Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55289 |
|---|---|
| ensemblid | ENSG00000153093.21 |
| hgncid | 25621 |
| symbol | ACOXL |
| name | acyl-CoA oxidase like |
| refseq_nuc | NM_001142807.4 |
| refseq_prot | NP_001136279.1 |
| ensembl_nuc | ENST00000439055.6 |
| ensembl_prot | ENSP00000407761.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 110732573 |
| end | 111118548 |
| strand | + |
| ver | v1.2 |
| region | chr2:110732573-111118548 |
| region5000 | chr2:110727573-111123548 |
| regionname0 | ACOXL_chr2_110732573_111118548 |
| regionname5000 | ACOXL_chr2_110727573_111123548 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000 | 0/0 | 0 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0001 | 1/0 | 580 | 93 | 40 | 16 | 22 | 6 | 8 | 13 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0002 | 0/1 | 580 | 21 | 6 | 6 | 7 | 0 | 1 | 5 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0003 | 0/0 | 580 | 10 | 0 | 2 | 8 | 0 | 0 | 4 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0004 | 0/0 | 567 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0005 | 0/0 | 580 | 3 | 1 | 1 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0006 | 0/0 | 580 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0007 | 0/0 | 580 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0008 | 0/0 | 567 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0009 | 0/0 | 580 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0010 | 0/0 | 576 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0011 | 0/0 | 580 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0012 | 0/0 | 580 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0013 | 0/0 | 580 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0014 | 0/0 | 580 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1743 | 79 | 40 | 11 | 15 | 5 | 7 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0002 | 0/1 | 1743 | 20 | 6 | 6 | 6 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0003 | 0/0 | 1743 | 12 | 0 | 5 | 7 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0004 | 0/0 | 1743 | 10 | 0 | 2 | 8 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0005 | 0/0 | 1704 | 8 | 7 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0006 | 0/0 | 1743 | 3 | 3 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0007 | 0/0 | 1743 | 3 | 1 | 1 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0008 | 0/0 | 1704 | 2 | 2 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0009 | 0/0 | 1743 | 2 | 0 | 0 | 0 | 1 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0010 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0011 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0012 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0013 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0014 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0015 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0016 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0017 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0018 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0019 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| c0020 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 957 | 95 | 40 | 20 | 19 | 5 | 9 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| t0002 | 0/0 | 956 | 46 | 21 | 5 | 14 | 3 | 3 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| t0003 | 0/0 | 957 | 3 | 0 | 0 | 3 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| t0004 | 0/0 | 956 | 3 | 0 | 1 | 2 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| t0005 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| t0006 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| t0007 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0013 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0000c0014 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0001c0001 | 1/0 | 1743 | 79 | 40 | 11 | 15 | 5 | 7 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0001c0003 | 0/0 | 1743 | 12 | 0 | 5 | 7 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0001c0012 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0001c0017 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0002c0002 | 0/1 | 1743 | 20 | 6 | 6 | 6 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0002c0019 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0003c0004 | 0/0 | 1743 | 10 | 0 | 2 | 8 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0004c0005 | 0/0 | 1704 | 8 | 7 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0005c0007 | 0/0 | 1743 | 3 | 1 | 1 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0006c0006 | 0/0 | 1743 | 3 | 3 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0007c0009 | 0/0 | 1743 | 2 | 0 | 0 | 0 | 1 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0008c0008 | 0/0 | 1704 | 2 | 2 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0009c0016 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0010c0015 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0011c0010 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0012c0018 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0013c0011 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0014c0020 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0013t0001 | 0/0 | 2660 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0000c0014t0001 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0001c0001t0001 | 1/0 | 2699 | 54 | 27 | 9 | 9 | 3 | 5 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0001c0001t0002 | 0/0 | 2698 | 23 | 11 | 2 | 6 | 2 | 2 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0001c0001t0005 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0001c0001t0006 | 0/0 | 2698 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0001c0003t0001 | 0/0 | 2699 | 8 | 0 | 5 | 3 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0001c0003t0002 | 0/0 | 2698 | 4 | 0 | 0 | 4 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0001c0012t0002 | 0/0 | 2698 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0001c0017t0002 | 0/0 | 2698 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0002c0002t0001 | 0/1 | 2699 | 11 | 3 | 4 | 2 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0002c0002t0002 | 0/0 | 2698 | 6 | 3 | 2 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0002c0002t0003 | 0/0 | 2699 | 2 | 0 | 0 | 2 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0002c0002t0004 | 0/0 | 2698 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0002c0019t0001 | 0/0 | 2699 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0003c0004t0001 | 0/0 | 2699 | 5 | 0 | 1 | 4 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0003c0004t0002 | 0/0 | 2698 | 3 | 0 | 0 | 3 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0003c0004t0003 | 0/0 | 2699 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0003c0004t0004 | 0/0 | 2698 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0004c0005t0001 | 0/0 | 2660 | 2 | 1 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0004c0005t0002 | 0/0 | 2659 | 5 | 5 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0004c0005t0007 | 0/0 | 2660 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0005c0007t0001 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0005c0007t0002 | 0/0 | 2698 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0005c0007t0004 | 0/0 | 2698 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0006c0006t0001 | 0/0 | 2699 | 2 | 2 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0006c0006t0002 | 0/0 | 2698 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0007c0009t0001 | 0/0 | 2699 | 2 | 0 | 0 | 0 | 1 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0008c0008t0001 | 0/0 | 2660 | 2 | 2 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0009c0016t0001 | 0/0 | 2699 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0010c0015t0001 | 0/0 | 2699 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0011c0010t0002 | 0/0 | 2698 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0012c0018t0001 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0013c0011t0001 | 0/0 | 2699 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| a0014c0020t0001 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | copy fasta | chr2 | 110727573 | 111123548 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0013t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0000c0014t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0012t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0001c0017t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0001g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0002c0019t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0003c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0003c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0003c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0003c0004t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0003c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0003c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0003c0004t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0003c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0003c0004t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0003c0004t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0004c0005t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0004c0005t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0004c0005t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0004c0005t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0004c0005t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0004c0005t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0004c0005t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0004c0005t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0005c0007t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0005c0007t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0005c0007t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0006c0006t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0006c0006t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0006c0006t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0007c0009t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0007c0009t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0008c0008t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0008c0008t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0009c0016t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0010c0015t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0011c0010t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0012c0018t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0013c0011t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| a0014c0020t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0065 | EUR | GBR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG00099 | hp2 | a0007 | c0009 | t0001 | g0106 | EUR | GBR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG00140 | hp2 | a0001 | c0017 | t0002 | g0073 | EUR | GBR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG00323 | hp1 | a0010 | c0015 | t0001 | g0074 | EUR | FIN | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG00423 | hp1 | a0002 | c0002 | t0004 | g0141 | EAS | CHS | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG00423 | hp2 | a0003 | c0004 | t0001 | g0027 | EAS | CHS | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG00438 | hp1 | a0003 | c0004 | t0003 | g0143 | EAS | CHS | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0084 | EAS | CHS | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG00673 | hp1 | a0005 | c0007 | t0004 | g0144 | EAS | CHS | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0091 | AMR | PUR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0081 | AMR | PUR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0087 | AMR | PUR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01175 | hp2 | a0005 | c0007 | t0002 | g0050 | AMR | PUR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01243 | hp2 | a0004 | c0005 | t0001 | g0134 | AMR | PUR | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0054 | AMR | CLM | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0148 | AMR | CLM | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0147 | AMR | CLM | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | CLM | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01496 | hp1 | a0003 | c0004 | t0001 | g0064 | AMR | CLM | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0089 | AMR | CLM | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0040 | EUR | IBS | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01891 | hp1 | a0004 | c0005 | t0002 | g0124 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01981 | hp1 | a0003 | c0004 | t0004 | g0140 | AMR | PEL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0090 | AMR | PEL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02040 | hp2 | a0003 | c0004 | t0001 | g0026 | EAS | KHV | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02080 | hp2 | a0003 | c0004 | t0002 | g0069 | EAS | KHV | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02145 | hp2 | a0008 | c0008 | t0001 | g0015 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02257 | hp1 | a0000 | c0014 | t0001 | g0072 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02257 | hp2 | a0014 | c0020 | t0001 | g0002 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02258 | hp1 | a0011 | c0010 | t0002 | g0009 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02451 | hp1 | a0004 | c0005 | t0002 | g0022 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0119 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02735 | hp1 | a0007 | c0009 | t0001 | g0092 | SAS | PJL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02886 | hp1 | a0004 | c0005 | t0002 | g0127 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02897 | hp1 | a0004 | c0005 | t0001 | g0070 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02897 | hp2 | a0006 | c0006 | t0001 | g0001 | AFR | GWD | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | ESN | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02976 | hp1 | a0006 | c0006 | t0002 | g0146 | AFR | ESN | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0132 | AFR | ESN | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03225 | hp2 | a0004 | c0005 | t0007 | g0133 | AFR | MSL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0103 | SAS | PJL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03516 | hp2 | a0006 | c0006 | t0001 | g0136 | AFR | ESN | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | MSL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03669 | hp2 | a0013 | c0011 | t0001 | g0130 | SAS | PJL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | STU | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG04115 | hp1 | a0009 | c0016 | t0001 | g0112 | SAS | STU | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG04115 | hp2 | a0001 | c0012 | t0002 | g0131 | SAS | STU | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | CHB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18612 | hp2 | a0002 | c0002 | t0003 | g0142 | EAS | CHB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18906 | hp2 | a0005 | c0007 | t0001 | g0062 | AFR | YRI | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18946 | hp1 | a0001 | c0003 | t0002 | g0104 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18950 | hp1 | a0001 | c0003 | t0002 | g0083 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18962 | hp1 | a0003 | c0004 | t0002 | g0098 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18993 | hp1 | a0001 | c0003 | t0001 | g0036 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18993 | hp2 | a0003 | c0004 | t0001 | g0093 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19002 | hp1 | a0003 | c0004 | t0002 | g0079 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19011 | hp1 | a0002 | c0019 | t0001 | g0095 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19011 | hp2 | a0002 | c0002 | t0003 | g0139 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19030 | hp2 | a0012 | c0018 | t0001 | g0053 | AFR | LWK | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19043 | hp1 | a0000 | c0013 | t0001 | g0046 | AFR | LWK | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | LWK | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19062 | hp1 | a0003 | c0004 | t0001 | g0030 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19088 | hp1 | a0001 | c0003 | t0002 | g0043 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | YRI | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | YRI | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ASW | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ASW | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02109 | hp1 | a0008 | c0008 | t0001 | g0016 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0135 | AFR | MSL | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG06807 | hp1 | a0004 | c0005 | t0002 | g0020 | AFR | USA | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | USA | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | USA | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| NA21309 | hp2 | a0004 | c0005 | t0002 | g0004 | AFR | LWK | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0099 | REF | REF | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | ACOXL_chr2_110727573_111123548 | ACOXL | chr2 | 110727573 | 111123548 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:110799040
|
C | T | 1 | a0014 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.487C>T | p.Arg163Trp | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/18 | 711/2699 | 487/1743 | 163/580 | chr2 | 110799040 | ||
| chr2:110801654
|
C | A | 1 | a0013 | 1 | HG03669.hp2 | missense_variant&splice_region_variant | MODERATE | c.550C>A | p.Leu184Met | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/18 | 774/2699 | 550/1743 | 184/580 | chr2 | 110801654 | ||
| chr2:110805298
|
C | T | 1 | a0007 | 2 | HG00099.hp2 HG02735.hp1 |
missense_variant | MODERATE | c.656C>T | p.Ser219Leu | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/18 | 880/2699 | 656/1743 | 219/580 | chr2 | 110805298 | ||
| chr2:110841381
|
C | T | 3 | a0002a0005a0008 | 26 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(23): Show |
missense_variant | MODERATE | c.764C>T | p.Thr255Met | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/18 | 988/2699 | 764/1743 | 255/580 | chr2 | 110841381 | ||
| chr2:110908790
|
C | T | 2 | a0006a0012 | 4 | HG02897.hp2 HG02976.hp1 HG03516.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.790C>T | p.Arg264Trp | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/18 | 1014/2699 | 790/1743 | 264/580 | chr2 | 110908790 | ||
| chr2:110995965
|
GGTTCTTC others(47): Show |
G | 3 | a0000a0004a0008 | 11 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
splice_donor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.1246_1281+18delCTT others(51): Show |
p.Leu416_Lys427del | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/18 | 1470/2699 | 1246/1743 | 416/580 | INFO_REALIGN_3_PRIME | chr2 | 110995965 | |
| chr2:110995975
|
C | T | 1 | a0011 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1252C>T | p.Arg418Trp | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/18 | 1476/2699 | 1252/1743 | 418/580 | chr2 | 110995975 | ||
| chr2:111092935
|
C | T | 1 | a0009 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.1511C>T | p.Thr504Ile | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/18 | 1735/2699 | 1511/1743 | 504/580 | chr2 | 111092935 | ||
| chr2:111092938
|
C | T | 2 | a0003a0005 | 13 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(10): Show |
missense_variant | MODERATE | c.1514C>T | p.Pro505Leu | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/18 | 1738/2699 | 1514/1743 | 505/580 | chr2 | 111092938 | ||
| chr2:111117797
|
A | G | 1 | a0012 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1724A>G | p.Lys575Arg | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 18/18 | 1948/2699 | 1724/1743 | 575/580 | chr2 | 111117797 | ||
| chr2:111117802
|
G | T | 1 | a0010 | 1 | HG00323.hp1 | stop_gained | HIGH | c.1729G>T | p.Gly577* | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 18/18 | 1953/2699 | 1729/1743 | 577/580 | chr2 | 111117802 | ||
| chr2:111117814
|
T | C | 1 | a0000 | 2 | HG02257.hp1 NA19043.hp1 |
stop_lost | HIGH | c.1741T>C | p.Ter581Glnext*? | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 18/18 | 1965/2699 | 1741/1743 | 581/580 | chr2 | 111117814 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:110793679
|
T | C | 1 | a0011c0010 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.189T>C | p.Gly63Gly | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 4/18 | 413/2699 | 189/1743 | 63/580 | chr2 | 110793679 | ||
| chr2:110933570
|
G | A | 2 | a0001c0003a0002c0019 | 13 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(10): Show |
synonymous_variant | LOW | c.987G>A | p.Ala329Ala | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/18 | 1211/2699 | 987/1743 | 329/580 | chr2 | 110933570 | ||
| chr2:110987161
|
A | C | 1 | a0001c0017 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.1113A>C | p.Pro371Pro | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/18 | 1337/2699 | 1113/1743 | 371/580 | chr2 | 110987161 | ||
| chr2:110987197
|
G | C | 1 | a0001c0012 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.1149G>C | p.Val383Val | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/18 | 1373/2699 | 1149/1743 | 383/580 | chr2 | 110987197 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:110732587
|
G | A | 1 | a0001c0001t0005 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-210G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/18 | 35803 | chr2 | 110732587 | |||||
| chr2:110732658
|
C | A | 5 | a0002c0002t0003a0002c0002t0004a0003c0004t0003others(2): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-139C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/18 | 35732 | chr2 | 110732658 | |||||
| chr2:110732702
|
C | G | 5 | a0002c0002t0003a0002c0002t0004a0003c0004t0003others(2): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-95C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/18 | 35688 | chr2 | 110732702 | |||||
| chr2:110732761
|
C | G | 1 | a0004c0005t0007 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-36C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/18 | 35629 | chr2 | 110732761 | |||||
| chr2:111118222
|
GA | G | 14 | a0001c0001t0002a0001c0001t0006a0001c0003t0002others(11): Show | 50 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*418delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 18/18 | 418 | INFO_REALIGN_3_PRIME | chr2 | 111118222 | ||||
| chr2:111118228
|
A | T | 13 | a0001c0001t0002a0001c0003t0002a0001c0012t0002others(10): Show | 49 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*412A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 18/18 | 412 | chr2 | 111118228 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:110732860
|
A | C | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+86A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110732860 | ||||||
| chr2:110732979
|
T | C | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+205T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110732979 | ||||||
| chr2:110733005
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-23+231C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110733005 | ||||||
| chr2:110733010
|
G | A | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-23+236G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110733010 | ||||||
| chr2:110733154
|
C | T | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0002c0002t0001g0135others(2): Show | 5 | HG01243.hp2 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+380C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110733154 | ||||||
| chr2:110733317
|
TAAG | T | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+549_-23+551del others(3): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110733317 | |||||
| chr2:110733529
|
G | A | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+755G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110733529 | ||||||
| chr2:110733844
|
G | A | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-23+1070G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110733844 | ||||||
| chr2:110734026
|
A | G | 1 | a0004c0005t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-23+1252A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110734026 | ||||||
| chr2:110734122
|
A | C | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-23+1348A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110734122 | ||||||
| chr2:110734301
|
A | G | 13 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(10): Show | 13 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.-23+1527A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110734301 | ||||||
| chr2:110734416
|
C | T | 2 | a0001c0012t0002g0131a0013c0011t0001g0130 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-23+1642C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110734416 | ||||||
| chr2:110734596
|
C | T | 15 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0121others(12): Show | 15 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-23+1822C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110734596 | ||||||
| chr2:110734622
|
C | T | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-23+1848C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110734622 | ||||||
| chr2:110734894
|
C | CT | 149 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.-23+2122dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110734894 | |||||
| chr2:110734904
|
T | C | 51 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.-23+2130T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110734904 | ||||||
| chr2:110735018
|
G | C | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-23+2244G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110735018 | ||||||
| chr2:110735088
|
A | G | 10 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0001g0132others(7): Show | 10 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23+2314A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110735088 | ||||||
| chr2:110735229
|
T | C | 13 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(10): Show | 13 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.-23+2455T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110735229 | ||||||
| chr2:110735280
|
T | C | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-23+2506T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110735280 | ||||||
| chr2:110735456
|
G | A | 1 | a0002c0002t0001g0023 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-23+2682G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110735456 | ||||||
| chr2:110735669
|
A | G | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-23+2895A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110735669 | ||||||
| chr2:110735893
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-23+3119C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110735893 | ||||||
| chr2:110736251
|
T | C | 11 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0121others(8): Show | 11 | HG01891.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-23+3477T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110736251 | ||||||
| chr2:110736436
|
G | A | 14 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0028others(11): Show | 14 | HG00323.hp2 HG00423.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23+3662G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110736436 | ||||||
| chr2:110736469
|
T | C | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+3695T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110736469 | ||||||
| chr2:110736619
|
CT | C | 94 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-23+3863delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110736619 | |||||
| chr2:110736619
|
CTT | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0145others(12): Show | 15 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.-23+3862_-23+3863d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110736619 | |||||
| chr2:110736744
|
T | C | 126 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(123): Show | 126 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-23+3970T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110736744 | ||||||
| chr2:110736818
|
C | T | 11 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0086others(8): Show | 11 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.-23+4044C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110736818 | ||||||
| chr2:110736841
|
C | T | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+4067C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110736841 | ||||||
| chr2:110736909
|
T | C | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+4135T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110736909 | ||||||
| chr2:110737176
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+4402T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110737176 | ||||||
| chr2:110737353
|
T | A | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+4579T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110737353 | ||||||
| chr2:110737432
|
C | T | 1 | a0001c0003t0001g0036 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-23+4658C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110737432 | ||||||
| chr2:110737728
|
T | A | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+4954T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110737728 | ||||||
| chr2:110737728
|
T | G | 6 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+4954T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110737728 | ||||||
| chr2:110737773
|
C | T | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-23+4999C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110737773 | ||||||
| chr2:110737984
|
G | C | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+5210G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110737984 | ||||||
| chr2:110738656
|
A | C | 1 | a0002c0002t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-23+5882A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110738656 | ||||||
| chr2:110739181
|
T | C | 1 | a0007c0009t0001g0092 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-23+6407T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110739181 | ||||||
| chr2:110739395
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-23+6621T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110739395 | ||||||
| chr2:110739750
|
A | C | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+6976A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110739750 | ||||||
| chr2:110739770
|
T | C | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+6996T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110739770 | ||||||
| chr2:110739777
|
G | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0037a0002c0002t0001g0023 | 3 | HG00544.hp2 NA18974.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-23+7003G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110739777 | ||||||
| chr2:110739870
|
C | T | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+7096C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110739870 | ||||||
| chr2:110739910
|
G | A | 1 | a0013c0011t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-23+7136G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110739910 | ||||||
| chr2:110739966
|
G | C | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+7192G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110739966 | ||||||
| chr2:110740190
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-23+7416C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110740190 | ||||||
| chr2:110740344
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-23+7570A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110740344 | ||||||
| chr2:110740406
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-23+7632G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110740406 | ||||||
| chr2:110740851
|
C | T | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+8077C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110740851 | ||||||
| chr2:110740890
|
C | G | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+8116C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110740890 | ||||||
| chr2:110741073
|
C | G | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-23+8299C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110741073 | ||||||
| chr2:110741226
|
G | A | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+8452G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110741226 | ||||||
| chr2:110741414
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-23+8640C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110741414 | ||||||
| chr2:110741489
|
T | G | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+8715T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110741489 | ||||||
| chr2:110742075
|
G | A | 11 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0002g0147others(8): Show | 11 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.-23+9301G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110742075 | ||||||
| chr2:110742283
|
T | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0002g0006others(2): Show | 5 | HG02451.hp2 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+9509T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110742283 | ||||||
| chr2:110742357
|
G | T | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-23+9583G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110742357 | ||||||
| chr2:110742526
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-23+9752C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110742526 | ||||||
| chr2:110742584
|
C | A | 2 | a0001c0001t0002g0076a0001c0003t0001g0075 | 2 | NA18950.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-23+9810C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110742584 | ||||||
| chr2:110742737
|
A | G | 1 | a0001c0017t0002g0073 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-23+9963A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110742737 | ||||||
| chr2:110742916
|
G | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+10142G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110742916 | ||||||
| chr2:110742951
|
G | C | 1 | a0010c0015t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-23+10177G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110742951 | ||||||
| chr2:110742955
|
A | G | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-23+10181A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110742955 | ||||||
| chr2:110742973
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-23+10199G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110742973 | ||||||
| chr2:110743558
|
A | G | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+10784A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110743558 | ||||||
| chr2:110743601
|
T | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.-23+10827T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110743601 | ||||||
| chr2:110743644
|
C | T | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-23+10870C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110743644 | ||||||
| chr2:110743847
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+11073C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110743847 | ||||||
| chr2:110743876
|
T | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+11102T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110743876 | ||||||
| chr2:110744001
|
C | T | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-23+11227C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110744001 | ||||||
| chr2:110744211
|
G | A | 3 | a0001c0001t0002g0094a0002c0019t0001g0095a0003c0004t0001g0093 | 3 | HG02040.hp1 NA18993.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-23+11437G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110744211 | ||||||
| chr2:110744554
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-23+11780C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110744554 | ||||||
| chr2:110744557
|
G | A | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+11783G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110744557 | ||||||
| chr2:110744628
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-23+11854C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110744628 | ||||||
| chr2:110744680
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0005g0149others(1): Show | 4 | HG01891.hp2 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+11906G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110744680 | ||||||
| chr2:110744830
|
A | C | 1 | a0009c0016t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-23+12056A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110744830 | ||||||
| chr2:110744880
|
T | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+12106T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110744880 | ||||||
| chr2:110744915
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-23+12141A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110744915 | ||||||
| chr2:110745105
|
G | T | 2 | a0000c0014t0001g0072a0001c0001t0002g0071 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-23+12331G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110745105 | ||||||
| chr2:110745312
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-23+12538G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110745312 | ||||||
| chr2:110745487
|
G | T | 1 | a0000c0014t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-23+12713G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110745487 | ||||||
| chr2:110745535
|
GAC | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0024others(27): Show | 30 | HG01167.hp1 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.-23+12762_-23+1276 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110745535 | ||||||
| chr2:110745727
|
C | CGTGCAAG others(27): Show |
1 | a0001c0001t0001g0038 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-23+12957_-23+1299 others(38): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110745727 | |||||
| chr2:110745741
|
A | G | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-23+12967A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110745741 | ||||||
| chr2:110746059
|
C | T | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-23+13285C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110746059 | ||||||
| chr2:110746209
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-23+13435G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110746209 | ||||||
| chr2:110746237
|
G | A | 1 | a0001c0001t0002g0040 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-23+13463G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110746237 | ||||||
| chr2:110746325
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-23+13551G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110746325 | ||||||
| chr2:110746407
|
A | G | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-23+13633A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110746407 | ||||||
| chr2:110746675
|
T | C | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-23+13901T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110746675 | ||||||
| chr2:110746791
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-23+14017C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110746791 | ||||||
| chr2:110746809
|
C | G | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-23+14035C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110746809 | ||||||
| chr2:110746936
|
A | G | 1 | a0004c0005t0002g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-23+14162A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110746936 | ||||||
| chr2:110746968
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-23+14194A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110746968 | ||||||
| chr2:110747014
|
G | C | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-23+14240G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110747014 | ||||||
| chr2:110747014
|
G | T | 3 | a0001c0001t0002g0094a0002c0019t0001g0095a0003c0004t0001g0093 | 3 | HG02040.hp1 NA18993.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-23+14240G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110747014 | ||||||
| chr2:110747467
|
C | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(14): Show | 17 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.-23+14693C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110747467 | ||||||
| chr2:110747823
|
G | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+15049G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110747823 | ||||||
| chr2:110747951
|
A | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+15177A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110747951 | ||||||
| chr2:110748204
|
G | C | 1 | a0001c0003t0001g0041 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-23+15430G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110748204 | ||||||
| chr2:110748635
|
A | G | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-23+15861A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110748635 | ||||||
| chr2:110748726
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-23+15952G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110748726 | ||||||
| chr2:110748779
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+16005C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110748779 | ||||||
| chr2:110748904
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+16130C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110748904 | ||||||
| chr2:110749250
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+16476A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110749250 | ||||||
| chr2:110749352
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-23+16578A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110749352 | ||||||
| chr2:110749369
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-23+16595C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110749369 | ||||||
| chr2:110749513
|
G | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-23+16739G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110749513 | ||||||
| chr2:110749584
|
T | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-23+16810T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110749584 | ||||||
| chr2:110749590
|
C | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-23+16816C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110749590 | ||||||
| chr2:110749596
|
C | T | 10 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0121others(7): Show | 10 | HG01891.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23+16822C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110749596 | ||||||
| chr2:110749798
|
G | A | 7 | a0001c0001t0005g0149a0002c0002t0003g0139a0002c0002t0003g0142others(4): Show | 7 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+17024G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110749798 | ||||||
| chr2:110749911
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-23+17137G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110749911 | ||||||
| chr2:110749990
|
C | T | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+17216C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110749990 | ||||||
| chr2:110750033
|
G | A | 1 | a0002c0002t0003g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-23+17259G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110750033 | ||||||
| chr2:110750213
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-23+17439G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110750213 | ||||||
| chr2:110750565
|
T | C | 7 | a0001c0001t0005g0149a0002c0002t0003g0139a0002c0002t0003g0142others(4): Show | 7 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+17791T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110750565 | ||||||
| chr2:110750683
|
GTA | G | 3 | a0001c0001t0001g0037a0001c0001t0001g0137a0001c0001t0005g0149 | 3 | HG00544.hp2 HG02922.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-22-17671_-22-1767 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110750683 | |||||
| chr2:110750685
|
A | G | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-17683A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110750685 | ||||||
| chr2:110750693
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-22-17675A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110750693 | ||||||
| chr2:110750694
|
T | C | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-22-17674T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110750694 | ||||||
| chr2:110750805
|
T | C | 1 | a0002c0002t0003g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-22-17563T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110750805 | ||||||
| chr2:110750923
|
G | A | 1 | a0003c0004t0004g0140 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-22-17445G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110750923 | ||||||
| chr2:110750950
|
T | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.-22-17418T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110750950 | ||||||
| chr2:110751240
|
G | A | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-17128G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110751240 | ||||||
| chr2:110751298
|
CA | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 13 | HG01257.hp2 HG01258.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.-22-17045delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110751298 | |||||
| chr2:110751322
|
A | T | 2 | a0001c0001t0006g0017a0008c0008t0001g0016 | 2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-22-17046A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110751322 | ||||||
| chr2:110751618
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-22-16750G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110751618 | ||||||
| chr2:110751624
|
T | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG02027.hp2 NA18950.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-16744T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110751624 | ||||||
| chr2:110751628
|
A | C | 1 | a0002c0019t0001g0095 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-22-16740A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110751628 | ||||||
| chr2:110752023
|
CT | C | 19 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.-22-16329delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110752023 | |||||
| chr2:110752097
|
T | A | 5 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0002g0147others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-16271T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110752097 | ||||||
| chr2:110752228
|
G | C | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-16140G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110752228 | ||||||
| chr2:110752339
|
C | T | 7 | a0001c0001t0005g0149a0002c0002t0003g0139a0002c0002t0003g0142others(4): Show | 7 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-16029C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110752339 | ||||||
| chr2:110752548
|
G | A | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-15820G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110752548 | ||||||
| chr2:110752732
|
G | A | 1 | a0001c0003t0002g0043 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-22-15636G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110752732 | ||||||
| chr2:110752939
|
G | A | 7 | a0001c0001t0005g0149a0002c0002t0003g0139a0002c0002t0003g0142others(4): Show | 7 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-15429G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110752939 | ||||||
| chr2:110753053
|
T | C | 56 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-22-15315T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110753053 | ||||||
| chr2:110753073
|
G | A | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-22-15295G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110753073 | ||||||
| chr2:110753092
|
G | A | 2 | a0001c0001t0001g0044a0001c0017t0002g0073 | 2 | HG00140.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-22-15276G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110753092 | ||||||
| chr2:110753136
|
C | T | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-15232C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110753136 | ||||||
| chr2:110753141
|
GCACCTCC others(27): Show |
G | 1 | a0001c0001t0001g0038 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-22-15224_-22-1519 others(38): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110753141 | |||||
| chr2:110753234
|
C | A | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-22-15134C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110753234 | ||||||
| chr2:110753266
|
A | G | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-15102A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110753266 | ||||||
| chr2:110753272
|
A | G | 24 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.-22-15096A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110753272 | ||||||
| chr2:110753542
|
T | A | 7 | a0001c0001t0005g0149a0002c0002t0003g0139a0002c0002t0003g0142others(4): Show | 7 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-14826T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110753542 | ||||||
| chr2:110753551
|
G | A | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-22-14817G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110753551 | ||||||
| chr2:110753714
|
A | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-22-14654A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110753714 | ||||||
| chr2:110753839
|
G | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0002g0006 | 3 | HG02451.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-22-14529G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110753839 | ||||||
| chr2:110754031
|
C | CGT | 2 | a0002c0002t0001g0066a0010c0015t0001g0074 | 2 | HG00323.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-22-14310_-22-1430 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110754031 | |||||
| chr2:110754031
|
CGT | C | 48 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.-22-14310_-22-1430 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110754031 | |||||
| chr2:110754031
|
CGTGT | C | 9 | a0000c0013t0001g0046a0001c0001t0001g0039a0001c0001t0001g0045others(6): Show | 9 | HG01257.hp2 HG01258.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22-14312_-22-1430 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110754031 | |||||
| chr2:110754031
|
CGTGTGT | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-22-14314_-22-1430 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110754031 | |||||
| chr2:110754070
|
A | ATTT | 5 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-14280_-22-1427 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110754070 | |||||
| chr2:110754287
|
G | C | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-22-14081G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110754287 | ||||||
| chr2:110754320
|
C | A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-22-14048C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110754320 | ||||||
| chr2:110754341
|
A | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.-22-14027A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110754341 | ||||||
| chr2:110754697
|
T | C | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-13671T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110754697 | ||||||
| chr2:110754879
|
A | G | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-22-13489A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110754879 | ||||||
| chr2:110755289
|
A | G | 5 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0002g0147others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-13079A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110755289 | ||||||
| chr2:110755451
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0002g0147others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-12917C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110755451 | ||||||
| chr2:110755906
|
T | TA | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-12454dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110755906 | |||||
| chr2:110756032
|
AT | A | 50 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-22-12334delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110756032 | |||||
| chr2:110756283
|
C | A | 7 | a0001c0001t0005g0149a0002c0002t0003g0139a0002c0002t0003g0142others(4): Show | 7 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-12085C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110756283 | ||||||
| chr2:110756418
|
C | T | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-11950C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110756418 | ||||||
| chr2:110756423
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0002g0033 | 2 | HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-22-11945C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110756423 | ||||||
| chr2:110756481
|
T | C | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-11887T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110756481 | ||||||
| chr2:110756608
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-22-11760A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110756608 | ||||||
| chr2:110756628
|
C | T | 7 | a0001c0001t0005g0149a0002c0002t0003g0139a0002c0002t0003g0142others(4): Show | 7 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-11740C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110756628 | ||||||
| chr2:110756902
|
C | CT | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-11459dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110756902 | |||||
| chr2:110756934
|
T | C | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-11434T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110756934 | ||||||
| chr2:110757062
|
C | A | 2 | a0001c0001t0001g0100a0002c0002t0001g0099 | 2 | HG01258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-22-11306C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110757062 | ||||||
| chr2:110757391
|
T | C | 1 | a0002c0002t0001g0023 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-22-10977T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110757391 | ||||||
| chr2:110757487
|
T | C | 127 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(124): Show | 127 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-22-10881T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110757487 | ||||||
| chr2:110757488
|
G | A | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-22-10880G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110757488 | ||||||
| chr2:110757551
|
C | T | 6 | a0001c0001t0001g0088a0001c0003t0001g0081a0001c0003t0001g0087others(3): Show | 6 | HG01081.hp2 HG01167.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-10817C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110757551 | ||||||
| chr2:110757600
|
A | G | 17 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0080others(14): Show | 17 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-22-10768A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110757600 | ||||||
| chr2:110757658
|
G | C | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-22-10710G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110757658 | ||||||
| chr2:110757783
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-22-10585C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110757783 | ||||||
| chr2:110757903
|
C | T | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-10465C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110757903 | ||||||
| chr2:110757908
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0002g0147others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-10460C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110757908 | ||||||
| chr2:110758099
|
T | C | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-10269T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110758099 | ||||||
| chr2:110758236
|
G | C | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0002c0002t0001g0135others(2): Show | 5 | HG01243.hp2 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22-10132G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110758236 | ||||||
| chr2:110758850
|
C | T | 2 | a0001c0001t0001g0063a0003c0004t0001g0064 | 2 | HG01496.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.-22-9518C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110758850 | ||||||
| chr2:110758895
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-22-9473C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110758895 | ||||||
| chr2:110758901
|
A | T | 1 | a0001c0001t0001g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-22-9467A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110758901 | ||||||
| chr2:110759015
|
T | A | 1 | a0001c0017t0002g0073 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-22-9353T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110759015 | ||||||
| chr2:110759191
|
C | G | 1 | a0001c0001t0002g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-22-9177C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110759191 | ||||||
| chr2:110759217
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-22-9151G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110759217 | ||||||
| chr2:110759737
|
C | T | 7 | a0001c0001t0005g0149a0002c0002t0003g0139a0002c0002t0003g0142others(4): Show | 7 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-8631C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110759737 | ||||||
| chr2:110760030
|
ATTTCT | A | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-8334_-22-8330d others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110760030 | |||||
| chr2:110760040
|
T | C | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-22-8328T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110760040 | ||||||
| chr2:110760070
|
A | G | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-22-8298A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110760070 | ||||||
| chr2:110760171
|
A | G | 12 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22-8197A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110760171 | ||||||
| chr2:110760303
|
T | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.-22-8065T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110760303 | ||||||
| chr2:110760390
|
C | T | 1 | a0009c0016t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-22-7978C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110760390 | ||||||
| chr2:110760433
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-22-7935C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110760433 | ||||||
| chr2:110760568
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-22-7800A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110760568 | ||||||
| chr2:110761362
|
T | A | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-22-7006T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110761362 | ||||||
| chr2:110761654
|
C | T | 2 | a0002c0002t0001g0061a0005c0007t0001g0062 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-22-6714C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110761654 | ||||||
| chr2:110761890
|
C | T | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.-22-6478C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110761890 | ||||||
| chr2:110762039
|
G | A | 2 | a0001c0001t0001g0035a0014c0020t0001g0002 | 2 | HG01257.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-22-6329G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110762039 | ||||||
| chr2:110762536
|
A | G | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-22-5832A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110762536 | ||||||
| chr2:110762576
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | NA18946.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-22-5792C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110762576 | ||||||
| chr2:110762585
|
T | A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-22-5783T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110762585 | ||||||
| chr2:110762676
|
G | A | 1 | a0002c0002t0002g0013 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-22-5692G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110762676 | ||||||
| chr2:110762822
|
A | G | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0002c0002t0001g0019others(3): Show | 6 | HG01167.hp1 HG01243.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-5546A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110762822 | ||||||
| chr2:110762896
|
A | G | 1 | a0001c0003t0001g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-22-5472A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110762896 | ||||||
| chr2:110762958
