41): Show |
48 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.431+2622T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398558 | |||||||
| chr10:45398616 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.431+2680C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398616 | |||||||
| chr10:45398761 | T | C | 6 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0034 others(3): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.431+2825T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398761 | |||||||
| chr10:45398803 | C | T | 1 | a0001c0007t0001g0133 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.431+2867C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398803 | |||||||
| chr10:45399180 | A | G | 1 | a0001c0001t0005g0043 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.431+3244A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45399180 | |||||||
| chr10:45399469 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.431+3533T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45399469 | |||||||
| chr10:45399496 | A | G | 6 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0003t0001g0175 others(3): Show |
6 | HG01258.hp1 HG01358.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+3560A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45399496 | |||||||
| chr10:45399751 | C | T | 5 | a0001c0003t0001g0018 a0001c0003t0001g0155 a0001c0003t0001g0156 others(2): Show |
6 | HG02486.hp1 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+3815C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45399751 | |||||||
| chr10:45400132 | T | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+4196T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400132 | |||||||
| chr10:45400142 | C | T | 1 | a0001c0001t0005g0096 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.431+4206C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400142 | |||||||
| chr10:45400325 | C | T | 7 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(4): Show |
8 | HG02809.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.431+4389C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400325 | |||||||
| chr10:45400326 | G | A | 13 | a0001c0003t0001g0056 a0001c0003t0001g0057 a0001c0003t0001g0059 others(10): Show |
13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.431+4390G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400326 | |||||||
| chr10:45400337 | C | T | 13 | a0001c0003t0001g0056 a0001c0003t0001g0057 a0001c0003t0001g0059 others(10): Show |
13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.431+4401C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400337 | |||||||
| chr10:45400400 | G | A | 2 | a0003c0010t0001g0244 a0003c0010t0001g0245 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.431+4464G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400400 | |||||||
| chr10:45400400 | GACCA | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+4468_431+4471d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45400400 | ||||||
| chr10:45400412 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.431+4476C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400412 | |||||||
| chr10:45400429 | A | G | 35 | a0001c0002t0002g0026 a0001c0002t0002g0027 a0001c0002t0002g0260 others(32): Show |
37 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.431+4493A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400429 | |||||||
| chr10:45400474 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG01361.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.431+4538C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400474 | |||||||
| chr10:45400521 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(90): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.431+4585C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400521 | |||||||
| chr10:45400579 | A | G | 1 | a0001c0003t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.431+4643A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400579 | |||||||
| chr10:45400759 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(253): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.431+4823G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400759 | |||||||
| chr10:45400803 | A | G | 69 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(66): Show |
74 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.431+4867A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400803 | |||||||
| chr10:45400869 | TATA | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+4936_431+4938d others(5): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45400869 | ||||||
| chr10:45401178 | A | G | 1 | a0001c0004t0001g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.431+5242A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401178 | |||||||
| chr10:45401223 | A | T | 1 | a0001c0002t0002g0291 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.431+5287A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401223 | |||||||
| chr10:45401279 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.431+5343T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401279 | |||||||
| chr10:45401358 | C | T | 4 | a0001c0004t0001g0038 a0001c0004t0001g0039 a0002c0005t0003g0040 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+5422C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401358 | |||||||
| chr10:45401359 | T | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+5423T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401359 | |||||||
| chr10:45401360 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+5424C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401360 | |||||||
| chr10:45401413 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02071.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.431+5477G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401413 | |||||||
| chr10:45401437 | T | C | 1 | a0001c0002t0006g0289 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.431+5501T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401437 | |||||||
| chr10:45401675 | G | A | 1 | a0001c0002t0002g0273 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.431+5739G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401675 | |||||||
| chr10:45401707 | A | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(265): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.431+5771A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401707 | |||||||
| chr10:45401825 | T | G | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.431+5889T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401825 | |||||||
| chr10:45401858 | G | A | 3 | a0001c0001t0002g0305 a0001c0008t0002g0258 a0001c0008t0002g0259 |
3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.431+5922G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401858 | |||||||
| chr10:45402004 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.431+6068G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402004 | |||||||
| chr10:45402036 | G | A | 2 | a0001c0001t0001g0079 a0001c0004t0001g0009 |
3 | HG02056.hp2 HG02083.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.431+6100G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402036 | |||||||
| chr10:45402072 | G | T | 26 | a0001c0003t0001g0006 a0001c0003t0001g0016 a0001c0003t0001g0017 others(23): Show |
31 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.431+6136G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402072 | |||||||
| chr10:45402073 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.431+6137C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402073 | |||||||
| chr10:45402086 | C | CA | 15 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0128 others(12): Show |
16 | HG01975.hp1 HG02040.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.431+6170dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45402086 | ||||||
| chr10:45402086 | C | CAA | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(188): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.431+6169_431+6170d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45402086 | ||||||
| chr10:45402086 | C | CAAA | 37 | a0001c0001t0001g0022 a0001c0001t0001g0117 a0001c0001t0001g0135 others(34): Show |
39 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.431+6168_431+6170d others(5): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45402086 | ||||||
| chr10:45402086 | CAAAAAA | C | 5 | a0001c0003t0001g0018 a0001c0003t0001g0155 a0001c0003t0001g0156 others(2): Show |
6 | HG02486.hp1 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+6165_431+6170d others(8): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45402086 | ||||||
| chr10:45402299 | T | C | 1 | a0001c0019t0001g0211 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.431+6363T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402299 | |||||||
| chr10:45402409 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+6473C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402409 | |||||||
| chr10:45402413 | G | A | 42 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(39): Show |
46 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.431+6477G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402413 | |||||||
| chr10:45402453 | GCATCTCG others(4): Show |
G | 1 | a0001c0001t0001g0195 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.431+6520_431+6530d others(13): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45402453 | ||||||
| chr10:45402601 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.431+6665G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402601 | |||||||
| chr10:45402693 | C | G | 1 | a0001c0001t0001g0241 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.431+6757C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402693 | |||||||
| chr10:45402701 | A | G | 2 | a0001c0002t0002g0267 a0001c0002t0002g0281 |
2 | HG01433.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.431+6765A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402701 | |||||||
| chr10:45402709 | ACT | A | 5 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | NA18954.hp1 NA18955.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.431+6776_431+6777d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45402709 | ||||||
| chr10:45402792 | C | T | 1 | a0001c0021t0006g0290 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.431+6856C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402792 | |||||||
| chr10:45402908 | C | A | 67 | a0001c0001t0001g0166 a0001c0001t0001g0183 a0001c0001t0001g0184 others(64): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.431+6972C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402908 | |||||||
| chr10:45402910 | C | G | 11 | a0001c0001t0001g0025 a0001c0001t0001g0170 a0001c0001t0001g0171 others(8): Show |
12 | HG00621.hp1 HG01106.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.431+6974C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402910 | |||||||
| chr10:45403034 | T | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+7098T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403034 | |||||||
| chr10:45403043 | G | A | 2 | a0001c0008t0002g0258 a0001c0008t0002g0259 |
2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.431+7107G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403043 | |||||||
| chr10:45403046 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.431+7110A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403046 | |||||||
| chr10:45403071 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0181 a0001c0001t0001g0182 |
6 | NA18944.hp2 NA18947.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+7135G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403071 | |||||||
| chr10:45403216 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+7280C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403216 | |||||||
| chr10:45403320 | C | G | 5 | a0001c0001t0001g0072 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.431+7384C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403320 | |||||||
| chr10:45403465 | G | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0036 others(18): Show |
22 | HG01069.hp1 HG02071.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.431+7529G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403465 | |||||||
| chr10:45403587 | G | A | 1 | a0001c0003t0001g0153 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.431+7651G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403587 | |||||||
| chr10:45403811 | G | A | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+7875G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403811 | |||||||
| chr10:45403901 | A | G | 1 | a0001c0002t0002g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.431+7965A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403901 | |||||||
| chr10:45403934 | C | T | 7 | a0001c0001t0001g0015 a0001c0004t0001g0131 a0001c0007t0001g0015 others(4): Show |
7 | NA18941.hp1 NA18949.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+7998C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403934 | |||||||
| chr10:45404147 | T | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-8044T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45404147 | |||||||
| chr10:45404255 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.432-7936A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45404255 | |||||||
| chr10:45404660 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.432-7531C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45404660 | |||||||
| chr10:45404885 | A | T | 1 | a0001c0001t0001g0116 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.432-7306A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45404885 | |||||||
| chr10:45404979 | A | G | 1 | a0001c0002t0002g0267 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.432-7212A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45404979 | |||||||
| chr10:45405042 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-7149C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405042 | |||||||
| chr10:45405244 | G | A | 5 | a0001c0001t0001g0072 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.432-6947G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405244 | |||||||
| chr10:45405281 | G | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(218): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.432-6910G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405281 | |||||||
| chr10:45405369 | C | T | 1 | a0001c0002t0007g0306 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.432-6822C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405369 | |||||||
| chr10:45405384 | T | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0227 others(1): Show |
7 | HG01255.hp2 HG01346.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.432-6807T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405384 | |||||||
| chr10:45405422 | A | G | 3 | a0001c0002t0002g0308 a0001c0002t0002g0309 a0001c0002t0002g0310 |
3 | HG01243.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.432-6769A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405422 | |||||||
| chr10:45405523 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.432-6668G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405523 | |||||||
| chr10:45405588 | A | G | 4 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0034 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.432-6603A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405588 | |||||||
| chr10:45405593 | T | A | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-6598T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405593 | |||||||
| chr10:45405641 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(180): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.432-6550A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405641 | |||||||
| chr10:45405653 | C | T | 13 | a0001c0003t0001g0056 a0001c0003t0001g0057 a0001c0003t0001g0059 others(10): Show |
13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.432-6538C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405653 | |||||||
| chr10:45405739 | C | CTTT | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-6439_432-6437d others(5): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45405739 | ||||||
| chr10:45405739 | CT | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(156): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.432-6437delT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45405739 | ||||||
| chr10:45405739 | CTT | C | 23 | a0001c0001t0001g0190 a0001c0001t0002g0305 a0001c0002t0002g0004 others(20): Show |
25 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.432-6438_432-6437d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45405739 | ||||||
| chr10:45406009 | G | T | 1 | a0001c0001t0001g0195 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.432-6182G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406009 | |||||||
| chr10:45406234 | G | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0004t0001g0038 others(3): Show |
6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-5957G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406234 | |||||||
| chr10:45406267 | C | A | 5 | a0001c0001t0001g0166 a0001c0004t0001g0038 a0001c0004t0001g0039 others(2): Show |
5 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.432-5924C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406267 | |||||||
| chr10:45406268 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0134 |
2 | NA19058.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.432-5923G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406268 | |||||||
| chr10:45406395 | G | A | 3 | a0001c0003t0001g0155 a0001c0003t0001g0164 a0001c0006t0009g0154 |
3 | HG02486.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.432-5796G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406395 | |||||||
| chr10:45406400 | A | G | 1 | a0001c0004t0001g0014 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.432-5791A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406400 | |||||||
| chr10:45406423 | T | A | 31 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0002g0304 others(28): Show |
33 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.432-5768T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406423 | |||||||
| chr10:45406492 | G | A | 13 | a0001c0003t0001g0056 a0001c0003t0001g0057 a0001c0003t0001g0059 others(10): Show |
13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.432-5699G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406492 | |||||||
| chr10:45406607 | A | G | 16 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
17 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.432-5584A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406607 | |||||||
| chr10:45406671 | T | C | 48 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(45): Show |
51 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.432-5520T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406671 | |||||||
| chr10:45406959 | T | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG02080.hp1 NA18975.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.432-5232T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406959 | |||||||
| chr10:45407064 | T | C | 2 | a0002c0005t0003g0122 a0002c0005t0003g0123 |
2 | NA18998.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.432-5127T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407064 | |||||||
| chr10:45407089 | G | T | 23 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(20): Show |
24 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.432-5102G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407089 | |||||||
| chr10:45407257 | C | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | NA18961.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.432-4934C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407257 | |||||||
| chr10:45407362 | T | A | 23 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(20): Show |
24 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.432-4829T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407362 | |||||||
| chr10:45407391 | CT | C | 61 | a0001c0001t0001g0101 a0001c0001t0001g0181 a0001c0002t0002g0026 others(58): Show |
68 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.432-4789delT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45407391 | ||||||
| chr10:45407400 | T | A | 1 | a0001c0002t0006g0289 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.432-4791T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407400 | |||||||
| chr10:45407402 | T | C | 5 | a0001c0001t0001g0081 a0001c0001t0002g0304 a0001c0002t0002g0269 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.432-4789T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407402 | |||||||
| chr10:45407403 | C | T | 19 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(16): Show |
20 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.432-4788C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407403 | |||||||
| chr10:45407404 | C | T | 23 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0183 others(20): Show |
24 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.432-4787C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407404 | |||||||
| chr10:45407438 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.432-4753C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407438 | |||||||
| chr10:45407464 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(265): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.432-4727A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407464 | |||||||
| chr10:45407490 | A | G | 1 | a0001c0002t0002g0296 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.432-4701A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407490 | |||||||
| chr10:45407587 | C | T | 3 | a0001c0004t0001g0007 a0001c0004t0001g0065 a0001c0004t0001g0066 |
4 | HG02258.hp1 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.432-4604C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407587 | |||||||
| chr10:45407785 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.432-4406C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407785 | |||||||
| chr10:45407905 | T | G | 1 | a0001c0002t0002g0269 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.432-4286T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407905 | |||||||
| chr10:45407919 | G | A | 24 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0107 others(21): Show |
26 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.432-4272G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407919 | |||||||
| chr10:45408230 | T | C | 2 | a0001c0011t0002g0256 a0001c0011t0002g0257 |
2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.432-3961T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408230 | |||||||
| chr10:45408231 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.432-3960G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408231 | |||||||
| chr10:45408239 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(137): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.432-3952C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408239 | |||||||
| chr10:45408318 | T | A | 20 | a0001c0001t0002g0305 a0001c0002t0002g0004 a0001c0002t0002g0262 others(17): Show |
22 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.432-3873T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408318 | |||||||
| chr10:45408539 | G | T | 20 | a0001c0001t0002g0305 a0001c0002t0002g0004 a0001c0002t0002g0262 others(17): Show |
22 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.432-3652G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408539 | |||||||
| chr10:45408568 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(137): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.432-3623A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408568 | |||||||
| chr10:45408578 | G | T | 4 | a0001c0004t0001g0038 a0001c0004t0001g0039 a0002c0005t0003g0040 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.432-3613G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408578 | |||||||
| chr10:45408593 | C | T | 1 | a0001c0004t0001g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.432-3598C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408593 | |||||||
| chr10:45408613 | G | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0101 |
2 | HG02965.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.432-3578G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408613 | |||||||
| chr10:45408817 | C | T | 1 | a0002c0005t0003g0240 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.432-3374C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408817 | |||||||
| chr10:45409266 | G | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(169): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.432-2925G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409266 | |||||||
| chr10:45409271 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.432-2920C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409271 | |||||||
| chr10:45409304 | T | C | 4 | a0001c0004t0001g0038 a0001c0004t0001g0039 a0002c0005t0003g0040 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.432-2887T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409304 | |||||||
| chr10:45409323 | A | ACT | 254 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(251): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.432-2867_432-2866d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409323 | ||||||
| chr10:45409411 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.432-2780T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409411 | |||||||
| chr10:45409432 | C | T | 1 | a0002c0005t0003g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.432-2759C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409432 | |||||||
| chr10:45409509 | G | GTC | 86 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0064 others(83): Show |
95 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.432-2658_432-2657d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409509 | ||||||
| chr10:45409509 | G | GTCTC | 14 | a0001c0001t0001g0166 a0001c0001t0001g0235 a0001c0002t0002g0291 others(11): Show |
14 | HG01123.hp1 HG01192.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.432-2660_432-2657d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409509 | ||||||
| chr10:45409509 | G | GTCTCTC | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(96): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.432-2662_432-2657d others(8): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409509 | ||||||
| chr10:45409509 | G | GTCTCTCT others(1): Show |
5 | a0001c0001t0001g0013 a0001c0001t0001g0127 a0001c0001t0001g0212 others(2): Show |
6 | HG01070.hp1 HG01071.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-2664_432-2657d others(10): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409509 | ||||||
| chr10:45409509 | G | GTCTCTCT others(3): Show |
2 | a0001c0001t0001g0044 a0001c0001t0001g0116 |
2 | HG02886.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.432-2666_432-2657d others(12): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409509 | ||||||
| chr10:45409509 | GTCTC | G | 11 | a0001c0003t0001g0056 a0001c0003t0001g0059 a0001c0003t0004g0048 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.432-2660_432-2657d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409509 | ||||||
| chr10:45409513 | C | G | 2 | a0002c0005t0003g0040 a0002c0005t0003g0041 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.432-2678C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409513 | |||||||
| chr10:45409527 | C | CTCTCTCT others(5): Show |
1 | a0001c0009t0001g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.432-2657_432-2656i others(14): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409527 | ||||||
| chr10:45409569 | TTCTC | T | 5 | a0001c0001t0008g0254 a0001c0004t0001g0038 a0001c0004t0001g0039 others(2): Show |
5 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.432-2606_432-2603d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409569 | ||||||
| chr10:45409593 | CTCTG | C | 20 | a0001c0001t0002g0305 a0001c0002t0002g0004 a0001c0002t0002g0262 others(17): Show |
22 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.432-2594_432-2591d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409593 | ||||||
| chr10:45409662 | C | T | 11 | a0001c0003t0001g0056 a0001c0003t0001g0059 a0001c0003t0004g0048 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.432-2529C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409662 | |||||||
| chr10:45409788 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.432-2403G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409788 | |||||||
| chr10:45409877 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0102 |
3 | HG01256.hp1 HG01258.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.432-2314G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409877 | |||||||
| chr10:45410076 | G | A | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.432-2115G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410076 | |||||||