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-22-5410A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110762958 | ||||||
| chr2:110763166
|
A | G | 6 | a0001c0001t0001g0044a0001c0001t0002g0060a0001c0012t0002g0131others(3): Show | 6 | HG00140.hp2 HG01168.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-5202A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110763166 | ||||||
| chr2:110763616
|
A | T | 5 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0002g0147others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-4752A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110763616 | ||||||
| chr2:110764271
|
C | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-22-4097C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110764271 | ||||||
| chr2:110764284
|
G | C | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-4084G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110764284 | ||||||
| chr2:110764532
|
T | C | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-22-3836T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110764532 | ||||||
| chr2:110764540
|
T | C | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-22-3828T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110764540 | ||||||
| chr2:110764743
|
G | A | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-22-3625G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110764743 | ||||||
| chr2:110764796
|
G | A | 5 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0002g0147others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-3572G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110764796 | ||||||
| chr2:110764832
|
C | A | 1 | a0001c0001t0001g0025 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-22-3536C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110764832 | ||||||
| chr2:110764846
|
T | C | 1 | a0001c0003t0001g0087 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-22-3522T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110764846 | ||||||
| chr2:110764911
|
T | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-22-3457T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110764911 | ||||||
| chr2:110765124
|
T | G | 1 | a0001c0001t0002g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-22-3244T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110765124 | ||||||
| chr2:110765207
|
T | C | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-3161T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110765207 | ||||||
| chr2:110765291
|
A | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-22-3077A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110765291 | ||||||
| chr2:110765361
|
A | G | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-22-3007A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110765361 | ||||||
| chr2:110765400
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-22-2968A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110765400 | ||||||
| chr2:110765836
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-2532T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110765836 | ||||||
| chr2:110765878
|
C | G | 1 | a0001c0001t0001g0042 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-22-2490C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110765878 | ||||||
| chr2:110766064
|
G | A | 5 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0002g0147others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-2304G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110766064 | ||||||
| chr2:110766086
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-22-2282A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110766086 | ||||||
| chr2:110766123
|
A | G | 2 | a0001c0001t0002g0076a0001c0003t0001g0075 | 2 | NA18950.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-22-2245A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110766123 | ||||||
| chr2:110766592
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-22-1776T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110766592 | ||||||
| chr2:110766752
|
C | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 5 | HG00323.hp1 HG02109.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22-1616C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110766752 | ||||||
| chr2:110766826
|
A | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.-22-1542A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110766826 | ||||||
| chr2:110766957
|
C | T | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-22-1411C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110766957 | ||||||
| chr2:110767194
|
G | A | 1 | a0003c0004t0001g0026 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-22-1174G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110767194 | ||||||
| chr2:110767440
|
A | C | 1 | a0001c0001t0001g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-22-928A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110767440 | ||||||
| chr2:110767444
|
C | T | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0002c0002t0001g0019others(3): Show | 6 | HG01167.hp1 HG01243.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-924C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110767444 | ||||||
| chr2:110767485
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0126a0001c0001t0001g0128others(3): Show | 6 | HG02145.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-883G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110767485 | ||||||
| chr2:110767488
|
C | T | 7 | a0001c0001t0005g0149a0002c0002t0003g0139a0002c0002t0003g0142others(4): Show | 7 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-880C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110767488 | ||||||
| chr2:110767632
|
A | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-22-736A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110767632 | ||||||
| chr2:110767922
|
AAACAC | A | 2 | a0002c0002t0001g0023a0004c0005t0001g0134 | 2 | HG01243.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-22-444_-22-440del others(5): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110767922 | |||||
| chr2:110767923
|
A | AAC | 6 | a0001c0001t0001g0038a0001c0001t0001g0044a0002c0002t0001g0135others(3): Show | 6 | HG02735.hp1 HG02735.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-389_-22-388dup others(2): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110767923 | |||||
| chr2:110767923
|
A | C | 1 | a0007c0009t0001g0106 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-22-445A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110767923 | ||||||
| chr2:110767923
|
AAC | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0024others(12): Show | 15 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-22-389_-22-388del others(2): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110767923 | |||||
| chr2:110767923
|
AACAC | A | 23 | a0000c0014t0001g0072a0001c0001t0001g0055a0001c0001t0001g0056others(20): Show | 23 | HG00438.hp2 HG01175.hp2 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.-22-391_-22-388del others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110767923 | |||||
| chr2:110767923
|
AACACAC | A | 46 | a0000c0013t0001g0046a0001c0001t0001g0025a0001c0001t0001g0029others(43): Show | 46 | HG00140.hp1 HG00673.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.-22-393_-22-388del others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110767923 | |||||
| chr2:110767923
|
AACACACA others(1): Show |
A | 19 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0021others(16): Show | 19 | HG00323.hp2 HG00423.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22-395_-22-388del others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110767923 | |||||
| chr2:110767923
|
AACACACA others(3): Show |
A | 5 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0067others(2): Show | 5 | HG00323.hp1 HG01081.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-397_-22-388del others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110767923 | |||||
| chr2:110767923
|
AACACACA others(7): Show |
A | 2 | a0001c0001t0001g0100a0002c0002t0001g0099 | 2 | HG01258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-22-401_-22-388del others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110767923 | |||||
| chr2:110767923
|
AACACACA others(9): Show |
A | 5 | a0001c0001t0001g0008a0001c0001t0006g0017a0008c0008t0001g0015others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-403_-22-388del others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110767923 | |||||
| chr2:110767923
|
AACACACA others(11): Show |
A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0145others(2): Show | 5 | HG01891.hp2 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-405_-22-388del others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110767923 | |||||
| chr2:110767923
|
AACACACA others(15): Show |
A | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-409_-22-388del others(22): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110767923 | |||||
| chr2:110767923
|
AACACACA others(23): Show |
A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-22-417_-22-388del others(30): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110767923 | |||||
| chr2:110767977
|
CACA | C | 2 | a0001c0001t0002g0065a0007c0009t0001g0106 | 2 | HG00099.hp1 HG00099.hp2 |
intron_variant | MODIFIER | c.-22-389_-22-387del others(3): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 110767977 | |||||
| chr2:110768081
|
G | A | 1 | a0002c0002t0003g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-22-287G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110768081 | ||||||
| chr2:110768098
|
C | T | 1 | a0002c0002t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-22-270C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110768098 | ||||||
| chr2:110768143
|
T | A | 51 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.-22-225T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110768143 | ||||||
| chr2:110768147
|
T | G | 33 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(30): Show | 33 | HG01167.hp1 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-22-221T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | chr2 | 110768147 | ||||||
| chr2:110768492
|
T | TTGTGTGT others(5): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.75+39_75+50dupTGTG others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110768492 | |||||
| chr2:110768492
|
T | TTGTGTGT others(7): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0012a0011c0010t0002g0009 | 3 | HG01891.hp2 HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.75+37_75+50dupTGTG others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110768492 | |||||
| chr2:110768492
|
T | TTGTGTGT others(11): Show |
1 | a0001c0001t0001g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.75+33_75+50dupTGTG others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110768492 | |||||
| chr2:110768492
|
T | TTGTGTGT others(15): Show |
4 | a0001c0001t0001g0150a0002c0002t0002g0147a0002c0002t0002g0148others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+29_75+50dupTGTG others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110768492 | |||||
| chr2:110768513
|
T | TGTGTGTG others(9): Show |
1 | a0002c0002t0003g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.75+50_75+51insTGTG others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110768513 | |||||
| chr2:110768513
|
T | TGTGTGTG others(9): Show |
5 | a0002c0002t0003g0142a0002c0002t0004g0141a0003c0004t0003g0143others(2): Show | 5 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+50_75+51insTGTG others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110768513 | |||||
| chr2:110768513
|
T | TGTGTGTG others(7): Show |
1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.75+50_75+51insTGTG others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110768513 | |||||
| chr2:110768513
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.75+50_75+51insTGTG others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110768513 | |||||
| chr2:110768513
|
TGA | T | 36 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(33): Show | 36 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.75+73_75+74delAG | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110768513 | |||||
| chr2:110768515
|
A | T | 3 | a0002c0002t0001g0132a0002c0002t0002g0147a0002c0002t0002g0148 | 3 | HG01257.hp2 HG01258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+51A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110768515 | ||||||
| chr2:110768669
|
C | T | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.75+205C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110768669 | ||||||
| chr2:110768712
|
T | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.75+248T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110768712 | ||||||
| chr2:110768727
|
C | T | 4 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0002g0052others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+263C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110768727 | ||||||
| chr2:110768729
|
C | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+265C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110768729 | ||||||
| chr2:110768738
|
A | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+274A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110768738 | ||||||
| chr2:110768906
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0126a0001c0001t0001g0128others(3): Show | 6 | HG02145.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+442G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110768906 | ||||||
| chr2:110769133
|
T | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.75+669T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110769133 | ||||||
| chr2:110769226
|
A | AAAAG | 15 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0109others(12): Show | 15 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+798_75+801dupGA others(2): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110769226 | |||||
| chr2:110769226
|
A | AAAAGAAA others(9): Show |
4 | a0001c0001t0001g0145a0001c0001t0006g0017a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+786_75+801dupGA others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110769226 | |||||
| chr2:110769226
|
A | AAAAGAAA others(13): Show |
1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+782_75+801dupGA others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110769226 | |||||
| chr2:110769226
|
AAAAG | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 24 | HG00140.hp1 HG01168.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.75+798_75+801delGA others(2): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110769226 | |||||
| chr2:110769564
|
A | T | 7 | a0001c0001t0005g0149a0002c0002t0003g0139a0002c0002t0003g0142others(4): Show | 7 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1100A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110769564 | ||||||
| chr2:110769610
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+1146G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110769610 | ||||||
| chr2:110769650
|
T | TAAAAC | 5 | a0001c0001t0001g0010a0001c0001t0001g0145a0001c0001t0001g0150others(2): Show | 5 | HG02922.hp2 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+1216_75+1220dup others(5): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110769650 | |||||
| chr2:110769650
|
T | TAAAACAA others(3): Show |
6 | a0001c0001t0001g0008a0001c0001t0001g0011a0002c0002t0002g0147others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+1211_75+1220dup others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110769650 | |||||
| chr2:110769650
|
T | TAAAACAA others(8): Show |
1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.75+1206_75+1220dup others(15): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110769650 | |||||
| chr2:110769650
|
TAAAAC | T | 2 | a0002c0002t0003g0142a0002c0002t0004g0141 | 2 | HG00423.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.75+1216_75+1220del others(5): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110769650 | |||||
| chr2:110769650
|
TAAAACAA others(3): Show |
T | 1 | a0004c0005t0002g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.75+1211_75+1220del others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110769650 | |||||
| chr2:110769775
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+1311G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110769775 | ||||||
| chr2:110769791
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.75+1327G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110769791 | ||||||
| chr2:110769914
|
AC | A | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.75+1452delC | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110769914 | |||||
| chr2:110770013
|
G | A | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.75+1549G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110770013 | ||||||
| chr2:110770078
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0002g0147others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+1614C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110770078 | ||||||
| chr2:110770681
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.75+2217A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110770681 | ||||||
| chr2:110770948
|
C | G | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.75+2484C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110770948 | ||||||
| chr2:110771126
|
C | A | 5 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0002g0147others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+2662C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110771126 | ||||||
| chr2:110771348
|
C | A | 1 | a0001c0001t0002g0033 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.75+2884C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110771348 | ||||||
| chr2:110771390
|
G | A | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.75+2926G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110771390 | ||||||
| chr2:110771413
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+2949A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110771413 | ||||||
| chr2:110771504
|
A | G | 3 | a0001c0001t0001g0110a0001c0001t0002g0101a0001c0003t0002g0104 | 3 | HG00438.hp2 HG02027.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.75+3040A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110771504 | ||||||
| chr2:110771561
|
C | G | 2 | a0001c0001t0001g0145a0006c0006t0002g0146 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.75+3097C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110771561 | ||||||
| chr2:110771780
|
G | A | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.75+3316G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110771780 | ||||||
| chr2:110771810
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG01081.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.75+3346A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110771810 | ||||||
| chr2:110771953
|
C | T | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0002c0002t0001g0019others(3): Show | 6 | HG01167.hp1 HG01243.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+3489C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110771953 | ||||||
| chr2:110771993
|
A | T | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0002c0002t0001g0019others(3): Show | 6 | HG01167.hp1 HG01243.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+3529A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110771993 | ||||||
| chr2:110772000
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.75+3536C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110772000 | ||||||
| chr2:110772017
|
A | G | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+3553A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110772017 | ||||||
| chr2:110772215
|
A | G | 5 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0002g0147others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+3751A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110772215 | ||||||
| chr2:110772264
|
T | C | 10 | a0001c0001t0005g0149a0001c0001t0006g0017a0002c0002t0003g0139others(7): Show | 10 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+3800T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110772264 | ||||||
| chr2:110772627
|
C | G | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.75+4163C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110772627 | ||||||
| chr2:110772769
|
C | G | 5 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0002g0147others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+4305C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110772769 | ||||||
| chr2:110772825
|
T | C | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.75+4361T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110772825 | ||||||
| chr2:110772876
|
A | G | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.75+4412A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110772876 | ||||||
| chr2:110773739
|
C | A | 1 | a0001c0003t0001g0036 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.75+5275C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110773739 | ||||||
| chr2:110774103
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.75+5639A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110774103 | ||||||
| chr2:110774184
|
A | C | 7 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+5720A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110774184 | ||||||
| chr2:110774189
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0002g0052 | 3 | HG02615.hp2 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.75+5725G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110774189 | ||||||
| chr2:110774380
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.75+5916G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110774380 | ||||||
| chr2:110775261
|
A | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.75+6797A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110775261 | ||||||
| chr2:110775556
|
C | G | 1 | a0001c0003t0001g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.75+7092C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110775556 | ||||||
| chr2:110775732
|
A | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.75+7268A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110775732 | ||||||
| chr2:110776008
|
C | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.75+7544C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110776008 | ||||||
| chr2:110776114
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.75+7650T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110776114 | ||||||
| chr2:110776125
|
G | A | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+7661G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110776125 | ||||||
| chr2:110776244
|
G | A | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.75+7780G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110776244 | ||||||
| chr2:110776527
|
C | G | 6 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0006g0017others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+8063C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110776527 | ||||||
| chr2:110776568
|
GC | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.75+8105delC | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110776568 | ||||||
| chr2:110776816
|
C | T | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.76-7916C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110776816 | ||||||
| chr2:110777009
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.76-7723G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777009 | ||||||
| chr2:110777025
|
C | T | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.76-7707C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777025 | ||||||
| chr2:110777280
|
G | C | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.76-7452G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777280 | ||||||
| chr2:110777318
|
A | G | 4 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-7414A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777318 | ||||||
| chr2:110777394
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.76-7338G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777394 | ||||||
| chr2:110777395
|
G | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.76-7337G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777395 | ||||||
| chr2:110777469
|
C | G | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.76-7263C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777469 | ||||||
| chr2:110777490
|
A | G | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.76-7242A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777490 | ||||||
| chr2:110777504
|
T | A | 1 | a0013c0011t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.76-7228T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777504 | ||||||
| chr2:110777508
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.76-7224C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777508 | ||||||
| chr2:110777552
|
CT | C | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-7177delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110777552 | |||||
| chr2:110777583
|
A | G | 6 | a0000c0014t0001g0072a0001c0001t0001g0042a0001c0001t0002g0057others(3): Show | 6 | HG01175.hp1 HG02257.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-7149A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777583 | ||||||
| chr2:110777714
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0126a0001c0001t0001g0128others(3): Show | 6 | HG02145.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-7018G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777714 | ||||||
| chr2:110777775
|
G | C | 1 | a0003c0004t0002g0069 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.76-6957G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777775 | ||||||
| chr2:110777824
|
T | C | 33 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0018others(30): Show | 33 | HG01167.hp1 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-6908T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110777824 | ||||||
| chr2:110778207
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.76-6525C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110778207 | ||||||
| chr2:110778367
|
A | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.76-6365A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110778367 | ||||||
| chr2:110778446
|
T | C | 32 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0021others(29): Show | 32 | HG01167.hp1 HG01243.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.76-6286T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110778446 | ||||||
| chr2:110778641
|
G | A | 1 | a0001c0017t0002g0073 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.76-6091G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110778641 | ||||||
| chr2:110778846
|
A | G | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.76-5886A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110778846 | ||||||
| chr2:110778935
|
A | G | 7 | a0001c0001t0001g0102a0002c0002t0003g0139a0002c0002t0003g0142others(4): Show | 7 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-5797A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110778935 | ||||||
| chr2:110779091
|
A | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.76-5641A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110779091 | ||||||
| chr2:110779662
|
C | T | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.76-5070C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110779662 | ||||||
| chr2:110779918
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.76-4814A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110779918 | ||||||
| chr2:110780770
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.76-3962A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110780770 | ||||||
| chr2:110780940
|
G | T | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.76-3792G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110780940 | ||||||
| chr2:110780980
|
C | T | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.76-3752C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110780980 | ||||||
| chr2:110781249
|
C | T | 7 | a0000c0013t0001g0046a0001c0001t0001g0039a0001c0001t0001g0045others(4): Show | 7 | HG02886.hp2 HG03139.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-3483C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110781249 | ||||||
| chr2:110781307
|
T | C | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.76-3425T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110781307 | ||||||
| chr2:110781511
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.76-3221G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110781511 | ||||||
| chr2:110781596
|
C | T | 1 | a0002c0002t0001g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.76-3136C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110781596 | ||||||
| chr2:110782090
|
AATT | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.76-2632_76-2630del others(3): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 110782090 | |||||
| chr2:110782305
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-2427C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110782305 | ||||||
| chr2:110782331
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.76-2401A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110782331 | ||||||
| chr2:110782476
|
G | T | 146 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.76-2256G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110782476 | ||||||
| chr2:110782527
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.76-2205A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110782527 | ||||||
| chr2:110782592
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-2140G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110782592 | ||||||
| chr2:110782966
|
G | A | 17 | a0001c0001t0001g0024a0001c0001t0001g0116a0001c0001t0001g0117others(14): Show | 17 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-1766G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110782966 | ||||||
| chr2:110783081
|
C | T | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0002g0071others(4): Show | 7 | HG01167.hp1 HG01243.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-1651C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110783081 | ||||||
| chr2:110783901
|
T | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-831T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110783901 | ||||||
| chr2:110784483
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0082 | 2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.76-249C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | 110784483 | ||||||
| chr2:110784856
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.159+41C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110784856 | ||||||
| chr2:110784989
|
G | C | 2 | a0001c0001t0001g0113a0002c0002t0001g0103 | 2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.159+174G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110784989 | ||||||
| chr2:110785142
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.159+327A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110785142 | ||||||
| chr2:110785280
|
A | G | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.159+465A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110785280 | ||||||
| chr2:110785370
|
T | TTG | 38 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0031others(35): Show | 38 | HG00423.hp2 HG00673.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.159+584_159+585dup others(2): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 110785370 | |||||
| chr2:110785370
|
T | TTGTG | 9 | a0001c0001t0001g0028a0001c0001t0002g0065a0001c0001t0006g0017others(6): Show | 9 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(6): Show |
intron_variant | MODIFIER | c.159+582_159+585dup others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 110785370 | |||||
| chr2:110785370
|
T | TTGTGTG | 2 | a0001c0001t0001g0010a0001c0001t0001g0012 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.159+580_159+585dup others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 110785370 | |||||
| chr2:110785370
|
T | TTGTGTGT others(1): Show |
2 | a0001c0001t0001g0011a0014c0020t0001g0002 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.159+578_159+585dup others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 110785370 | |||||
| chr2:110785370
|
T | TTGTGTGT others(3): Show |
4 | a0001c0001t0001g0008a0001c0001t0001g0145a0001c0001t0001g0150others(1): Show | 4 | HG02258.hp1 HG03195.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+576_159+585dup others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 110785370 | |||||
| chr2:110785370
|
T | TTGTGTGT others(5): Show |
1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.159+574_159+585dup others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 110785370 | |||||
| chr2:110785424
|
T | C | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.159+609T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110785424 | ||||||
| chr2:110785650
|
A | C | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.159+835A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110785650 | ||||||
| chr2:110785770
|
C | T | 3 | a0001c0001t0002g0094a0002c0019t0001g0095a0003c0004t0001g0093 | 3 | HG02040.hp1 NA18993.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.159+955C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110785770 | ||||||
| chr2:110785833
|
A | G | 1 | a0003c0004t0004g0140 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.159+1018A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110785833 | ||||||
| chr2:110785898
|
G | A | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.159+1083G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110785898 | ||||||
| chr2:110785910
|
C | T | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.159+1095C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110785910 | ||||||
| chr2:110786025
|
C | G | 2 | a0001c0001t0001g0145a0006c0006t0002g0146 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.159+1210C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110786025 | ||||||
| chr2:110786036
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.159+1221G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110786036 | ||||||
| chr2:110786290
|
G | T | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.159+1475G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110786290 | ||||||
| chr2:110786720
|
G | A | 2 | a0002c0002t0001g0061a0005c0007t0001g0062 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.159+1905G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110786720 | ||||||
| chr2:110787260
|
T | C | 25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.159+2445T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110787260 | ||||||
| chr2:110787406
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.159+2591C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110787406 | ||||||
| chr2:110787533
|
C | CAA | 6 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.159+2736_159+2737d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 110787533 | |||||
| chr2:110787533
|
CA | C | 6 | a0001c0001t0002g0060a0001c0003t0001g0041a0001c0003t0001g0087others(3): Show | 6 | HG01168.hp1 HG01168.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+2737delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 110787533 | |||||
| chr2:110787661
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.159+2846G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110787661 | ||||||
| chr2:110787802
|
C | T | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.159+2987C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110787802 | ||||||
| chr2:110787807
|
T | C | 4 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+2992T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110787807 | ||||||
| chr2:110787828
|
G | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0001g0103others(1): Show | 4 | HG02976.hp1 HG03195.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+3013G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110787828 | ||||||
| chr2:110787909
|
A | G | 1 | a0001c0003t0002g0084 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.159+3094A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110787909 | ||||||
| chr2:110787979
|
G | A | 1 | a0003c0004t0002g0079 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.159+3164G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110787979 | ||||||
| chr2:110788100
|
A | G | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.159+3285A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110788100 | ||||||
| chr2:110788408
|
A | G | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.159+3593A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110788408 | ||||||
| chr2:110788413
|
T | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.159+3598T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110788413 | ||||||
| chr2:110788509
|
T | C | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.159+3694T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110788509 | ||||||
| chr2:110788898
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.159+4083G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110788898 | ||||||
| chr2:110788938
|
G | C | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.159+4123G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110788938 | ||||||
| chr2:110789015
|
C | G | 1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.159+4200C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110789015 | ||||||
| chr2:110789147
|
G | A | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.159+4332G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110789147 | ||||||
| chr2:110789701
|
A | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-3949A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110789701 | ||||||
| chr2:110789767
|
A | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.160-3883A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110789767 | ||||||
| chr2:110790010
|
T | C | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.160-3640T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110790010 | ||||||
| chr2:110790178
|
C | T | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.160-3472C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110790178 | ||||||
| chr2:110790192
|
C | T | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.160-3458C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110790192 | ||||||
| chr2:110790259
|
C | T | 2 | a0001c0001t0001g0145a0006c0006t0002g0146 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.160-3391C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110790259 | ||||||
| chr2:110790410
|
C | T | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0002g0071others(3): Show | 6 | HG01243.hp2 HG02922.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-3240C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110790410 | ||||||
| chr2:110790415
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.160-3235G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110790415 | ||||||
| chr2:110790439
|
T | C | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.160-3211T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110790439 | ||||||
| chr2:110790859
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.160-2791G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110790859 | ||||||
| chr2:110791577
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.160-2073G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110791577 | ||||||
| chr2:110791726
|
G | A | 11 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0121others(8): Show | 11 | HG01891.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.160-1924G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110791726 | ||||||
| chr2:110792164
|
G | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.160-1486G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110792164 | ||||||
| chr2:110792471
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.160-1179C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110792471 | ||||||
| chr2:110792504
|
G | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-1146G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110792504 | ||||||
| chr2:110792557
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.160-1093A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110792557 | ||||||
| chr2:110792717
|
T | G | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.160-933T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110792717 | ||||||
| chr2:110792736
|
A | G | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.160-914A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110792736 | ||||||
| chr2:110792769
|
A | G | 4 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0002g0052others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-881A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110792769 | ||||||
| chr2:110792832
|
G | A | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.160-818G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110792832 | ||||||
| chr2:110792975
|
T | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.160-675T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110792975 | ||||||
| chr2:110793120
|
A | G | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.160-530A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110793120 | ||||||
| chr2:110793277
|
C | CAG | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.160-373_160-372ins others(2): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110793277 | ||||||
| chr2:110793293
|
G | A | 1 | a0002c0002t0001g0061 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.160-357G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110793293 | ||||||
| chr2:110793376
|
A | G | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.160-274A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110793376 | ||||||
| chr2:110793586
|
G | A | 3 | a0001c0001t0002g0078a0001c0003t0001g0041a0003c0004t0002g0098 | 3 | NA18962.hp1 NA18962.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.160-64G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | chr2 | 110793586 | ||||||
| chr2:110794009
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0002g0006 | 3 | HG02451.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.247-67C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 4/17 | chr2 | 110794009 | ||||||
| chr2:110794186
|
A | G | 42 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.345+12A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110794186 | ||||||
| chr2:110794339
|
T | C | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.345+165T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110794339 | ||||||
| chr2:110794600
|
G | C | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.345+426G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110794600 | ||||||
| chr2:110794625
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.345+451A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110794625 | ||||||
| chr2:110794694
|
G | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+520G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110794694 | ||||||
| chr2:110794836
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.345+662G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110794836 | ||||||
| chr2:110795114
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.345+940C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110795114 | ||||||
| chr2:110795388
|
T | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.345+1214T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110795388 | ||||||
| chr2:110795793
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.345+1619G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110795793 | ||||||
| chr2:110795807
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.345+1633A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110795807 | ||||||
| chr2:110795929
|
C | T | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.345+1755C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110795929 | ||||||
| chr2:110796075
|
G | C | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.345+1901G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110796075 | ||||||
| chr2:110796189
|
T | G | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.345+2015T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110796189 | ||||||
| chr2:110796515
|
T | C | 1 | a0001c0003t0002g0084 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.346-2095T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110796515 | ||||||
| chr2:110796611
|
A | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.346-1999A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110796611 | ||||||
| chr2:110796631
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.346-1979G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110796631 | ||||||
| chr2:110796914
|
T | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.346-1696T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110796914 | ||||||
| chr2:110797015
|
ACT | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.346-1590_346-1589d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 110797015 | |||||
| chr2:110797171
|
A | G | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.346-1439A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110797171 | ||||||
| chr2:110797201
|
C | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.346-1409C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110797201 | ||||||
| chr2:110797344
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.346-1266C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110797344 | ||||||
| chr2:110797523
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.346-1087T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110797523 | ||||||
| chr2:110797585
|
G | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.346-1025G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110797585 | ||||||
| chr2:110797602
|
T | C | 1 | a0002c0002t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.346-1008T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110797602 | ||||||
| chr2:110797705
|
C | T | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.346-905C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110797705 | ||||||
| chr2:110797753
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.346-857G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110797753 | ||||||
| chr2:110797764
|
C | T | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.346-846C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110797764 | ||||||
| chr2:110798053
|
A | G | 4 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.346-557A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110798053 | ||||||
| chr2:110798168
|
G | A | 34 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(31): Show | 34 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.346-442G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | chr2 | 110798168 | ||||||
| chr2:110798258
|
CT | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.346-336delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 110798258 | |||||
| chr2:110798766
|
A | C | 1 | a0004c0005t0001g0070 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.460+42A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 6/17 | chr2 | 110798766 | ||||||
| chr2:110798946
|
T | C | 2 | a0001c0012t0002g0131a0013c0011t0001g0130 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.461-68T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 6/17 | chr2 | 110798946 | ||||||
| chr2:110798949
|
T | C | 4 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-65T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 6/17 | chr2 | 110798949 | ||||||
| chr2:110799133
|
C | G | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.547+33C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110799133 | ||||||
| chr2:110799179
|
G | A | 2 | a0001c0001t0001g0008a0011c0010t0002g0009 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.547+79G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110799179 | ||||||
| chr2:110799244
|
C | T | 2 | a0001c0012t0002g0131a0013c0011t0001g0130 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.547+144C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110799244 | ||||||
| chr2:110799413
|
C | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.547+313C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110799413 | ||||||
| chr2:110799428
|
T | G | 1 | a0001c0001t0001g0063 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.547+328T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110799428 | ||||||
| chr2:110799435
|
T | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.547+335T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110799435 | ||||||
| chr2:110799566
|
C | T | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.547+466C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110799566 | ||||||
| chr2:110799751
|
C | T | 1 | a0001c0003t0001g0089 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.547+651C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110799751 | ||||||
| chr2:110799896
|
C | T | 1 | a0004c0005t0002g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.547+796C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110799896 | ||||||
| chr2:110799934
|
C | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.547+834C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110799934 | ||||||
| chr2:110800063
|
A | G | 1 | a0000c0014t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.547+963A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110800063 | ||||||
| chr2:110800406
|
T | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG02109.hp2 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.548-1246T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110800406 | ||||||
| chr2:110800511
|
A | AT | 19 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.548-1127dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 110800511 | |||||
| chr2:110800524
|
T | G | 6 | a0001c0001t0001g0110a0001c0001t0002g0101a0001c0001t0002g0105others(3): Show | 6 | HG00438.hp2 HG02027.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.548-1128T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110800524 | ||||||
| chr2:110800610
|
A | C | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.548-1042A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110800610 | ||||||
| chr2:110800739
|
T | C | 4 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.548-913T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110800739 | ||||||
| chr2:110800789
|
C | G | 2 | a0001c0001t0002g0040a0005c0007t0002g0050 | 2 | HG01175.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.548-863C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110800789 | ||||||
| chr2:110801029
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.548-623G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110801029 | ||||||
| chr2:110801075
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.548-577C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110801075 | ||||||
| chr2:110801220
|
G | A | 1 | a0002c0002t0003g0142 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.548-432G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 7/17 | chr2 | 110801220 | ||||||
| chr2:110801843
|
G | A | 1 | a0010c0015t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.620+119G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110801843 | ||||||
| chr2:110801975
|
C | G | 1 | a0002c0002t0001g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.620+251C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110801975 | ||||||
| chr2:110802225
|
T | C | 4 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0005g0149others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.620+501T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110802225 | ||||||
| chr2:110802273
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.620+549G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110802273 | ||||||
| chr2:110802572
|
G | GA | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.620+854dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 110802572 | |||||
| chr2:110802735
|
A | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.620+1011A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110802735 | ||||||
| chr2:110802781
|
C | T | 20 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 20 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.620+1057C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110802781 | ||||||
| chr2:110803194
|
A | G | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.620+1470A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110803194 | ||||||
| chr2:110803941
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG01081.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.621-1322G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110803941 | ||||||
| chr2:110803985
|
C | CTT | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.621-1260_621-1259d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 110803985 | |||||
| chr2:110804348
|
A | G | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.621-915A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110804348 | ||||||
| chr2:110804413
|
C | T | 2 | a0002c0002t0001g0061a0005c0007t0001g0062 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.621-850C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110804413 | ||||||
| chr2:110804575
|
T | C | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.621-688T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110804575 | ||||||
| chr2:110804576
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.621-687A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110804576 | ||||||
| chr2:110804626
|
C | CATTTTTA others(15): Show |
1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.621-635_621-634ins others(22): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 110804626 | |||||
| chr2:110804630
|
C | G | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.621-633C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110804630 | ||||||
| chr2:110804973
|
T | A | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.621-290T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110804973 | ||||||
| chr2:110805064
|
C | T | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.621-199C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110805064 | ||||||
| chr2:110805129
|
C | T | 3 | a0000c0013t0001g0046a0001c0001t0001g0039a0001c0001t0001g0045 | 3 | HG03139.hp1 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.621-134C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110805129 | ||||||
| chr2:110805159
|
A | G | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.621-104A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110805159 | ||||||
| chr2:110805205
|
C | T | 1 | a0005c0007t0004g0144 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.621-58C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | chr2 | 110805205 | ||||||
| chr2:110805445
|
A | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.753+50A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110805445 | ||||||
| chr2:110805473
|
C | G | 1 | a0001c0001t0002g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.753+78C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110805473 | ||||||
| chr2:110805570
|
C | T | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.753+175C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110805570 | ||||||
| chr2:110805623
|
G | A | 1 | a0005c0007t0002g0050 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.753+228G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110805623 | ||||||
| chr2:110805788
|
T | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0126a0001c0001t0001g0128others(3): Show | 6 | HG02145.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+393T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110805788 | ||||||
| chr2:110806198
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.753+803G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110806198 | ||||||
| chr2:110806711
|
G | A | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.753+1316G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110806711 | ||||||
| chr2:110806724
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.753+1329C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110806724 | ||||||
| chr2:110806785
|
T | C | 1 | a0005c0007t0004g0144 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.753+1390T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110806785 | ||||||
| chr2:110806884
|
G | T | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+1489G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110806884 | ||||||
| chr2:110807479
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.753+2084G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110807479 | ||||||
| chr2:110808949
|
A | T | 1 | a0004c0005t0001g0070 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.753+3554A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110808949 | ||||||
| chr2:110809144
|
C | G | 1 | a0001c0001t0002g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.753+3749C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110809144 | ||||||
| chr2:110809238
|
C | T | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+3843C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110809238 | ||||||
| chr2:110809289
|
T | C | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.753+3894T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110809289 | ||||||
| chr2:110809435
|
A | T | 1 | a0001c0001t0002g0105 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.753+4040A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110809435 | ||||||
| chr2:110809615
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.753+4220T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110809615 | ||||||
| chr2:110809938
|
C | T | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+4543C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110809938 | ||||||
| chr2:110810204
|
C | T | 12 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0002g0060others(9): Show | 12 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(9): Show |
intron_variant | MODIFIER | c.753+4809C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110810204 | ||||||
| chr2:110810349
|
T | C | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.753+4954T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110810349 | ||||||
| chr2:110810473
|
G | A | 7 | a0001c0001t0005g0149a0002c0002t0003g0139a0002c0002t0003g0142others(4): Show | 7 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+5078G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110810473 | ||||||
| chr2:110810522
|
A | AT | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+5128dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110810522 | |||||
| chr2:110810560
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.753+5165A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110810560 | ||||||
| chr2:110810657
|
A | G | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.753+5262A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110810657 | ||||||
| chr2:110811082
|
A | G | 1 | a0013c0011t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.753+5687A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110811082 | ||||||
| chr2:110811288
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.753+5893A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110811288 | ||||||
| chr2:110811727
|
GCATACAC others(5): Show |
G | 4 | a0001c0001t0001g0008a0001c0001t0001g0010a0002c0002t0003g0139others(1): Show | 4 | HG01981.hp1 HG03225.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.753+6335_753+6346d others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811727 | |||||
| chr2:110811727
|
GCATACAC others(7): Show |
G | 4 | a0001c0001t0001g0012a0002c0002t0003g0142a0002c0002t0004g0141others(1): Show | 4 | HG00423.hp1 HG00673.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.753+6335_753+6348d others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811727 | |||||
| chr2:110811727
|
GCATACAC others(9): Show |
G | 1 | a0003c0004t0003g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.753+6335_753+6350d others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811727 | |||||
| chr2:110811727
|
GCATACAC others(11): Show |
G | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.753+6335_753+6352d others(20): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811727 | |||||
| chr2:110811727
|
GCATACAC others(13): Show |
G | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.753+6335_753+6354d others(22): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811727 | |||||
| chr2:110811730
|
T | C | 1 | a0004c0005t0002g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.753+6335T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110811730 | ||||||
| chr2:110811730
|
T | TAC | 11 | a0001c0001t0001g0055a0001c0001t0001g0113a0001c0001t0002g0006others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.753+6390_753+6391d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
T | TACAC | 19 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0021others(16): Show | 19 | HG00323.hp2 HG01168.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.753+6388_753+6391d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
T | TACACAC | 23 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0037others(20): Show | 23 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.753+6386_753+6391d others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
T | TACACACA others(1): Show |
18 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0034others(15): Show | 18 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.753+6384_753+6391d others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
T | TACACACA others(3): Show |
16 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0001t0001g0049others(13): Show | 16 | HG00438.hp2 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.753+6382_753+6391d others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
T | TACACACA others(5): Show |
8 | a0001c0001t0001g0086a0001c0001t0002g0118a0001c0001t0005g0149others(5): Show | 8 | HG01496.hp2 HG02040.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.753+6380_753+6391d others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
T | TACACACA others(7): Show |
11 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0117others(8): Show | 11 | HG00423.hp2 HG01255.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.753+6378_753+6391d others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
T | TACACACA others(9): Show |
9 | a0001c0001t0001g0031a0001c0001t0001g0067a0001c0001t0001g0097others(6): Show | 9 | HG00140.hp1 HG01081.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.753+6376_753+6391d others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
T | TACACACA others(11): Show |
2 | a0001c0001t0001g0058a0001c0001t0002g0101 | 2 | HG02027.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.753+6374_753+6391d others(20): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
T | TACACACA others(13): Show |
2 | a0001c0001t0001g0137a0001c0001t0002g0105 | 2 | HG03688.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.753+6372_753+6391d others(22): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
TAC | T | 5 | a0001c0001t0001g0128a0001c0001t0002g0065a0001c0003t0002g0043others(2): Show | 5 | HG00099.hp1 NA18522.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+6390_753+6391d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
TACAC | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0082a0004c0005t0002g0127 | 3 | HG01928.hp2 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.753+6388_753+6391d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.753+6382_753+6391d others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
TACACACA others(5): Show |
T | 1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.753+6380_753+6391d others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811730
|
TACACACA others(7): Show |
T | 2 | a0001c0001t0001g0145a0001c0001t0001g0150 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.753+6378_753+6391d others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811730 | |||||
| chr2:110811783
|
A | G | 1 | a0003c0004t0003g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.753+6388A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110811783 | ||||||
| chr2:110811785
|
A | ACACACAC others(3): Show |
1 | a0001c0017t0002g0073 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.753+6391_753+6392i others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110811785 | |||||
| chr2:110811785
|
A | G | 9 | a0001c0001t0001g0145a0001c0001t0001g0150a0002c0002t0003g0139others(6): Show | 9 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.753+6390A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110811785 | ||||||
| chr2:110811788
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.753+6393C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110811788 | ||||||
| chr2:110811832
|
A | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.753+6437A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110811832 | ||||||
| chr2:110811909
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.753+6514G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110811909 | ||||||
| chr2:110811991
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0002g0006others(2): Show | 5 | HG02451.hp2 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+6596C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110811991 | ||||||
| chr2:110812309
|
CT | C | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.753+6919delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110812309 | |||||
| chr2:110812446
|
C | G | 1 | a0003c0004t0001g0026 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.753+7051C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110812446 | ||||||
| chr2:110812467
|
A | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.753+7072A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110812467 | ||||||
| chr2:110812516
|
C | A | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.753+7121C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110812516 | ||||||
| chr2:110812547
|
G | C | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.753+7152G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110812547 | ||||||
| chr2:110813649
|
A | G | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+8254A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110813649 | ||||||
| chr2:110813770
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | HG01891.hp2 HG02258.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+8375A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110813770 | ||||||
| chr2:110813956
|
A | T | 1 | a0000c0014t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.753+8561A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110813956 | ||||||
| chr2:110814508
|
T | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.753+9113T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110814508 | ||||||
| chr2:110814602
|
T | C | 1 | a0005c0007t0002g0050 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.753+9207T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110814602 | ||||||
| chr2:110815112
|
T | C | 1 | a0004c0005t0001g0070 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.753+9717T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110815112 | ||||||
| chr2:110815237
|
G | A | 2 | a0002c0002t0003g0142a0002c0002t0004g0141 | 2 | HG00423.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.753+9842G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110815237 | ||||||
| chr2:110815314
|
T | C | 2 | a0002c0002t0001g0061a0005c0007t0001g0062 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.753+9919T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110815314 | ||||||
| chr2:110815593
|
T | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0126a0001c0001t0001g0128others(3): Show | 6 | HG02145.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+10198T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110815593 | ||||||
| chr2:110815767
|
G | C | 5 | a0001c0001t0006g0017a0002c0002t0002g0147a0002c0002t0002g0148others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+10372G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110815767 | ||||||
| chr2:110816017
|
A | G | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.753+10622A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110816017 | ||||||
| chr2:110816137
|
A | T | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.753+10742A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110816137 | ||||||
| chr2:110816214
|
T | TGATG | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.753+10844_753+1084 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110816214 | |||||
| chr2:110816308
|
A | G | 10 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.753+10913A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110816308 | ||||||
| chr2:110816533
|
C | A | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.753+11138C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110816533 | ||||||
| chr2:110816535
|
A | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.753+11140A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110816535 | ||||||
| chr2:110816710
|
G | T | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.753+11315G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110816710 | ||||||
| chr2:110816808
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0002g0006 | 3 | HG02451.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.753+11413T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110816808 | ||||||
| chr2:110816925
|
G | A | 2 | a0002c0002t0001g0114a0004c0005t0007g0133 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.753+11530G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110816925 | ||||||
| chr2:110817018
|
G | C | 3 | a0001c0001t0002g0094a0001c0003t0001g0036a0002c0019t0001g0095 | 3 | HG02040.hp1 NA18993.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.753+11623G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110817018 | ||||||
| chr2:110817068
|
C | T | 2 | a0001c0001t0002g0033a0002c0002t0001g0066 | 2 | HG01346.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.753+11673C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110817068 | ||||||
| chr2:110817204
|
C | G | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.753+11809C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110817204 | ||||||
| chr2:110817228
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.753+11833G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110817228 | ||||||
| chr2:110817442
|
G | C | 1 | a0002c0002t0001g0023 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.753+12047G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110817442 | ||||||
| chr2:110817484
|
A | G | 1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.753+12089A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110817484 | ||||||
| chr2:110817582
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.753+12187C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110817582 | ||||||
| chr2:110817584
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.753+12189A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110817584 | ||||||
| chr2:110817691
|
A | G | 139 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.753+12296A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110817691 | ||||||
| chr2:110817895
|
G | A | 1 | a0003c0004t0001g0026 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.753+12500G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110817895 | ||||||
| chr2:110817952
|
C | CT | 12 | a0001c0001t0001g0077a0001c0001t0002g0071a0001c0001t0002g0094others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.753+12577dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110817952 | |||||
| chr2:110817952
|
CT | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0003t0001g0036others(2): Show | 5 | HG01175.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+12577delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110817952 | |||||
| chr2:110818091
|
TGA | T | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.753+12700_753+1270 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110818091 | |||||
| chr2:110818117
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.753+12722G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818117 | ||||||
| chr2:110818126
|
G | C | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.753+12731G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818126 | ||||||
| chr2:110818318
|
C | T | 1 | a0002c0002t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.753+12923C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818318 | ||||||
| chr2:110818393
|
CA | C | 120 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0011others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.753+13014delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110818393 | |||||
| chr2:110818408
|
A | AC | 9 | a0000c0013t0001g0046a0001c0001t0001g0029a0001c0001t0001g0045others(6): Show | 9 | HG00673.hp2 HG02027.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.753+13013_753+1301 others(5): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818408 | ||||||
| chr2:110818408
|
A | ACAT | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.753+13013_753+1301 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818408 | ||||||
| chr2:110818410
|
C | T | 11 | a0000c0013t0001g0046a0001c0001t0001g0029a0001c0001t0001g0045others(8): Show | 11 | HG00673.hp2 HG02027.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.753+13015C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818410 | ||||||
| chr2:110818417
|
A | G | 3 | a0001c0001t0001g0012a0001c0001t0005g0149a0014c0020t0001g0002 | 3 | HG01891.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.753+13022A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818417 | ||||||
| chr2:110818417
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.753+13024_753+1303 others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110818417 | |||||
| chr2:110818419
|
A | ATGTGTGT others(3): Show |
1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.753+13025_753+1302 others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110818419 | |||||
| chr2:110818419
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0001g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.753+13025_753+1302 others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110818419 | |||||
| chr2:110818419
|
A | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+13024A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818419 | ||||||
| chr2:110818421
|
A | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.753+13026A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818421 | ||||||
| chr2:110818423
|
A | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.753+13028A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818423 | ||||||
| chr2:110818423
|
ATG | A | 3 | a0001c0001t0001g0056a0001c0001t0002g0052a0001c0001t0002g0101 | 3 | HG02027.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.753+13056_753+1305 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110818423 | |||||
| chr2:110818425
|
G | A | 109 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.753+13030G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818425 | ||||||
| chr2:110818427
|
G | A | 7 | a0001c0001t0001g0035a0002c0002t0003g0139a0002c0002t0003g0142others(4): Show | 7 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+13032G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818427 | ||||||
| chr2:110818429
|
G | A | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+13034G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818429 | ||||||
| chr2:110818451
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0002g0094a0001c0003t0001g0036others(1): Show | 4 | HG02027.hp2 HG02040.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.753+13056G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818451 | ||||||
| chr2:110818451
|
G | GTA | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.753+13070_753+1307 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110818451 | |||||
| chr2:110818451
|
G | GTGTGTGT others(5): Show |
1 | a0001c0001t0001g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.753+13057_753+1305 others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110818451 | |||||
| chr2:110818451
|
GTA | G | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.753+13070_753+1307 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110818451 | |||||
| chr2:110818453
|
A | G | 29 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.753+13058A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818453 | ||||||
| chr2:110818455
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0138a0001c0001t0005g0149others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.753+13060A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818455 | ||||||
| chr2:110818457
|
A | G | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.753+13062A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818457 | ||||||
| chr2:110818469
|
A | T | 1 | a0001c0001t0001g0086 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.753+13074A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818469 | ||||||
| chr2:110818523
|
GTA | G | 137 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.753+13138_753+1313 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110818523 | |||||
| chr2:110818523
|
GTATA | G | 2 | a0001c0001t0001g0008a0011c0010t0002g0009 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.753+13136_753+1313 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110818523 | |||||
| chr2:110818827
|
CTGATGTC others(225): Show |
C | 30 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(27): Show | 30 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.753+13437_753+1366 others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110818827 | |||||
| chr2:110818932
|
C | T | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.753+13537C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110818932 | ||||||
| chr2:110819535
|
A | G | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.753+14140A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110819535 | ||||||
| chr2:110819747
|
C | G | 10 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.753+14352C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110819747 | ||||||
| chr2:110819790
|
G | T | 1 | a0001c0001t0001g0067 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.753+14395G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110819790 | ||||||
| chr2:110820079
|
C | T | 2 | a0001c0001t0002g0076a0001c0001t0002g0078 | 2 | NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.753+14684C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110820079 | ||||||
| chr2:110820225
|
A | C | 1 | a0002c0002t0001g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.753+14830A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110820225 | ||||||
| chr2:110820450
|
A | G | 1 | a0002c0019t0001g0095 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.753+15055A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110820450 | ||||||
| chr2:110820777
|
G | A | 7 | a0001c0001t0001g0025a0001c0001t0001g0055a0001c0001t0001g0082others(4): Show | 7 | HG00099.hp1 HG01255.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.753+15382G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110820777 | ||||||
| chr2:110821004
|
C | T | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.753+15609C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110821004 | ||||||
| chr2:110821057
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.753+15662A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110821057 | ||||||
| chr2:110821206
|
G | C | 17 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0077others(14): Show | 17 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.753+15811G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110821206 | ||||||
| chr2:110821285
|
C | CT | 8 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.753+15899dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110821285 | |||||
| chr2:110821287
|
T | C | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.753+15892T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110821287 | ||||||
| chr2:110821480
|
A | G | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0002g0071others(4): Show | 7 | HG01167.hp1 HG01243.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+16085A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110821480 | ||||||
| chr2:110821603
|
G | A | 6 | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+16208G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110821603 | ||||||
| chr2:110822016
|
C | A | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.753+16621C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110822016 | ||||||
| chr2:110822199
|
ATG | A | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.753+16810_753+1681 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110822199 | |||||
| chr2:110822594
|
A | G | 1 | a0002c0002t0001g0066 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.753+17199A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110822594 | ||||||
| chr2:110822732
|
G | A | 2 | a0001c0001t0002g0076a0001c0001t0002g0078 | 2 | NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.753+17337G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110822732 | ||||||
| chr2:110822785
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.753+17390C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110822785 | ||||||
| chr2:110823301
|
G | A | 1 | a0002c0002t0002g0059 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.753+17906G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110823301 | ||||||
| chr2:110823886
|
T | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.754-17485T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110823886 | ||||||
| chr2:110825566
|
T | G | 2 | a0003c0004t0003g0143a0003c0004t0004g0140 | 2 | HG00438.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.754-15805T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110825566 | ||||||
| chr2:110825576
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.754-15795A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110825576 | ||||||
| chr2:110826085
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.754-15286G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110826085 | ||||||
| chr2:110826185
|
T | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00438.hp1 HG01891.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.754-15186T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110826185 | ||||||
| chr2:110826477
|
G | C | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.754-14894G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110826477 | ||||||
| chr2:110826751
|
GCTTTTTT others(10): Show |
G | 8 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG01891.hp2 HG02257.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.754-14608_754-1459 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110826751 | |||||
| chr2:110826753
|
TTTTTTTT others(9): Show |
T | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.754-14607_754-1459 others(20): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110826753 | |||||
| chr2:110826960
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.754-14411A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110826960 | ||||||
| chr2:110827227
|
A | G | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.754-14144A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110827227 | ||||||
| chr2:110827362
|
AAAGGTAG others(5): Show |
A | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.754-14008_754-1399 others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110827362 | ||||||
| chr2:110827383
|
G | A | 2 | a0003c0004t0003g0143a0003c0004t0004g0140 | 2 | HG00438.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.754-13988G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110827383 | ||||||
| chr2:110827707
|
G | C | 3 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.754-13664G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110827707 | ||||||
| chr2:110827729
|
G | A | 51 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(48): Show | 51 | HG00438.hp1 HG00544.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.754-13642G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110827729 | ||||||
| chr2:110827908
|
A | T | 1 | a0002c0002t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.754-13463A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110827908 | ||||||
| chr2:110828187
|
G | A | 1 | a0002c0002t0002g0119 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.754-13184G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110828187 | ||||||
| chr2:110828637
|
C | T | 18 | a0001c0001t0001g0035a0001c0001t0001g0063a0001c0001t0001g0085others(15): Show | 18 | HG00099.hp2 HG00438.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.754-12734C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110828637 | ||||||
| chr2:110828750
|
G | T | 46 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0021others(43): Show | 46 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.754-12621G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110828750 | ||||||
| chr2:110828760
|
A | C | 1 | a0002c0002t0001g0066 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.754-12611A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110828760 | ||||||
| chr2:110828937
|
G | A | 5 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0012t0002g0131others(2): Show | 5 | HG00140.hp2 HG01346.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.754-12434G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110828937 | ||||||
| chr2:110829038
|
C | T | 1 | a0002c0002t0001g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.754-12333C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110829038 | ||||||
| chr2:110829091
|
G | A | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.754-12280G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110829091 | ||||||
| chr2:110829091
|
G | T | 1 | a0002c0002t0004g0141 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.754-12280G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110829091 | ||||||
| chr2:110829193
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.754-12178G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110829193 | ||||||
| chr2:110829327
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.754-12044G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110829327 | ||||||
| chr2:110829392
|
G | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(25): Show | 28 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.754-11979G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110829392 | ||||||
| chr2:110829417
|
G | A | 3 | a0001c0001t0001g0113a0002c0002t0002g0013a0002c0002t0002g0014 | 3 | HG03831.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.754-11954G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110829417 | ||||||
| chr2:110829439
|
T | C | 81 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(78): Show | 81 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.754-11932T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110829439 | ||||||
| chr2:110829465
|
T | C | 2 | a0001c0001t0001g0010a0014c0020t0001g0002 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.754-11906T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110829465 | ||||||
| chr2:110829914
|
T | C | 1 | a0009c0016t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.754-11457T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110829914 | ||||||
| chr2:110830514
|
G | C | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.754-10857G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110830514 | ||||||
| chr2:110830588
|
C | CA | 2 | a0002c0002t0001g0019a0002c0002t0001g0135 | 2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.754-10782dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110830588 | |||||
| chr2:110831520
|
A | G | 3 | a0001c0001t0001g0097a0007c0009t0001g0092a0007c0009t0001g0106 | 3 | HG00099.hp2 HG01517.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.754-9851A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110831520 | ||||||
| chr2:110831592
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0005g0149others(1): Show | 4 | HG01891.hp2 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-9779C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110831592 | ||||||
| chr2:110832068
|
A | C | 42 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0028others(39): Show | 42 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.754-9303A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110832068 | ||||||
| chr2:110832118
|
T | C | 16 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(13): Show | 16 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(13): Show |
intron_variant | MODIFIER | c.754-9253T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110832118 | ||||||
| chr2:110832370
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.754-9001C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110832370 | ||||||
| chr2:110832395
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.754-8976G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110832395 | ||||||
| chr2:110832462
|
C | T | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.754-8909C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110832462 | ||||||
| chr2:110832923
|
G | A | 26 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(23): Show | 26 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.754-8448G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110832923 | ||||||
| chr2:110832929
|
A | G | 1 | a0009c0016t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.754-8442A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110832929 | ||||||
| chr2:110832983
|
A | G | 77 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(74): Show | 77 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.754-8388A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110832983 | ||||||
| chr2:110833091
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.754-8280A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110833091 | ||||||
| chr2:110833193
|
T | G | 2 | a0001c0001t0001g0138a0003c0004t0004g0140 | 2 | HG01981.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.754-8178T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110833193 | ||||||
| chr2:110833459
|
A | G | 82 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(79): Show | 82 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.754-7912A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110833459 | ||||||
| chr2:110833533
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.754-7838T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110833533 | ||||||
| chr2:110833627
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.754-7744C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110833627 | ||||||
| chr2:110833754
|
A | G | 78 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(75): Show | 78 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.754-7617A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110833754 | ||||||
| chr2:110833781
|
T | C | 1 | a0001c0001t0002g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.754-7590T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110833781 | ||||||
| chr2:110833847
|
G | A | 1 | a0010c0015t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.754-7524G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110833847 | ||||||
| chr2:110834061
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.754-7310C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110834061 | ||||||
| chr2:110834078
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0005g0149others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-7293C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110834078 | ||||||
| chr2:110834200
|
A | G | 80 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.754-7171A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110834200 | ||||||
| chr2:110834352
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.754-7019G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110834352 | ||||||
| chr2:110834387
|
T | C | 3 | a0000c0013t0001g0046a0001c0001t0001g0039a0001c0001t0001g0045 | 3 | HG03139.hp1 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.754-6984T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110834387 | ||||||
| chr2:110834590
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.754-6781C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110834590 | ||||||
| chr2:110834671
|
TC | T | 2 | a0002c0002t0002g0013a0002c0002t0002g0014 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.754-6699delC | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110834671 | ||||||
| chr2:110834697
|
C | G | 79 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.754-6674C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110834697 | ||||||
| chr2:110834747
|
G | T | 1 | a0001c0001t0002g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.754-6624G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110834747 | ||||||
| chr2:110834830
|
G | T | 44 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0028others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.754-6541G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110834830 | ||||||
| chr2:110835029
|
C | A | 44 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0028others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.754-6342C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110835029 | ||||||
| chr2:110835263
|
G | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0005g0149others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-6108G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110835263 | ||||||
| chr2:110835350
|
CT | C | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.754-6020delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110835350 | ||||||
| chr2:110835754
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0005g0149others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-5617C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110835754 | ||||||
| chr2:110836212
|
G | A | 1 | a0002c0002t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.754-5159G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110836212 | ||||||
| chr2:110836308
|
C | A | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.754-5063C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110836308 | ||||||
| chr2:110836912
|
C | G | 1 | a0004c0005t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.754-4459C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110836912 | ||||||
| chr2:110837132
|
G | A | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.754-4239G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110837132 | ||||||
| chr2:110837241
|
G | A | 2 | a0001c0001t0001g0010a0014c0020t0001g0002 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.754-4130G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110837241 | ||||||
| chr2:110837352
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.754-4019G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110837352 | ||||||
| chr2:110837451
|
TA | T | 17 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0080others(14): Show | 17 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.754-3914delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110837451 | |||||
| chr2:110837529
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0005g0149others(1): Show | 4 | HG01891.hp2 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-3842G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110837529 | ||||||
| chr2:110837912
|
A | G | 57 | a0000c0013t0001g0046a0001c0001t0001g0010a0001c0001t0001g0011others(54): Show | 57 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.754-3459A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110837912 | ||||||
| chr2:110838065
|
A | C | 9 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0012others(6): Show | 9 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.754-3306A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110838065 | ||||||
| chr2:110838161
|
A | G | 80 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.754-3210A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110838161 | ||||||
| chr2:110838360
|
G | A | 92 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.754-3011G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110838360 | ||||||
| chr2:110839132
|
G | GT | 7 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0145others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.754-2227dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110839132 | |||||
| chr2:110839714
|
C | T | 15 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0088others(12): Show | 15 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.754-1657C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110839714 | ||||||
| chr2:110839919
|
T | C | 3 | a0001c0001t0001g0034a0001c0012t0002g0131a0013c0011t0001g0130 | 3 | HG01346.hp2 HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.754-1452T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110839919 | ||||||
| chr2:110839971
|
G | GGTTTGTT others(9): Show |
95 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.754-1379_754-1364d others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 110839971 | |||||
| chr2:110840012
|
C | T | 36 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 36 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.754-1359C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110840012 | ||||||
| chr2:110840020
|
C | T | 2 | a0001c0012t0002g0131a0013c0011t0001g0130 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.754-1351C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110840020 | ||||||
| chr2:110840045
|
G | A | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.754-1326G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110840045 | ||||||
| chr2:110840059
|
A | G | 95 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.754-1312A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110840059 | ||||||
| chr2:110840123
|
C | T | 94 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.754-1248C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110840123 | ||||||
| chr2:110840284
|
A | T | 5 | a0000c0013t0001g0046a0001c0001t0001g0018a0001c0001t0001g0039others(2): Show | 5 | HG02280.hp1 HG02280.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.754-1087A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110840284 | ||||||
| chr2:110840414
|
A | G | 32 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0042others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.754-957A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110840414 | ||||||
| chr2:110840638
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.754-733A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110840638 | ||||||
| chr2:110840788
|
T | C | 94 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.754-583T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110840788 | ||||||
| chr2:110840789
|
G | A | 94 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.754-582G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110840789 | ||||||
| chr2:110840830
|
C | T | 24 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.754-541C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110840830 | ||||||
| chr2:110840909
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.754-462C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110840909 | ||||||
| chr2:110841146
|
A | G | 6 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0137others(3): Show | 6 | HG02027.hp2 HG03688.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-225A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110841146 | ||||||
| chr2:110841184
|
A | G | 1 | a0001c0001t0002g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.754-187A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | 110841184 | ||||||
| chr2:110841602
|
A | C | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.788+197A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110841602 | ||||||
| chr2:110841705
|
G | C | 68 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.788+300G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110841705 | ||||||
| chr2:110841822
|
G | C | 3 | a0001c0001t0001g0034a0001c0012t0002g0131a0013c0011t0001g0130 | 3 | HG01346.hp2 HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.788+417G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110841822 | ||||||
| chr2:110842024
|
A | G | 27 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.788+619A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110842024 | ||||||
| chr2:110842103
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.788+698C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110842103 | ||||||
| chr2:110842129
|
G | A | 67 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.788+724G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110842129 | ||||||
| chr2:110842132
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.788+727A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110842132 | ||||||
| chr2:110842139
|
T | G | 1 | a0001c0001t0001g0082 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.788+734T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110842139 | ||||||
| chr2:110842384
|
A | G | 2 | a0002c0002t0003g0142a0002c0002t0004g0141 | 2 | HG00423.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.788+979A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110842384 | ||||||
| chr2:110842400
|
G | A | 16 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0088others(13): Show | 16 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.788+995G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110842400 | ||||||
| chr2:110842478
|
T | C | 1 | a0000c0013t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.788+1073T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110842478 | ||||||
| chr2:110842890
|
G | A | 1 | a0002c0002t0001g0066 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.788+1485G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110842890 | ||||||
| chr2:110842942
|
C | T | 26 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0051others(23): Show | 26 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.788+1537C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110842942 | ||||||
| chr2:110842945
|
G | A | 1 | a0013c0011t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.788+1540G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110842945 | ||||||
| chr2:110843218
|
C | T | 4 | a0000c0013t0001g0046a0001c0001t0001g0018a0001c0001t0001g0039others(1): Show | 4 | HG02280.hp2 HG03139.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+1813C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110843218 | ||||||
| chr2:110843417
|
T | A | 27 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.788+2012T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110843417 | ||||||
| chr2:110843665
|
G | A | 16 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0088others(13): Show | 16 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.788+2260G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110843665 | ||||||
| chr2:110843761
|
A | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0145a0004c0005t0002g0020others(1): Show | 4 | HG02451.hp1 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+2356A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110843761 | ||||||
| chr2:110843796
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.788+2391G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110843796 | ||||||
| chr2:110843851
|
TAAAC | T | 6 | a0001c0001t0001g0042a0001c0001t0001g0121a0001c0001t0001g0122others(3): Show | 6 | HG01175.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.788+2454_788+2457d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110843851 | |||||
| chr2:110843901
|
G | A | 66 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0011others(63): Show | 66 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.788+2496G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110843901 | ||||||
| chr2:110844032
|
G | T | 1 | a0006c0006t0001g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.788+2627G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110844032 | ||||||
| chr2:110844221
|
A | G | 26 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0051others(23): Show | 26 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.788+2816A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110844221 | ||||||
| chr2:110844365
|
C | G | 94 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.788+2960C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110844365 | ||||||
| chr2:110844469
|
C | T | 27 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.788+3064C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110844469 | ||||||
| chr2:110844550
|
CT | C | 28 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0031others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.788+3160delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110844550 | |||||
| chr2:110844555
|
T | C | 12 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0003t0001g0041others(9): Show | 12 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.788+3150T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110844555 | ||||||
| chr2:110844613
|
T | G | 20 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0080others(17): Show | 20 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.788+3208T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110844613 | ||||||
| chr2:110844658
|
A | G | 6 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0137others(3): Show | 6 | HG02027.hp2 HG03688.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.788+3253A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110844658 | ||||||
| chr2:110845024
|
G | T | 40 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0011others(37): Show | 40 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.788+3619G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110845024 | ||||||
| chr2:110845070
|
G | A | 1 | a0005c0007t0004g0144 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.788+3665G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110845070 | ||||||
| chr2:110845153
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0145a0004c0005t0002g0020others(1): Show | 4 | HG02451.hp1 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+3748T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110845153 | ||||||
| chr2:110845161
|
C | G | 1 | a0001c0001t0002g0120 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.788+3756C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110845161 | ||||||
| chr2:110845238
|
G | A | 3 | a0002c0002t0001g0132a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.788+3833G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110845238 | ||||||
| chr2:110845369
|
C | T | 1 | a0002c0002t0002g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.788+3964C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110845369 | ||||||
| chr2:110845397
|
G | A | 94 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.788+3992G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110845397 | ||||||
| chr2:110845432
|
A | G | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.788+4027A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110845432 | ||||||
| chr2:110845445
|
C | G | 1 | a0002c0002t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.788+4040C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110845445 | ||||||
| chr2:110845801
|
A | T | 1 | a0005c0007t0002g0050 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.788+4396A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110845801 | ||||||
| chr2:110845849
|
C | T | 2 | a0001c0001t0001g0138a0003c0004t0004g0140 | 2 | HG01981.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.788+4444C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110845849 | ||||||
| chr2:110846161
|
T | C | 2 | a0001c0001t0002g0076a0001c0001t0002g0078 | 2 | NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.788+4756T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110846161 | ||||||
| chr2:110846428
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0005g0149 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.788+5023C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110846428 | ||||||
| chr2:110846484
|
C | A | 6 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0137others(3): Show | 6 | HG02027.hp2 HG03688.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.788+5079C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110846484 | ||||||
| chr2:110846536
|
A | G | 94 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.788+5131A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110846536 | ||||||
| chr2:110846636
|
T | TACACACA others(11): Show |
2 | a0001c0001t0001g0080a0002c0002t0001g0051 | 2 | HG03831.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.788+5235_788+5236i others(20): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846636 | |||||
| chr2:110846636
|
T | TACACACA others(13): Show |
3 | a0001c0001t0001g0088a0001c0003t0001g0041a0001c0003t0001g0090 | 3 | HG01981.hp2 HG02004.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.788+5235_788+5236i others(22): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846636 | |||||
| chr2:110846636
|
T | TACACACA others(15): Show |
2 | a0001c0003t0001g0089a0001c0003t0001g0091 | 2 | HG01081.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.788+5235_788+5236i others(24): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846636 | |||||
| chr2:110846636
|
T | TACACACA others(17): Show |
3 | a0001c0003t0001g0081a0001c0003t0002g0083a0001c0003t0002g0104 | 3 | HG01167.hp2 NA18946.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.788+5235_788+5236i others(26): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846636 | |||||
| chr2:110846636
|
T | TACACACA others(21): Show |
1 | a0001c0003t0002g0084 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.788+5235_788+5236i others(30): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846636 | |||||
| chr2:110846636
|
T | TACACACA others(23): Show |
1 | a0001c0003t0002g0043 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.788+5235_788+5236i others(32): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846636 | |||||
| chr2:110846641
|
G | A | 12 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0003t0001g0041others(9): Show | 12 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.788+5236G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110846641 | ||||||
| chr2:110846641
|
G | GCA | 21 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0049others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.788+5269_788+5270d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCACA | 7 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG02258.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.788+5267_788+5270d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCACACAC others(1): Show |
8 | a0001c0001t0001g0024a0001c0001t0001g0056a0001c0001t0001g0058others(5): Show | 8 | HG02145.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.788+5263_788+5270d others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCACACAC others(3): Show |
1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.788+5261_788+5270d others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCACACAC others(5): Show |
3 | a0001c0001t0001g0008a0002c0002t0001g0132a0002c0002t0002g0014 | 3 | HG03195.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.788+5259_788+5270d others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCACACAC others(7): Show |
9 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0006g0017others(6): Show | 9 | HG00423.hp1 HG01257.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.788+5257_788+5270d others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCACACAC others(9): Show |
5 | a0001c0001t0001g0137a0001c0001t0001g0150a0002c0002t0002g0147others(2): Show | 5 | HG00673.hp1 HG01175.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.788+5255_788+5270d others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCACACAC others(11): Show |
10 | a0001c0001t0001g0138a0001c0001t0002g0076a0001c0001t0002g0078others(7): Show | 10 | HG01255.hp2 HG01981.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.788+5253_788+5270d others(20): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCACACAC others(13): Show |
9 | a0001c0001t0001g0021a0001c0001t0001g0113a0002c0002t0001g0019others(6): Show | 9 | HG01167.hp1 HG01243.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.788+5251_788+5270d others(22): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCACACAC others(15): Show |
4 | a0001c0001t0001g0145a0002c0002t0001g0066a0002c0002t0003g0139others(1): Show | 4 | HG01346.hp1 HG03195.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+5249_788+5270d others(24): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCACACAC others(17): Show |
3 | a0002c0002t0001g0099a0002c0002t0002g0013a0002c0002t0002g0119 | 3 | HG02615.hp1 HG06807.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.788+5247_788+5270d others(26): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCGCACA | 3 | a0001c0001t0001g0086a0001c0017t0002g0073a0003c0004t0001g0093 | 3 | HG00140.hp2 NA18993.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.788+5237_788+5238i others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCGCACAC others(1): Show |
14 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0031others(11): Show | 14 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(11): Show |
intron_variant | MODIFIER | c.788+5237_788+5238i others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCGCACAC others(5): Show |
6 | a0001c0001t0002g0040a0001c0001t0002g0060a0001c0001t0005g0149others(3): Show | 6 | HG01168.hp1 HG01517.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.788+5237_788+5238i others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCGCACAC others(7): Show |
1 | a0001c0001t0001g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.788+5237_788+5238i others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCGCACAC others(9): Show |
2 | a0001c0001t0001g0055a0001c0001t0001g0082 | 2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.788+5237_788+5238i others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCGCACAC others(11): Show |
1 | a0002c0002t0001g0023 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.788+5237_788+5238i others(20): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
G | GCGCGCGC others(3): Show |
1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.788+5237_788+5238i others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846641
|
GCACACAC others(1): Show |
G | 4 | a0000c0013t0001g0046a0001c0001t0001g0018a0001c0001t0001g0039others(1): Show | 4 | HG02280.hp2 HG03139.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+5263_788+5270d others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846641 | |||||
| chr2:110846643
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.788+5238A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110846643 | ||||||
| chr2:110846787
|
T | TG | 19 | a0002c0002t0001g0023a0002c0002t0001g0051a0002c0002t0001g0054others(16): Show | 19 | HG00673.hp1 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.788+5390dupG | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110846787 | |||||
| chr2:110846969
|
A | G | 4 | a0000c0013t0001g0046a0001c0001t0001g0018a0001c0001t0001g0039others(1): Show | 4 | HG02280.hp2 HG03139.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+5564A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110846969 | ||||||
| chr2:110847065
|
T | C | 94 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.788+5660T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110847065 | ||||||
| chr2:110847133
|
C | T | 1 | a0001c0003t0001g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.788+5728C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110847133 | ||||||
| chr2:110847414
|
T | C | 1 | a0001c0001t0002g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.788+6009T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110847414 | ||||||
| chr2:110847661
|
A | C | 26 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0051others(23): Show | 26 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.788+6256A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110847661 | ||||||
| chr2:110847668
|
C | T | 41 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0011others(38): Show | 41 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.788+6263C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110847668 | ||||||
| chr2:110847716
|
C | T | 2 | a0001c0012t0002g0131a0013c0011t0001g0130 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.788+6311C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110847716 | ||||||
| chr2:110848330
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.788+6925C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110848330 | ||||||
| chr2:110848934
|
G | A | 2 | a0001c0012t0002g0131a0013c0011t0001g0130 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.788+7529G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110848934 | ||||||
| chr2:110849014
|
G | C | 94 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.788+7609G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849014 | ||||||
| chr2:110849020
|
C | T | 1 | a0002c0002t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.788+7615C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849020 | ||||||
| chr2:110849023
|
C | T | 16 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0088others(13): Show | 16 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.788+7618C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849023 | ||||||
| chr2:110849026
|
C | T | 26 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0051others(23): Show | 26 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.788+7621C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849026 | ||||||
| chr2:110849121
|
A | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.788+7716A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849121 | ||||||
| chr2:110849207
|
C | T | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.788+7802C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849207 | ||||||
| chr2:110849307
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.788+7902T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849307 | ||||||
| chr2:110849411
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.788+8006A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849411 | ||||||
| chr2:110849462
|
A | G | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.788+8057A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849462 | ||||||
| chr2:110849624
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.788+8219G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849624 | ||||||
| chr2:110849672
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.788+8267T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849672 | ||||||
| chr2:110849673
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.788+8268G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849673 | ||||||
| chr2:110849682
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.788+8277C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849682 | ||||||
| chr2:110849749
|
A | AAAAC | 23 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0113others(20): Show | 23 | HG01167.hp1 HG01981.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.788+8372_788+8375d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110849749 | |||||
| chr2:110849749
|
A | AAAACAAA others(1): Show |
4 | a0000c0013t0001g0046a0001c0001t0001g0011a0001c0001t0001g0039others(1): Show | 4 | HG03139.hp1 NA19043.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.788+8368_788+8375d others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110849749 | |||||
| chr2:110849749
|
A | AAAACAAA others(5): Show |
1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.788+8364_788+8375d others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110849749 | |||||
| chr2:110849749
|
AAAAC | A | 25 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(22): Show | 25 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.788+8372_788+8375d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110849749 | |||||
| chr2:110849781
|
A | G | 27 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.788+8376A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849781 | ||||||
| chr2:110849824
|
C | T | 94 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.788+8419C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849824 | ||||||
| chr2:110849888
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.788+8483A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110849888 | ||||||
| chr2:110850099
|