| chr10:45410097 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.432-2094T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410097 | |||||||
| chr10:45410122 | A | G | 1 | a0001c0021t0006g0290 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.432-2069A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410122 | |||||||
| chr10:45410240 | G | A | 2 | a0001c0001t0002g0304 a0001c0008t0002g0258 |
2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.432-1951G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410240 | |||||||
| chr10:45410274 | G | T | 2 | a0001c0001t0001g0068 a0001c0015t0001g0063 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.432-1917G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410274 | |||||||
| chr10:45410352 | A | G | 8 | a0001c0002t0002g0004 a0001c0002t0002g0262 a0001c0002t0002g0284 others(5): Show |
10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.432-1839A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410352 | |||||||
| chr10:45410446 | T | C | 11 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(8): Show |
12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.432-1745T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410446 | |||||||
| chr10:45410551 | C | A | 1 | a0001c0006t0009g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.432-1640C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410551 | |||||||
| chr10:45410584 | A | C | 1 | a0001c0021t0006g0290 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.432-1607A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410584 | |||||||
| chr10:45410926 | G | C | 1 | a0002c0005t0003g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.432-1265G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410926 | |||||||
| chr10:45411064 | T | C | 2 | a0001c0011t0002g0256 a0001c0011t0002g0257 |
2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.432-1127T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411064 | |||||||
| chr10:45411125 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(69): Show |
82 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.432-1066G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411125 | |||||||
| chr10:45411171 | A | C | 8 | a0001c0002t0002g0004 a0001c0002t0002g0262 a0001c0002t0002g0284 others(5): Show |
10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.432-1020A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411171 | |||||||
| chr10:45411245 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.432-946G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411245 | |||||||
| chr10:45411516 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0162 |
2 | HG01099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.432-675C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411516 | |||||||
| chr10:45411688 | G | T | 26 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0107 others(23): Show |
28 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.432-503G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411688 | |||||||
| chr10:45411754 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.432-437C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411754 | |||||||
| chr10:45411839 | C | A | 1 | a0001c0001t0001g0116 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.432-352C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411839 | |||||||
| chr10:45411914 | A | G | 11 | a0001c0007t0001g0109 a0002c0005t0003g0037 a0002c0005t0003g0114 others(8): Show |
11 | HG02040.hp1 HG02080.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.432-277A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411914 | |||||||
| chr10:45411952 | A | G | 36 | a0001c0001t0001g0067 a0001c0001t0001g0158 a0001c0002t0002g0026 others(33): Show |
39 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.432-239A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411952 | |||||||
| chr10:45412006 | G | C | 42 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0064 others(39): Show |
46 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.432-185G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45412006 | |||||||
| chr10:45412078 | G | A | 10 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(7): Show |
12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.432-113G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45412078 | |||||||
| chr10:45412088 | A | G | 1 | a0001c0003t0001g0152 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.432-103A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45412088 | |||||||
| chr10:45412106 | G | A | 1 | a0001c0006t0001g0005 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.432-85G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45412106 | |||||||
| chr10:45412314 | G | A | 1 | a0001c0003t0001g0149 | 1 | HG02717.hp2 | splice_donor_variant&intron_variant | HIGH | c.554+1G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412314 | |||||||
| chr10:45412474 | G | A | 1 | a0001c0002t0002g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.554+161G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412474 | |||||||
| chr10:45412526 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.554+213A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412526 | |||||||
| chr10:45412730 | G | T | 1 | a0001c0001t0001g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.554+417G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412730 | |||||||
| chr10:45412768 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.554+455T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412768 | |||||||
| chr10:45412954 | G | A | 3 | a0001c0003t0001g0155 a0001c0003t0001g0164 a0001c0006t0009g0154 |
3 | HG02486.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.554+641G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412954 | |||||||
| chr10:45412977 | T | C | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.554+664T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412977 | |||||||
| chr10:45413312 | T | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(251): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.554+999T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413312 | |||||||
| chr10:45413314 | G | A | 4 | a0001c0004t0001g0038 a0001c0004t0001g0039 a0002c0005t0003g0040 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+1001G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413314 | |||||||
| chr10:45413546 | C | T | 1 | a0001c0004t0001g0008 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.554+1233C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413546 | |||||||
| chr10:45413569 | C | T | 7 | a0001c0002t0002g0004 a0001c0002t0002g0262 a0001c0002t0002g0284 others(4): Show |
9 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+1256C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413569 | |||||||
| chr10:45413570 | A | G | 8 | a0001c0002t0002g0004 a0001c0002t0002g0262 a0001c0002t0002g0284 others(5): Show |
10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.554+1257A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413570 | |||||||
| chr10:45413644 | A | G | 10 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(7): Show |
12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.554+1331A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413644 | |||||||
| chr10:45413656 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0022 others(64): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.554+1343C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413656 | |||||||
| chr10:45413698 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.554+1385C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413698 | |||||||
| chr10:45413798 | AACAG | A | 20 | a0001c0001t0002g0305 a0001c0002t0002g0004 a0001c0002t0002g0262 others(17): Show |
22 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.554+1494_554+1497d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45413798 | ||||||
| chr10:45413807 | A | C | 1 | a0001c0001t0001g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.554+1494A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413807 | |||||||
| chr10:45413826 | A | G | 11 | a0001c0003t0001g0056 a0001c0003t0001g0059 a0001c0003t0004g0048 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.554+1513A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413826 | |||||||
| chr10:45413913 | C | G | 4 | a0001c0004t0001g0038 a0001c0004t0001g0039 a0002c0005t0003g0040 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+1600C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413913 | |||||||
| chr10:45413987 | T | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.554+1674T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413987 | |||||||
| chr10:45414120 | G | A | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0002g0304 others(1): Show |
4 | HG01192.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+1807G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414120 | |||||||
| chr10:45414187 | A | G | 3 | a0001c0002t0002g0308 a0001c0002t0002g0309 a0001c0002t0002g0310 |
3 | HG01243.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.554+1874A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414187 | |||||||
| chr10:45414193 | C | T | 11 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(8): Show |
13 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.554+1880C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414193 | |||||||
| chr10:45414398 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2085A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414398 | |||||||
| chr10:45414400 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2087G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414400 | |||||||
| chr10:45414403 | G | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2090G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414403 | |||||||
| chr10:45414404 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2091G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414404 | |||||||
| chr10:45414409 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2096C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414409 | |||||||
| chr10:45414413 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2100C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414413 | |||||||
| chr10:45414421 | T | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2108T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414421 | |||||||
| chr10:45414436 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2123T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414436 | |||||||
| chr10:45414444 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2131G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414444 | |||||||
| chr10:45414452 | T | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2139T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414452 | |||||||
| chr10:45414459 | A | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2146A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414459 | |||||||
| chr10:45414461 | G | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2148G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414461 | |||||||
| chr10:45414463 | T | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2150T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414463 | |||||||
| chr10:45414468 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2155C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414468 | |||||||
| chr10:45414472 | A | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2159A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414472 | |||||||
| chr10:45414475 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2162C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414475 | |||||||
| chr10:45414476 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2163A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414476 | |||||||
| chr10:45414484 | C | T | 20 | a0001c0001t0002g0305 a0001c0002t0002g0004 a0001c0002t0002g0262 others(17): Show |
22 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.554+2171C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414484 | |||||||
| chr10:45414521 | G | A | 1 | a0001c0011t0002g0256 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.554+2208G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414521 | |||||||
| chr10:45414585 | A | G | 8 | a0001c0002t0002g0004 a0001c0002t0002g0262 a0001c0002t0002g0284 others(5): Show |
10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.554+2272A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414585 | |||||||
| chr10:45414642 | T | G | 3 | a0001c0011t0002g0256 a0001c0011t0002g0257 a0001c0015t0001g0063 |
3 | HG00741.hp2 HG01192.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.554+2329T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414642 | |||||||
| chr10:45414822 | A | G | 7 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(4): Show |
8 | HG02109.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.554+2509A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414822 | |||||||
| chr10:45414840 | A | G | 1 | a0001c0002t0002g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.554+2527A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414840 | |||||||
| chr10:45414894 | T | C | 2 | a0001c0003t0001g0155 a0001c0006t0009g0154 |
2 | HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.554+2581T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414894 | |||||||
| chr10:45414952 | T | A | 2 | a0001c0001t0001g0253 a0001c0001t0008g0254 |
2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.554+2639T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414952 | |||||||
| chr10:45414992 | G | A | 2 | a0001c0004t0001g0008 a0001c0004t0001g0069 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.554+2679G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414992 | |||||||
| chr10:45415099 | G | T | 2 | a0002c0005t0003g0040 a0002c0005t0003g0041 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.554+2786G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415099 | |||||||
| chr10:45415148 | T | C | 8 | a0001c0002t0002g0004 a0001c0002t0002g0262 a0001c0002t0002g0284 others(5): Show |
10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.554+2835T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415148 | |||||||
| chr10:45415328 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.554+3015C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415328 | |||||||
| chr10:45415581 | T | TA | 158 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(155): Show |