A | T | 26 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0051others(23): Show | 26 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.788+8694A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110850099 | ||||||
| chr2:110850150
|
G | A | 1 | a0004c0005t0002g0127 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.788+8745G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110850150 | ||||||
| chr2:110850255
|
A | G | 67 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0011others(64): Show | 67 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.788+8850A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110850255 | ||||||
| chr2:110850512
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.788+9107G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110850512 | ||||||
| chr2:110850530
|
T | A | 3 | a0001c0001t0001g0034a0001c0012t0002g0131a0013c0011t0001g0130 | 3 | HG01346.hp2 HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.788+9125T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110850530 | ||||||
| chr2:110850603
|
A | T | 1 | a0001c0001t0002g0125 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.788+9198A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110850603 | ||||||
| chr2:110850609
|
T | C | 3 | a0002c0002t0001g0132a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG02109.hp1 HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.788+9204T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110850609 | ||||||
| chr2:110850760
|
A | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0002g0006others(1): Show | 4 | HG02451.hp2 HG02717.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+9355A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110850760 | ||||||
| chr2:110850813
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0145others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.788+9408C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110850813 | ||||||
| chr2:110850938
|
A | G | 1 | a0001c0003t0002g0083 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.788+9533A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110850938 | ||||||
| chr2:110850957
|
T | C | 95 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.788+9552T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110850957 | ||||||
| chr2:110851532
|
G | A | 1 | a0003c0004t0001g0026 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.788+10127G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110851532 | ||||||
| chr2:110851579
|
G | A | 5 | a0002c0002t0001g0019a0002c0002t0001g0132a0002c0002t0001g0135others(2): Show | 5 | HG01167.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.788+10174G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110851579 | ||||||
| chr2:110851706
|
C | T | 16 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0088others(13): Show | 16 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.788+10301C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110851706 | ||||||
| chr2:110851808
|
C | T | 25 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(22): Show | 25 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.788+10403C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110851808 | ||||||
| chr2:110851854
|
A | G | 1 | a0004c0005t0002g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.788+10449A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110851854 | ||||||
| chr2:110851863
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.788+10458C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110851863 | ||||||
| chr2:110851897
|
G | A | 3 | a0001c0001t0001g0034a0001c0012t0002g0131a0013c0011t0001g0130 | 3 | HG01346.hp2 HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.788+10492G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110851897 | ||||||
| chr2:110851973
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0005g0149 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.788+10568C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110851973 | ||||||
| chr2:110851993
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0145others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.788+10588A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110851993 | ||||||
| chr2:110852042
|
G | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.788+10637G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110852042 | ||||||
| chr2:110852061
|
A | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.788+10656A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110852061 | ||||||
| chr2:110852113
|
G | A | 95 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.788+10708G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110852113 | ||||||
| chr2:110852130
|
G | C | 1 | a0002c0002t0002g0013 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.788+10725G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110852130 | ||||||
| chr2:110852181
|
G | A | 95 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.788+10776G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110852181 | ||||||
| chr2:110852323
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.788+10918G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110852323 | ||||||
| chr2:110852354
|
G | GCCCTGGC others(1): Show |
7 | a0001c0001t0001g0008a0001c0001t0001g0113a0001c0001t0001g0138others(4): Show | 7 | HG01981.hp1 HG02258.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+10959_788+1096 others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110852354 | |||||
| chr2:110852366
|
T | C | 28 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.788+10961T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110852366 | ||||||
| chr2:110852621
|
A | G | 2 | a0001c0001t0001g0037a0001c0001t0002g0094 | 2 | HG00544.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.788+11216A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110852621 | ||||||
| chr2:110852637
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.788+11232A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110852637 | ||||||
| chr2:110852700
|
G | C | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.788+11295G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110852700 | ||||||
| chr2:110852847
|
G | A | 1 | a0002c0002t0001g0066 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.788+11442G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110852847 | ||||||
| chr2:110853111
|
C | T | 1 | a0002c0002t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.788+11706C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110853111 | ||||||
| chr2:110853239
|
G | T | 47 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0011others(44): Show | 47 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.788+11834G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110853239 | ||||||
| chr2:110853250
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.788+11845G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110853250 | ||||||
| chr2:110853521
|
C | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.788+12116C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110853521 | ||||||
| chr2:110853764
|
A | G | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.788+12359A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110853764 | ||||||
| chr2:110853807
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.788+12402G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110853807 | ||||||
| chr2:110853913
|
GT | G | 94 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.788+12524delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110853913 | |||||
| chr2:110853960
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0145others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.788+12555A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110853960 | ||||||
| chr2:110854101
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.788+12696G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110854101 | ||||||
| chr2:110854420
|
A | G | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.788+13015A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110854420 | ||||||
| chr2:110854435
|
A | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0150a0001c0012t0002g0131others(1): Show | 4 | HG01346.hp2 HG03669.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.788+13030A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110854435 | ||||||
| chr2:110854473
|
T | TTCCC | 28 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.788+13070_788+1307 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110854473 | |||||
| chr2:110855457
|
C | G | 2 | a0001c0001t0001g0012a0001c0001t0005g0149 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.788+14052C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110855457 | ||||||
| chr2:110855461
|
GA | G | 5 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0137others(2): Show | 5 | HG02027.hp2 HG03688.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.788+14058delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110855461 | |||||
| chr2:110855568
|
T | C | 28 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.788+14163T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110855568 | ||||||
| chr2:110855730
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0113a0001c0001t0001g0138others(4): Show | 7 | HG01981.hp1 HG02258.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+14325G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110855730 | ||||||
| chr2:110855900
|
A | G | 2 | a0001c0003t0001g0036a0001c0003t0001g0075 | 2 | NA18993.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.788+14495A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110855900 | ||||||
| chr2:110856002
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0005g0149 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.788+14597A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110856002 | ||||||
| chr2:110856159
|
A | G | 95 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.788+14754A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110856159 | ||||||
| chr2:110856618
|
C | T | 2 | a0001c0001t0001g0063a0003c0004t0001g0064 | 2 | HG01496.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.788+15213C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110856618 | ||||||
| chr2:110856867
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0082 | 2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.788+15462C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110856867 | ||||||
| chr2:110856887
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.788+15482C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110856887 | ||||||
| chr2:110857115
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.788+15710C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110857115 | ||||||
| chr2:110857136
|
G | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0113a0001c0001t0001g0138others(4): Show | 7 | HG01981.hp1 HG02258.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+15731G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110857136 | ||||||
| chr2:110857189
|
G | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0038others(11): Show | 14 | HG01981.hp1 HG02027.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.788+15784G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110857189 | ||||||
| chr2:110857348
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0005g0149 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.788+15943C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110857348 | ||||||
| chr2:110857438
|
A | G | 95 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.788+16033A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110857438 | ||||||
| chr2:110857502
|
T | G | 95 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.788+16097T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110857502 | ||||||
| chr2:110857571
|
G | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0126a0001c0001t0001g0128others(4): Show | 7 | HG02145.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.788+16166G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110857571 | ||||||
| chr2:110857704
|
T | A | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.788+16299T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110857704 | ||||||
| chr2:110857844
|
G | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.788+16439G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110857844 | ||||||
| chr2:110858289
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.788+16884C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110858289 | ||||||
| chr2:110858348
|
T | C | 95 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.788+16943T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110858348 | ||||||
| chr2:110858410
|
C | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.788+17005C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110858410 | ||||||
| chr2:110858527
|
G | A | 27 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0051others(24): Show | 27 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.788+17122G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110858527 | ||||||
| chr2:110858564
|
C | T | 67 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0011others(64): Show | 67 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.788+17159C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110858564 | ||||||
| chr2:110858618
|
G | A | 20 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0080others(17): Show | 20 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.788+17213G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110858618 | ||||||
| chr2:110858727
|
C | T | 94 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.788+17322C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110858727 | ||||||
| chr2:110858782
|
A | C | 2 | a0001c0001t0002g0076a0001c0001t0002g0078 | 2 | NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.788+17377A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110858782 | ||||||
| chr2:110858988
|
C | T | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.788+17583C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110858988 | ||||||
| chr2:110859005
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.788+17600C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110859005 | ||||||
| chr2:110859042
|
T | C | 48 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.788+17637T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110859042 | ||||||
| chr2:110859069
|
C | T | 1 | a0002c0002t0002g0013 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.788+17664C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110859069 | ||||||
| chr2:110859115
|
T | C | 90 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.788+17710T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110859115 | ||||||
| chr2:110859335
|
G | A | 35 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0056others(32): Show | 35 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.788+17930G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110859335 | ||||||
| chr2:110859438
|
A | G | 7 | a0001c0001t0001g0021a0001c0001t0001g0145a0001c0001t0001g0150others(4): Show | 7 | HG02451.hp1 HG02818.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.788+18033A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110859438 | ||||||
| chr2:110859574
|
G | A | 32 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(29): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.788+18169G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110859574 | ||||||
| chr2:110859842
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.788+18437C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110859842 | ||||||
| chr2:110860101
|
G | A | 6 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0013others(3): Show | 6 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.788+18696G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110860101 | ||||||
| chr2:110860345
|
A | C | 30 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.788+18940A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110860345 | ||||||
| chr2:110860348
|
T | C | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.788+18943T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110860348 | ||||||
| chr2:110860364
|
G | A | 1 | a0002c0002t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.788+18959G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110860364 | ||||||
| chr2:110860372
|
A | G | 8 | a0000c0014t0001g0072a0001c0001t0001g0010a0002c0002t0001g0061others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.788+18967A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110860372 | ||||||
| chr2:110860408
|
C | T | 5 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0119others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.788+19003C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110860408 | ||||||
| chr2:110860425
|
A | G | 4 | a0001c0001t0001g0096a0001c0012t0002g0131a0002c0002t0001g0066others(1): Show | 4 | HG01346.hp1 HG03209.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.788+19020A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110860425 | ||||||
| chr2:110860598
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.788+19193G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110860598 | ||||||
| chr2:110860985
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.788+19580C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110860985 | ||||||
| chr2:110861403
|
C | T | 36 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(33): Show | 36 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.788+19998C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110861403 | ||||||
| chr2:110861604
|
TCA | T | 29 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.788+20204_788+2020 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110861604 | |||||
| chr2:110861704
|
G | A | 1 | a0002c0002t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.788+20299G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110861704 | ||||||
| chr2:110861870
|
C | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.788+20465C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110861870 | ||||||
| chr2:110861945
|
T | C | 29 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.788+20540T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110861945 | ||||||
| chr2:110862414
|
T | C | 1 | a0006c0006t0001g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.788+21009T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110862414 | ||||||
| chr2:110862673
|
G | A | 29 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.788+21268G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110862673 | ||||||
| chr2:110862850
|
G | A | 2 | a0002c0002t0001g0019a0002c0002t0001g0135 | 2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.788+21445G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110862850 | ||||||
| chr2:110862939
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.788+21534A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110862939 | ||||||
| chr2:110863376
|
T | A | 30 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.788+21971T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110863376 | ||||||
| chr2:110863541
|
T | A | 30 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.788+22136T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110863541 | ||||||
| chr2:110863663
|
A | G | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.788+22258A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110863663 | ||||||
| chr2:110863674
|
C | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.788+22269C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110863674 | ||||||
| chr2:110863939
|
G | A | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.788+22534G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110863939 | ||||||
| chr2:110863986
|
T | C | 30 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.788+22581T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110863986 | ||||||
| chr2:110864005
|
T | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0108a0001c0001t0002g0111others(1): Show | 4 | HG00140.hp2 HG01255.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.788+22600T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110864005 | ||||||
| chr2:110864319
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.788+22914C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110864319 | ||||||
| chr2:110864524
|
A | G | 5 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0119others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.788+23119A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110864524 | ||||||
| chr2:110864623
|
C | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.788+23218C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110864623 | ||||||
| chr2:110864650
|
G | A | 1 | a0002c0002t0001g0103 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.788+23245G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110864650 | ||||||
| chr2:110864651
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG02027.hp2 NA18950.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+23246G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110864651 | ||||||
| chr2:110864858
|
C | T | 21 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0063others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.788+23453C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110864858 | ||||||
| chr2:110864888
|
C | T | 3 | a0001c0001t0001g0011a0012c0018t0001g0053a0014c0020t0001g0002 | 3 | HG02257.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.788+23483C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110864888 | ||||||
| chr2:110864967
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG02027.hp2 NA18950.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+23562G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110864967 | ||||||
| chr2:110865028
|
A | AGCTTT | 3 | a0001c0001t0001g0011a0012c0018t0001g0053a0014c0020t0001g0002 | 3 | HG02257.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.788+23624_788+2362 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110865028 | |||||
| chr2:110865028
|
A | AGTTTT | 38 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0018others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.788+23627_788+2362 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110865028 | |||||
| chr2:110865107
|
A | G | 1 | a0003c0004t0001g0030 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.788+23702A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110865107 | ||||||
| chr2:110865211
|
T | C | 37 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.788+23806T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110865211 | ||||||
| chr2:110865295
|
C | T | 3 | a0001c0012t0002g0131a0002c0002t0001g0066a0013c0011t0001g0130 | 3 | HG01346.hp1 HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.788+23890C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110865295 | ||||||
| chr2:110865346
|
C | G | 5 | a0001c0001t0006g0017a0002c0002t0001g0132a0006c0006t0001g0001others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.788+23941C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110865346 | ||||||
| chr2:110865416
|
A | G | 1 | a0001c0001t0002g0120 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.788+24011A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110865416 | ||||||
| chr2:110865653
|
A | C | 29 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.788+24248A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110865653 | ||||||
| chr2:110865723
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.788+24318C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110865723 | ||||||
| chr2:110865835
|
GT | G | 24 | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0077others(21): Show | 24 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.788+24440delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110865835 | |||||
| chr2:110866295
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.788+24890A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110866295 | ||||||
| chr2:110866460
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.788+25055G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110866460 | ||||||
| chr2:110866878
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.788+25473A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110866878 | ||||||
| chr2:110867005
|
T | C | 100 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.788+25600T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110867005 | ||||||
| chr2:110867021
|
C | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.788+25616C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110867021 | ||||||
| chr2:110867071
|
A | G | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.788+25666A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110867071 | ||||||
| chr2:110867132
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.788+25727G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110867132 | ||||||
| chr2:110867173
|
G | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.788+25768G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110867173 | ||||||
| chr2:110867189
|
A | G | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.788+25784A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110867189 | ||||||
| chr2:110867585
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.788+26180A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110867585 | ||||||
| chr2:110867770
|
C | A | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.788+26365C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110867770 | ||||||
| chr2:110867935
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.788+26530G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110867935 | ||||||
| chr2:110868029
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.788+26624G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110868029 | ||||||
| chr2:110868114
|
A | G | 37 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.788+26709A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110868114 | ||||||
| chr2:110868641
|
T | TGCACTGG others(22): Show |
1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.788+27254_788+2725 others(33): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110868641 | |||||
| chr2:110868771
|
A | T | 37 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.788+27366A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110868771 | ||||||
| chr2:110869157
|
T | C | 106 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(103): Show | 106 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.788+27752T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110869157 | ||||||
| chr2:110869290
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0082 | 2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.788+27885C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110869290 | ||||||
| chr2:110869518
|
C | T | 8 | a0000c0013t0001g0046a0001c0001t0001g0024a0001c0001t0001g0039others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.788+28113C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110869518 | ||||||
| chr2:110869546
|
T | A | 37 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.788+28141T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110869546 | ||||||
| chr2:110869663
|
T | C | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.788+28258T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110869663 | ||||||
| chr2:110869698
|
C | T | 1 | a0009c0016t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.788+28293C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110869698 | ||||||
| chr2:110869723
|
G | A | 24 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.788+28318G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110869723 | ||||||
| chr2:110870285
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.788+28880C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110870285 | ||||||
| chr2:110870340
|
C | CT | 37 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.788+28949dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110870340 | |||||
| chr2:110870411
|
A | G | 24 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.788+29006A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110870411 | ||||||
| chr2:110870417
|
G | T | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.788+29012G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110870417 | ||||||
| chr2:110870453
|
C | G | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.788+29048C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110870453 | ||||||
| chr2:110870831
|
G | C | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.788+29426G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110870831 | ||||||
| chr2:110870878
|
C | G | 100 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.788+29473C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110870878 | ||||||
| chr2:110870903
|
C | G | 37 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.788+29498C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110870903 | ||||||
| chr2:110870945
|
G | A | 27 | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0077others(24): Show | 27 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.788+29540G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110870945 | ||||||
| chr2:110870975
|
T | C | 39 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0018others(36): Show | 39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.788+29570T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110870975 | ||||||
| chr2:110871086
|
G | A | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.788+29681G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110871086 | ||||||
| chr2:110871159
|
G | T | 37 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.788+29754G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110871159 | ||||||
| chr2:110871231
|
G | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.788+29826G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110871231 | ||||||
| chr2:110871490
|
G | A | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.788+30085G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110871490 | ||||||
| chr2:110871548
|
G | T | 55 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0024others(52): Show | 55 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.788+30143G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110871548 | ||||||
| chr2:110871571
|
A | G | 2 | a0004c0005t0002g0004a0004c0005t0002g0124 | 2 | HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.788+30166A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110871571 | ||||||
| chr2:110871664
|
A | G | 1 | a0002c0002t0001g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.788+30259A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110871664 | ||||||
| chr2:110871770
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0102 | 2 | HG00140.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.788+30365T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110871770 | ||||||
| chr2:110871980
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.788+30575C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110871980 | ||||||
| chr2:110872051
|
C | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.788+30646C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110872051 | ||||||
| chr2:110872057
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.788+30652G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110872057 | ||||||
| chr2:110872292
|
G | A | 1 | a0003c0004t0004g0140 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.788+30887G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110872292 | ||||||
| chr2:110872354
|
G | A | 5 | a0001c0001t0006g0017a0002c0002t0001g0132a0006c0006t0001g0001others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.788+30949G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110872354 | ||||||
| chr2:110872691
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.788+31286C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110872691 | ||||||
| chr2:110872912
|
G | T | 31 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0029others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.788+31507G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110872912 | ||||||
| chr2:110873402
|
C | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.788+31997C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110873402 | ||||||
| chr2:110873562
|
G | T | 1 | a0002c0002t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.788+32157G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110873562 | ||||||
| chr2:110873789
|
C | T | 5 | a0001c0001t0006g0017a0002c0002t0001g0132a0006c0006t0001g0001others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.788+32384C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110873789 | ||||||
| chr2:110874003
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.788+32598G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110874003 | ||||||
| chr2:110874213
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.788+32808G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110874213 | ||||||
| chr2:110874214
|
G | T | 1 | a0001c0001t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.788+32809G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110874214 | ||||||
| chr2:110874392
|
TC | T | 10 | a0000c0013t0001g0046a0001c0001t0001g0024a0001c0001t0001g0039others(7): Show | 10 | HG02145.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.788+32990delC | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110874392 | |||||
| chr2:110874547
|
T | C | 1 | a0001c0003t0002g0084 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.788+33142T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110874547 | ||||||
| chr2:110874652
|
G | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0138a0003c0004t0004g0140 | 3 | HG01981.hp1 HG03669.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.788+33247G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110874652 | ||||||
| chr2:110874658
|
A | G | 37 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.788+33253A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110874658 | ||||||
| chr2:110874755
|
G | A | 28 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0042others(25): Show | 28 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.788+33350G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110874755 | ||||||
| chr2:110874783
|
C | A | 2 | a0001c0001t0001g0067a0001c0001t0002g0123 | 2 | HG01081.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.788+33378C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110874783 | ||||||
| chr2:110874870
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0002g0094 | 2 | HG00544.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.788+33465C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110874870 | ||||||
| chr2:110874886
|
T | G | 2 | a0001c0001t0001g0063a0003c0004t0001g0064 | 2 | HG01496.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.788+33481T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110874886 | ||||||
| chr2:110874964
|
C | T | 2 | a0001c0001t0001g0067a0001c0001t0002g0123 | 2 | HG01081.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.788+33559C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110874964 | ||||||
| chr2:110874990
|
C | T | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.788+33585C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110874990 | ||||||
| chr2:110875107
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0012c0018t0001g0053others(1): Show | 4 | HG02257.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-33682C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110875107 | ||||||
| chr2:110875192
|
G | A | 1 | a0001c0001t0002g0040 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.789-33597G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110875192 | ||||||
| chr2:110875340
|
A | G | 24 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.789-33449A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110875340 | ||||||
| chr2:110875401
|
A | G | 1 | a0002c0002t0001g0103 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.789-33388A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110875401 | ||||||
| chr2:110875638
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.789-33151A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110875638 | ||||||
| chr2:110875805
|
T | C | 1 | a0001c0003t0001g0075 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.789-32984T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110875805 | ||||||
| chr2:110875850
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.789-32939T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110875850 | ||||||
| chr2:110875978
|
A | G | 2 | a0008c0008t0001g0015a0008c0008t0001g0016 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.789-32811A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110875978 | ||||||
| chr2:110876084
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-32705C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110876084 | ||||||
| chr2:110876197
|
T | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0145a0001c0001t0005g0149others(2): Show | 5 | HG02451.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.789-32592T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110876197 | ||||||
| chr2:110876261
|
A | G | 2 | a0002c0002t0001g0019a0002c0002t0001g0135 | 2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.789-32528A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110876261 | ||||||
| chr2:110876290
|
G | A | 29 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.789-32499G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110876290 | ||||||
| chr2:110876315
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0150a0002c0002t0002g0014 | 3 | HG02280.hp2 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.789-32474C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110876315 | ||||||
| chr2:110876331
|
T | C | 2 | a0001c0003t0001g0036a0001c0003t0001g0075 | 2 | NA18993.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.789-32458T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110876331 | ||||||
| chr2:110876393
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-32396C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110876393 | ||||||
| chr2:110876434
|
C | T | 31 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0029others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.789-32355C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110876434 | ||||||
| chr2:110876466
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG02027.hp2 NA18950.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.789-32323G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110876466 | ||||||
| chr2:110876777
|
ATGTT | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0150 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.789-32005_789-3200 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110876777 | |||||
| chr2:110877011
|
A | C | 39 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(36): Show | 39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.789-31778A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110877011 | ||||||
| chr2:110877308
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.789-31481G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110877308 | ||||||
| chr2:110877386
|
C | G | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.789-31403C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110877386 | ||||||
| chr2:110877451
|
G | T | 1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.789-31338G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110877451 | ||||||
| chr2:110877502
|
C | T | 31 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0029others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.789-31287C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110877502 | ||||||
| chr2:110877503
|
G | A | 1 | a0002c0002t0001g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.789-31286G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110877503 | ||||||
| chr2:110877620
|
G | A | 102 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.789-31169G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110877620 | ||||||
| chr2:110877802
|
C | T | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-30987C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110877802 | ||||||
| chr2:110877819
|
G | A | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.789-30970G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110877819 | ||||||
| chr2:110877986
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0145others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.789-30803C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110877986 | ||||||
| chr2:110878030
|
C | T | 4 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0119others(1): Show | 4 | HG02257.hp1 HG02615.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-30759C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110878030 | ||||||
| chr2:110878455
|
T | C | 2 | a0001c0003t0001g0036a0001c0003t0001g0075 | 2 | NA18993.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.789-30334T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110878455 | ||||||
| chr2:110878485
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.789-30304C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110878485 | ||||||
| chr2:110878631
|
G | A | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.789-30158G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110878631 | ||||||
| chr2:110878707
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.789-30082G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110878707 | ||||||
| chr2:110878913
|
C | A | 31 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0029others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.789-29876C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110878913 | ||||||
| chr2:110878998
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0145others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.789-29791G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110878998 | ||||||
| chr2:110879054
|
T | TA | 23 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(20): Show | 23 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.789-29720dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110879054 | |||||
| chr2:110879259
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0150 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.789-29530G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110879259 | ||||||
| chr2:110879715
|
G | C | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.789-29074G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110879715 | ||||||
| chr2:110879744
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.789-29045A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110879744 | ||||||
| chr2:110879753
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0145others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.789-29036C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110879753 | ||||||
| chr2:110879754
|
G | T | 1 | a0005c0007t0002g0050 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.789-29035G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110879754 | ||||||
| chr2:110879965
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.789-28824G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110879965 | ||||||
| chr2:110879999
|
A | T | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.789-28790A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110879999 | ||||||
| chr2:110880107
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.789-28682T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110880107 | ||||||
| chr2:110880150
|
AAAC | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0145others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.789-28636_789-2863 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110880150 | |||||
| chr2:110880153
|
C | CA | 5 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0003t0001g0075others(2): Show | 5 | HG03225.hp1 NA18906.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.789-28617dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110880153 | |||||
| chr2:110880153
|
CA | C | 13 | a0000c0013t0001g0046a0001c0001t0001g0024a0001c0001t0001g0039others(10): Show | 13 | HG01168.hp2 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.789-28617delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110880153 | |||||
| chr2:110880153
|
CAAA | C | 28 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.789-28619_789-2861 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110880153 | |||||
| chr2:110880157
|
A | C | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-28632A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110880157 | ||||||
| chr2:110880279
|
C | A | 31 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0029others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.789-28510C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110880279 | ||||||
| chr2:110880294
|
C | A | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-28495C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110880294 | ||||||
| chr2:110880350
|
A | T | 31 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0029others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.789-28439A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110880350 | ||||||
| chr2:110880486
|
T | G | 31 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0029others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.789-28303T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110880486 | ||||||
| chr2:110880540
|
A | G | 2 | a0001c0001t0001g0010a0014c0020t0001g0002 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.789-28249A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110880540 | ||||||
| chr2:110880600
|
C | T | 1 | a0005c0007t0002g0050 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.789-28189C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110880600 | ||||||
| chr2:110880814
|
A | G | 11 | a0001c0001t0001g0088a0001c0003t0001g0041a0001c0003t0001g0081others(8): Show | 11 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.789-27975A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110880814 | ||||||
| chr2:110880894
|
G | A | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-27895G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110880894 | ||||||
| chr2:110881079
|
T | G | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-27710T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881079 | ||||||
| chr2:110881176
|
C | T | 2 | a0001c0001t0001g0008a0011c0010t0002g0009 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.789-27613C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881176 | ||||||
| chr2:110881190
|
A | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0145others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.789-27599A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881190 | ||||||
| chr2:110881198
|
C | T | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-27591C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881198 | ||||||
| chr2:110881321
|
A | G | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-27468A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881321 | ||||||
| chr2:110881418
|
A | G | 2 | a0001c0001t0001g0008a0011c0010t0002g0009 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.789-27371A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881418 | ||||||
| chr2:110881453
|
A | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0002g0101 | 3 | HG00438.hp2 HG02027.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.789-27336A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881453 | ||||||
| chr2:110881523
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0150 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.789-27266A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881523 | ||||||
| chr2:110881543
|
A | G | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-27246A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881543 | ||||||
| chr2:110881652
|
G | A | 1 | a0009c0016t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.789-27137G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881652 | ||||||
| chr2:110881658
|
T | C | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-27131T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881658 | ||||||
| chr2:110881862
|
A | T | 105 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.789-26927A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881862 | ||||||
| chr2:110881884
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.789-26905A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881884 | ||||||
| chr2:110881891
|
G | GTT | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-26889_789-2688 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110881891 | |||||
| chr2:110881906
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.789-26883G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881906 | ||||||
| chr2:110881913
|
G | A | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.789-26876G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881913 | ||||||
| chr2:110881968
|
G | A | 1 | a0002c0002t0001g0061 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.789-26821G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110881968 | ||||||
| chr2:110882012
|
T | C | 39 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(36): Show | 39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.789-26777T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110882012 | ||||||
| chr2:110882169
|
T | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0145others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.789-26620T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110882169 | ||||||
| chr2:110882247
|
G | T | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.789-26542G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110882247 | ||||||
| chr2:110882306
|
A | G | 1 | a0001c0012t0002g0131 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.789-26483A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110882306 | ||||||
| chr2:110882595
|
A | G | 1 | a0001c0012t0002g0131 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.789-26194A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110882595 | ||||||
| chr2:110882686
|
T | C | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.789-26103T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110882686 | ||||||
| chr2:110882716
|
C | G | 39 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(36): Show | 39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.789-26073C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110882716 | ||||||
| chr2:110883031
|
A | G | 39 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(36): Show | 39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.789-25758A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110883031 | ||||||
| chr2:110883107
|
G | GT | 9 | a0001c0001t0001g0058a0001c0001t0001g0080a0001c0001t0001g0110others(6): Show | 9 | HG00438.hp2 HG01175.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.789-25660dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110883107 | |||||
| chr2:110883107
|
G | GTTT | 30 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0028others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.789-25662_789-2566 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110883107 | |||||
| chr2:110883107
|
G | GTTTT | 5 | a0001c0001t0001g0029a0001c0001t0001g0150a0003c0004t0001g0027others(2): Show | 5 | HG00423.hp2 HG00673.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.789-25663_789-2566 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110883107 | |||||
| chr2:110883133
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-25656A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110883133 | ||||||
| chr2:110883390
|
A | G | 39 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(36): Show | 39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.789-25399A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110883390 | ||||||
| chr2:110883435
|
T | TC | 37 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.789-25352dupC | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110883435 | |||||
| chr2:110883561
|
T | C | 24 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.789-25228T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110883561 | ||||||
| chr2:110883686
|
T | C | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-25103T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110883686 | ||||||
| chr2:110883726
|
G | A | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-25063G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110883726 | ||||||
| chr2:110883813
|
C | T | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-24976C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110883813 | ||||||
| chr2:110883922
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.789-24867T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110883922 | ||||||
| chr2:110883952
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.789-24837A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110883952 | ||||||
| chr2:110883961
|
G | C | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-24828G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110883961 | ||||||
| chr2:110884013
|
G | T | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-24776G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110884013 | ||||||
| chr2:110884109
|
G | A | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.789-24680G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110884109 | ||||||
| chr2:110884275
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.789-24514G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110884275 | ||||||
| chr2:110884313
|
G | A | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-24476G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110884313 | ||||||
| chr2:110884580
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-24209A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110884580 | ||||||
| chr2:110884756
|
A | G | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-24033A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110884756 | ||||||
| chr2:110885488
|
A | T | 37 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0028others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.789-23301A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110885488 | ||||||
| chr2:110885491
|
T | A | 2 | a0000c0014t0001g0072a0001c0001t0001g0011 | 2 | HG02257.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.789-23298T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110885491 | ||||||
| chr2:110885502
|
T | G | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-23287T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110885502 | ||||||
| chr2:110885512
|
C | T | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-23277C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110885512 | ||||||
| chr2:110885607
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.789-23182C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110885607 | ||||||
| chr2:110885635
|
A | G | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-23154A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110885635 | ||||||
| chr2:110885677
|
C | G | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-23112C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110885677 | ||||||
| chr2:110885715
|
C | A | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-23074C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110885715 | ||||||
| chr2:110885778
|
G | A | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-23011G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110885778 | ||||||
| chr2:110885910
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0145others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.789-22879G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110885910 | ||||||
| chr2:110885982
|
CAAATCAA others(17): Show |
C | 7 | a0001c0001t0001g0042a0001c0001t0001g0117a0001c0001t0001g0121others(4): Show | 7 | HG01175.hp1 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.789-22798_789-2277 others(28): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110885982 | |||||
| chr2:110886036
|
A | G | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-22753A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110886036 | ||||||
| chr2:110886046
|
C | T | 1 | a0009c0016t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.789-22743C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110886046 | ||||||
| chr2:110886112
|
C | T | 2 | a0002c0002t0001g0019a0002c0002t0001g0135 | 2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.789-22677C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110886112 | ||||||
| chr2:110886168
|
G | A | 141 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.789-22621G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110886168 | ||||||
| chr2:110886268
|
A | T | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.789-22521A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110886268 | ||||||
| chr2:110886362
|
T | C | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-22427T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110886362 | ||||||
| chr2:110886380
|
C | CT | 5 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0077others(2): Show | 5 | HG02027.hp2 HG02257.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-22392dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110886380 | |||||
| chr2:110886380
|
C | CTTT | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.789-22394_789-2239 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110886380 | |||||
| chr2:110886386
|
T | C | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.789-22403T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110886386 | ||||||
| chr2:110886543
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-22246G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110886543 | ||||||
| chr2:110886671
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0145others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.789-22118G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110886671 | ||||||
| chr2:110886882
|
G | A | 12 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0003t0001g0041others(9): Show | 12 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.789-21907G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110886882 | ||||||
| chr2:110886898
|
C | T | 24 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.789-21891C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110886898 | ||||||
| chr2:110886914
|
TA | T | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.789-21873delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110886914 | |||||
| chr2:110887018
|
C | T | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-21771C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110887018 | ||||||
| chr2:110887046
|
C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0145others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.789-21743C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110887046 | ||||||
| chr2:110887058
|
G | C | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.789-21731G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110887058 | ||||||
| chr2:110887345
|
A | G | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.789-21444A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110887345 | ||||||
| chr2:110887385
|
G | A | 1 | a0002c0002t0002g0059 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.789-21404G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110887385 | ||||||
| chr2:110887579
|
T | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-21210T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110887579 | ||||||
| chr2:110887955
|
T | C | 5 | a0001c0001t0006g0017a0002c0002t0001g0132a0006c0006t0001g0001others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-20834T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110887955 | ||||||
| chr2:110888153
|
A | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-20636A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110888153 | ||||||
| chr2:110888331
|
T | G | 1 | a0000c0014t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.789-20458T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110888331 | ||||||
| chr2:110888481
|
TAAACAC | T | 2 | a0004c0005t0002g0004a0004c0005t0002g0124 | 2 | HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.789-20305_789-2030 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110888481 | |||||
| chr2:110888595
|
G | A | 1 | a0002c0002t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.789-20194G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110888595 | ||||||
| chr2:110888650
|
G | T | 1 | a0001c0001t0002g0105 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.789-20139G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110888650 | ||||||
| chr2:110888745
|
A | G | 1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.789-20044A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110888745 | ||||||
| chr2:110888842
|
A | G | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.789-19947A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110888842 | ||||||
| chr2:110889060
|
C | T | 2 | a0001c0001t0001g0011a0014c0020t0001g0002 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.789-19729C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110889060 | ||||||
| chr2:110889151
|
A | G | 1 | a0001c0003t0001g0090 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.789-19638A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110889151 | ||||||
| chr2:110889190
|
C | T | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.789-19599C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110889190 | ||||||
| chr2:110889313
|
AT | A | 32 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(29): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.789-19468delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110889313 | |||||
| chr2:110889457
|
C | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.789-19332C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110889457 | ||||||
| chr2:110889660
|
A | G | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-19129A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110889660 | ||||||
| chr2:110889685
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.789-19104A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110889685 | ||||||
| chr2:110889697
|
G | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-19092G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110889697 | ||||||
| chr2:110889710
|
T | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-19079T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110889710 | ||||||
| chr2:110889946
|
A | G | 1 | a0001c0003t0001g0036 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.789-18843A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110889946 | ||||||
| chr2:110889961
|
A | C | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.789-18828A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110889961 | ||||||
| chr2:110889972
|
C | T | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-18817C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110889972 | ||||||
| chr2:110890200
|
A | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.789-18589A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110890200 | ||||||
| chr2:110890270
|
C | G | 6 | a0001c0001t0001g0010a0001c0001t0006g0017a0002c0002t0001g0132others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.789-18519C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110890270 | ||||||
| chr2:110890297
|
TGAC | T | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-18488_789-1848 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110890297 | |||||
| chr2:110890437
|
T | C | 24 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.789-18352T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110890437 | ||||||
| chr2:110890655
|
A | T | 4 | a0001c0001t0001g0096a0001c0012t0002g0131a0002c0002t0001g0066others(1): Show | 4 | HG01346.hp1 HG03209.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-18134A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110890655 | ||||||
| chr2:110890677
|
T | C | 56 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0024others(53): Show | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.789-18112T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110890677 | ||||||
| chr2:110890744
|
G | T | 1 | a0006c0006t0001g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.789-18045G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110890744 | ||||||
| chr2:110890797
|
C | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.789-17992C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110890797 | ||||||
| chr2:110890820
|
C | T | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-17969C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110890820 | ||||||
| chr2:110890943
|
C | T | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-17846C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110890943 | ||||||
| chr2:110891030
|
A | T | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.789-17759A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110891030 | ||||||
| chr2:110891059
|
A | AATTC | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-17727_789-1772 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110891059 | |||||
| chr2:110891086
|
A | G | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-17703A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110891086 | ||||||
| chr2:110891407
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0150 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.789-17382A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110891407 | ||||||
| chr2:110891442
|
A | G | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-17347A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110891442 | ||||||
| chr2:110891691
|
T | C | 1 | a0003c0004t0002g0098 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.789-17098T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110891691 | ||||||
| chr2:110891802
|
G | A | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-16987G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110891802 | ||||||
| chr2:110891903
|
G | C | 146 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.789-16886G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110891903 | ||||||
| chr2:110891907
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0150 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.789-16882C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110891907 | ||||||
| chr2:110892011
|
G | A | 40 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0018others(37): Show | 40 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.789-16778G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110892011 | ||||||
| chr2:110892255
|
A | G | 34 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.789-16534A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110892255 | ||||||
| chr2:110892375
|
C | A | 34 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.789-16414C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110892375 | ||||||
| chr2:110892394
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.789-16395C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110892394 | ||||||
| chr2:110892553
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.789-16236G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110892553 | ||||||
| chr2:110892834
|
A | G | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-15955A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110892834 | ||||||
| chr2:110892961
|
T | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-15828T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110892961 | ||||||
| chr2:110893052
|
C | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-15737C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110893052 | ||||||
| chr2:110893188
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.789-15601C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110893188 | ||||||
| chr2:110893366
|
AATT | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-15418_789-1541 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110893366 | |||||
| chr2:110893413
|
A | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.789-15376A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110893413 | ||||||
| chr2:110893433
|
T | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.789-15356T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110893433 | ||||||
| chr2:110893672
|
A | C | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.789-15117A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110893672 | ||||||
| chr2:110893926
|
A | G | 32 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(29): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.789-14863A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110893926 | ||||||
| chr2:110893945
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0002g0111 | 2 | HG01255.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.789-14844G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110893945 | ||||||
| chr2:110894065
|
A | G | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.789-14724A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110894065 | ||||||
| chr2:110894089
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.789-14700A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110894089 | ||||||
| chr2:110894090
|
T | C | 5 | a0001c0001t0006g0017a0002c0002t0001g0132a0006c0006t0001g0001others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-14699T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110894090 | ||||||
| chr2:110894119
|
A | G | 1 | a0004c0005t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.789-14670A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110894119 | ||||||
| chr2:110894332
|
C | CA | 38 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-14443dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110894332 | |||||
| chr2:110894536
|
C | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.789-14253C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110894536 | ||||||
| chr2:110894755
|
A | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.789-14034A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110894755 | ||||||
| chr2:110894818
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-13971G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110894818 | ||||||
| chr2:110894824
|
C | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.789-13965C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110894824 | ||||||
| chr2:110894999
|
C | T | 56 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0024others(53): Show | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.789-13790C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110894999 | ||||||
| chr2:110895122
|
G | A | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-13667G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110895122 | ||||||
| chr2:110895175
|
G | A | 34 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.789-13614G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110895175 | ||||||
| chr2:110895451
|
T | A | 4 | a0001c0001t0001g0096a0001c0012t0002g0131a0002c0002t0001g0066others(1): Show | 4 | HG01346.hp1 HG03209.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-13338T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110895451 | ||||||
| chr2:110895667
|
T | TAGAG | 9 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.789-13106_789-1310 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110895667 | |||||
| chr2:110895667
|
T | TAGAGAG | 23 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(20): Show | 23 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.789-13108_789-1310 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110895667 | |||||
| chr2:110896008
|
T | C | 34 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.789-12781T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896008 | ||||||
| chr2:110896042
|
A | G | 1 | a0002c0002t0001g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.789-12747A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896042 | ||||||
| chr2:110896064
|
T | G | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-12725T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896064 | ||||||
| chr2:110896108
|
C | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-12681C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896108 | ||||||
| chr2:110896228
|
C | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0108a0001c0001t0002g0111others(1): Show | 4 | HG00140.hp2 HG01255.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-12561C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896228 | ||||||
| chr2:110896290
|
T | A | 1 | a0001c0017t0002g0073 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.789-12499T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896290 | ||||||
| chr2:110896360
|
G | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-12429G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896360 | ||||||
| chr2:110896426
|
T | G | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-12363T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896426 | ||||||
| chr2:110896544
|
G | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-12245G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896544 | ||||||
| chr2:110896640
|
T | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-12149T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896640 | ||||||
| chr2:110896674
|
A | T | 10 | a0000c0013t0001g0046a0001c0001t0001g0024a0001c0001t0001g0039others(7): Show | 10 | HG02145.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.789-12115A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896674 | ||||||
| chr2:110896708
|
C | G | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.789-12081C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896708 | ||||||
| chr2:110896719
|
G | A | 5 | a0001c0001t0006g0017a0002c0002t0001g0132a0006c0006t0001g0001others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-12070G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896719 | ||||||
| chr2:110896727
|
C | T | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-12062C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110896727 | ||||||
| chr2:110897092
|
T | G | 34 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.789-11697T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110897092 | ||||||
| chr2:110897559
|
A | C | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.789-11230A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110897559 | ||||||
| chr2:110897592
|
C | T | 1 | a0002c0002t0003g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.789-11197C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110897592 | ||||||
| chr2:110897956
|
C | T | 1 | a0007c0009t0001g0092 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.789-10833C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110897956 | ||||||
| chr2:110897965
|
ACT | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0037others(7): Show | 10 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(7): Show |
intron_variant | MODIFIER | c.789-10821_789-1082 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110897965 | |||||
| chr2:110897990
|
TTAGAG | T | 2 | a0001c0001t0001g0011a0014c0020t0001g0002 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.789-10796_789-1079 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110897990 | |||||
| chr2:110898010
|
G | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-10779G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110898010 | ||||||
| chr2:110898057
|
T | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-10732T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110898057 | ||||||
| chr2:110898184
|
T | TC | 97 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.789-10604dupC | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110898184 | |||||
| chr2:110898267
|
G | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-10522G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110898267 | ||||||
| chr2:110898376
|
A | G | 25 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0029others(22): Show | 25 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.789-10413A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110898376 | ||||||
| chr2:110898695
|
G | T | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-10094G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110898695 | ||||||
| chr2:110898709
|
T | C | 1 | a0005c0007t0002g0050 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.789-10080T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110898709 | ||||||
| chr2:110898744
|
A | G | 5 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0119others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-10045A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110898744 | ||||||
| chr2:110898940
|
C | T | 1 | a0007c0009t0001g0092 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.789-9849C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110898940 | ||||||
| chr2:110899074
|
A | G | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-9715A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110899074 | ||||||
| chr2:110899218
|
G | A | 1 | a0002c0002t0002g0059 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.789-9571G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110899218 | ||||||
| chr2:110899289
|
T | C | 34 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.789-9500T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110899289 | ||||||
| chr2:110899387
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.789-9402G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110899387 | ||||||
| chr2:110899449
|
G | T | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.789-9340G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110899449 | ||||||
| chr2:110899559
|
C | G | 5 | a0001c0001t0006g0017a0002c0002t0001g0132a0006c0006t0001g0001others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-9230C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110899559 | ||||||
| chr2:110899612
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.789-9177A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110899612 | ||||||
| chr2:110899737
|
T | A | 41 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.789-9052T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110899737 | ||||||
| chr2:110899913
|
C | T | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.789-8876C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110899913 | ||||||
| chr2:110900074
|
CACACACA others(5): Show |
C | 1 | a0001c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.789-8703_789-8692d others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900074 | |||||
| chr2:110900076
|
CACACACA others(3): Show |
C | 2 | a0001c0001t0002g0048a0014c0020t0001g0002 | 2 | HG02257.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.789-8703_789-8694d others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900076 | |||||
| chr2:110900082
|
CACAT | C | 2 | a0001c0001t0001g0096a0001c0001t0005g0149 | 2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.789-8703_789-8700d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900082 | |||||
| chr2:110900086
|
T | TAC | 17 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(14): Show | 17 | HG01255.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.789-8660_789-8659d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900086 | |||||
| chr2:110900086
|
T | TACAC | 9 | a0001c0001t0001g0056a0001c0001t0001g0068a0002c0002t0001g0051others(6): Show | 9 | HG00673.hp1 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.789-8662_789-8659d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900086 | |||||
| chr2:110900086
|
T | TACACAC | 5 | a0002c0002t0001g0023a0002c0002t0001g0114a0002c0002t0002g0059others(2): Show | 5 | HG01175.hp2 HG01243.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-8664_789-8659d others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900086 | |||||
| chr2:110900086
|
T | TACACACA others(1): Show |
4 | a0002c0002t0001g0061a0002c0002t0002g0013a0005c0007t0001g0062others(1): Show | 4 | HG02258.hp1 HG06807.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-8666_789-8659d others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900086 | |||||
| chr2:110900086
|
TAC | T | 12 | a0001c0001t0001g0011a0001c0001t0001g0113a0001c0001t0001g0116others(9): Show | 12 | HG00544.hp1 HG01081.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.789-8660_789-8659d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900086 | |||||
| chr2:110900086
|
TACAC | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0077others(16): Show | 19 | HG01167.hp1 HG01167.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.789-8662_789-8659d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900086 | |||||
| chr2:110900086
|
TACACAC | T | 21 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0063others(18): Show | 21 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.789-8664_789-8659d others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900086 | |||||
| chr2:110900086
|
TACACACA others(1): Show |
T | 5 | a0001c0001t0001g0012a0001c0001t0001g0102a0001c0003t0001g0036others(2): Show | 5 | HG00140.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-8666_789-8659d others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900086 | |||||
| chr2:110900086
|
TACACACA others(3): Show |
T | 4 | a0001c0001t0001g0021a0006c0006t0001g0136a0006c0006t0002g0146others(1): Show | 4 | HG02818.hp1 HG02976.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-8668_789-8659d others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900086 | |||||
| chr2:110900086
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-8670_789-8659d others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900086 | |||||
| chr2:110900086
|
TACACACA others(11): Show |
T | 5 | a0001c0001t0006g0017a0002c0002t0001g0132a0006c0006t0001g0001others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-8676_789-8659d others(20): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900086 | |||||
| chr2:110900086
|
TACACACA others(17): Show |
T | 22 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.789-8682_789-8659d others(26): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900086 | |||||
| chr2:110900092
|
C | T | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.789-8697C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110900092 | ||||||
| chr2:110900137
|
T | TA | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-8646dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900137 | |||||
| chr2:110900217
|
C | CT | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-8569dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110900217 | |||||
| chr2:110900263
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-8526A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110900263 | ||||||
| chr2:110900284
|
A | T | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-8505A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110900284 | ||||||
| chr2:110900311
|
G | T | 23 | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0077others(20): Show | 23 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.789-8478G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110900311 | ||||||
| chr2:110900433
|
A | G | 30 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.789-8356A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110900433 | ||||||
| chr2:110900783
|
T | C | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.789-8006T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110900783 | ||||||
| chr2:110900807
|
A | C | 1 | a0001c0001t0001g0058 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.789-7982A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110900807 | ||||||
| chr2:110900906
|
A | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | HG01981.hp1 HG03669.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.789-7883A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110900906 | ||||||
| chr2:110900976
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.789-7813G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110900976 | ||||||
| chr2:110901018
|
A | G | 5 | a0001c0001t0006g0017a0002c0002t0001g0132a0006c0006t0001g0001others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-7771A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110901018 | ||||||
| chr2:110901034
|
G | A | 22 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.789-7755G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110901034 | ||||||
| chr2:110901491
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.789-7298G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110901491 | ||||||
| chr2:110901521
|
G | C | 141 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.789-7268G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110901521 | ||||||
| chr2:110901641
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.789-7148G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110901641 | ||||||
| chr2:110901642
|
C | CCA | 11 | a0001c0001t0001g0012a0001c0001t0006g0017a0001c0012t0002g0131others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.789-7116_789-7115d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110901642 | |||||
| chr2:110901642
|
C | CCACA | 7 | a0001c0001t0001g0018a0001c0001t0001g0145a0001c0001t0001g0150others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.789-7118_789-7115d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110901642 | |||||
| chr2:110901642
|
C | CCACACAC others(1): Show |
3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.789-7122_789-7115d others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110901642 | |||||
| chr2:110901642
|
C | CCACACAC others(3): Show |
3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.789-7124_789-7115d others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110901642 | |||||
| chr2:110901642
|
CCA | C | 82 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.789-7116_789-7115d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110901642 | |||||
| chr2:110901642
|
CCACACA | C | 2 | a0001c0001t0001g0138a0003c0004t0004g0140 | 2 | HG01981.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.789-7120_789-7115d others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110901642 | |||||
| chr2:110901674
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.789-7115A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110901674 | ||||||
| chr2:110901685
|
C | T | 3 | a0006c0006t0001g0136a0006c0006t0002g0146a0012c0018t0001g0053 | 3 | HG02976.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.789-7104C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110901685 | ||||||
| chr2:110902032
|
C | CA | 25 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0068others(22): Show | 25 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.789-6746dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110902032 | |||||
| chr2:110902083
|
G | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-6706G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110902083 | ||||||
| chr2:110902271
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.789-6518A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110902271 | ||||||
| chr2:110902289
|
A | G | 34 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.789-6500A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110902289 | ||||||
| chr2:110902328
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-6461G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110902328 | ||||||
| chr2:110902405
|
G | T | 5 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0119others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-6384G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110902405 | ||||||
| chr2:110902747
|
C | T | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.789-6042C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110902747 | ||||||
| chr2:110902770
|
T | C | 43 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0018others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.789-6019T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110902770 | ||||||
| chr2:110902985
|
A | G | 34 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.789-5804A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110902985 | ||||||
| chr2:110903079
|
C | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0145others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.789-5710C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110903079 | ||||||
| chr2:110903133
|
T | A | 36 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(33): Show | 36 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.789-5656T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110903133 | ||||||
| chr2:110903261
|
C | T | 2 | a0001c0001t0001g0068a0002c0002t0001g0114 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.789-5528C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110903261 | ||||||
| chr2:110903450
|
C | T | 1 | a0013c0011t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.789-5339C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110903450 | ||||||
| chr2:110903809
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.789-4980G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110903809 | ||||||
| chr2:110903825
|
A | G | 5 | a0001c0001t0006g0017a0002c0002t0001g0132a0006c0006t0001g0001others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-4964A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110903825 | ||||||
| chr2:110903947
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-4842C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110903947 | ||||||
| chr2:110904107
|
C | G | 30 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.789-4682C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110904107 | ||||||
| chr2:110904172
|
CT | C | 43 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0018others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.789-4616delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110904172 | ||||||
| chr2:110904233
|
G | T | 30 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.789-4556G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110904233 | ||||||
| chr2:110904344
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-4445G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110904344 | ||||||
| chr2:110904705
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-4084A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110904705 | ||||||
| chr2:110904878
|
G | C | 30 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.789-3911G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110904878 | ||||||
| chr2:110905047
|
C | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0145others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.789-3742C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110905047 | ||||||
| chr2:110905364
|
A | G | 142 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.789-3425A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110905364 | ||||||
| chr2:110905369
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.789-3420A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110905369 | ||||||
| chr2:110905548
|
A | G | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-3241A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110905548 | ||||||
| chr2:110905931
|
C | T | 30 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.789-2858C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110905931 | ||||||
| chr2:110906016
|
G | A | 3 | a0006c0006t0001g0136a0006c0006t0002g0146a0012c0018t0001g0053 | 3 | HG02976.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.789-2773G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110906016 | ||||||
| chr2:110906034
|
A | T | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.789-2755A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110906034 | ||||||
| chr2:110906184
|
T | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.789-2605T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110906184 | ||||||
| chr2:110906293
|
G | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0018others(37): Show | 40 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.789-2496G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110906293 | ||||||
| chr2:110906363
|
C | T | 22 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.789-2426C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110906363 | ||||||
| chr2:110906537
|
C | CA | 19 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0042others(16): Show | 19 | HG01175.hp1 HG01175.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.789-2233dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110906537 | |||||
| chr2:110906537
|
CA | C | 17 | a0000c0013t0001g0046a0001c0001t0001g0011a0001c0001t0001g0024others(14): Show | 17 | HG01167.hp1 HG01167.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.789-2233delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110906537 | |||||
| chr2:110906537
|
CAA | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.789-2234_789-2233d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110906537 | |||||
| chr2:110906537
|
CAAA | C | 22 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.789-2235_789-2233d others(5): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110906537 | |||||
| chr2:110906586
|
C | CA | 12 | a0000c0014t0001g0072a0001c0001t0001g0077a0001c0001t0001g0097others(9): Show | 12 | HG01175.hp2 HG01517.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.789-2185dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110906586 | |||||
| chr2:110906586
|
C | CAA | 6 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0067others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.789-2186_789-2185d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110906586 | |||||
| chr2:110906586
|
C | CAAA | 5 | a0001c0001t0001g0012a0001c0001t0001g0145a0001c0001t0005g0149others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.789-2187_789-2185d others(5): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110906586 | |||||
| chr2:110906586
|
CA | C | 21 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.789-2185delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110906586 | |||||
| chr2:110906586
|
CAA | C | 13 | a0001c0001t0001g0088a0001c0001t0001g0113a0001c0001t0001g0138others(10): Show | 13 | HG00544.hp1 HG01081.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.789-2186_789-2185d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 110906586 | |||||
| chr2:110906633
|
A | C | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.789-2156A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110906633 | ||||||
| chr2:110906745
|
C | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0058 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.789-2044C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110906745 | ||||||
| chr2:110906788
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0002g0123 | 2 | HG01081.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.789-2001G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110906788 | ||||||
| chr2:110907103
|
C | T | 30 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.789-1686C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110907103 | ||||||
| chr2:110907154
|
T | G | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.789-1635T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110907154 | ||||||
| chr2:110907179
|
A | G | 42 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0018others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.789-1610A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110907179 | ||||||
| chr2:110907456
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.789-1333C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110907456 | ||||||
| chr2:110907560
|
A | G | 31 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.789-1229A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110907560 | ||||||
| chr2:110907675
|
C | T | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.789-1114C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110907675 | ||||||
| chr2:110907684
|
G | T | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.789-1105G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110907684 | ||||||
| chr2:110908204
|
T | G | 31 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.789-585T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110908204 | ||||||
| chr2:110908236
|
C | T | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.789-553C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110908236 | ||||||
| chr2:110908502
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.789-287T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110908502 | ||||||
| chr2:110908586
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789-203T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110908586 | ||||||
| chr2:110908762
|
A | G | 5 | a0001c0001t0001g0067a0001c0001t0002g0123a0002c0002t0001g0132others(2): Show | 5 | HG01081.hp1 HG01891.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-27A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | 110908762 | ||||||
| chr2:110908977
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.905+72G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110908977 | ||||||
| chr2:110908984
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0005g0149 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.905+79C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110908984 | ||||||
| chr2:110909034
|
G | A | 1 | a0000c0014t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.905+129G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110909034 | ||||||
| chr2:110909096
|
A | G | 1 | a0002c0002t0001g0066 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.905+191A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110909096 | ||||||
| chr2:110909352
|
G | A | 24 | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0077others(21): Show | 24 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.905+447G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110909352 | ||||||
| chr2:110909359
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.905+454A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110909359 | ||||||
| chr2:110909621
|
G | A | 60 | a0000c0014t0001g0072a0001c0001t0001g0012a0001c0001t0001g0018others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.905+716G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110909621 | ||||||
| chr2:110909977
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.905+1072T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110909977 | ||||||
| chr2:110910083
|
A | G | 103 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.905+1178A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110910083 | ||||||
| chr2:110910126
|
G | A | 3 | a0002c0002t0001g0061a0002c0002t0002g0119a0005c0007t0001g0062 | 3 | HG02615.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.905+1221G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110910126 | ||||||
| chr2:110910159
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.905+1254C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110910159 | ||||||
| chr2:110910610
|
T | C | 1 | a0001c0003t0001g0036 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.905+1705T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110910610 | ||||||
| chr2:110910698
|
T | C | 24 | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0077others(21): Show | 24 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.905+1793T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110910698 | ||||||
| chr2:110910813
|
T | C | 1 | a0010c0015t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.905+1908T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110910813 | ||||||
| chr2:110910921
|
G | T | 1 | a0001c0001t0001g0086 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.905+2016G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110910921 | ||||||
| chr2:110911164
|
C | T | 6 | a0001c0001t0001g0096a0001c0012t0002g0131a0002c0002t0001g0019others(3): Show | 6 | HG01167.hp1 HG01346.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+2259C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110911164 | ||||||
| chr2:110911223
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.905+2318A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110911223 | ||||||
| chr2:110911617
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.905+2712G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110911617 | ||||||
| chr2:110911907
|
G | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0145others(7): Show | 10 | HG02280.hp2 HG02451.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.905+3002G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110911907 | ||||||
| chr2:110912203
|
T | C | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.905+3298T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110912203 | ||||||
| chr2:110912480
|
A | G | 24 | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0077others(21): Show | 24 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.905+3575A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110912480 | ||||||
| chr2:110912744
|
G | A | 21 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0018others(18): Show | 21 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.905+3839G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110912744 | ||||||
| chr2:110912961
|
T | G | 1 | a0008c0008t0001g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.905+4056T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110912961 | ||||||
| chr2:110913002
|
A | C | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.905+4097A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110913002 | ||||||
| chr2:110913003
|
A | G | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+4098A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110913003 | ||||||
| chr2:110913231
|
T | C | 6 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0014others(3): Show | 6 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.905+4326T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110913231 | ||||||
| chr2:110913518
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.905+4613A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110913518 | ||||||
| chr2:110913712
|
G | A | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+4807G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110913712 | ||||||
| chr2:110913751
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.905+4846C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110913751 | ||||||
| chr2:110913953
|
T | C | 2 | a0001c0003t0001g0036a0001c0003t0001g0075 | 2 | NA18993.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.905+5048T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110913953 | ||||||
| chr2:110914094
|
T | C | 72 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.905+5189T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110914094 | ||||||
| chr2:110914176
|
GAGAA | G | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+5275_905+5278d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110914176 | |||||
| chr2:110914382
|
T | C | 12 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0006g0017others(9): Show | 12 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.905+5477T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110914382 | ||||||
| chr2:110914447
|
G | T | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.905+5542G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110914447 | ||||||
| chr2:110914557
|
C | A | 22 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0018others(19): Show | 22 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.905+5652C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110914557 | ||||||
| chr2:110914645
|
A | G | 6 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0014others(3): Show | 6 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.905+5740A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110914645 | ||||||
| chr2:110914974
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.905+6069C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110914974 | ||||||
| chr2:110914992
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.905+6087G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110914992 | ||||||
| chr2:110915002
|
A | G | 8 | a0000c0013t0001g0046a0001c0001t0001g0024a0001c0001t0001g0039others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.905+6097A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915002 | ||||||
| chr2:110915062
|
CA | C | 6 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0014others(3): Show | 6 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.905+6158delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915062 | ||||||
| chr2:110915065
|
C | T | 1 | a0003c0004t0002g0079 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.905+6160C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915065 | ||||||
| chr2:110915110
|
A | G | 2 | a0001c0012t0002g0131a0013c0011t0001g0130 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.905+6205A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915110 | ||||||
| chr2:110915334
|
T | TTATATAT others(3): Show |
1 | a0000c0014t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.905+6430_905+6431i others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915334 | |||||
| chr2:110915334
|
T | TTATATAT others(7): Show |
2 | a0002c0002t0002g0119a0005c0007t0001g0062 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905+6430_905+6431i others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915334 | |||||
| chr2:110915334
|
T | TTATATAT others(9): Show |
1 | a0002c0002t0001g0061 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.905+6430_905+6431i others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915334 | |||||
| chr2:110915336
|
T | A | 5 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0119others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.905+6431T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915336 | ||||||
| chr2:110915336
|
T | TTA | 3 | a0004c0005t0002g0124a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | HG01891.hp1 HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.905+6445_905+6446d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915336 | |||||
| chr2:110915336
|
T | TTATA | 4 | a0001c0001t0001g0011a0001c0001t0006g0017a0004c0005t0002g0004others(1): Show | 4 | HG02280.hp1 HG02897.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+6443_905+6446d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915336 | |||||
| chr2:110915336
|
TTA | T | 21 | a0001c0001t0001g0137a0001c0001t0002g0040a0002c0002t0001g0023others(18): Show | 21 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.905+6445_905+6446d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915336 | |||||
| chr2:110915348
|
ATATG | A | 3 | a0001c0001t0001g0080a0001c0001t0002g0032a0003c0004t0003g0143 | 3 | HG00438.hp1 HG03831.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.905+6445_905+6448d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915348 | |||||
| chr2:110915350
|
A | ATATATAT others(3): Show |
1 | a0009c0016t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.905+6446_905+6447i others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915350 | |||||
| chr2:110915350
|
A | ATG | 2 | a0001c0001t0001g0067a0001c0001t0002g0123 | 2 | HG01081.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.905+6475_905+6476d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915350 | |||||
| chr2:110915350
|
A | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0021others(7): Show | 10 | HG01243.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.905+6445A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915350 | ||||||
| chr2:110915350
|
ATG | A | 29 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.905+6475_905+6476d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915350 | |||||
| chr2:110915350
|
ATGTG | A | 14 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0086others(11): Show | 14 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.905+6473_905+6476d others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915350 | |||||
| chr2:110915350
|
ATGTGTGT others(1): Show |
A | 2 | a0001c0001t0001g0008a0011c0010t0002g0009 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.905+6469_905+6476d others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915350 | |||||
| chr2:110915350
|
ATGTGTGT others(7): Show |
A | 8 | a0000c0013t0001g0046a0001c0001t0001g0024a0001c0001t0001g0039others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.905+6463_905+6476d others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915350 | |||||
| chr2:110915352
|
G | A | 9 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0006g0017others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.905+6447G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915352 | ||||||
| chr2:110915354
|
G | A | 5 | a0001c0001t0001g0011a0006c0006t0001g0001a0008c0008t0001g0015others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.905+6449G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915354 | ||||||
| chr2:110915356
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0058others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+6451G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915356 | ||||||
| chr2:110915407
|
C | CAT | 2 | a0001c0001t0001g0042a0004c0005t0002g0127 | 2 | HG01175.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.905+6523_905+6524d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915407 | |||||
| chr2:110915407
|
CAT | C | 27 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0029others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.905+6523_905+6524d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915407 | |||||
| chr2:110915419
|
TA | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0150 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.905+6515delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915419 | ||||||
| chr2:110915420
|
A | T | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.905+6515A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915420 | ||||||
| chr2:110915421
|
TATA | T | 5 | a0001c0001t0001g0011a0001c0001t0006g0017a0006c0006t0001g0136others(2): Show | 5 | HG02280.hp1 HG02976.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.905+6517_905+6519d others(5): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915421 | ||||||
| chr2:110915422
|
A | T | 14 | a0000c0013t0001g0046a0001c0001t0001g0018a0001c0001t0001g0021others(11): Show | 14 | HG02145.hp1 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.905+6517A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915422 | ||||||
| chr2:110915423
|
TATA | T | 4 | a0006c0006t0001g0001a0008c0008t0001g0015a0008c0008t0001g0016others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+6519_905+6521d others(5): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915423 | ||||||
| chr2:110915424
|
A | T | 20 | a0000c0013t0001g0046a0001c0001t0001g0018a0001c0001t0001g0021others(17): Show | 20 | HG02027.hp2 HG02145.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.905+6519A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915424 | ||||||
| chr2:110915425
|
TATA | T | 3 | a0001c0001t0001g0044a0002c0002t0001g0061a0009c0016t0001g0112 | 3 | HG02735.hp2 HG04115.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.905+6521_905+6523d others(5): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915425 | ||||||
| chr2:110915426
|
A | AT | 3 | a0001c0001t0001g0010a0001c0001t0001g0056a0002c0002t0001g0103 | 3 | HG02622.hp2 HG03225.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.905+6522dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110915426 | |||||
| chr2:110915426
|
A | T | 47 | a0000c0013t0001g0046a0001c0001t0001g0011a0001c0001t0001g0018others(44): Show | 47 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.905+6521A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915426 | ||||||
| chr2:110915427
|
TA | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0113 | 2 | HG01081.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.905+6523delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915427 | ||||||
| chr2:110915428
|
A | T | 118 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.905+6523A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915428 | ||||||
| chr2:110915430
|
T | A | 1 | a0001c0001t0001g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.905+6525T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915430 | ||||||
| chr2:110915637
|
A | G | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905+6732A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915637 | ||||||
| chr2:110915708
|
G | A | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.905+6803G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110915708 | ||||||
| chr2:110916239
|
CT | C | 21 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0018others(18): Show | 21 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.905+7344delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110916239 | |||||
| chr2:110916905
|
G | A | 3 | a0006c0006t0001g0136a0006c0006t0002g0146a0012c0018t0001g0053 | 3 | HG02976.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.905+8000G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110916905 | ||||||
| chr2:110916909
|
G | A | 23 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0006g0017others(20): Show | 23 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.905+8004G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110916909 | ||||||
| chr2:110917023
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.905+8118T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110917023 | ||||||
| chr2:110917330
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(8): Show | 11 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.905+8425A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110917330 | ||||||
| chr2:110917537
|
T | C | 1 | a0002c0002t0001g0103 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.905+8632T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110917537 | ||||||
| chr2:110917632
|
C | T | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.905+8727C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110917632 | ||||||
| chr2:110917633
|
A | G | 34 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0049others(31): Show | 34 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.905+8728A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110917633 | ||||||
| chr2:110917962
|
C | T | 1 | a0002c0002t0001g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.905+9057C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110917962 | ||||||
| chr2:110917980
|
G | A | 1 | a0009c0016t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.905+9075G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110917980 | ||||||
| chr2:110917998
|
A | T | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.905+9093A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110917998 | ||||||
| chr2:110918055
|
C | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0058 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.905+9150C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110918055 | ||||||
| chr2:110918258
|
A | T | 11 | a0001c0001t0001g0088a0001c0003t0001g0041a0001c0003t0001g0081others(8): Show | 11 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.905+9353A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110918258 | ||||||
| chr2:110918329
|
A | G | 1 | a0002c0002t0001g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.905+9424A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110918329 | ||||||
| chr2:110918843
|
C | G | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.905+9938C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110918843 | ||||||
| chr2:110918864
|
C | T | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.905+9959C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110918864 | ||||||
| chr2:110919016
|
C | T | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.905+10111C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110919016 | ||||||
| chr2:110919101
|
CAGGT | C | 69 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0012others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.905+10202_905+1020 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110919101 | |||||
| chr2:110919170
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0002g0123 | 2 | HG01081.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.905+10265T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110919170 | ||||||
| chr2:110919180
|
G | C | 1 | a0001c0001t0002g0033 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.905+10275G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110919180 | ||||||
| chr2:110919272
|
T | G | 1 | a0006c0006t0001g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.905+10367T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110919272 | ||||||
| chr2:110919394
|
C | T | 1 | a0003c0004t0003g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.905+10489C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110919394 | ||||||
| chr2:110919409
|
G | T | 3 | a0006c0006t0001g0136a0006c0006t0002g0146a0012c0018t0001g0053 | 3 | HG02976.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.905+10504G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110919409 | ||||||
| chr2:110919412
|
G | T | 2 | a0001c0001t0001g0068a0002c0002t0001g0114 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.905+10507G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110919412 | ||||||
| chr2:110919461
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.905+10556A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110919461 | ||||||
| chr2:110919533
|
G | A | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+10628G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110919533 | ||||||
| chr2:110919559
|
T | TA | 11 | a0000c0014t0001g0072a0001c0001t0001g0056a0001c0001t0001g0058others(8): Show | 11 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.905+10661dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110919559 | |||||
| chr2:110919567
|
T | A | 106 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(103): Show | 106 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.905+10662T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110919567 | ||||||
| chr2:110919616
|
C | T | 22 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0018others(19): Show | 22 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.905+10711C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110919616 | ||||||
| chr2:110920440
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.905+11535G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110920440 | ||||||
| chr2:110920489
|
A | G | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+11584A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110920489 | ||||||
| chr2:110920937
|
A | T | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.905+12032A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110920937 | ||||||
| chr2:110921089
|
G | A | 5 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0119others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.905+12184G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110921089 | ||||||
| chr2:110921136
|
T | A | 1 | a0007c0009t0001g0106 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.905+12231T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110921136 | ||||||
| chr2:110921227
|
G | A | 11 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(8): Show | 11 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.906-12262G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110921227 | ||||||
| chr2:110921266
|
T | G | 1 | a0001c0001t0001g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.906-12223T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110921266 | ||||||
| chr2:110921342
|
GTTGCTCT others(3): Show |
G | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.906-12135_906-1212 others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110921342 | |||||
| chr2:110921364
|
C | G | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-12125C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110921364 | ||||||
| chr2:110921388
|
A | AC | 33 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0031others(30): Show | 33 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.906-12089dupC | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110921388 | |||||
| chr2:110921388
|
A | ACC | 13 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0088others(10): Show | 13 | HG01175.hp2 HG01496.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.906-12090_906-1208 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110921388 | |||||