174 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.554+3277dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45415581 | ||||||
| chr10:45415583 | A | AT | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0022 others(67): Show |
80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.554+3270_554+3271i others(3): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415583 | |||||||
| chr10:45415599 | C | T | 4 | a0001c0003t0001g0006 a0001c0003t0001g0033 a0001c0003t0001g0034 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.554+3286C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415599 | |||||||
| chr10:45415603 | A | G | 4 | a0001c0004t0001g0038 a0001c0004t0001g0039 a0002c0005t0003g0040 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+3290A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415603 | |||||||
| chr10:45415653 | G | A | 14 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0165 others(11): Show |
16 | HG01192.hp1 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.554+3340G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415653 | |||||||
| chr10:45415690 | C | A | 1 | a0001c0021t0006g0290 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.554+3377C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415690 | |||||||
| chr10:45415844 | G | A | 10 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(7): Show |
12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.554+3531G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415844 | |||||||
| chr10:45415871 | T | C | 1 | a0001c0004t0001g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.554+3558T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415871 | |||||||
| chr10:45416240 | A | C | 7 | a0001c0002t0002g0004 a0001c0002t0002g0262 a0001c0002t0002g0284 others(4): Show |
9 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+3927A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416240 | |||||||
| chr10:45416354 | A | G | 1 | a0001c0021t0006g0290 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.554+4041A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416354 | |||||||
| chr10:45416383 | A | G | 5 | a0001c0001t0001g0210 a0001c0001t0001g0228 a0001c0001t0001g0229 others(2): Show |
5 | NA18939.hp2 NA18944.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.554+4070A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416383 | |||||||
| chr10:45416438 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.554+4125C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416438 | |||||||
| chr10:45416516 | A | G | 2 | a0001c0001t0002g0304 a0001c0008t0002g0258 |
2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.554+4203A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416516 | |||||||
| chr10:45416671 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.554+4358G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416671 | |||||||
| chr10:45416706 | GATGA | G | 24 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0107 others(21): Show |
26 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.554+4397_554+4400d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45416706 | ||||||
| chr10:45416761 | A | G | 3 | a0001c0003t0001g0155 a0001c0003t0001g0164 a0001c0006t0009g0154 |
3 | HG02486.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.554+4448A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416761 | |||||||
| chr10:45416789 | T | C | 24 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0107 others(21): Show |
26 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.554+4476T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416789 | |||||||
| chr10:45416817 | GGATGGAT others(20): Show |
G | 5 | a0001c0001t0001g0166 a0001c0004t0001g0038 a0001c0004t0001g0039 others(2): Show |
5 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.554+4520_554+4546d others(29): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45416817 | ||||||
| chr10:45416987 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0106 |
3 | NA18983.hp2 NA18991.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.554+4674A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416987 | |||||||
| chr10:45416991 | T | A | 1 | a0001c0020t0001g0221 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.554+4678T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416991 | |||||||
| chr10:45417056 | G | A | 7 | a0001c0002t0002g0004 a0001c0002t0002g0262 a0001c0002t0002g0284 others(4): Show |
9 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+4743G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417056 | |||||||
| chr10:45417323 | T | G | 27 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0107 others(24): Show |
29 | HG00099.hp1 HG00323.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.554+5010T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417323 | |||||||
| chr10:45417700 | A | G | 10 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(7): Show |
12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.554+5387A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417700 | |||||||
| chr10:45417728 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.554+5415G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417728 | |||||||
| chr10:45417872 | A | G | 10 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(7): Show |
12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.554+5559A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417872 | |||||||
| chr10:45417879 | C | T | 3 | a0001c0011t0002g0256 a0001c0011t0002g0257 a0001c0015t0001g0063 |
3 | HG00741.hp2 HG01192.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.554+5566C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417879 | |||||||
| chr10:45417964 | C | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0158 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+5651C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417964 | |||||||
| chr10:45418288 | G | A | 2 | a0001c0001t0005g0043 a0001c0001t0005g0096 |
2 | HG01346.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.555-5753G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45418288 | |||||||
| chr10:45418429 | G | A | 1 | a0001c0002t0002g0270 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.555-5612G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45418429 | |||||||
| chr10:45418437 | C | CT | 10 | a0001c0003t0001g0056 a0001c0003t0001g0059 a0001c0003t0004g0048 others(7): Show |
10 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.555-5603dupT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45418437 | ||||||
| chr10:45418690 | A | C | 10 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(7): Show |
12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-5351A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45418690 | |||||||
| chr10:45418691 | G | C | 10 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0168 others(7): Show |
12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-5350G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45418691 | |||||||
| chr10:45418839 | G | C | 1 | a0001c0002t0002g0276 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.555-5202G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45418839 | |||||||
| chr10:45419055 | C | T | 1 | a0001c0002t0002g0295 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.555-4986C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419055 | |||||||
| chr10:45419079 | C | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(201): Show |
226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.555-4962C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419079 | |||||||
| chr10:45419250 | C | T | 1 | a0001c0006t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.555-4791C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419250 | |||||||
| chr10:45419296 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(142): Show |
161 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.555-4745G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419296 | |||||||
| chr10:45419302 | G | C | 2 | a0001c0001t0002g0305 a0001c0006t0001g0143 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.555-4739G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419302 | |||||||
| chr10:45419305 | CG | C | 93 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0047 others(90): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.555-4729delG | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45419305 | ||||||
| chr10:45419324 | G | A | 13 | a0001c0001t0001g0064 a0001c0001t0001g0168 a0001c0004t0001g0007 others(10): Show |
16 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.555-4717G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419324 | |||||||
| chr10:45419426 | A | G | 4 | a0001c0002t0002g0308 a0001c0003t0001g0155 a0001c0003t0001g0164 others(1): Show |
4 | HG02970.hp1 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-4615A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419426 | |||||||
| chr10:45419455 | G | A | 2 | a0001c0004t0001g0038 a0001c0004t0001g0069 |
2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.555-4586G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419455 | |||||||
| chr10:45419471 | G | C | 1 | a0001c0001t0001g0204 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.555-4570G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419471 | |||||||
| chr10:45419666 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.555-4375G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419666 | |||||||
| chr10:45419707 | C | A | 12 | a0001c0001t0001g0064 a0001c0001t0001g0070 a0001c0001t0001g0168 others(9): Show |
14 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.555-4334C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419707 | |||||||
| chr10:45419710 | G | T | 11 | a0001c0001t0001g0064 a0001c0001t0001g0168 a0001c0004t0001g0007 others(8): Show |
13 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.555-4331G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419710 | |||||||
| chr10:45419737 | T | TCAAAAGA others(6): Show |
252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.555-4298_555-4297i others(15): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45419737 | ||||||
| chr10:45419804 | G | C | 17 | a0001c0001t0001g0064 a0001c0001t0001g0070 a0001c0001t0001g0168 others(14): Show |
21 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.555-4237G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419804 | |||||||
| chr10:45419816 | A | C | 17 | a0001c0006t0001g0005 a0002c0005t0003g0037 a0002c0005t0003g0040 others(14): Show |
18 | HG01243.hp2 HG01884.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.555-4225A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419816 | |||||||
| chr10:45419871 | G | C | 11 | a0001c0001t0001g0064 a0001c0001t0001g0168 a0001c0004t0001g0007 others(8): Show |
13 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.555-4170G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419871 | |||||||
| chr10:45419886 | G | C | 1 | a0001c0006t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.555-4155G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419886 | |||||||
| chr10:45419892 | A | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(235): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.555-4149A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419892 | |||||||
| chr10:45419923 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.555-4118G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419923 | |||||||
| chr10:45420206 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.555-3835G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420206 | |||||||
| chr10:45420245 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.555-3796C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420245 | |||||||
| chr10:45420304 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.555-3737G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420304 | |||||||
| chr10:45420321 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0070 others(1): Show |
5 | HG01070.hp1 HG01071.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-3720A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420321 | |||||||
| chr10:45420374 | C | G | 1 | a0001c0020t0001g0221 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.555-3667C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420374 | |||||||
| chr10:45420398 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0006t0009g0154 |
3 | HG02486.hp1 HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.555-3643G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420398 | |||||||
| chr10:45420407 | C | T | 1 | a0001c0021t0006g0290 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.555-3634C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420407 | |||||||
| chr10:45420477 | C | A | 1 | a0001c0001t0001g0196 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.555-3564C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420477 | |||||||
| chr10:45420493 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(195): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.555-3548C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420493 | |||||||
| chr10:45420540 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.555-3501C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420540 | |||||||
| chr10:45420680 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.555-3361C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420680 | |||||||
| chr10:45420778 | T | A | 14 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0107 others(11): Show |
15 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.555-3263T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420778 | |||||||
| chr10:45420788 | G | A | 14 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0107 others(11): Show |
15 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.555-3253G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420788 | |||||||
| chr10:45420818 | G | A | 2 | a0001c0002t0002g0276 a0001c0002t0002g0296 |
2 | HG00099.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.555-3223G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420818 | |||||||
| chr10:45420837 | G | A | 4 | a0001c0002t0002g0309 a0001c0002t0002g0310 a0001c0003t0001g0016 others(1): Show |
5 | HG01243.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-3204G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420837 | |||||||
| chr10:45420901 | C | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0214 |
2 | NA18946.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.555-3140C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420901 | |||||||