| chr2:110921388
|
AC | A | 13 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0049others(10): Show | 13 | HG01243.hp2 HG02622.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.906-12089delC | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110921388 | |||||
| chr2:110921388
|
ACC | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0001g0122others(10): Show | 13 | HG02027.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.906-12090_906-1208 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110921388 | |||||
| chr2:110921397
|
C | G | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.906-12092C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110921397 | ||||||
| chr2:110921400
|
CT | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0005g0149others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-12079delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110921400 | |||||
| chr2:110921401
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.906-12088T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110921401 | ||||||
| chr2:110921567
|
G | T | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.906-11922G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110921567 | ||||||
| chr2:110921600
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.906-11889A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110921600 | ||||||
| chr2:110921673
|
A | G | 5 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048others(2): Show | 5 | HG02040.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-11816A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110921673 | ||||||
| chr2:110921688
|
T | C | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-11801T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110921688 | ||||||
| chr2:110921883
|
C | T | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.906-11606C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110921883 | ||||||
| chr2:110921973
|
T | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.906-11516T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110921973 | ||||||
| chr2:110922291
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.906-11198G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110922291 | ||||||
| chr2:110922572
|
C | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0145others(7): Show | 10 | HG02280.hp2 HG02451.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.906-10917C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110922572 | ||||||
| chr2:110922578
|
T | C | 24 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(21): Show |
intron_variant | MODIFIER | c.906-10911T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110922578 | ||||||
| chr2:110922616
|
C | T | 5 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0119others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-10873C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110922616 | ||||||
| chr2:110922677
|
C | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0145others(7): Show | 10 | HG02280.hp2 HG02451.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.906-10812C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110922677 | ||||||
| chr2:110923092
|
A | G | 5 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0119others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-10397A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110923092 | ||||||
| chr2:110923241
|
A | G | 22 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.906-10248A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110923241 | ||||||
| chr2:110923586
|
A | G | 1 | a0002c0002t0002g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.906-9903A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110923586 | ||||||
| chr2:110923746
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.906-9743C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110923746 | ||||||
| chr2:110923755
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.906-9734G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110923755 | ||||||
| chr2:110923796
|
C | T | 4 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0119others(1): Show | 4 | HG02257.hp1 HG02615.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-9693C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110923796 | ||||||
| chr2:110923860
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.906-9629C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110923860 | ||||||
| chr2:110923893
|
A | G | 67 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0011others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.906-9596A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110923893 | ||||||
| chr2:110924190
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.906-9299T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110924190 | ||||||
| chr2:110924261
|
G | T | 66 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0012others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.906-9228G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110924261 | ||||||
| chr2:110924327
|
C | T | 5 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0119others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-9162C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110924327 | ||||||
| chr2:110924334
|
A | G | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-9155A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110924334 | ||||||
| chr2:110924405
|
G | A | 2 | a0003c0004t0001g0093a0003c0004t0002g0079 | 2 | NA18993.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.906-9084G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110924405 | ||||||
| chr2:110924454
|
C | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0145others(7): Show | 10 | HG02280.hp2 HG02451.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.906-9035C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110924454 | ||||||
| chr2:110924536
|
C | G | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.906-8953C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110924536 | ||||||
| chr2:110924603
|
A | G | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.906-8886A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110924603 | ||||||
| chr2:110924785
|
T | TGAATCAC others(291): Show |
13 | a0001c0001t0001g0080a0002c0002t0001g0023a0002c0002t0001g0051others(10): Show | 13 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.906-8687_906-8686i others(300): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110924785 | |||||
| chr2:110924785
|
T | TGAATCAC others(291): Show |
1 | a0002c0002t0001g0103 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.906-8687_906-8686i others(300): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110924785 | |||||
| chr2:110924785
|
T | TGAATCAC others(292): Show |
3 | a0001c0001t0001g0068a0002c0002t0001g0114a0002c0002t0002g0059 | 3 | HG01243.hp1 HG02723.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.906-8687_906-8686i others(301): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110924785 | |||||
| chr2:110924785
|
T | TGAATCAC others(304): Show |
1 | a0001c0001t0001g0038 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.906-8687_906-8686i others(313): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110924785 | |||||
| chr2:110924785
|
T | TGAATCAC others(305): Show |
3 | a0001c0001t0001g0077a0001c0001t0002g0076a0001c0001t0002g0078 | 3 | HG02027.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.906-8687_906-8686i others(314): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110924785 | |||||
| chr2:110924904
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.906-8585T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110924904 | ||||||
| chr2:110925144
|
C | G | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-8345C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110925144 | ||||||
| chr2:110925354
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(8): Show | 11 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.906-8135A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110925354 | ||||||
| chr2:110925380
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.906-8109G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110925380 | ||||||
| chr2:110925415
|
G | A | 1 | a0001c0001t0002g0076 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.906-8074G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110925415 | ||||||
| chr2:110925466
|
C | T | 21 | a0001c0001t0001g0008a0001c0001t0001g0113a0001c0001t0001g0137others(18): Show | 21 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.906-8023C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110925466 | ||||||
| chr2:110925800
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.906-7689C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110925800 | ||||||
| chr2:110925827
|
T | C | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.906-7662T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110925827 | ||||||
| chr2:110925853
|
C | CT | 78 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.906-7615dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110925853 | |||||
| chr2:110925853
|
C | CTT | 5 | a0001c0001t0001g0011a0001c0001t0001g0138a0001c0001t0002g0076others(2): Show | 5 | HG02258.hp1 HG03669.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-7616_906-7615d others(4): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110925853 | |||||
| chr2:110925853
|
CT | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0021others(11): Show | 14 | HG01243.hp2 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.906-7615delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 110925853 | |||||
| chr2:110926016
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(8): Show | 11 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.906-7473A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110926016 | ||||||
| chr2:110926159
|
AG | A | 2 | a0001c0001t0001g0008a0011c0010t0002g0009 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.906-7329delG | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110926159 | ||||||
| chr2:110926192
|
G | A | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-7297G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110926192 | ||||||
| chr2:110926208
|
C | T | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.906-7281C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110926208 | ||||||
| chr2:110926215
|
A | G | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.906-7274A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110926215 | ||||||
| chr2:110926409
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0002g0006others(2): Show | 5 | HG02451.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-7080G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110926409 | ||||||
| chr2:110926480
|
C | T | 48 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(45): Show | 48 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.906-7009C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110926480 | ||||||
| chr2:110926513
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0102 | 2 | HG00140.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.906-6976G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110926513 | ||||||
| chr2:110926674
|
A | G | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.906-6815A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110926674 | ||||||
| chr2:110926796
|
C | T | 3 | a0006c0006t0001g0136a0006c0006t0002g0146a0012c0018t0001g0053 | 3 | HG02976.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.906-6693C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110926796 | ||||||
| chr2:110926822
|
C | A | 3 | a0006c0006t0001g0136a0006c0006t0002g0146a0012c0018t0001g0053 | 3 | HG02976.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.906-6667C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110926822 | ||||||
| chr2:110926870
|
C | T | 4 | a0001c0001t0001g0008a0002c0002t0002g0147a0002c0002t0002g0148others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-6619C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110926870 | ||||||
| chr2:110926871
|
G | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0018others(10): Show | 13 | HG00099.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.906-6618G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110926871 | ||||||
| chr2:110927008
|
A | G | 47 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.906-6481A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110927008 | ||||||
| chr2:110927223
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.906-6266G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110927223 | ||||||
| chr2:110927257
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.906-6232C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110927257 | ||||||
| chr2:110927258
|
G | A | 1 | a0002c0002t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.906-6231G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110927258 | ||||||
| chr2:110927361
|
G | A | 1 | a0003c0004t0001g0027 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.906-6128G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110927361 | ||||||
| chr2:110927410
|
C | T | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.906-6079C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110927410 | ||||||
| chr2:110927705
|
G | A | 1 | a0003c0004t0001g0093 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.906-5784G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110927705 | ||||||
| chr2:110927840
|
C | T | 22 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.906-5649C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110927840 | ||||||
| chr2:110927864
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.906-5625A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110927864 | ||||||
| chr2:110928057
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.906-5432G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110928057 | ||||||
| chr2:110928125
|
A | G | 1 | a0010c0015t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.906-5364A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110928125 | ||||||
| chr2:110928212
|
C | T | 69 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0011others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.906-5277C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110928212 | ||||||
| chr2:110928241
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.906-5248T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110928241 | ||||||
| chr2:110928322
|
G | T | 21 | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0077others(18): Show | 21 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.906-5167G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110928322 | ||||||
| chr2:110928480
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.906-5009C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110928480 | ||||||
| chr2:110928601
|
T | A | 22 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.906-4888T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110928601 | ||||||
| chr2:110928814
|
G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0145a0001c0001t0005g0149others(2): Show | 5 | HG02451.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-4675G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110928814 | ||||||
| chr2:110928856
|
C | A | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.906-4633C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110928856 | ||||||
| chr2:110928950
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.906-4539C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110928950 | ||||||
| chr2:110929058
|
G | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0145others(7): Show | 10 | HG02280.hp2 HG02451.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.906-4431G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110929058 | ||||||
| chr2:110929268
|
T | A | 2 | a0001c0001t0001g0145a0001c0001t0005g0149 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.906-4221T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110929268 | ||||||
| chr2:110929334
|
C | T | 4 | a0001c0001t0001g0096a0001c0012t0002g0131a0002c0002t0001g0066others(1): Show | 4 | HG01346.hp1 HG03209.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-4155C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110929334 | ||||||
| chr2:110929398
|
A | G | 2 | a0002c0002t0001g0019a0002c0002t0001g0135 | 2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.906-4091A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110929398 | ||||||
| chr2:110929618
|
G | A | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.906-3871G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110929618 | ||||||
| chr2:110929690
|
A | T | 1 | a0001c0001t0002g0123 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.906-3799A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110929690 | ||||||
| chr2:110929762
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.906-3727C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110929762 | ||||||
| chr2:110930026
|
G | A | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.906-3463G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110930026 | ||||||
| chr2:110930187
|
G | A | 5 | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0119others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-3302G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110930187 | ||||||
| chr2:110930325
|
C | G | 1 | a0001c0003t0001g0090 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.906-3164C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110930325 | ||||||
| chr2:110930412
|
G | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0002g0047others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-3077G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110930412 | ||||||
| chr2:110930414
|
T | C | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.906-3075T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110930414 | ||||||
| chr2:110930483
|
A | G | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.906-3006A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110930483 | ||||||
| chr2:110930662
|
T | C | 8 | a0002c0002t0001g0023a0002c0002t0001g0051a0002c0002t0001g0054others(5): Show | 8 | HG00673.hp1 HG01255.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.906-2827T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110930662 | ||||||
| chr2:110931110
|
C | T | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.906-2379C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110931110 | ||||||
| chr2:110931391
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.906-2098A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110931391 | ||||||
| chr2:110931418
|
A | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0002g0047others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-2071A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110931418 | ||||||
| chr2:110931579
|
G | A | 15 | a0001c0001t0001g0008a0001c0003t0001g0036a0001c0003t0001g0041others(12): Show | 15 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.906-1910G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110931579 | ||||||
| chr2:110931895
|
C | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0145others(7): Show | 10 | HG02280.hp2 HG02451.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.906-1594C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110931895 | ||||||
| chr2:110932022
|
A | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0002g0047others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-1467A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110932022 | ||||||
| chr2:110932349
|
A | G | 1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.906-1140A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110932349 | ||||||
| chr2:110932570
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.906-919G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110932570 | ||||||
| chr2:110932964
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.906-525C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110932964 | ||||||
| chr2:110933047
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.906-442T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110933047 | ||||||
| chr2:110933091
|
G | A | 1 | a0002c0002t0002g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.906-398G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110933091 | ||||||
| chr2:110933213
|
C | G | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.906-276C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110933213 | ||||||
| chr2:110933476
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.906-13C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | 110933476 | ||||||
| chr2:110933785
|
C | T | 10 | a0000c0013t0001g0046a0001c0001t0001g0024a0001c0001t0001g0039others(7): Show | 10 | HG02145.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1059+143C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110933785 | ||||||
| chr2:110933891
|
C | A | 22 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.1059+249C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110933891 | ||||||
| chr2:110933953
|
G | C | 16 | a0001c0001t0001g0068a0001c0001t0001g0080a0002c0002t0001g0023others(13): Show | 16 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.1059+311G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110933953 | ||||||
| chr2:110933964
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1059+322A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110933964 | ||||||
| chr2:110934166
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1059+524G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110934166 | ||||||
| chr2:110934358
|
C | T | 22 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.1059+716C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110934358 | ||||||
| chr2:110935004
|
C | T | 25 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0024others(22): Show | 25 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1059+1362C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110935004 | ||||||
| chr2:110935472
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1059+1830G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110935472 | ||||||
| chr2:110935579
|
C | T | 10 | a0000c0013t0001g0046a0001c0001t0001g0024a0001c0001t0001g0039others(7): Show | 10 | HG02145.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1059+1937C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110935579 | ||||||
| chr2:110935867
|
C | T | 2 | a0001c0001t0002g0047a0001c0001t0002g0071 | 2 | HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1059+2225C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110935867 | ||||||
| chr2:110935955
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0006g0017a0006c0006t0001g0001others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+2313C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110935955 | ||||||
| chr2:110936076
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0006g0017a0006c0006t0001g0001others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+2434C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110936076 | ||||||
| chr2:110936753
|
G | A | 99 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1059+3111G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110936753 | ||||||
| chr2:110936803
|
G | A | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1059+3161G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110936803 | ||||||
| chr2:110936836
|
C | A | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1059+3194C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110936836 | ||||||
| chr2:110936850
|
AT | A | 56 | a0000c0014t0001g0072a0001c0001t0001g0012a0001c0001t0001g0018others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1059+3223delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110936850 | |||||
| chr2:110936923
|
C | T | 21 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0037others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+3281C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110936923 | ||||||
| chr2:110936925
|
A | G | 99 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1059+3283A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110936925 | ||||||
| chr2:110937103
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1059+3461A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110937103 | ||||||
| chr2:110937172
|
G | T | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+3530G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110937172 | ||||||
| chr2:110937204
|
A | G | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1059+3562A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110937204 | ||||||
| chr2:110937220
|
G | C | 21 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0037others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+3578G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110937220 | ||||||
| chr2:110937235
|
T | C | 32 | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0024others(29): Show | 32 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.1059+3593T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110937235 | ||||||
| chr2:110937379
|
A | ATC | 58 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0012others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1059+3737_1059+373 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110937379 | ||||||
| chr2:110937762
|
A | T | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1059+4120A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110937762 | ||||||
| chr2:110937767
|
T | G | 21 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0037others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+4125T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110937767 | ||||||
| chr2:110937842
|
T | A | 99 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1059+4200T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110937842 | ||||||
| chr2:110937902
|
C | A | 58 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0012others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1059+4260C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110937902 | ||||||
| chr2:110937967
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1059+4325G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110937967 | ||||||
| chr2:110938274
|
C | T | 1 | a0003c0004t0001g0027 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1059+4632C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110938274 | ||||||
| chr2:110938277
|
T | A | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1059+4635T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110938277 | ||||||
| chr2:110938338
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1059+4696C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110938338 | ||||||
| chr2:110938691
|
GAATGAAT others(9): Show |
G | 3 | a0003c0004t0001g0027a0003c0004t0001g0093a0003c0004t0002g0079 | 3 | HG00423.hp2 NA18993.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1059+5060_1059+507 others(20): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110938691 | |||||
| chr2:110938707
|
A | AAATG | 3 | a0002c0002t0001g0132a0004c0005t0002g0004a0004c0005t0002g0124 | 3 | HG01891.hp1 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1059+5084_1059+508 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110938707 | |||||
| chr2:110938730
|
A | T | 1 | a0004c0005t0002g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1059+5088A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110938730 | ||||||
| chr2:110938839
|
CT | C | 30 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0029others(27): Show | 30 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+5209delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110938839 | |||||
| chr2:110938852
|
A | T | 1 | a0001c0012t0002g0131 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1059+5210A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110938852 | ||||||
| chr2:110938969
|
A | C | 93 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1059+5327A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110938969 | ||||||
| chr2:110939012
|
T | C | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1059+5370T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110939012 | ||||||
| chr2:110939040
|
G | C | 1 | a0002c0002t0001g0023 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1059+5398G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110939040 | ||||||
| chr2:110939163
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+5521G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110939163 | ||||||
| chr2:110939993
|
C | A | 1 | a0005c0007t0004g0144 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1059+6351C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110939993 | ||||||
| chr2:110940085
|
T | C | 1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1059+6443T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110940085 | ||||||
| chr2:110940353
|
G | A | 3 | a0001c0001t0001g0097a0007c0009t0001g0092a0007c0009t0001g0106 | 3 | HG00099.hp2 HG01517.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1059+6711G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110940353 | ||||||
| chr2:110940354
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1059+6712G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110940354 | ||||||
| chr2:110940463
|
A | C | 26 | a0000c0014t0001g0072a0001c0001t0001g0029a0001c0001t0001g0038others(23): Show | 26 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1059+6821A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110940463 | ||||||
| chr2:110940501
|
C | T | 93 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1059+6859C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110940501 | ||||||
| chr2:110941482
|
T | C | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+7840T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110941482 | ||||||
| chr2:110941648
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+8006A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110941648 | ||||||
| chr2:110941695
|
A | C | 1 | a0001c0001t0001g0025 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1059+8053A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110941695 | ||||||
| chr2:110941793
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1059+8151A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110941793 | ||||||
| chr2:110941862
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1059+8220T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110941862 | ||||||
| chr2:110942591
|
A | C | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1059+8949A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110942591 | ||||||
| chr2:110942726
|
T | TA | 21 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0037others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+9098dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110942726 | |||||
| chr2:110942726
|
TA | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+9098delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110942726 | |||||
| chr2:110942860
|
G | C | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1059+9218G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110942860 | ||||||
| chr2:110942886
|
A | T | 1 | a0002c0002t0002g0013 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1059+9244A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110942886 | ||||||
| chr2:110942886
|
AAAGG | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+9249_1059+925 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110942886 | |||||
| chr2:110943005
|
GGAAA | G | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+9370_1059+937 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110943005 | |||||
| chr2:110943040
|
G | GAAGGAAG others(10): Show |
28 | a0000c0014t0001g0072a0001c0001t0001g0029a0001c0001t0001g0038others(25): Show | 28 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.1059+9406_1059+942 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110943040 | |||||
| chr2:110943063
|
A | AGGAAGAA others(7): Show |
8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+9422_1059+942 others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110943063 | |||||
| chr2:110943162
|
GA | G | 45 | a0000c0014t0001g0072a0001c0001t0001g0028a0001c0001t0001g0029others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.1059+9525delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110943162 | |||||
| chr2:110943166
|
A | AAGG | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+9525_1059+952 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110943166 | |||||
| chr2:110943166
|
A | G | 45 | a0000c0014t0001g0072a0001c0001t0001g0028a0001c0001t0001g0029others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.1059+9524A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110943166 | ||||||
| chr2:110943172
|
G | A | 16 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0080others(13): Show | 16 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.1059+9530G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110943172 | ||||||
| chr2:110943249
|
AAAG | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0002g0006others(1): Show | 4 | HG02451.hp2 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+9610_1059+961 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110943249 | |||||
| chr2:110943253
|
AAAAG | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+9616_1059+961 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110943253 | |||||
| chr2:110943273
|
GGAAA | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+9639_1059+964 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110943273 | |||||
| chr2:110943321
|
A | AAAAG | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+9682_1059+968 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110943321 | |||||
| chr2:110943457
|
G | C | 1 | a0003c0004t0002g0079 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1059+9815G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110943457 | ||||||
| chr2:110943494
|
A | T | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+9852A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110943494 | ||||||
| chr2:110943673
|
G | A | 13 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0080others(10): Show | 13 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1059+10031G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110943673 | ||||||
| chr2:110943746
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1059+10104G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110943746 | ||||||
| chr2:110943764
|
C | T | 16 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0080others(13): Show | 16 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.1059+10122C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110943764 | ||||||
| chr2:110943765
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1059+10123G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110943765 | ||||||
| chr2:110943774
|
A | ACAG | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+10135_1059+10 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110943774 | |||||
| chr2:110943899
|
C | CT | 93 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1059+10259dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110943899 | |||||
| chr2:110943949
|
A | G | 2 | a0004c0005t0002g0020a0004c0005t0002g0022 | 2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1059+10307A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110943949 | ||||||
| chr2:110944139
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1059+10497C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110944139 | ||||||
| chr2:110944207
|
A | C | 57 | a0000c0014t0001g0072a0001c0001t0001g0012a0001c0001t0001g0018others(54): Show | 57 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1059+10565A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110944207 | ||||||
| chr2:110944403
|
A | G | 21 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0037others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+10761A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110944403 | ||||||
| chr2:110944554
|
C | T | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+10912C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110944554 | ||||||
| chr2:110944616
|
G | A | 21 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0037others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+10974G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110944616 | ||||||
| chr2:110944712
|
T | C | 58 | a0000c0014t0001g0072a0001c0001t0001g0012a0001c0001t0001g0018others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1059+11070T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110944712 | ||||||
| chr2:110944746
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1059+11104T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110944746 | ||||||
| chr2:110944811
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1059+11169G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110944811 | ||||||
| chr2:110944938
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1059+11296G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110944938 | ||||||
| chr2:110944968
|
G | A | 21 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0037others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+11326G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110944968 | ||||||
| chr2:110945197
|
T | C | 24 | a0000c0014t0001g0072a0001c0001t0001g0029a0001c0001t0001g0038others(21): Show | 24 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1059+11555T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110945197 | ||||||
| chr2:110945283
|
G | A | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1059+11641G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110945283 | ||||||
| chr2:110945642
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+12000C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110945642 | ||||||
| chr2:110945753
|
G | T | 4 | a0001c0001t0006g0017a0006c0006t0001g0001a0008c0008t0001g0015others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+12111G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110945753 | ||||||
| chr2:110945755
|
A | G | 24 | a0000c0014t0001g0072a0001c0001t0001g0029a0001c0001t0001g0038others(21): Show | 24 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1059+12113A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110945755 | ||||||
| chr2:110945909
|
T | A | 21 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0037others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+12267T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110945909 | ||||||
| chr2:110945942
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1059+12300T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110945942 | ||||||
| chr2:110946157
|
C | A | 133 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1059+12515C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110946157 | ||||||
| chr2:110946562
|
T | C | 49 | a0000c0014t0001g0072a0001c0001t0001g0028a0001c0001t0001g0029others(46): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1059+12920T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110946562 | ||||||
| chr2:110946618
|
T | C | 133 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1059+12976T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110946618 | ||||||
| chr2:110947183
|
G | A | 21 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0037others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+13541G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110947183 | ||||||
| chr2:110947226
|
G | A | 1 | a0002c0002t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1059+13584G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110947226 | ||||||
| chr2:110947255
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+13613C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110947255 | ||||||
| chr2:110947542
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1059+13900A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110947542 | ||||||
| chr2:110947784
|
C | T | 3 | a0001c0003t0001g0036a0001c0003t0001g0075a0009c0016t0001g0112 | 3 | HG04115.hp1 NA18993.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1059+14142C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110947784 | ||||||
| chr2:110947850
|
T | C | 64 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0012others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.1059+14208T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110947850 | ||||||
| chr2:110947898
|
G | A | 1 | a0002c0002t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1059+14256G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110947898 | ||||||
| chr2:110947960
|
T | G | 1 | a0002c0002t0002g0059 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1059+14318T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110947960 | ||||||
| chr2:110948092
|
AAAG | A | 3 | a0001c0001t0001g0008a0006c0006t0002g0146a0011c0010t0002g0009 | 3 | HG02258.hp1 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1059+14456_1059+14 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110948092 | |||||
| chr2:110948100
|
A | G | 2 | a0002c0002t0001g0114a0002c0002t0001g0132 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1059+14458A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110948100 | ||||||
| chr2:110948161
|
G | A | 106 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(103): Show | 106 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1059+14519G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110948161 | ||||||
| chr2:110948508
|
A | G | 18 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(15): Show | 18 | HG01167.hp1 HG01346.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1059+14866A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110948508 | ||||||
| chr2:110948519
|
T | A | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1059+14877T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110948519 | ||||||
| chr2:110948649
|
T | G | 26 | a0001c0001t0001g0067a0001c0001t0001g0113a0001c0001t0001g0137others(23): Show | 26 | HG00544.hp1 HG01081.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1059+15007T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110948649 | ||||||
| chr2:110948703
|
TA | T | 40 | a0001c0001t0001g0067a0001c0001t0001g0077a0001c0001t0001g0096others(37): Show | 40 | HG00323.hp1 HG00544.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.1059+15086delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110948703 | |||||
| chr2:110948703
|
TAA | T | 20 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0044others(17): Show | 20 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.1059+15085_1059+15 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110948703 | |||||
| chr2:110948753
|
G | C | 2 | a0002c0002t0003g0142a0002c0002t0004g0141 | 2 | HG00423.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1059+15111G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110948753 | ||||||
| chr2:110948776
|
C | T | 1 | a0003c0004t0002g0079 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1059+15134C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110948776 | ||||||
| chr2:110948906
|
T | C | 21 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0037others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+15264T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110948906 | ||||||
| chr2:110949169
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1059+15527G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110949169 | ||||||
| chr2:110949317
|
C | CT | 18 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(15): Show | 18 | HG01167.hp1 HG01346.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1059+15678dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110949317 | |||||
| chr2:110949391
|
C | CTTTT | 99 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1059+15750_1059+15 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110949391 | |||||
| chr2:110949649
|
T | A | 1 | a0001c0001t0002g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1059+16007T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110949649 | ||||||
| chr2:110949650
|
T | A | 29 | a0000c0013t0001g0046a0001c0001t0001g0011a0001c0001t0001g0028others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1059+16008T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110949650 | ||||||
| chr2:110949806
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1059+16164C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110949806 | ||||||
| chr2:110949823
|
T | G | 1 | a0001c0001t0002g0105 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1059+16181T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110949823 | ||||||
| chr2:110949828
|
C | T | 49 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(46): Show | 49 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1059+16186C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110949828 | ||||||
| chr2:110950016
|
CTCTG | C | 2 | a0008c0008t0001g0015a0008c0008t0001g0016 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1059+16378_1059+16 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950016 | |||||
| chr2:110950124
|
ATGTGCCA others(5): Show |
A | 1 | a0001c0001t0001g0035 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1059+16483_1059+16 others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110950124 | ||||||
| chr2:110950803
|
G | C | 53 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(50): Show | 53 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.1059+17161G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110950803 | ||||||
| chr2:110950810
|
G | GGA | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0028others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1059+17192_1059+17 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950810
|
G | GGAGAGA | 14 | a0000c0014t0001g0072a0001c0001t0001g0012a0001c0001t0001g0021others(11): Show | 14 | HG01167.hp1 HG01346.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1059+17188_1059+17 others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950810
|
G | GGAGAGAG others(1): Show |
6 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0126others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+17186_1059+17 others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950810
|
G | GGAGAGAG others(3): Show |
2 | a0008c0008t0001g0015a0008c0008t0001g0016 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1059+17184_1059+17 others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950810
|
G | GGAGAGAG others(5): Show |
1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1059+17182_1059+17 others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950810
|
G | GGAGAGAG others(7): Show |
9 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0113others(6): Show | 9 | HG01081.hp1 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+17180_1059+17 others(20): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950810
|
G | GGAGAGAG others(9): Show |
4 | a0001c0003t0001g0036a0002c0002t0001g0114a0002c0002t0001g0132others(1): Show | 4 | HG01243.hp1 HG03195.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+17178_1059+17 others(22): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950810
|
G | GGAGAGAG others(27): Show |
2 | a0002c0019t0001g0095a0009c0016t0001g0112 | 2 | HG04115.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1059+17193_1059+17 others(40): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950810
|
G | GGAGAGAG others(29): Show |
1 | a0001c0003t0002g0104 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1059+17193_1059+17 others(42): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950810
|
G | GGAGAGAG others(31): Show |
5 | a0001c0003t0001g0075a0001c0003t0001g0087a0001c0003t0001g0089others(2): Show | 5 | HG01168.hp2 HG01496.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+17193_1059+17 others(44): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950810
|
G | GGAGAGAG others(33): Show |
1 | a0001c0003t0001g0041 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1059+17193_1059+17 others(46): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950810
|
G | GGAGAGAG others(35): Show |
1 | a0001c0003t0001g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1059+17193_1059+17 others(48): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950810
|
G | GGAGAGAG others(37): Show |
1 | a0001c0003t0001g0081 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1059+17193_1059+17 others(50): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950810
|
GGA | G | 3 | a0001c0001t0001g0008a0006c0006t0002g0146a0011c0010t0002g0009 | 3 | HG02258.hp1 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1059+17192_1059+17 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950810 | |||||
| chr2:110950834
|
A | AGAGAGAG others(35): Show |
1 | a0001c0003t0002g0084 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1059+17193_1059+17 others(48): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110950834 | |||||
| chr2:110950836
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1059+17194G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110950836 | ||||||
| chr2:110950874
|
T | C | 1 | a0006c0006t0001g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1059+17232T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110950874 | ||||||
| chr2:110951101
|
C | T | 10 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0038others(7): Show | 10 | HG02027.hp2 HG02257.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.1059+17459C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110951101 | ||||||
| chr2:110951397
|
A | T | 19 | a0001c0001t0001g0067a0001c0003t0001g0036a0001c0003t0001g0041others(16): Show | 19 | HG00544.hp1 HG01081.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1059+17755A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110951397 | ||||||
| chr2:110951422
|
C | A | 21 | a0001c0001t0001g0067a0001c0003t0001g0036a0001c0003t0001g0041others(18): Show | 21 | HG00544.hp1 HG01081.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+17780C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110951422 | ||||||
| chr2:110951496
|
G | T | 3 | a0001c0001t0001g0008a0006c0006t0002g0146a0011c0010t0002g0009 | 3 | HG02258.hp1 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1059+17854G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110951496 | ||||||
| chr2:110951570
|
T | G | 18 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(15): Show | 18 | HG01167.hp1 HG01346.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1059+17928T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110951570 | ||||||
| chr2:110951600
|
C | T | 53 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(50): Show | 53 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.1059+17958C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110951600 | ||||||
| chr2:110951689
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1059+18047A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110951689 | ||||||
| chr2:110952251
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1059+18609A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110952251 | ||||||
| chr2:110952442
|
A | G | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1059+18800A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110952442 | ||||||
| chr2:110952468
|
T | C | 71 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1059+18826T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110952468 | ||||||
| chr2:110952544
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1059+18902A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110952544 | ||||||
| chr2:110952851
|
A | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0002g0101 | 3 | HG00438.hp2 HG02027.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1059+19209A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110952851 | ||||||
| chr2:110953286
|
G | C | 39 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0018others(36): Show | 39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1059+19644G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110953286 | ||||||
| chr2:110953295
|
CTTG | C | 18 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0063others(15): Show | 18 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1059+19662_1059+19 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110953295 | |||||
| chr2:110953307
|
A | G | 4 | a0001c0001t0001g0096a0002c0002t0001g0066a0002c0002t0001g0103others(1): Show | 4 | HG01346.hp1 HG03209.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+19665A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110953307 | ||||||
| chr2:110953331
|
CAT | C | 37 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(34): Show | 37 | HG00544.hp1 HG01081.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.1059+19704_1059+19 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110953331 | |||||
| chr2:110953348
|
T | A | 2 | a0001c0001t0001g0128a0002c0002t0002g0014 | 2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1059+19706T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110953348 | ||||||
| chr2:110953512
|
A | G | 17 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(14): Show | 17 | HG01346.hp1 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1059+19870A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110953512 | ||||||
| chr2:110953570
|
T | G | 3 | a0001c0001t0001g0055a0001c0001t0001g0082a0001c0001t0001g0088 | 3 | HG01928.hp2 HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1059+19928T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110953570 | ||||||
| chr2:110953769
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1059+20127A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110953769 | ||||||
| chr2:110953959
|
T | C | 70 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1059+20317T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110953959 | ||||||
| chr2:110954109
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1059+20467C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110954109 | ||||||
| chr2:110954546
|
T | C | 32 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(29): Show | 32 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1059+20904T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110954546 | ||||||
| chr2:110954609
|
C | T | 1 | a0002c0002t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1059+20967C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110954609 | ||||||
| chr2:110954665
|
G | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.1059+21023G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110954665 | ||||||
| chr2:110954674
|
A | G | 70 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1059+21032A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110954674 | ||||||
| chr2:110954713
|
T | C | 19 | a0001c0001t0001g0067a0001c0003t0001g0036a0001c0003t0001g0041others(16): Show | 19 | HG00544.hp1 HG01081.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1059+21071T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110954713 | ||||||
| chr2:110954821
|
T | TG | 134 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1059+21181dupG | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110954821 | |||||
| chr2:110955025
|
GTATTT | G | 21 | a0001c0001t0001g0067a0001c0003t0001g0036a0001c0003t0001g0041others(18): Show | 21 | HG00544.hp1 HG01081.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+21389_1059+21 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110955025 | |||||
| chr2:110955030
|
T | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.1059+21388T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110955030 | ||||||
| chr2:110955126
|
C | T | 91 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(88): Show | 91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1059+21484C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110955126 | ||||||
| chr2:110955253
|
G | A | 21 | a0001c0001t0001g0067a0001c0003t0001g0036a0001c0003t0001g0041others(18): Show | 21 | HG00544.hp1 HG01081.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+21611G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110955253 | ||||||
| chr2:110955429
|
CCT | C | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0018others(15): Show | 18 | HG01346.hp1 HG01891.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1059+21812_1059+21 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110955429 | |||||
| chr2:110955429
|
CCTCT | C | 52 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1059+21810_1059+21 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110955429 | |||||
| chr2:110955469
|
T | G | 70 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1059+21827T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110955469 | ||||||
| chr2:110955480
|
T | C | 91 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(88): Show | 91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1059+21838T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110955480 | ||||||
| chr2:110955644
|
C | G | 1 | a0001c0001t0002g0040 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1059+22002C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110955644 | ||||||
| chr2:110955733
|
G | A | 1 | a0002c0002t0001g0103 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1059+22091G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110955733 | ||||||
| chr2:110955933
|
A | AT | 25 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 25 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.1059+22314dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110955933 | |||||
| chr2:110955933
|
A | ATT | 5 | a0001c0001t0001g0035a0001c0001t0001g0110a0001c0001t0002g0033others(2): Show | 5 | HG00438.hp2 HG01167.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+22313_1059+22 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110955933 | |||||
| chr2:110955933
|
AT | A | 26 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0018others(23): Show | 26 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1059+22314delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110955933 | |||||
| chr2:110955933
|
ATT | A | 19 | a0001c0001t0001g0067a0001c0003t0001g0036a0001c0003t0001g0041others(16): Show | 19 | HG00544.hp1 HG01081.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1059+22313_1059+22 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110955933 | |||||
| chr2:110955969
|
C | T | 69 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1059+22327C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110955969 | ||||||
| chr2:110955994
|
A | G | 26 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0113others(23): Show | 26 | HG00544.hp1 HG01081.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1059+22352A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110955994 | ||||||
| chr2:110956018
|
T | A | 99 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1059+22376T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110956018 | ||||||
| chr2:110956078
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1059+22436G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110956078 | ||||||
| chr2:110956084
|
T | C | 99 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1059+22442T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110956084 | ||||||
| chr2:110956093
|
G | A | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1059+22451G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110956093 | ||||||
| chr2:110956147
|
T | C | 91 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(88): Show | 91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1059+22505T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110956147 | ||||||
| chr2:110956300
|
G | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.1059+22658G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110956300 | ||||||
| chr2:110956544
|
T | A | 1 | a0001c0001t0002g0040 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1059+22902T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110956544 | ||||||
| chr2:110956588
|
G | A | 2 | a0007c0009t0001g0092a0007c0009t0001g0106 | 2 | HG00099.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1059+22946G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110956588 | ||||||
| chr2:110956752
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1059+23110C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110956752 | ||||||
| chr2:110956772
|
A | G | 18 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(15): Show | 18 | HG01346.hp1 HG01891.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1059+23130A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110956772 | ||||||