| chr10:45420902 | G | C | 18 | a0001c0001t0001g0165 a0001c0006t0001g0145 a0002c0005t0003g0037 others(15): Show |
18 | HG01243.hp2 HG02040.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.555-3139G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420902 | |||||||
| chr10:45421386 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(241): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.555-2655T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421386 | |||||||
| chr10:45421465 | C | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(241): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.555-2576C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421465 | |||||||
| chr10:45421466 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0070 others(1): Show |
5 | HG01070.hp1 HG01071.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-2575G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421466 | |||||||
| chr10:45421639 | A | G | 1 | a0001c0002t0002g0293 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.555-2402A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421639 | |||||||
| chr10:45421644 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(239): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.555-2397A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421644 | |||||||
| chr10:45421669 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(210): Show |
238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.555-2372T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421669 | |||||||
| chr10:45421751 | A | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0061 others(15): Show |
19 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.555-2290A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421751 | |||||||
| chr10:45421868 | T | C | 18 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0061 others(15): Show |
19 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.555-2173T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421868 | |||||||
| chr10:45421895 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.555-2146C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421895 | |||||||
| chr10:45421928 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(207): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.555-2113C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421928 | |||||||
| chr10:45422033 | G | A | 4 | a0001c0002t0002g0309 a0001c0002t0002g0310 a0001c0003t0001g0016 others(1): Show |
5 | HG01243.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-2008G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422033 | |||||||
| chr10:45422094 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0212 |
3 | HG01361.hp2 HG01516.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.555-1947T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422094 | |||||||
| chr10:45422293 | C | G | 33 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0061 others(30): Show |
34 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.555-1748C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422293 | |||||||
| chr10:45422299 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.555-1742G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422299 | |||||||
| chr10:45422379 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.555-1662G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422379 | |||||||
| chr10:45422409 | C | A | 1 | a0001c0006t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.555-1632C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422409 | |||||||
| chr10:45422628 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(255): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.555-1413A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422628 | |||||||
| chr10:45422645 | C | T | 15 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0002g0304 others(12): Show |
15 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.555-1396C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422645 | |||||||
| chr10:45422646 | G | A | 1 | a0001c0002t0002g0282 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.555-1395G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422646 | |||||||
| chr10:45422831 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(255): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.555-1210C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422831 | |||||||
| chr10:45422932 | C | T | 21 | a0001c0001t0001g0192 a0001c0001t0001g0253 a0001c0003t0001g0057 others(18): Show |
25 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(22): Show |
intron_variant | MODIFIER | c.555-1109C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422932 | |||||||
| chr10:45423033 | G | A | 1 | a0001c0006t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.555-1008G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423033 | |||||||
| chr10:45423051 | C | T | 1 | a0001c0004t0001g0014 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.555-990C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423051 | |||||||
| chr10:45423264 | G | A | 1 | a0001c0003t0001g0142 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.555-777G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423264 | |||||||
| chr10:45423283 | A | G | 1 | a0001c0006t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.555-758A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423283 | |||||||
| chr10:45423366 | C | T | 1 | a0001c0001t0001g0021 | 2 | NA18945.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.555-675C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423366 | |||||||
| chr10:45423567 | G | A | 1 | a0001c0002t0002g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.555-474G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423567 | |||||||
| chr10:45423609 | A | G | 33 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0061 others(30): Show |
34 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.555-432A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423609 | |||||||
| chr10:45423628 | A | C | 1 | a0001c0002t0002g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.555-413A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423628 | |||||||
| chr10:45423666 | G | T | 1 | a0001c0008t0002g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.555-375G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423666 | |||||||
| chr10:45423668 | C | G | 1 | a0001c0001t0001g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.555-373C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423668 | |||||||
| chr10:45423686 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.555-355C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423686 | |||||||
| chr10:45423711 | G | C | 33 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0061 others(30): Show |
34 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.555-330G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423711 | |||||||
| chr10:45423885 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.555-156G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423885 | |||||||
| chr10:45423941 | G | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0070 others(8): Show |
12 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.555-100G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423941 | |||||||
| chr10:45423945 | G | A | 4 | a0001c0002t0002g0309 a0001c0002t0002g0310 a0001c0003t0001g0016 others(1): Show |
5 | HG01243.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-96G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423945 | |||||||
| chr10:45423976 | T | C | 1 | a0002c0005t0003g0118 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.555-65T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423976 | |||||||
| chr10:45423983 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.555-58G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423983 | |||||||
| chr10:45424168 | C | T | 2 | a0001c0001t0005g0043 a0001c0001t0005g0096 |
2 | HG01346.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.661+21C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424168 | |||||||
| chr10:45424274 | T | C | 33 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(30): Show |
36 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.661+127T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424274 | |||||||
| chr10:45424279 | C | G | 4 | a0001c0002t0002g0309 a0001c0002t0002g0310 a0001c0003t0001g0016 others(1): Show |
5 | HG01243.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+132C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424279 | |||||||
| chr10:45424378 | C | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0061 others(15): Show |
19 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.661+231C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424378 | |||||||
| chr10:45424528 | A | G | 4 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0113 others(1): Show |
4 | HG01099.hp2 HG02622.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+381A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424528 | |||||||
| chr10:45424651 | G | C | 1 | a0001c0001t0001g0214 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.662-309G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424651 | |||||||
| chr10:45424657 | C | A | 1 | a0001c0008t0002g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.662-303C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424657 | |||||||
| chr10:45424680 | C | T | 1 | a0001c0001t0005g0043 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.662-280C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424680 | |||||||
| chr10:45424791 | G | C | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.662-169G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424791 | |||||||
| chr10:45424830 | G | A | 1 | a0001c0002t0002g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.662-130G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424830 | |||||||
| chr10:45424897 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.662-63G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424897 | |||||||
| chr10:45425257 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(212): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.834+125C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425257 | |||||||
| chr10:45425366 | G | A | 30 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0070 others(27): Show |
32 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.834+234G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425366 | |||||||
| chr10:45425396 | A | G | 15 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0002g0304 others(12): Show |
15 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.834+264A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425396 | |||||||
| chr10:45425461 | A | C | 1 | a0001c0001t0001g0075 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.834+329A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425461 | |||||||
| chr10:45425570 | C | A | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.834+438C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425570 | |||||||
| chr10:45425744 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.834+612C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425744 | |||||||
| chr10:45425895 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.834+763G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425895 | |||||||
| chr10:45425903 | G | T | 14 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0004g0201 others(11): Show |
14 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.834+771G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425903 | |||||||
| chr10:45426095 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.834+963C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426095 | |||||||
| chr10:45426291 | T | TG | 30 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0070 others(27): Show |
32 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.834+1161dupG | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 45426291 | ||||||
| chr10:45426315 | G | A | 1 | a0001c0003t0001g0164 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.834+1183G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426315 | |||||||
| chr10:45426333 | A | G | 1 | a0001c0021t0006g0290 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.834+1201A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426333 | |||||||
| chr10:45426417 | A | C | 30 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0070 others(27): Show |
32 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.834+1285A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426417 | |||||||
| chr10:45426418 | A | C | 30 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0070 others(27): Show |
32 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.834+1286A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426418 | |||||||
| chr10:45426429 | C | T | 57 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0024 others(54): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.834+1297C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426429 | |||||||
| chr10:45426534 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(212): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.834+1402A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426534 | |||||||
| chr10:45426582 | G | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0075 a0001c0001t0001g0248 |
4 | NA18939.hp1 NA18950.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+1450G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426582 | |||||||
| chr10:45426586 | G | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0227 others(1): Show |
7 | HG01255.hp2 HG01346.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.834+1454G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426586 | |||||||
| chr10:45426742 | G | A | 15 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0002g0304 others(12): Show |
15 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.834+1610G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426742 | |||||||
| chr10:45426763 | T | G | 1 | a0001c0009t0001g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.834+1631T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426763 | |||||||
| chr10:45426927 | A | G | 1 | a0001c0002t0002g0280 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.835-1691A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426927 | |||||||
| chr10:45426938 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.835-1680A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426938 | |||||||
| chr10:45427023 | G | C | 1 | a0001c0004t0001g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.835-1595G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427023 | |||||||
| chr10:45427179 | C | T | 15 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0002g0304 others(12): Show |
15 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.835-1439C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427179 | |||||||
| chr10:45427282 | C | T | 13 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0107 others(10): Show |
14 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.835-1336C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427282 | |||||||
| chr10:45427353 | C | A | 1 | a0001c0001t0001g0247 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.835-1265C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427353 | |||||||
| chr10:45427506 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG01361.hp1 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.835-1112C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427506 | |||||||
| chr10:45427529 | C | T | 4 | a0001c0002t0002g0309 a0001c0002t0002g0310 a0001c0003t0001g0016 others(1): Show |
5 | HG01243.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.835-1089C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427529 | |||||||
| chr10:45427576 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.835-1042G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427576 | |||||||
| chr10:45427577 | G | A | 1 | a0001c0006t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.835-1041G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427577 | |||||||
| chr10:45427617 | A | C | 12 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0070 others(9): Show |
13 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.835-1001A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427617 | |||||||
| chr10:45427720 | C | T | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.835-898C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427720 | |||||||
| chr10:45428023 | C | T | 1 | a0001c0006t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.835-595C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428023 | |||||||
| chr10:45428063 | T | C | 41 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(38): Show |
44 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.835-555T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428063 | |||||||
| chr10:45428080 | C | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(201): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.835-538C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428080 | |||||||
| chr10:45428098 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.835-520C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428098 | |||||||
| chr10:45428133 | G | C | 1 | a0001c0001t0001g0191 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.835-485G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428133 | |||||||
| chr10:45428322 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(224): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.835-296A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428322 | |||||||
| chr10:45428575 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(247): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.835-43G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428575 | |||||||
| chr10:45428808 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(239): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.981+44T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45428808 | |||||||
| chr10:45428909 | A | T | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+145A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45428909 | |||||||
| chr10:45429029 | C | T | 1 | a0001c0006t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.981+265C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429029 | |||||||
| chr10:45429235 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.981+471C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429235 | |||||||
| chr10:45429366 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.981+602G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429366 | |||||||
| chr10:45429436 | C | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0070 others(19): Show |
23 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.981+672C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429436 | |||||||
| chr10:45429439 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.981+675T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429439 | |||||||
| chr10:45429448 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.981+684T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429448 | |||||||
| chr10:45429504 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0121 |
2 | HG01106.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.981+740C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429504 | |||||||
| chr10:45429520 | C | A | 30 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0061 others(27): Show |
32 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.981+756C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429520 | |||||||
| chr10:45429629 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.981+865G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429629 | |||||||
| chr10:45429751 | A | T | 1 | a0001c0006t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.981+987A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429751 | |||||||
| chr10:45429758 | T | G | 2 | a0002c0005t0003g0136 a0002c0005t0003g0240 |
2 | NA18945.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.981+994T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429758 | |||||||
| chr10:45429767 | T | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(150): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.981+1003T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429767 | |||||||
| chr10:45429816 | G | A | 1 | a0001c0006t0009g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.981+1052G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429816 | |||||||
| chr10:45430054 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.981+1290G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45430054 | |||||||
| chr10:45430116 | G | C | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.981+1352G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45430116 | |||||||
| chr10:45430141 | A | G | 1 | a0001c0001t0002g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.981+1377A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45430141 | |||||||
| chr10:45430218 | T | C | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+1454T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45430218 | |||||||
| chr10:45430358 | C | A | 1 | a0001c0002t0002g0279 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.981+1594C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45430358 | |||||||
| chr10:45430428 | GA | G | 12 | a0001c0001t0001g0220 a0001c0001t0004g0201 a0001c0002t0007g0306 others(9): Show |
12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.981+1674delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45430428 | ||||||
| chr10:45430631 | TA | T | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+1879delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45430631 | ||||||
| chr10:45430777 | G | A | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+2013G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45430777 | |||||||
| chr10:45430796 | CACAGCGA others(26): Show |
C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | NA18961.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.981+2038_981+2070d others(35): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45430796 | ||||||
| chr10:45431452 | G | A | 1 | a0001c0006t0009g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.981+2688G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431452 | |||||||
| chr10:45431548 | G | GTTAT | 21 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0084 others(18): Show |
22 | HG01109.hp1 HG01256.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.981+2823_981+2826d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | ||||||
| chr10:45431548 | G | GTTATTTA others(1): Show |
5 | a0001c0001t0001g0085 a0001c0001t0001g0092 a0001c0001t0001g0187 others(2): Show |
5 | NA18955.hp1 NA18956.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+2819_981+2826d others(10): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | ||||||
| chr10:45431548 | GTTAT | G | 36 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0044 others(33): Show |
41 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.981+2823_981+2826d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | ||||||
| chr10:45431548 | GTTATTTA others(1): Show |
G | 15 | a0001c0001t0001g0021 a0001c0001t0001g0190 a0001c0001t0001g0207 others(12): Show |
17 | HG01243.hp1 HG01261.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.981+2819_981+2826d others(10): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | ||||||
| chr10:45431548 | GTTATTTA others(5): Show |
G | 2 | a0001c0004t0001g0069 a0001c0004t0001g0177 |
2 | HG03225.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.981+2815_981+2826d others(14): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | ||||||
| chr10:45431548 | GTTATTTA others(9): Show |
G | 2 | a0001c0006t0001g0035 a0001c0008t0002g0258 |
2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.981+2811_981+2826d others(18): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | ||||||
| chr10:45431548 | GTTATTTA others(13): Show |
G | 17 | a0001c0006t0001g0145 a0002c0005t0003g0037 a0002c0005t0003g0040 others(14): Show |
17 | HG01243.hp2 HG02040.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.981+2807_981+2826d others(22): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | ||||||
| chr10:45431588 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG01891.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.981+2824T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431588 | |||||||
| chr10:45431627 | C | T | 1 | a0001c0003t0001g0057 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.981+2863C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431627 | |||||||
| chr10:45431666 | A | G | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+2902A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431666 | |||||||
| chr10:45431682 | C | T | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+2918C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431682 | |||||||
| chr10:45431794 | G | A | 21 | a0001c0001t0001g0192 a0001c0001t0001g0253 a0001c0003t0001g0057 others(18): Show |
25 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(22): Show |
intron_variant | MODIFIER | c.981+3030G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431794 | |||||||
| chr10:45431861 | C | T | 12 | a0001c0001t0001g0168 a0001c0004t0001g0007 a0001c0004t0001g0008 others(9): Show |
16 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.981+3097C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431861 | |||||||
| chr10:45431868 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.981+3104G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431868 | |||||||
| chr10:45432027 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0207 |
2 | NA19056.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.981+3263G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432027 | |||||||
| chr10:45432028 | TG | T | 5 | a0001c0002t0002g0309 a0001c0002t0002g0310 a0001c0003t0001g0016 others(2): Show |
7 | HG01243.hp1 HG02572.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.981+3269delG | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45432028 | ||||||
| chr10:45432187 | TA | T | 6 | a0001c0001t0001g0223 a0001c0001t0001g0243 a0001c0001t0008g0254 others(3): Show |
6 | HG01891.hp2 HG03239.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.981+3437delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45432187 | ||||||
| chr10:45432187 | TAA | T | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+3436_981+3437d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45432187 | ||||||
| chr10:45432341 | C | G | 28 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(25): Show |
28 | HG01243.hp2 HG01261.hp2 HG01928.hp2 others(25): Show |
intron_variant | MODIFIER | c.981+3577C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432341 | |||||||
| chr10:45432343 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.981+3579G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432343 | |||||||
| chr10:45432360 | TA | T | 14 | a0001c0001t0001g0082 a0001c0001t0001g0107 a0001c0001t0001g0170 others(11): Show |
14 | HG00741.hp1 HG01069.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.981+3613delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45432360 | ||||||
| chr10:45432697 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.981+3933G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432697 | |||||||
| chr10:45432747 | A | G | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+3983A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432747 | |||||||
| chr10:45432754 | C | T | 6 | a0001c0001t0001g0168 a0001c0004t0001g0008 a0001c0004t0001g0029 others(3): Show |
8 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.981+3990C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432754 | |||||||
| chr10:45432785 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0172 a0001c0001t0001g0193 others(4): Show |
8 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(5): Show |
intron_variant | MODIFIER | c.981+4021G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432785 | |||||||
| chr10:45432813 | T | A | 6 | a0001c0001t0001g0192 a0001c0004t0001g0002 a0001c0004t0001g0131 others(3): Show |
8 | HG00140.hp1 NA18941.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.981+4049T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432813 | |||||||
| chr10:45432943 | T | A | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+4179T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432943 | |||||||
| chr10:45432944 | C | A | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+4180C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432944 | |||||||
| chr10:45432974 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.981+4210C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432974 | |||||||