| chr2:110956849
|
T | C | 6 | a0000c0013t0001g0046a0001c0001t0001g0039a0001c0001t0001g0045others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+23207T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110956849 | ||||||
| chr2:110956939
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1059+23297G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110956939 | ||||||
| chr2:110957000
|
C | T | 28 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0028others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1059+23358C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110957000 | ||||||
| chr2:110957259
|
A | G | 1 | a0001c0012t0002g0131 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1059+23617A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110957259 | ||||||
| chr2:110957452
|
C | A | 21 | a0001c0001t0001g0067a0001c0003t0001g0036a0001c0003t0001g0041others(18): Show | 21 | HG00544.hp1 HG01081.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+23810C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110957452 | ||||||
| chr2:110957753
|
T | C | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1059+24111T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110957753 | ||||||
| chr2:110957798
|
G | T | 1 | a0001c0001t0002g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1059+24156G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110957798 | ||||||
| chr2:110957869
|
C | A | 1 | a0001c0003t0002g0084 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1059+24227C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110957869 | ||||||
| chr2:110957998
|
C | T | 23 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0031others(20): Show | 23 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.1059+24356C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110957998 | ||||||
| chr2:110957999
|
A | G | 148 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1059+24357A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110957999 | ||||||
| chr2:110958045
|
G | A | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1059+24403G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110958045 | ||||||
| chr2:110958049
|
C | CA | 33 | a0000c0013t0001g0046a0001c0001t0001g0011a0001c0001t0001g0012others(30): Show | 33 | HG00673.hp1 HG00673.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1059+24426dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110958049 | |||||
| chr2:110958049
|
CA | C | 33 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(30): Show | 33 | HG00544.hp1 HG00544.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1059+24426delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110958049 | |||||
| chr2:110958049
|
CAA | C | 21 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0044others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1059+24425_1059+24 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110958049 | |||||
| chr2:110958080
|
A | G | 74 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1059+24438A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110958080 | ||||||
| chr2:110958120
|
C | T | 6 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0126others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+24478C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110958120 | ||||||
| chr2:110958135
|
G | A | 1 | a0001c0012t0002g0131 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1059+24493G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110958135 | ||||||
| chr2:110958299
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1059+24657C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110958299 | ||||||
| chr2:110958303
|
C | T | 6 | a0000c0013t0001g0046a0001c0001t0001g0039a0001c0001t0001g0045others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+24661C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110958303 | ||||||
| chr2:110958507
|
A | G | 109 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1059+24865A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110958507 | ||||||
| chr2:110958766
|
A | G | 6 | a0000c0013t0001g0046a0001c0001t0001g0039a0001c0001t0001g0045others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+25124A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110958766 | ||||||
| chr2:110958993
|
C | CAGGCCTG others(33): Show |
1 | a0001c0001t0001g0035 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1059+25352_1059+25 others(46): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110958993 | |||||
| chr2:110959418
|
G | A | 22 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0044others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.1059+25776G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110959418 | ||||||
| chr2:110959502
|
G | A | 2 | a0001c0001t0002g0076a0001c0001t0002g0078 | 2 | NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1059+25860G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110959502 | ||||||
| chr2:110959523
|
G | A | 85 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1059+25881G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110959523 | ||||||
| chr2:110960101
|
G | A | 20 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0044others(17): Show | 20 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1059+26459G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110960101 | ||||||
| chr2:110960427
|
C | T | 134 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1060-26681C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110960427 | ||||||
| chr2:110960474
|
T | A | 107 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(104): Show | 107 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1060-26634T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110960474 | ||||||
| chr2:110960666
|
G | GT | 28 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0080others(25): Show | 28 | HG00544.hp1 HG00544.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1060-26430dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110960666 | |||||
| chr2:110960666
|
GT | G | 56 | a0000c0013t0001g0046a0001c0001t0001g0011a0001c0001t0001g0012others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1060-26430delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110960666 | |||||
| chr2:110960694
|
T | TG | 16 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(13): Show | 16 | HG01346.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1060-26411dupG | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110960694 | |||||
| chr2:110960697
|
GTT | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.1060-26401_1060-26 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110960697 | |||||
| chr2:110960856
|
T | C | 85 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1060-26252T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110960856 | ||||||
| chr2:110960922
|
G | C | 22 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0049others(19): Show | 22 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1060-26186G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110960922 | ||||||
| chr2:110960944
|
T | C | 1 | a0000c0014t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1060-26164T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110960944 | ||||||
| chr2:110961193
|
A | C | 1 | a0002c0002t0001g0061 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1060-25915A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110961193 | ||||||
| chr2:110961309
|
G | A | 85 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1060-25799G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110961309 | ||||||
| chr2:110961536
|
G | A | 1 | a0001c0003t0002g0084 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1060-25572G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110961536 | ||||||
| chr2:110961804
|
T | A | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1060-25304T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110961804 | ||||||
| chr2:110961828
|
C | T | 3 | a0001c0001t0005g0149a0006c0006t0002g0146a0012c0018t0001g0053 | 3 | HG02922.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1060-25280C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110961828 | ||||||
| chr2:110961829
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1060-25279G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110961829 | ||||||
| chr2:110962063
|
G | A | 27 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0080others(24): Show | 27 | HG00544.hp1 HG00544.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1060-25045G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962063 | ||||||
| chr2:110962089
|
T | C | 15 | a0001c0003t0001g0036a0001c0003t0001g0041a0001c0003t0001g0075others(12): Show | 15 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1060-25019T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962089 | ||||||
| chr2:110962091
|
A | G | 85 | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1060-25017A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962091 | ||||||
| chr2:110962228
|
T | A | 1 | a0001c0001t0001g0035 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1060-24880T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962228 | ||||||
| chr2:110962251
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1060-24857C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962251 | ||||||
| chr2:110962278
|
C | G | 1 | a0001c0001t0001g0035 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1060-24830C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962278 | ||||||
| chr2:110962279
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1060-24829G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962279 | ||||||
| chr2:110962287
|
C | T | 1 | a0006c0006t0001g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1060-24821C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962287 | ||||||
| chr2:110962306
|
C | A | 84 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0011others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1060-24802C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962306 | ||||||
| chr2:110962384
|
A | G | 6 | a0000c0013t0001g0046a0001c0001t0001g0039a0001c0001t0001g0045others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-24724A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962384 | ||||||
| chr2:110962675
|
A | C | 67 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1060-24433A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962675 | ||||||
| chr2:110962678
|
G | A | 11 | a0001c0001t0001g0021a0001c0001t0001g0128a0001c0001t0002g0052others(8): Show | 11 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1060-24430G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962678 | ||||||
| chr2:110962717
|
T | C | 1 | a0002c0002t0003g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1060-24391T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962717 | ||||||
| chr2:110962744
|
A | T | 1 | a0001c0001t0001g0035 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1060-24364A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962744 | ||||||
| chr2:110962822
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1060-24286C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962822 | ||||||
| chr2:110962866
|
C | T | 1 | a0002c0002t0002g0013 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1060-24242C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110962866 | ||||||
| chr2:110963193
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1060-23915A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110963193 | ||||||
| chr2:110963307
|
T | G | 31 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1060-23801T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110963307 | ||||||
| chr2:110963319
|
T | TA | 56 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0031others(53): Show | 56 | HG00438.hp1 HG00544.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.1060-23779dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110963319 | |||||
| chr2:110963394
|
A | G | 1 | a0000c0013t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1060-23714A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110963394 | ||||||
| chr2:110963565
|
A | ATG | 4 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0002g0006others(1): Show | 4 | HG02451.hp2 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-23505_1060-23 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110963565 | |||||
| chr2:110963565
|
A | ATGTG | 3 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0002g0101 | 3 | HG00438.hp2 HG02027.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1060-23507_1060-23 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110963565 | |||||
| chr2:110963565
|
ATG | A | 2 | a0001c0001t0001g0034a0007c0009t0001g0106 | 2 | HG00099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1060-23505_1060-23 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110963565 | |||||
| chr2:110963565
|
ATGTG | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0056others(2): Show | 5 | HG01255.hp1 HG02622.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-23507_1060-23 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110963565 | |||||
| chr2:110963565
|
ATGTGTG | A | 34 | a0001c0001t0001g0055a0001c0001t0001g0067a0001c0001t0001g0082others(31): Show | 34 | HG00140.hp2 HG00544.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.1060-23509_1060-23 others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110963565 | |||||
| chr2:110963565
|
ATGTGTGT others(1): Show |
A | 28 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0031others(25): Show | 28 | HG00438.hp1 HG01175.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1060-23511_1060-23 others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110963565 | |||||
| chr2:110963565
|
ATGTGTGT others(3): Show |
A | 13 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0128others(10): Show | 13 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1060-23513_1060-23 others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110963565 | |||||
| chr2:110963565
|
ATGTGTGT others(13): Show |
A | 15 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0096others(12): Show | 15 | HG00099.hp1 HG00423.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1060-23523_1060-23 others(26): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110963565 | |||||
| chr2:110963579
|
G | C | 2 | a0003c0004t0004g0140a0005c0007t0002g0050 | 2 | HG01175.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1060-23529G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110963579 | ||||||
| chr2:110963595
|
GTGTGTGT others(3): Show |
G | 2 | a0001c0001t0002g0076a0001c0001t0002g0078 | 2 | NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1060-23511_1060-23 others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110963595 | |||||
| chr2:110963601
|
G | T | 2 | a0002c0002t0001g0061a0005c0007t0001g0062 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1060-23507G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110963601 | ||||||
| chr2:110963603
|
G | T | 42 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0011others(39): Show | 42 | HG00438.hp1 HG01175.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.1060-23505G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110963603 | ||||||
| chr2:110963812
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0002g0006others(1): Show | 4 | HG02451.hp2 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-23296G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110963812 | ||||||
| chr2:110963990
|
A | G | 10 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0082others(7): Show | 10 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1060-23118A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110963990 | ||||||
| chr2:110964094
|
C | T | 1 | a0006c0006t0001g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1060-23014C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110964094 | ||||||
| chr2:110964191
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1060-22917G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110964191 | ||||||
| chr2:110964387
|
A | G | 27 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(24): Show | 27 | HG01175.hp2 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1060-22721A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110964387 | ||||||
| chr2:110964421
|
T | G | 20 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(17): Show | 20 | HG00438.hp1 HG01257.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1060-22687T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110964421 | ||||||
| chr2:110964526
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1060-22582C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110964526 | ||||||
| chr2:110964541
|
A | G | 45 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1060-22567A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110964541 | ||||||
| chr2:110964608
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1060-22500A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110964608 | ||||||
| chr2:110964745
|
C | G | 28 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(25): Show | 28 | HG01175.hp2 HG01243.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1060-22363C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110964745 | ||||||
| chr2:110964748
|
T | C | 45 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1060-22360T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110964748 | ||||||
| chr2:110964787
|
A | G | 3 | a0001c0001t0001g0077a0001c0001t0002g0076a0001c0001t0002g0078 | 3 | HG02027.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1060-22321A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110964787 | ||||||
| chr2:110965058
|
A | G | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1060-22050A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110965058 | ||||||
| chr2:110965061
|
G | A | 116 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.1060-22047G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110965061 | ||||||
| chr2:110965183
|
C | T | 1 | a0001c0003t0002g0084 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1060-21925C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110965183 | ||||||
| chr2:110965380
|
T | C | 2 | a0000c0014t0001g0072a0006c0006t0001g0001 | 2 | HG02257.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1060-21728T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110965380 | ||||||
| chr2:110965653
|
A | G | 27 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(24): Show | 27 | HG01175.hp2 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1060-21455A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110965653 | ||||||
| chr2:110965815
|
C | G | 97 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1060-21293C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110965815 | ||||||
| chr2:110965891
|
T | C | 45 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1060-21217T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110965891 | ||||||
| chr2:110965974
|
A | C | 97 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1060-21134A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110965974 | ||||||
| chr2:110966042
|
G | C | 45 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1060-21066G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110966042 | ||||||
| chr2:110966055
|
A | G | 1 | a0002c0002t0002g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1060-21053A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110966055 | ||||||
| chr2:110966246
|
C | T | 4 | a0001c0001t0001g0010a0002c0002t0001g0061a0005c0007t0001g0062others(1): Show | 4 | HG03225.hp1 HG03516.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-20862C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110966246 | ||||||
| chr2:110966253
|
G | A | 45 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1060-20855G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110966253 | ||||||
| chr2:110966369
|
G | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0126others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-20739G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110966369 | ||||||
| chr2:110966406
|
G | A | 1 | a0001c0003t0002g0083 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1060-20702G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110966406 | ||||||
| chr2:110966451
|
T | C | 74 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0038others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1060-20657T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110966451 | ||||||
| chr2:110966460
|
G | C | 1 | a0002c0002t0002g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1060-20648G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110966460 | ||||||
| chr2:110966694
|
T | C | 97 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1060-20414T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110966694 | ||||||
| chr2:110966762
|
G | A | 45 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1060-20346G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110966762 | ||||||
| chr2:110966798
|
C | T | 74 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0038others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1060-20310C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110966798 | ||||||
| chr2:110966845
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1060-20263A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110966845 | ||||||
| chr2:110967515
|
A | G | 11 | a0001c0001t0001g0031a0001c0001t0001g0086a0001c0001t0002g0032others(8): Show | 11 | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1060-19593A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110967515 | ||||||
| chr2:110967619
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0006g0017 | 3 | HG02280.hp1 HG03139.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1060-19489T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110967619 | ||||||
| chr2:110967666
|
G | C | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1060-19442G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110967666 | ||||||
| chr2:110967822
|
C | T | 1 | a0002c0002t0001g0023 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1060-19286C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110967822 | ||||||
| chr2:110967887
|
G | A | 27 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(24): Show | 27 | HG01175.hp2 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1060-19221G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110967887 | ||||||
| chr2:110967980
|
T | C | 1 | a0010c0015t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1060-19128T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110967980 | ||||||
| chr2:110968085
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1060-19023A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110968085 | ||||||
| chr2:110968195
|
G | A | 27 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(24): Show | 27 | HG01175.hp2 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1060-18913G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110968195 | ||||||
| chr2:110968234
|
A | G | 45 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1060-18874A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110968234 | ||||||
| chr2:110968379
|
T | C | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1060-18729T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110968379 | ||||||
| chr2:110968524
|
G | A | 18 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(15): Show | 18 | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.1060-18584G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110968524 | ||||||
| chr2:110968778
|
C | CA | 18 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(15): Show | 18 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1060-18315dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110968778 | |||||
| chr2:110968778
|
C | CAAAA | 34 | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0067others(31): Show | 34 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.1060-18318_1060-18 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110968778 | |||||
| chr2:110968778
|
C | CAAAAA | 27 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(24): Show | 27 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1060-18319_1060-18 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110968778 | |||||
| chr2:110968778
|
C | CAAAAAA | 13 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0056others(10): Show | 13 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1060-18320_1060-18 others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110968778 | |||||
| chr2:110968847
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1060-18261C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110968847 | ||||||
| chr2:110968879
|
A | G | 2 | a0001c0001t0001g0011a0004c0005t0002g0124 | 2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1060-18229A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110968879 | ||||||
| chr2:110969063
|
A | C | 97 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1060-18045A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110969063 | ||||||
| chr2:110969152
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1060-17956G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110969152 | ||||||
| chr2:110969668
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1060-17440G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110969668 | ||||||
| chr2:110969747
|
G | A | 4 | a0001c0001t0001g0097a0002c0002t0001g0066a0007c0009t0001g0092others(1): Show | 4 | HG00099.hp2 HG01346.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-17361G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110969747 | ||||||
| chr2:110969810
|
C | CA | 52 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0044others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1060-17289dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110969810 | |||||
| chr2:110970127
|
A | T | 2 | a0002c0002t0001g0061a0005c0007t0001g0062 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1060-16981A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110970127 | ||||||
| chr2:110970343
|
A | G | 132 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.1060-16765A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110970343 | ||||||
| chr2:110970383
|
G | A | 27 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(24): Show | 27 | HG01175.hp2 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1060-16725G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110970383 | ||||||
| chr2:110970497
|
A | AAAAG | 45 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1060-16610_1060-16 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110970497 | |||||
| chr2:110970536
|
G | A | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1060-16572G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110970536 | ||||||
| chr2:110970701
|
G | A | 3 | a0001c0001t0001g0077a0001c0001t0002g0076a0001c0001t0002g0078 | 3 | HG02027.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1060-16407G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110970701 | ||||||
| chr2:110970905
|
C | T | 73 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0038others(70): Show | 73 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1060-16203C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110970905 | ||||||
| chr2:110970915
|
G | A | 1 | a0002c0002t0002g0014 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1060-16193G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110970915 | ||||||
| chr2:110971152
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1060-15956T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110971152 | ||||||
| chr2:110971228
|
T | C | 1 | a0001c0001t0002g0076 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1060-15880T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110971228 | ||||||
| chr2:110971396
|
C | T | 27 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(24): Show | 27 | HG01175.hp2 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1060-15712C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110971396 | ||||||
| chr2:110971762
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0002g0076a0001c0001t0002g0078 | 3 | HG02027.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1060-15346T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110971762 | ||||||
| chr2:110971912
|
G | C | 35 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0067others(32): Show | 35 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1060-15196G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110971912 | ||||||
| chr2:110972049
|
T | C | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1060-15059T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110972049 | ||||||
| chr2:110972614
|
GTCTC | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0117a0001c0001t0001g0121others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-14489_1060-14 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110972614 | |||||
| chr2:110972633
|
G | A | 1 | a0000c0013t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1060-14475G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110972633 | ||||||
| chr2:110972646
|
C | T | 17 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0031others(14): Show | 17 | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.1060-14462C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110972646 | ||||||
| chr2:110972649
|
G | GCA | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1060-14432_1060-14 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110972649 | |||||
| chr2:110972649
|
GCA | G | 25 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(22): Show | 25 | HG00099.hp2 HG00438.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.1060-14432_1060-14 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110972649 | |||||
| chr2:110972649
|
GCACA | G | 26 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(23): Show | 26 | HG01175.hp2 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1060-14434_1060-14 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110972649 | |||||
| chr2:110972649
|
GCACACA | G | 48 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(45): Show | 48 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.1060-14436_1060-14 others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110972649 | |||||
| chr2:110972660
|
C | T | 20 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(17): Show | 20 | HG00438.hp1 HG01496.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.1060-14448C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110972660 | ||||||
| chr2:110972662
|
C | T | 1 | a0003c0004t0001g0030 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1060-14446C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110972662 | ||||||
| chr2:110972680
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1060-14428A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110972680 | ||||||
| chr2:110972707
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0002g0076a0001c0001t0002g0078 | 3 | HG02027.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1060-14401C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110972707 | ||||||
| chr2:110972722
|
A | G | 72 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0038others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-14386A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110972722 | ||||||
| chr2:110972936
|
C | T | 149 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1060-14172C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110972936 | ||||||
| chr2:110973275
|
C | T | 20 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0031others(17): Show | 20 | HG00438.hp1 HG01496.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.1060-13833C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110973275 | ||||||
| chr2:110973292
|
A | C | 1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1060-13816A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110973292 | ||||||
| chr2:110973407
|
G | T | 73 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0038others(70): Show | 73 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1060-13701G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110973407 | ||||||
| chr2:110973705
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1060-13403C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110973705 | ||||||
| chr2:110973923
|
T | A | 1 | a0001c0003t0002g0084 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1060-13185T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110973923 | ||||||
| chr2:110974012
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1060-13096G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110974012 | ||||||
| chr2:110974136
|
T | C | 35 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0067others(32): Show | 35 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1060-12972T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110974136 | ||||||
| chr2:110974328
|
C | T | 17 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0031others(14): Show | 17 | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.1060-12780C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110974328 | ||||||
| chr2:110974357
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0082 | 2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1060-12751T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110974357 | ||||||
| chr2:110974408
|
C | T | 18 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(15): Show | 18 | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.1060-12700C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110974408 | ||||||
| chr2:110974621
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0005g0149 | 2 | HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1060-12487C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110974621 | ||||||
| chr2:110974936
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1060-12172C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110974936 | ||||||
| chr2:110975022
|
G | T | 2 | a0001c0001t0001g0056a0001c0001t0005g0149 | 2 | HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1060-12086G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110975022 | ||||||
| chr2:110975142
|
A | G | 1 | a0003c0004t0001g0064 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1060-11966A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110975142 | ||||||
| chr2:110975216
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1060-11892A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110975216 | ||||||
| chr2:110975314
|
C | T | 15 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0045others(12): Show | 15 | HG01175.hp2 HG01981.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1060-11794C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110975314 | ||||||
| chr2:110975333
|
C | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1060-11775C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110975333 | ||||||
| chr2:110975415
|
A | AGT | 33 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0063others(30): Show | 33 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.1060-11673_1060-11 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110975415 | |||||
| chr2:110975415
|
A | AGTGT | 11 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0082others(8): Show | 11 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1060-11675_1060-11 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110975415 | |||||
| chr2:110975415
|
AGT | A | 49 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(46): Show | 49 | HG00438.hp1 HG01175.hp2 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.1060-11673_1060-11 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110975415 | |||||
| chr2:110975524
|
T | G | 3 | a0001c0001t0001g0077a0001c0001t0002g0076a0001c0001t0002g0078 | 3 | HG02027.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1060-11584T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110975524 | ||||||
| chr2:110975808
|
C | CA | 5 | a0001c0001t0001g0056a0001c0001t0001g0077a0001c0001t0005g0149others(2): Show | 5 | HG02027.hp2 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-11287dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110975808 | |||||
| chr2:110975808
|
CA | C | 18 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(15): Show | 18 | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.1060-11287delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110975808 | |||||
| chr2:110975994
|
C | A | 18 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(15): Show | 18 | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.1060-11114C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110975994 | ||||||
| chr2:110976735
|
A | G | 18 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(15): Show | 18 | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.1060-10373A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110976735 | ||||||
| chr2:110977202
|
C | T | 35 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0067others(32): Show | 35 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1060-9906C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110977202 | ||||||
| chr2:110977396
|
G | GA | 45 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1060-9706dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110977396 | |||||
| chr2:110977511
|
G | A | 145 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1060-9597G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110977511 | ||||||
| chr2:110977552
|
T | G | 64 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0038others(61): Show | 64 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1060-9556T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110977552 | ||||||
| chr2:110977724
|
C | T | 18 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(15): Show | 18 | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.1060-9384C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110977724 | ||||||
| chr2:110977725
|
A | G | 145 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1060-9383A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110977725 | ||||||
| chr2:110978187
|
C | T | 94 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1060-8921C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110978187 | ||||||
| chr2:110978321
|
C | A | 2 | a0001c0001t0001g0037a0003c0004t0001g0027 | 2 | HG00423.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.1060-8787C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110978321 | ||||||
| chr2:110978355
|
A | C | 74 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0038others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1060-8753A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110978355 | ||||||
| chr2:110978394
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1060-8714C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110978394 | ||||||
| chr2:110978531
|
T | C | 10 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0082others(7): Show | 10 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1060-8577T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110978531 | ||||||
| chr2:110978596
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1060-8512G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110978596 | ||||||
| chr2:110978709
|
T | G | 1 | a0001c0001t0002g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1060-8399T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110978709 | ||||||
| chr2:110978806
|
C | CT | 63 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0038others(60): Show | 63 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1060-8301dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110978806 | |||||
| chr2:110979101
|
A | AAC | 35 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0067others(32): Show | 35 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1060-8007_1060-800 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110979101 | ||||||
| chr2:110979102
|
G | A | 35 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0067others(32): Show | 35 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1060-8006G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110979102 | ||||||
| chr2:110979105
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1060-8003G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110979105 | ||||||
| chr2:110979246
|
A | G | 63 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0038others(60): Show | 63 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1060-7862A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110979246 | ||||||
| chr2:110979595
|
G | A | 18 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(15): Show | 18 | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.1060-7513G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110979595 | ||||||
| chr2:110979602
|
A | C | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1060-7506A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110979602 | ||||||
| chr2:110979698
|
G | A | 63 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0038others(60): Show | 63 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1060-7410G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110979698 | ||||||
| chr2:110979817
|
A | C | 1 | a0002c0019t0001g0095 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1060-7291A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110979817 | ||||||
| chr2:110979888
|
A | T | 1 | a0002c0002t0001g0103 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1060-7220A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110979888 | ||||||
| chr2:110980110
|
T | C | 17 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0031others(14): Show | 17 | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.1060-6998T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110980110 | ||||||
| chr2:110980376
|
C | T | 20 | a0001c0001t0001g0067a0001c0001t0002g0105a0001c0003t0001g0036others(17): Show | 20 | HG00544.hp1 HG01081.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1060-6732C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110980376 | ||||||
| chr2:110980402
|
C | A | 3 | a0001c0001t0001g0077a0001c0001t0002g0076a0001c0001t0002g0078 | 3 | HG02027.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1060-6706C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110980402 | ||||||
| chr2:110980419
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0117a0001c0001t0001g0121others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-6689T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110980419 | ||||||
| chr2:110980510
|
C | T | 1 | a0006c0006t0001g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1060-6598C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110980510 | ||||||
| chr2:110980684
|
G | A | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1060-6424G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110980684 | ||||||
| chr2:110980756
|
C | T | 11 | a0001c0001t0001g0031a0001c0001t0001g0086a0001c0001t0002g0032others(8): Show | 11 | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1060-6352C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110980756 | ||||||
| chr2:110980794
|
G | A | 36 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0067others(33): Show | 36 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.1060-6314G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110980794 | ||||||
| chr2:110981149
|
G | C | 20 | a0001c0001t0001g0067a0001c0001t0002g0105a0001c0003t0001g0036others(17): Show | 20 | HG00544.hp1 HG01081.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1060-5959G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110981149 | ||||||
| chr2:110981441
|
T | C | 36 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0067others(33): Show | 36 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.1060-5667T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110981441 | ||||||
| chr2:110981462
|
G | A | 36 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0067others(33): Show | 36 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.1060-5646G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110981462 | ||||||
| chr2:110981836
|
G | A | 3 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1060-5272G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110981836 | ||||||
| chr2:110981888
|
G | T | 3 | a0001c0001t0001g0077a0001c0001t0002g0076a0001c0001t0002g0078 | 3 | HG02027.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1060-5220G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110981888 | ||||||
| chr2:110982183
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1060-4925G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110982183 | ||||||
| chr2:110982323
|
T | C | 1 | a0002c0002t0003g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1060-4785T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110982323 | ||||||
| chr2:110982365
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0002g0076a0001c0001t0002g0078 | 3 | HG02027.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1060-4743C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110982365 | ||||||
| chr2:110982381
|
G | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1060-4727G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110982381 | ||||||
| chr2:110982450
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1060-4658C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110982450 | ||||||
| chr2:110982644
|
A | G | 74 | a0000c0013t0001g0046a0001c0001t0001g0011a0001c0001t0001g0012others(71): Show | 74 | HG00140.hp2 HG00544.hp1 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.1060-4464A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110982644 | ||||||
| chr2:110982705
|
G | C | 20 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0031others(17): Show | 20 | HG00438.hp1 HG01496.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.1060-4403G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110982705 | ||||||
| chr2:110982713
|
A | T | 90 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(87): Show | 90 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-4395A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110982713 | ||||||
| chr2:110982818
|
C | T | 2 | a0000c0014t0001g0072a0006c0006t0001g0001 | 2 | HG02257.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1060-4290C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110982818 | ||||||
| chr2:110982831
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0002g0076a0001c0001t0002g0078 | 3 | HG00673.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1060-4277A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110982831 | ||||||
| chr2:110982961
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0067a0002c0002t0001g0114others(2): Show | 5 | HG01081.hp1 HG01243.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-4147C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110982961 | ||||||
| chr2:110983015
|
T | A | 1 | a0001c0001t0002g0040 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1060-4093T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110983015 | ||||||
| chr2:110983094
|
C | T | 12 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0034others(9): Show | 12 | HG00140.hp1 HG00323.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1060-4014C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110983094 | ||||||
| chr2:110983193
|
G | C | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1060-3915G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110983193 | ||||||
| chr2:110983482
|
G | T | 2 | a0002c0002t0001g0061a0005c0007t0001g0062 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1060-3626G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110983482 | ||||||
| chr2:110983515
|
A | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-3593A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110983515 | ||||||
| chr2:110983623
|
A | G | 18 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(15): Show | 18 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1060-3485A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110983623 | ||||||
| chr2:110983896
|
C | T | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1060-3212C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110983896 | ||||||
| chr2:110984137
|
C | T | 11 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0045others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1060-2971C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110984137 | ||||||
| chr2:110984491
|
T | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1060-2617T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110984491 | ||||||
| chr2:110984734
|
C | G | 50 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.1060-2374C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110984734 | ||||||
| chr2:110984752
|
T | A | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1060-2356T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110984752 | ||||||
| chr2:110984785
|
G | C | 1 | a0001c0001t0002g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1060-2323G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110984785 | ||||||
| chr2:110985106
|
A | G | 60 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(57): Show | 60 | HG00140.hp2 HG00438.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.1060-2002A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110985106 | ||||||
| chr2:110985170
|
AT | A | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1060-1936delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 110985170 | |||||
| chr2:110985465
|
T | C | 5 | a0001c0003t0001g0041a0001c0003t0002g0043a0001c0003t0002g0083others(2): Show | 5 | HG00544.hp1 NA18946.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-1643T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110985465 | ||||||
| chr2:110985569
|
T | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0116others(6): Show | 9 | HG02451.hp2 HG02615.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-1539T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110985569 | ||||||
| chr2:110985966
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1060-1142T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110985966 | ||||||
| chr2:110986385
|
A | T | 11 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0045others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1060-723A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110986385 | ||||||
| chr2:110986409
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-699G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110986409 | ||||||
| chr2:110986489
|
G | A | 9 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0088others(6): Show | 9 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.1060-619G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110986489 | ||||||
| chr2:110986604
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1060-504G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110986604 | ||||||
| chr2:110986747
|
A | C | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1060-361A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110986747 | ||||||
| chr2:110986829
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0100others(2): Show | 5 | HG00140.hp1 HG00323.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-279G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110986829 | ||||||
| chr2:110986858
|
A | C | 60 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(57): Show | 60 | HG00140.hp2 HG00438.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.1060-250A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110986858 | ||||||
| chr2:110986925
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1060-183T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | 110986925 | ||||||
| chr2:110987230
|
C | T | 3 | a0001c0001t0001g0037a0002c0002t0003g0142a0003c0004t0001g0027 | 3 | HG00423.hp2 HG00544.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1169+13C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110987230 | ||||||
| chr2:110987374
|
C | T | 1 | a0002c0002t0001g0023 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1169+157C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110987374 | ||||||
| chr2:110987407
|
T | A | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1169+190T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110987407 | ||||||
| chr2:110987736
|
A | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1169+519A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110987736 | ||||||
| chr2:110987981
|
A | G | 11 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0045others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1169+764A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110987981 | ||||||
| chr2:110988039
|
A | G | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1169+822A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110988039 | ||||||
| chr2:110988140
|
G | C | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1169+923G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110988140 | ||||||
| chr2:110988218
|
G | A | 2 | a0001c0001t0001g0068a0014c0020t0001g0002 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1169+1001G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110988218 | ||||||
| chr2:110988282
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1169+1065A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110988282 | ||||||
| chr2:110988401
|
C | G | 21 | a0000c0013t0001g0046a0001c0001t0001g0012a0001c0001t0001g0018others(18): Show | 21 | HG01167.hp1 HG01243.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1169+1184C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110988401 | ||||||
| chr2:110988719
|
T | A | 1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1169+1502T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110988719 | ||||||
| chr2:110988728
|
A | T | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1169+1511A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110988728 | ||||||
| chr2:110988857
|
T | TTG | 11 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0082others(8): Show | 11 | HG00423.hp2 HG00673.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1169+1676_1169+167 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110988857 | |||||
| chr2:110988857
|
T | TTGTG | 33 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(30): Show | 33 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1169+1674_1169+167 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110988857 | |||||
| chr2:110988857
|
T | TTGTGTG | 7 | a0001c0001t0001g0031a0001c0001t0001g0067a0002c0002t0001g0103others(4): Show | 7 | HG01081.hp1 HG02080.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.1169+1672_1169+167 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110988857 | |||||
| chr2:110988857
|
T | TTGTGTGT others(1): Show |
5 | a0001c0001t0001g0137a0001c0001t0002g0033a0003c0004t0001g0064others(2): Show | 5 | HG00673.hp1 HG01496.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1169+1670_1169+167 others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110988857 | |||||
| chr2:110988857
|
T | TTGTGTGT others(3): Show |
20 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0096others(17): Show | 20 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.1169+1668_1169+167 others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110988857 | |||||
| chr2:110988857
|
T | TTGTGTGT others(5): Show |
3 | a0001c0001t0001g0086a0002c0002t0004g0141a0003c0004t0001g0093 | 3 | HG00423.hp1 NA18993.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1169+1666_1169+167 others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110988857 | |||||
| chr2:110988857
|
T | TTGTGTGT others(7): Show |
2 | a0002c0002t0001g0135a0006c0006t0001g0001 | 2 | HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1169+1664_1169+167 others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110988857 | |||||
| chr2:110988857
|
T | TTGTGTGT others(11): Show |
1 | a0003c0004t0001g0026 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1169+1660_1169+167 others(22): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110988857 | |||||
| chr2:110988857
|
TTGTG | T | 30 | a0000c0013t0001g0046a0001c0001t0001g0018a0001c0001t0001g0024others(27): Show | 30 | HG00140.hp2 HG01167.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1169+1674_1169+167 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110988857 | |||||
| chr2:110988857
|
TTGTGTG | T | 20 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0039others(17): Show | 20 | HG00438.hp2 HG01243.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1169+1672_1169+167 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110988857 | |||||
| chr2:110988857
|
TTGTGTGT others(1): Show |
T | 2 | a0001c0001t0001g0058a0001c0001t0002g0052 | 2 | HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1169+1670_1169+167 others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110988857 | |||||
| chr2:110989013
|
A | C | 17 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(14): Show | 17 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1169+1796A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110989013 | ||||||
| chr2:110989051
|
T | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169+1834T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110989051 | ||||||
| chr2:110989279
|
A | G | 114 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1169+2062A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110989279 | ||||||
| chr2:110989295
|
C | T | 50 | a0000c0013t0001g0046a0001c0001t0001g0012a0001c0001t0001g0018others(47): Show | 50 | HG00140.hp2 HG01167.hp1 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.1169+2078C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110989295 | ||||||
| chr2:110989332
|
C | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169+2115C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110989332 | ||||||
| chr2:110989548
|
G | A | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1169+2331G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110989548 | ||||||
| chr2:110989783
|
C | G | 4 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0002g0048others(1): Show | 4 | HG02622.hp2 HG03579.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169+2566C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110989783 | ||||||
| chr2:110989838
|
T | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0045 | 2 | HG03139.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1169+2621T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110989838 | ||||||
| chr2:110989864
|
A | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0002g0101 | 3 | HG00438.hp2 HG02027.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1169+2647A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110989864 | ||||||
| chr2:110989872
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1169+2655C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110989872 | ||||||
| chr2:110990265
|
T | G | 56 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1169+3048T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110990265 | ||||||
| chr2:110990290
|
T | G | 1 | a0002c0002t0003g0142 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1169+3073T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110990290 | ||||||
| chr2:110990428
|
T | G | 61 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1169+3211T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110990428 | ||||||
| chr2:110990536
|
A | G | 62 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1169+3319A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110990536 | ||||||
| chr2:110990705
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169+3488G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110990705 | ||||||
| chr2:110990894
|
G | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1169+3677G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110990894 | ||||||
| chr2:110990954
|
A | G | 62 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1169+3737A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110990954 | ||||||
| chr2:110990987
|
T | G | 52 | a0000c0013t0001g0046a0001c0001t0001g0012a0001c0001t0001g0018others(49): Show | 52 | HG00140.hp2 HG00438.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.1169+3770T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110990987 | ||||||
| chr2:110990988
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1169+3771C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110990988 | ||||||
| chr2:110991192
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1169+3975T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110991192 | ||||||