| chr10:45432981 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.981+4217A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432981 | |||||||
| chr10:45433168 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.981+4404C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433168 | |||||||
| chr10:45433210 | T | G | 21 | a0001c0001t0001g0192 a0001c0001t0001g0253 a0001c0003t0001g0057 others(18): Show |
25 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(22): Show |
intron_variant | MODIFIER | c.981+4446T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433210 | |||||||
| chr10:45433239 | A | C | 17 | a0001c0006t0001g0145 a0002c0005t0003g0037 a0002c0005t0003g0040 others(14): Show |
17 | HG01243.hp2 HG02040.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.981+4475A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433239 | |||||||
| chr10:45433258 | G | A | 1 | a0001c0002t0002g0309 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.981+4494G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433258 | |||||||
| chr10:45433344 | G | A | 1 | a0001c0003t0004g0051 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.981+4580G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433344 | |||||||
| chr10:45433345 | C | T | 2 | a0001c0003t0001g0018 a0001c0003t0001g0156 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.981+4581C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433345 | |||||||
| chr10:45433346 | G | A | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+4582G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433346 | |||||||
| chr10:45433374 | C | T | 41 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(38): Show |
44 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.981+4610C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433374 | |||||||
| chr10:45433456 | T | G | 28 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(25): Show |
28 | HG01243.hp2 HG01261.hp2 HG01928.hp2 others(25): Show |
intron_variant | MODIFIER | c.981+4692T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433456 | |||||||
| chr10:45433463 | C | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(219): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.981+4699C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433463 | |||||||
| chr10:45433528 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.981+4764G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433528 | |||||||
| chr10:45433548 | A | T | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+4784A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433548 | |||||||
| chr10:45433655 | C | T | 1 | a0001c0002t0002g0284 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.981+4891C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433655 | |||||||
| chr10:45433675 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.981+4911G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433675 | |||||||
| chr10:45433785 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.981+5021C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433785 | |||||||
| chr10:45433865 | G | C | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+5101G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433865 | |||||||
| chr10:45434277 | C | T | 1 | a0001c0007t0001g0132 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.981+5513C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434277 | |||||||
| chr10:45434515 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.981+5751C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434515 | |||||||
| chr10:45434517 | T | C | 29 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(26): Show |
29 | HG01243.hp2 HG01261.hp2 HG01928.hp2 others(26): Show |
intron_variant | MODIFIER | c.981+5753T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434517 | |||||||
| chr10:45434536 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.981+5772T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434536 | |||||||
| chr10:45434693 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.982-5737G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434693 | |||||||
| chr10:45434887 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.982-5543G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434887 | |||||||
| chr10:45434906 | T | TTTTC | 12 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(9): Show |
12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-5518_982-5515d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45434906 | ||||||
| chr10:45434938 | G | A | 12 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(9): Show |
12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-5492G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434938 | |||||||
| chr10:45434951 | G | A | 12 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(9): Show |
12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-5479G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434951 | |||||||
| chr10:45435015 | A | G | 1 | a0001c0002t0002g0291 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.982-5415A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435015 | |||||||
| chr10:45435033 | A | G | 12 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(9): Show |
12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-5397A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435033 | |||||||
| chr10:45435049 | T | C | 1 | a0002c0005t0003g0122 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.982-5381T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435049 | |||||||
| chr10:45435262 | G | GT | 40 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0061 others(37): Show |
42 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.982-5155dupT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45435262 | ||||||
| chr10:45435266 | T | TG | 2 | a0001c0001t0001g0013 a0001c0001t0001g0044 |
3 | HG01070.hp1 HG01071.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.982-5164_982-5163i others(3): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435266 | |||||||
| chr10:45435274 | T | A | 1 | a0001c0006t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.982-5156T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435274 | |||||||
| chr10:45435275 | T | A | 12 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(9): Show |
12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-5155T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435275 | |||||||
| chr10:45435331 | G | T | 1 | a0001c0004t0001g0014 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.982-5099G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435331 | |||||||
| chr10:45435337 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(221): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.982-5093T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435337 | |||||||
| chr10:45435357 | T | C | 70 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(67): Show |
73 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.982-5073T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435357 | |||||||
| chr10:45435357 | T | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0181 a0001c0001t0001g0182 |
6 | NA18944.hp2 NA18947.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.982-5073T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435357 | |||||||
| chr10:45435382 | A | G | 1 | a0001c0002t0002g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.982-5048A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435382 | |||||||
| chr10:45435397 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.982-5033C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435397 | |||||||
| chr10:45435417 | C | A | 1 | a0001c0002t0006g0289 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.982-5013C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435417 | |||||||
| chr10:45435612 | A | C | 32 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(29): Show |
35 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.982-4818A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435612 | |||||||
| chr10:45435622 | A | G | 53 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(50): Show |
56 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.982-4808A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435622 | |||||||
| chr10:45435654 | T | C | 53 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(50): Show |
56 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.982-4776T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435654 | |||||||
| chr10:45435812 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.982-4618G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435812 | |||||||
| chr10:45435980 | G | A | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.982-4450G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435980 | |||||||
| chr10:45436022 | T | A | 1 | a0001c0004t0001g0029 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.982-4408T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436022 | |||||||
| chr10:45436026 | G | A | 1 | a0005c0014t0001g0097 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.982-4404G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436026 | |||||||
| chr10:45436030 | G | A | 71 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(68): Show |
74 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.982-4400G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436030 | |||||||
| chr10:45436116 | G | T | 16 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0064 others(13): Show |
18 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.982-4314G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436116 | |||||||
| chr10:45436177 | A | C | 2 | a0001c0006t0001g0143 a0001c0006t0009g0154 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.982-4253A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436177 | |||||||
| chr10:45436351 | C | G | 1 | a0001c0006t0001g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.982-4079C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436351 | |||||||
| chr10:45436412 | A | G | 1 | a0001c0003t0002g0255 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.982-4018A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436412 | |||||||
| chr10:45436415 | G | A | 1 | a0001c0003t0001g0146 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.982-4015G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436415 | |||||||
| chr10:45436451 | C | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(56): Show |
62 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.982-3979C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436451 | |||||||
| chr10:45436516 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.982-3914C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436516 | |||||||
| chr10:45436552 | G | A | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.982-3878G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436552 | |||||||
| chr10:45436552 | G | T | 1 | a0001c0006t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.982-3878G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436552 | |||||||
| chr10:45436732 | C | T | 2 | a0001c0006t0001g0143 a0001c0008t0002g0258 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.982-3698C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436732 | |||||||
| chr10:45436816 | T | C | 70 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(67): Show |
73 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.982-3614T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436816 | |||||||
| chr10:45436885 | A | G | 1 | a0001c0008t0002g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.982-3545A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436885 | |||||||
| chr10:45436892 | C | G | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.982-3538C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436892 | |||||||
| chr10:45437001 | C | A | 2 | a0001c0001t0001g0107 a0001c0002t0002g0265 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.982-3429C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437001 | |||||||
| chr10:45437090 | C | T | 1 | a0002c0005t0003g0118 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.982-3340C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437090 | |||||||
| chr10:45437214 | G | A | 1 | a0001c0002t0006g0289 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.982-3216G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437214 | |||||||
| chr10:45437416 | G | GT | 12 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(9): Show |
12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-3004dupT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45437416 | ||||||
| chr10:45437471 | G | C | 18 | a0001c0001t0001g0085 a0001c0001t0001g0197 a0001c0002t0002g0026 others(15): Show |
19 | HG02027.hp2 HG02132.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.982-2959G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437471 | |||||||
| chr10:45437703 | T | C | 1 | a0001c0019t0001g0211 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.982-2727T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437703 | |||||||
| chr10:45437757 | C | T | 9 | a0001c0001t0001g0070 a0001c0001t0001g0165 a0001c0001t0002g0304 others(6): Show |
9 | HG01099.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.982-2673C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437757 | |||||||
| chr10:45437890 | C | T | 7 | a0001c0001t0001g0165 a0001c0003t0001g0144 a0001c0003t0001g0146 others(4): Show |
7 | HG01099.hp1 HG02258.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.982-2540C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437890 | |||||||
| chr10:45438129 | CT | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(248): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.982-2288delT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45438129 | ||||||
| chr10:45438291 | A | G | 2 | a0001c0006t0001g0143 a0001c0006t0009g0154 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.982-2139A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438291 | |||||||
| chr10:45438378 | G | A | 1 | a0001c0003t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.982-2052G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438378 | |||||||
| chr10:45438394 | T | C | 1 | a0001c0006t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.982-2036T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438394 | |||||||
| chr10:45438431 | A | T | 1 | a0001c0007t0001g0109 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.982-1999A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438431 | |||||||
| chr10:45438485 | GTCAGGAA others(21): Show |
G | 59 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(56): Show |
62 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.982-1901_982-1874d others(30): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45438485 | ||||||
| chr10:45438710 | C | T | 1 | a0001c0002t0002g0291 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.982-1720C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438710 | |||||||
| chr10:45438794 | A | G | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.982-1636A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438794 | |||||||
| chr10:45438863 | C | G | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.982-1567C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438863 | |||||||
| chr10:45438883 | C | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(150): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.982-1547C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438883 | |||||||
| chr10:45438890 | C | A | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.982-1540C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438890 | |||||||
| chr10:45438924 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(150): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.982-1506G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438924 | |||||||
| chr10:45438989 | G | A | 48 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(45): Show |
51 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.982-1441G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438989 | |||||||
| chr10:45439070 | A | C | 1 | a0001c0006t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.982-1360A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439070 | |||||||
| chr10:45439081 | T | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(150): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.982-1349T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439081 | |||||||
| chr10:45439347 | G | A | 47 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(44): Show |
50 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.982-1083G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439347 | |||||||
| chr10:45439433 | C | A | 57 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0044 others(54): Show |
60 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.982-997C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439433 | |||||||
| chr10:45439474 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.982-956C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439474 | |||||||
| chr10:45439518 | C | T | 7 | a0001c0001t0001g0165 a0001c0003t0001g0144 a0001c0003t0001g0146 others(4): Show |
7 | HG01099.hp1 HG02258.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.982-912C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439518 | |||||||
| chr10:45439613 | G | A | 1 | a0001c0002t0002g0273 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.982-817G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439613 | |||||||
| chr10:45440028 | A | C | 1 | a0001c0008t0002g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.982-402A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45440028 | |||||||
| chr10:45440077 | G | A | 1 | a0001c0006t0009g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.982-353G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45440077 | |||||||
| chr10:45440101 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0220 |
2 | NA18747.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.982-329G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45440101 | |||||||
| chr10:45440115 | G | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(220): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.982-315G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45440115 | |||||||
| chr10:45440296 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(150): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.982-134C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45440296 | |||||||
| chr10:45440648 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1185+15C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45440648 | |||||||
| chr10:45440715 | G | GA | 12 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0107 others(9): Show |
13 | HG00642.hp2 HG01069.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1185+83dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 45440715 | ||||||
| chr10:45440776 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(208): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.1185+143A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45440776 | |||||||
| chr10:45440878 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1185+245T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45440878 | |||||||
| chr10:45440911 | G | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(207): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1185+278G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45440911 | |||||||
| chr10:45440958 | C | T | 1 | a0001c0007t0001g0133 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1185+325C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45440958 | |||||||
| chr10:45441020 | T | C | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1186-324T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45441020 | |||||||
| chr10:45441186 | G | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0215 a0001c0001t0001g0218 others(1): Show |
4 | HG01070.hp2 HG01261.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1186-158G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45441186 | |||||||
| chr10:45441250 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0099 |
2 | HG00323.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1186-94A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45441250 | |||||||
| chr10:45441277 | C | T | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1186-67C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45441277 | |||||||
| chr10:45441479 | C | T | 1 | a0001c0008t0002g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1272+49C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441479 | |||||||
| chr10:45441489 | C | A | 1 | a0001c0001t0001g0239 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1272+59C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441489 | |||||||
| chr10:45441510 | C | G | 11 | a0001c0001t0004g0201 a0001c0002t0007g0306 a0001c0002t0007g0307 others(8): Show |
11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1272+80C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441510 | |||||||
| chr10:45441625 | C | A | 1 | a0001c0007t0001g0109 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1272+195C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441625 | |||||||
| chr10:45441626 | A | C | 1 | a0001c0007t0001g0109 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1272+196A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441626 | |||||||
| chr10:45441627 | C | A | 1 | a0001c0007t0001g0109 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1272+197C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441627 | |||||||
| chr10:45441750 | A | G | 1 | a0001c0004t0001g0014 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1272+320A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441750 | |||||||
| chr10:45441751 | C | T | 1 | a0001c0008t0002g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1272+321C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441751 | |||||||
| chr10:45441975 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(159): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1272+545C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441975 | |||||||
| chr10:45442019 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0214 |
2 | NA18946.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1272+589G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442019 | |||||||
| chr10:45442030 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1272+600T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442030 | |||||||
| chr10:45442130 | C | T | 5 | a0001c0003t0001g0034 a0001c0004t0001g0007 a0001c0004t0001g0014 others(2): Show |
7 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1272+700C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442130 | |||||||
| chr10:45442280 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1273-758T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442280 | |||||||
| chr10:45442409 | C | A | 1 | a0001c0004t0001g0086 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1273-629C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442409 | |||||||
| chr10:45442459 | C | T | 5 | a0001c0004t0001g0008 a0001c0004t0001g0029 a0001c0004t0001g0039 others(2): Show |
7 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1273-579C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442459 | |||||||
| chr10:45442466 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1273-572G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442466 | |||||||
| chr10:45442477 | A | ATG | 4 | a0001c0001t0001g0180 a0001c0001t0001g0215 a0001c0001t0001g0218 others(1): Show |
4 | HG01070.hp2 HG01261.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273-550_1273-549d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 45442477 | ||||||
| chr10:45442538 | A | T | 3 | a0001c0001t0001g0064 a0001c0003t0001g0155 a0001c0003t0001g0164 |
3 | HG03486.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1273-500A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442538 | |||||||
| chr10:45442544 | A | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(178): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1273-494A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442544 | |||||||
| chr10:45442647 | CTG | C | 44 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0047 others(41): Show |
46 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.1273-390_1273-389d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442647 | |||||||
| chr10:45442791 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(205): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1273-247T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442791 | |||||||
| chr10:45442799 | T | G | 52 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0085 others(49): Show |
55 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1273-239T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442799 | |||||||
| chr10:45442827 | T | C | 1 | a0001c0004t0001g0008 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1273-211T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442827 | |||||||
| chr10:45442831 | T | C | 1 | a0001c0006t0001g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1273-207T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442831 | |||||||
| chr10:45442853 | G | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(204): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1273-185G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442853 | |||||||
| chr10:45443229 | G | A | 3 | a0001c0002t0002g0028 a0001c0002t0002g0292 a0001c0002t0002g0293 |
4 | HG00323.hp2 HG01175.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1451+13G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 10/13 | chr10 | 45443229 | |||||||
| chr10:45443239 | T | C | 4 | a0001c0002t0002g0309 a0001c0002t0002g0310 a0001c0003t0001g0016 others(1): Show |
5 | HG01243.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1451+23T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 10/13 | chr10 | 45443239 | |||||||
| chr10:45443298 | C | T | 50 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0047 others(47): Show |
52 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1451+82C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 10/13 | chr10 | 45443298 | |||||||
| chr10:45443553 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1573+16C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 11/13 | chr10 | 45443553 | |||||||
| chr10:45443559 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1573+22C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 11/13 | chr10 | 45443559 | |||||||
| chr10:45443631 | C | T | 5 | a0001c0004t0001g0008 a0001c0004t0001g0029 a0001c0004t0001g0039 others(2): Show |
7 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1573+94C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 11/13 | chr10 | 45443631 | |||||||
| chr10:45443688 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(242): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.1574-40T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 11/13 | chr10 | 45443688 | |||||||
| chr10:45443889 | G | A | 2 | a0001c0003t0001g0006 a0001c0003t0001g0033 |
3 | HG03453.hp2 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1674+61G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 12/13 | chr10 | 45443889 | |||||||
| chr10:45444370 | C | T | 34 | a0001c0004t0001g0002 a0001c0004t0001g0007 a0001c0004t0001g0008 others(31): Show |
42 | HG00280.hp2 HG00408.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1845+84C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45444370 | |||||||
| chr10:45444533 | T | G | 6 | a0002c0005t0003g0037 a0002c0005t0003g0114 a0002c0005t0003g0124 others(3): Show |
6 | HG02040.hp1 HG02155.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1845+247T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45444533 | |||||||
| chr10:45444543 | C | T | 45 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0047 others(42): Show |
47 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.1845+257C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45444543 | |||||||
| chr10:45444728 | G | A | 1 | a0001c0007t0001g0126 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1845+442G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45444728 | |||||||
| chr10:45444827 | T | G | 3 | a0001c0004t0001g0007 a0001c0004t0001g0065 a0001c0004t0001g0066 |
4 | HG02258.hp1 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1845+541T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45444827 | |||||||
| chr10:45445142 | C | G | 1 | a0001c0006t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1846-366C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45445142 | |||||||
| chr10:45445174 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1846-334G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45445174 |