| chr2:110991333
|
G | T | 1 | a0004c0005t0002g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1169+4116G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110991333 | ||||||
| chr2:110991436
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169+4219C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110991436 | ||||||
| chr2:110991566
|
CATTAG | C | 22 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0067others(19): Show | 22 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.1170-4325_1170-432 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110991566 | |||||
| chr2:110991623
|
T | C | 62 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1170-4270T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110991623 | ||||||
| chr2:110991624
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0002g0032a0001c0001t0002g0094 | 3 | HG02040.hp1 HG02080.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1170-4269G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110991624 | ||||||
| chr2:110991655
|
C | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0024others(7): Show | 10 | HG01167.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1170-4238C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110991655 | ||||||
| chr2:110991677
|
T | C | 58 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1170-4216T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110991677 | ||||||
| chr2:110991691
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1170-4202T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110991691 | ||||||
| chr2:110991731
|
T | A | 1 | a0001c0001t0002g0078 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1170-4162T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110991731 | ||||||
| chr2:110991954
|
C | T | 8 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0088others(5): Show | 8 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1170-3939C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110991954 | ||||||
| chr2:110992081
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1170-3812G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110992081 | ||||||
| chr2:110992133
|
A | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170-3760A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110992133 | ||||||
| chr2:110992344
|
A | C | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1170-3549A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110992344 | ||||||
| chr2:110992451
|
A | G | 52 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1170-3442A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110992451 | ||||||
| chr2:110992476
|
A | C | 17 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(14): Show | 17 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1170-3417A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110992476 | ||||||
| chr2:110992937
|
A | G | 3 | a0002c0002t0001g0114a0002c0002t0001g0132a0006c0006t0001g0136 | 3 | HG01243.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1170-2956A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110992937 | ||||||
| chr2:110992972
|
C | T | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1170-2921C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110992972 | ||||||
| chr2:110992992
|
T | C | 114 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1170-2901T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110992992 | ||||||
| chr2:110992993
|
A | G | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1170-2900A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110992993 | ||||||
| chr2:110993033
|
C | A | 1 | a0001c0001t0001g0042 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1170-2860C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110993033 | ||||||
| chr2:110993166
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1170-2727C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110993166 | ||||||
| chr2:110993167
|
G | A | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1170-2726G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110993167 | ||||||
| chr2:110993285
|
C | G | 51 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1170-2608C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110993285 | ||||||
| chr2:110993295
|
A | T | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1170-2598A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110993295 | ||||||
| chr2:110993386
|
G | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1170-2507G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110993386 | ||||||
| chr2:110993415
|
G | A | 12 | a0001c0001t0001g0082a0001c0003t0001g0041a0001c0003t0001g0081others(9): Show | 12 | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1170-2478G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110993415 | ||||||
| chr2:110993561
|
C | T | 114 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1170-2332C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110993561 | ||||||
| chr2:110993617
|
A | G | 2 | a0001c0001t0002g0071a0001c0001t0005g0149 | 2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1170-2276A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110993617 | ||||||
| chr2:110993702
|
G | A | 3 | a0001c0001t0001g0037a0002c0002t0003g0142a0003c0004t0001g0027 | 3 | HG00423.hp2 HG00544.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1170-2191G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110993702 | ||||||
| chr2:110993709
|
C | T | 1 | a0000c0013t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1170-2184C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110993709 | ||||||
| chr2:110993847
|
A | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1170-2046A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110993847 | ||||||
| chr2:110993917
|
A | G | 2 | a0002c0002t0001g0135a0006c0006t0002g0146 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1170-1976A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110993917 | ||||||
| chr2:110994074
|
A | T | 1 | a0002c0002t0004g0141 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1170-1819A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110994074 | ||||||
| chr2:110994345
|
A | C | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1170-1548A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110994345 | ||||||
| chr2:110994414
|
G | A | 2 | a0002c0002t0001g0135a0006c0006t0002g0146 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1170-1479G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110994414 | ||||||
| chr2:110994447
|
G | GT | 123 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.1170-1437dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110994447 | |||||
| chr2:110994447
|
G | GTT | 5 | a0001c0001t0001g0031a0001c0012t0002g0131a0002c0002t0001g0114others(2): Show | 5 | HG01243.hp1 HG02080.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1170-1438_1170-143 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110994447 | |||||
| chr2:110994704
|
T | G | 1 | a0001c0003t0001g0075 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1170-1189T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110994704 | ||||||
| chr2:110994839
|
G | A | 21 | a0000c0013t0001g0046a0001c0001t0001g0012a0001c0001t0001g0018others(18): Show | 21 | HG01167.hp1 HG01243.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1170-1054G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110994839 | ||||||
| chr2:110994988
|
G | A | 1 | a0003c0004t0003g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1170-905G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110994988 | ||||||
| chr2:110995080
|
TA | T | 63 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1170-812delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110995080 | ||||||
| chr2:110995122
|
T | G | 2 | a0001c0001t0001g0058a0001c0001t0002g0052 | 2 | HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1170-771T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110995122 | ||||||
| chr2:110995138
|
G | C | 2 | a0001c0001t0001g0008a0001c0001t0006g0017 | 2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1170-755G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110995138 | ||||||
| chr2:110995306
|
C | T | 9 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0024others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1170-587C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110995306 | ||||||
| chr2:110995345
|
C | A | 43 | a0000c0013t0001g0046a0001c0001t0001g0012a0001c0001t0001g0018others(40): Show | 43 | HG00140.hp2 HG01168.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.1170-548C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110995345 | ||||||
| chr2:110995373
|
G | A | 9 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0088others(6): Show | 9 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170-520G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110995373 | ||||||
| chr2:110995379
|
A | T | 2 | a0002c0002t0001g0061a0005c0007t0001g0062 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1170-514A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110995379 | ||||||
| chr2:110995455
|
G | A | 17 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(14): Show | 17 | HG00438.hp1 HG01175.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1170-438G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110995455 | ||||||
| chr2:110995499
|
C | CAAAAAAA | 15 | a0000c0013t0001g0046a0001c0001t0001g0086a0002c0002t0001g0061others(12): Show | 15 | HG00438.hp1 HG01175.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1170-381_1170-375d others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110995499 | |||||
| chr2:110995499
|
C | CAAAAAAA others(1): Show |
64 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1170-382_1170-375d others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110995499 | |||||
| chr2:110995499
|
C | CAAAAAAA others(2): Show |
33 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0024others(30): Show | 33 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1170-383_1170-375d others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110995499 | |||||
| chr2:110995499
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0012a0001c0001t0002g0048a0001c0001t0002g0101others(1): Show | 4 | HG01891.hp2 HG02027.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170-384_1170-375d others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110995499 | |||||
| chr2:110995499
|
C | CAAAAAAA others(4): Show |
8 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0058others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1170-385_1170-375d others(13): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110995499 | |||||
| chr2:110995499
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0080a0001c0001t0001g0113 | 2 | HG03831.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1170-386_1170-375d others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110995499 | |||||
| chr2:110995499
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0038 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1170-387_1170-375d others(15): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 110995499 | |||||
| chr2:110995651
|
C | A | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1170-242C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110995651 | ||||||
| chr2:110995826
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1170-67A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110995826 | ||||||
| chr2:110995868
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170-25G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110995868 | ||||||
| chr2:110995872
|
G | C | 59 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.1170-21G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | 110995872 | ||||||
| chr2:110996394
|
A | T | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1281+390A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110996394 | ||||||
| chr2:110996528
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+524C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110996528 | ||||||
| chr2:110996569
|
A | T | 107 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.1281+565A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110996569 | ||||||
| chr2:110996968
|
G | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1281+964G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110996968 | ||||||
| chr2:110996971
|
T | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1281+967T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110996971 | ||||||
| chr2:110997344
|
C | T | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+1340C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110997344 | ||||||
| chr2:110997346
|
G | GA | 70 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1281+1350dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 110997346 | |||||
| chr2:110997546
|
G | A | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+1542G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110997546 | ||||||
| chr2:110997720
|
G | A | 12 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0045others(9): Show | 12 | HG01257.hp2 HG01258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1281+1716G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110997720 | ||||||
| chr2:110997780
|
C | T | 1 | a0004c0005t0002g0127 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1281+1776C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110997780 | ||||||
| chr2:110997804
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1281+1800C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110997804 | ||||||
| chr2:110997961
|
C | G | 70 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1281+1957C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110997961 | ||||||
| chr2:110997999
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1281+1995C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110997999 | ||||||
| chr2:110998007
|
C | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1281+2003C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110998007 | ||||||
| chr2:110998032
|
CAG | C | 54 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(51): Show | 54 | HG00140.hp2 HG00438.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.1281+2036_1281+203 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 110998032 | |||||
| chr2:110998042
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0002g0052 | 2 | HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1281+2038C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110998042 | ||||||
| chr2:110998107
|
A | T | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1281+2103A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110998107 | ||||||
| chr2:110998180
|
A | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+2176A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110998180 | ||||||
| chr2:110998248
|
G | C | 54 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(51): Show | 54 | HG00140.hp2 HG00438.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.1281+2244G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110998248 | ||||||
| chr2:110998445
|
C | T | 58 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(55): Show | 58 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.1281+2441C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110998445 | ||||||
| chr2:110998472
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1281+2468G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110998472 | ||||||
| chr2:110999023
|
G | A | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1281+3019G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110999023 | ||||||
| chr2:110999028
|
A | C | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1281+3024A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110999028 | ||||||
| chr2:110999224
|
A | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0085a0001c0001t0001g0110others(2): Show | 5 | HG00438.hp2 HG02027.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+3220A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110999224 | ||||||
| chr2:110999272
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1281+3268C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110999272 | ||||||
| chr2:110999336
|
A | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(14): Show | 17 | HG00438.hp1 HG01175.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1281+3332A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110999336 | ||||||
| chr2:110999494
|
A | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(14): Show | 17 | HG00438.hp1 HG01175.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1281+3490A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110999494 | ||||||
| chr2:110999504
|
T | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0024others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1281+3500T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110999504 | ||||||
| chr2:110999522
|
A | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1281+3518A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110999522 | ||||||
| chr2:110999856
|
T | C | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+3852T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110999856 | ||||||
| chr2:110999865
|
C | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(14): Show | 17 | HG00438.hp1 HG01175.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1281+3861C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 110999865 | ||||||
| chr2:111000021
|
A | G | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1281+4017A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111000021 | ||||||
| chr2:111000226
|
C | T | 18 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0045others(15): Show | 18 | HG00438.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1281+4222C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111000226 | ||||||
| chr2:111000233
|
G | A | 3 | a0002c0002t0001g0114a0002c0002t0001g0132a0006c0006t0001g0136 | 3 | HG01243.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1281+4229G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111000233 | ||||||
| chr2:111000341
|
T | C | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+4337T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111000341 | ||||||
| chr2:111000392
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1281+4388A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111000392 | ||||||
| chr2:111000529
|
C | G | 1 | a0000c0013t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1281+4525C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111000529 | ||||||
| chr2:111000709
|
C | G | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1281+4705C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111000709 | ||||||
| chr2:111001002
|
T | C | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+4998T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111001002 | ||||||
| chr2:111001047
|
A | G | 26 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(23): Show | 26 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1281+5043A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111001047 | ||||||
| chr2:111001120
|
A | G | 1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1281+5116A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111001120 | ||||||
| chr2:111001138
|
T | G | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1281+5134T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111001138 | ||||||
| chr2:111001197
|
T | C | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+5193T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111001197 | ||||||
| chr2:111001387
|
A | AAAAAC | 16 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0067others(13): Show | 16 | HG00438.hp1 HG01081.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.1281+5408_1281+541 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111001387 | |||||
| chr2:111001387
|
A | AAAAACAA others(3): Show |
31 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(28): Show | 31 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1281+5403_1281+541 others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111001387 | |||||
| chr2:111001387
|
A | AAAAACAA others(8): Show |
4 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0102others(1): Show | 4 | HG00140.hp1 HG01257.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+5398_1281+541 others(19): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111001387 | |||||
| chr2:111001387
|
AAAAAC | A | 57 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(54): Show | 57 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1281+5408_1281+541 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111001387 | |||||
| chr2:111001508
|
C | G | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1281+5504C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111001508 | ||||||
| chr2:111001963
|
G | A | 57 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(54): Show | 57 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1281+5959G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111001963 | ||||||
| chr2:111002013
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+6009C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111002013 | ||||||
| chr2:111002029
|
T | TTC | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0024others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1281+6041_1281+604 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111002029 | |||||
| chr2:111002084
|
G | T | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+6080G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111002084 | ||||||
| chr2:111002110
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+6106G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111002110 | ||||||
| chr2:111002258
|
AT | A | 57 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(54): Show | 57 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1281+6262delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111002258 | |||||
| chr2:111002313
|
T | C | 1 | a0001c0003t0001g0075 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1281+6309T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111002313 | ||||||
| chr2:111002409
|
G | A | 57 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(54): Show | 57 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1281+6405G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111002409 | ||||||
| chr2:111002477
|
A | C | 2 | a0002c0002t0001g0114a0002c0002t0001g0132 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1281+6473A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111002477 | ||||||
| chr2:111002504
|
G | A | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+6500G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111002504 | ||||||
| chr2:111002801
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1281+6797G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111002801 | ||||||
| chr2:111002810
|
A | C | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1281+6806A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111002810 | ||||||
| chr2:111002815
|
G | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+6811G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111002815 | ||||||
| chr2:111003214
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+7210G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111003214 | ||||||
| chr2:111003376
|
C | T | 1 | a0007c0009t0001g0106 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1281+7372C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111003376 | ||||||
| chr2:111003410
|
A | G | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+7406A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111003410 | ||||||
| chr2:111003443
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1281+7439C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111003443 | ||||||
| chr2:111003512
|
C | T | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+7508C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111003512 | ||||||
| chr2:111003518
|
T | A | 1 | a0003c0004t0002g0069 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1281+7514T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111003518 | ||||||
| chr2:111003550
|
C | CAAAA | 11 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0088others(8): Show | 11 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1281+7572_1281+757 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
C | CAAAAAA | 14 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0109others(11): Show | 14 | HG00544.hp2 HG00673.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1281+7570_1281+757 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
C | CAAAAAAA | 18 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0108others(15): Show | 18 | HG00323.hp1 HG00423.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1281+7569_1281+757 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
C | CAAAAAAA others(1): Show |
14 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.1281+7568_1281+757 others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
C | CAAAAAAA others(3): Show |
1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1281+7566_1281+757 others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0058 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1281+7564_1281+757 others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0128a0001c0001t0002g0052a0011c0010t0002g0009 | 3 | HG02258.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1281+7563_1281+757 others(17): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0113 | 3 | HG03831.hp1 HG03831.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1281+7562_1281+757 others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0029a0001c0001t0001g0077 | 2 | HG00673.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.1281+7558_1281+757 others(22): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1281+7554_1281+757 others(26): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
C | CAAAAAAA others(16): Show |
3 | a0001c0001t0001g0049a0001c0001t0002g0048a0001c0001t0002g0101 | 3 | HG02027.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1281+7553_1281+757 others(27): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
CAAAAA | C | 21 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(18): Show | 21 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1281+7571_1281+757 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1281+7566_1281+757 others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
CAAAAAAA others(4): Show |
C | 15 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0086others(12): Show | 15 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.1281+7565_1281+757 others(15): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003550
|
CAAAAAAA others(5): Show |
C | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1281+7564_1281+757 others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111003550 | |||||
| chr2:111003661
|
T | C | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+7657T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111003661 | ||||||
| chr2:111003679
|
G | A | 1 | a0003c0004t0001g0027 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1281+7675G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111003679 | ||||||
| chr2:111003714
|
A | C | 111 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1281+7710A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111003714 | ||||||
| chr2:111003803
|
G | A | 6 | a0001c0001t0001g0082a0001c0003t0001g0081a0001c0003t0001g0087others(3): Show | 6 | HG01081.hp2 HG01167.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281+7799G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111003803 | ||||||
| chr2:111004000
|
G | T | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1281+7996G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111004000 | ||||||
| chr2:111004315
|
CA | C | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+8314delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111004315 | |||||
| chr2:111004356
|
C | T | 53 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.1281+8352C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111004356 | ||||||
| chr2:111004357
|
C | T | 26 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(23): Show | 26 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1281+8353C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111004357 | ||||||
| chr2:111004466
|
T | C | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+8462T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111004466 | ||||||
| chr2:111004583
|
C | T | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+8579C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111004583 | ||||||
| chr2:111004658
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1281+8654A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111004658 | ||||||
| chr2:111004709
|
A | G | 2 | a0001c0001t0002g0076a0001c0001t0002g0078 | 2 | NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1281+8705A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111004709 | ||||||
| chr2:111004828
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1281+8824G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111004828 | ||||||
| chr2:111004832
|
C | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1281+8828C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111004832 | ||||||
| chr2:111004927
|
T | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1281+8923T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111004927 | ||||||
| chr2:111005024
|
G | T | 52 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1281+9020G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111005024 | ||||||
| chr2:111005084
|
C | A | 1 | a0001c0001t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1281+9080C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111005084 | ||||||
| chr2:111005088
|
T | C | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1281+9084T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111005088 | ||||||
| chr2:111005137
|
C | G | 2 | a0004c0005t0002g0020a0004c0005t0002g0022 | 2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1281+9133C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111005137 | ||||||
| chr2:111005164
|
C | A | 1 | a0003c0004t0003g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1281+9160C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111005164 | ||||||
| chr2:111005245
|
C | T | 58 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0011others(55): Show | 58 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.1281+9241C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111005245 | ||||||
| chr2:111005349
|
C | T | 57 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0011others(54): Show | 57 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1281+9345C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111005349 | ||||||
| chr2:111005383
|
AG | A | 6 | a0004c0005t0001g0134a0004c0005t0002g0020a0004c0005t0002g0022others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1281+9381delG | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111005383 | |||||
| chr2:111005633
|
C | T | 1 | a0001c0003t0001g0075 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1281+9629C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111005633 | ||||||
| chr2:111005754
|
G | C | 3 | a0001c0001t0002g0123a0002c0002t0002g0014a0014c0020t0001g0002 | 3 | HG02257.hp2 HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1281+9750G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111005754 | ||||||
| chr2:111005840
|
A | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(14): Show | 17 | HG00438.hp1 HG01175.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1281+9836A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111005840 | ||||||
| chr2:111005913
|
T | A | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+9909T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111005913 | ||||||
| chr2:111006429
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1281+10425C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111006429 | ||||||
| chr2:111006447
|
A | G | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1281+10443A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111006447 | ||||||
| chr2:111006716
|
G | A | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1281+10712G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111006716 | ||||||
| chr2:111006750
|
G | A | 58 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(55): Show | 58 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.1281+10746G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111006750 | ||||||
| chr2:111006760
|
T | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(14): Show | 17 | HG00438.hp1 HG01175.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1281+10756T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111006760 | ||||||
| chr2:111006818
|
C | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(14): Show | 17 | HG00438.hp1 HG01175.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1281+10814C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111006818 | ||||||
| chr2:111006929
|
T | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+10925T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111006929 | ||||||
| chr2:111006949
|
C | CT | 111 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1281+10951dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111006949 | |||||
| chr2:111007506
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1281+11502T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111007506 | ||||||
| chr2:111007759
|
C | A | 17 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(14): Show | 17 | HG00438.hp1 HG01175.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1281+11755C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111007759 | ||||||
| chr2:111007765
|
C | T | 9 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0024others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1281+11761C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111007765 | ||||||
| chr2:111007838
|
A | G | 1 | a0000c0013t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1281+11834A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111007838 | ||||||
| chr2:111008062
|
G | A | 57 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(54): Show | 57 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1281+12058G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111008062 | ||||||
| chr2:111008212
|
T | C | 3 | a0002c0002t0001g0114a0002c0002t0001g0132a0006c0006t0001g0136 | 3 | HG01243.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1281+12208T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111008212 | ||||||
| chr2:111008224
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1281+12220A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111008224 | ||||||
| chr2:111008427
|
G | A | 1 | a0002c0002t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1281+12423G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111008427 | ||||||
| chr2:111008542
|
C | T | 111 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1281+12538C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111008542 | ||||||
| chr2:111008550
|
C | A | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+12546C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111008550 | ||||||
| chr2:111009006
|
T | G | 8 | a0000c0014t0001g0072a0001c0001t0001g0042a0001c0001t0001g0117others(5): Show | 8 | HG01175.hp1 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281+13002T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111009006 | ||||||
| chr2:111009070
|
A | G | 19 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0067others(16): Show | 19 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(16): Show |
intron_variant | MODIFIER | c.1281+13066A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111009070 | ||||||
| chr2:111009198
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0002g0032 | 2 | HG02080.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1281+13194A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111009198 | ||||||
| chr2:111009513
|
CA | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(14): Show | 17 | HG00438.hp1 HG01175.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1281+13524delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111009513 | |||||
| chr2:111009513
|
CAA | C | 57 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(54): Show | 57 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1281+13523_1281+13 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111009513 | |||||
| chr2:111009575
|
T | C | 110 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.1281+13571T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111009575 | ||||||
| chr2:111010511
|
TGAGAGAG others(11): Show |
T | 3 | a0001c0001t0001g0077a0001c0001t0002g0076a0001c0001t0002g0078 | 3 | HG02027.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1281+14510_1281+14 others(24): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111010511 | |||||
| chr2:111010616
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1281+14612C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111010616 | ||||||
| chr2:111010633
|
A | C | 1 | a0003c0004t0003g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1281+14629A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111010633 | ||||||
| chr2:111010643
|
C | T | 58 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(55): Show | 58 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.1281+14639C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111010643 | ||||||
| chr2:111010700
|
A | T | 2 | a0001c0001t0002g0071a0001c0001t0005g0149 | 2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1281+14696A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111010700 | ||||||
| chr2:111010762
|
T | C | 57 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(54): Show | 57 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1281+14758T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111010762 | ||||||
| chr2:111010796
|
G | A | 111 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1281+14792G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111010796 | ||||||
| chr2:111010843
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1281+14839C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111010843 | ||||||
| chr2:111010846
|
G | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1281+14842G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111010846 | ||||||
| chr2:111010865
|
T | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0126others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1281+14861T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111010865 | ||||||
| chr2:111010880
|
A | G | 57 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(54): Show | 57 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1281+14876A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111010880 | ||||||
| chr2:111010908
|
A | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1281+14904A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111010908 | ||||||
| chr2:111011075
|
T | C | 111 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1281+15071T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111011075 | ||||||
| chr2:111011256
|
CTA | C | 2 | a0001c0001t0001g0145a0002c0002t0001g0019 | 2 | HG01167.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1281+15255_1281+15 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111011256 | |||||
| chr2:111011457
|
A | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1281+15453A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111011457 | ||||||
| chr2:111011625
|
G | A | 3 | a0001c0001t0001g0037a0002c0002t0003g0142a0003c0004t0001g0027 | 3 | HG00423.hp2 HG00544.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1281+15621G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111011625 | ||||||
| chr2:111011628
|
G | A | 111 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1281+15624G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111011628 | ||||||
| chr2:111011649
|
A | G | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1281+15645A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111011649 | ||||||
| chr2:111011714
|
C | T | 22 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(19): Show | 22 | HG00438.hp2 HG00673.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1281+15710C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111011714 | ||||||
| chr2:111011881
|
T | TAAA | 14 | a0001c0001t0001g0086a0002c0002t0001g0061a0002c0002t0001g0114others(11): Show | 14 | HG00438.hp1 HG01243.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1281+15899_1281+15 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111011881 | |||||
| chr2:111011881
|
TAA | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0096a0001c0001t0001g0100others(2): Show | 5 | HG00140.hp1 HG01258.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.1281+15900_1281+15 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111011881 | |||||
| chr2:111011881
|
TAAA | T | 46 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 46 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.1281+15899_1281+15 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111011881 | |||||
| chr2:111011881
|
TAAAA | T | 20 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0024others(17): Show | 20 | HG00140.hp2 HG00323.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1281+15898_1281+15 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111011881 | |||||
| chr2:111011881
|
TAAAAA | T | 32 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0029others(29): Show | 32 | HG00673.hp2 HG01175.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1281+15897_1281+15 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111011881 | |||||
| chr2:111011891
|
AAAAAAAA others(9): Show |
A | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1281+15889_1281+15 others(22): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111011891 | |||||
| chr2:111011900
|
AAAAAAGG | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0001g0085others(3): Show | 6 | HG00438.hp2 HG02027.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281+15898_1281+15 others(13): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111011900 | |||||
| chr2:111011916
|
A | T | 8 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0088others(5): Show | 8 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281+15912A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111011916 | ||||||
| chr2:111011936
|
T | G | 1 | a0006c0006t0001g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1281+15932T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111011936 | ||||||
| chr2:111012010
|
T | TA | 111 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1281+16011dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111012010 | |||||
| chr2:111012585
|
A | T | 7 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0001g0085others(4): Show | 7 | HG00438.hp2 HG02027.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1281+16581A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111012585 | ||||||
| chr2:111013241
|
G | T | 11 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0045others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1281+17237G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111013241 | ||||||
| chr2:111013244
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1281+17240G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111013244 | ||||||
| chr2:111013393
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1281+17389G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111013393 | ||||||
| chr2:111013522
|
C | CA | 6 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0003t0002g0083others(3): Show | 6 | HG00423.hp2 HG01175.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1281+17541dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111013522 | |||||
| chr2:111013522
|
C | CAAA | 17 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0096others(14): Show | 17 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(14): Show |
intron_variant | MODIFIER | c.1281+17539_1281+17 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111013522 | |||||
| chr2:111013522
|
CA | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0067a0002c0002t0001g0099others(2): Show | 5 | HG00323.hp2 HG01081.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+17541delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111013522 | |||||
| chr2:111013522
|
CAAA | C | 13 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0024others(10): Show | 13 | HG00438.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1281+17539_1281+17 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111013522 | |||||
| chr2:111013522
|
CAAAA | C | 26 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0029others(23): Show | 26 | HG00673.hp2 HG01175.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1281+17538_1281+17 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111013522 | |||||
| chr2:111013522
|
CAAAAA | C | 16 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0045others(13): Show | 16 | HG00140.hp2 HG01168.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1281+17537_1281+17 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111013522 | |||||
| chr2:111013844
|
ACAAATAT others(4): Show |
A | 58 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(55): Show | 58 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.1282-17780_1282-17 others(17): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111013844 | |||||
| chr2:111013859
|
G | C | 58 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(55): Show | 58 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.1282-17768G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111013859 | ||||||
| chr2:111013860
|
A | T | 58 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(55): Show | 58 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.1282-17767A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111013860 | ||||||
| chr2:111013947
|
G | A | 57 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(54): Show | 57 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1282-17680G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111013947 | ||||||
| chr2:111013952
|
T | A | 1 | a0001c0001t0001g0055 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1282-17675T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111013952 | ||||||
| chr2:111013975
|
G | A | 1 | a0002c0002t0001g0103 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1282-17652G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111013975 | ||||||
| chr2:111014070
|
A | G | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1282-17557A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111014070 | ||||||
| chr2:111014139
|
T | C | 17 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(14): Show | 17 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1282-17488T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111014139 | ||||||
| chr2:111014234
|
G | A | 17 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(14): Show | 17 | HG00438.hp1 HG01175.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1282-17393G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111014234 | ||||||
| chr2:111014234
|
G | T | 8 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0088others(5): Show | 8 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282-17393G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111014234 | ||||||
| chr2:111014296
|
C | T | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1282-17331C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111014296 | ||||||
| chr2:111014316
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1282-17311C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111014316 | ||||||
| chr2:111014450
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1282-17177C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111014450 | ||||||
| chr2:111014964
|
A | T | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1282-16663A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111014964 | ||||||
| chr2:111015028
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1282-16599T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111015028 | ||||||
| chr2:111015208
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1282-16419C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111015208 | ||||||
| chr2:111015283
|
A | T | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1282-16344A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111015283 | ||||||
| chr2:111015584
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1282-16043C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111015584 | ||||||
| chr2:111015896
|
A | G | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1282-15731A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111015896 | ||||||
| chr2:111015911
|
A | G | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1282-15716A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111015911 | ||||||
| chr2:111015916
|
T | A | 1 | a0001c0001t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1282-15711T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111015916 | ||||||
| chr2:111015955
|
C | T | 9 | a0001c0001t0001g0086a0003c0004t0001g0026a0003c0004t0001g0030others(6): Show | 9 | HG01175.hp2 HG01496.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1282-15672C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111015955 | ||||||
| chr2:111015993
|
T | G | 57 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(54): Show | 57 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1282-15634T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111015993 | ||||||
| chr2:111016046
|
C | T | 11 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0045others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1282-15581C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111016046 | ||||||
| chr2:111016108
|
A | AT | 54 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1282-15508dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111016108 | |||||
| chr2:111016108
|
A | ATT | 57 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0018others(54): Show | 57 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1282-15509_1282-15 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111016108 | |||||
| chr2:111016108
|
A | ATTT | 17 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(14): Show | 17 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1282-15510_1282-15 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111016108 | |||||
| chr2:111016333
|
G | A | 57 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(54): Show | 57 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1282-15294G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111016333 | ||||||
| chr2:111016383
|
G | A | 111 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1282-15244G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111016383 | ||||||
| chr2:111016539
|
G | A | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1282-15088G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111016539 | ||||||
| chr2:111016552
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1282-15075G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111016552 | ||||||
| chr2:111016656
|
G | A | 1 | a0001c0003t0001g0081 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1282-14971G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111016656 | ||||||
| chr2:111016779
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0002g0101 | 3 | HG00438.hp2 HG02027.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1282-14848G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111016779 | ||||||
| chr2:111016930
|
G | GA | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1282-14696dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111016930 | |||||
| chr2:111017061
|
C | T | 128 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1282-14566C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111017061 | ||||||
| chr2:111017264
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-14363C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111017264 | ||||||
| chr2:111017530
|
A | G | 32 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0038others(29): Show | 32 | HG00438.hp1 HG00673.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1282-14097A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111017530 | ||||||
| chr2:111017629
|
G | A | 43 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1282-13998G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111017629 | ||||||
| chr2:111017872
|
G | C | 27 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(24): Show | 27 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1282-13755G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111017872 | ||||||
| chr2:111017882
|
G | C | 27 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0063others(24): Show | 27 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.1282-13745G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111017882 | ||||||
| chr2:111018577
|
C | T | 27 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0063others(24): Show | 27 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.1282-13050C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111018577 | ||||||
| chr2:111018680
|
G | C | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1282-12947G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111018680 | ||||||
| chr2:111018708
|
T | TG | 8 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0088others(5): Show | 8 | HG00140.hp2 HG01168.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282-12917dupG | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111018708 | |||||
| chr2:111018708
|
T | TGG | 6 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0110others(3): Show | 6 | HG00438.hp2 HG01255.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.1282-12918_1282-12 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111018708 | |||||
| chr2:111018710
|
GA | G | 33 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0038others(30): Show | 33 | HG00438.hp1 HG00673.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1282-12916delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111018710 | ||||||
| chr2:111018711
|
A | G | 95 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.1282-12916A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111018711 | ||||||
| chr2:111018713
|
G | GC | 27 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(24): Show | 27 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1282-12914_1282-12 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111018713 | ||||||
| chr2:111018900
|
G | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.1282-12727G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111018900 | ||||||
| chr2:111019125
|
C | T | 33 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0038others(30): Show | 33 | HG00438.hp1 HG00673.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1282-12502C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111019125 | ||||||
| chr2:111019435
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-12192G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111019435 | ||||||
| chr2:111019613
|
G | A | 3 | a0002c0002t0001g0114a0002c0002t0001g0132a0006c0006t0001g0136 | 3 | HG01243.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1282-12014G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111019613 | ||||||
| chr2:111019632
|
C | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(23): Show | 26 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.1282-11995C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111019632 | ||||||
| chr2:111019664
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1282-11963C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111019664 | ||||||
| chr2:111019702
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1282-11925C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111019702 | ||||||
| chr2:111019963
|
C | T | 33 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0038others(30): Show | 33 | HG00438.hp1 HG00673.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1282-11664C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111019963 | ||||||
| chr2:111020218
|
C | T | 113 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.1282-11409C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111020218 | ||||||
| chr2:111020336
|
A | G | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1282-11291A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111020336 | ||||||
| chr2:111020561
|
G | A | 8 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0088others(5): Show | 8 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282-11066G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111020561 | ||||||
| chr2:111020569
|
G | T | 3 | a0001c0001t0001g0056a0001c0001t0002g0071a0001c0001t0005g0149 | 3 | HG02622.hp2 HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1282-11058G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111020569 | ||||||
| chr2:111020664
|
T | C | 3 | a0002c0002t0001g0114a0002c0002t0001g0132a0006c0006t0001g0136 | 3 | HG01243.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1282-10963T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111020664 | ||||||
| chr2:111020987
|
C | T | 95 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.1282-10640C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111020987 | ||||||
| chr2:111021215
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1282-10412A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111021215 | ||||||
| chr2:111021295
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0024others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1282-10332A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111021295 | ||||||
| chr2:111021302
|
T | A | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1282-10325T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111021302 | ||||||
| chr2:111021325
|
G | A | 145 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1282-10302G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111021325 | ||||||
| chr2:111021334
|
G | T | 1 | a0001c0001t0002g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1282-10293G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111021334 | ||||||
| chr2:111021519
|
C | T | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1282-10108C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111021519 | ||||||
| chr2:111021581
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1282-10046C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111021581 | ||||||
| chr2:111021594
|
C | T | 11 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0045others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1282-10033C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111021594 | ||||||
| chr2:111021752
|
G | A | 4 | a0001c0001t0001g0145a0002c0002t0001g0019a0002c0002t0001g0135others(1): Show | 4 | HG01167.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282-9875G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111021752 | ||||||
| chr2:111021781
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1282-9846A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111021781 | ||||||
| chr2:111022005
|
G | A | 26 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(23): Show | 26 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.1282-9622G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111022005 | ||||||
| chr2:111022118
|
C | T | 15 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG00673.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1282-9509C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111022118 | ||||||
| chr2:111022353
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-9274G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111022353 | ||||||
| chr2:111022421
|
T | TCA | 8 | a0001c0001t0001g0145a0001c0001t0002g0052a0001c0003t0001g0075others(5): Show | 8 | HG01167.hp1 HG01168.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1282-9179_1282-917 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111022421 | |||||
| chr2:111022421
|
T | TCACA | 19 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0024others(16): Show | 19 | HG00438.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1282-9181_1282-917 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111022421 | |||||
| chr2:111022421
|
T | TCACACAC others(3): Show |
10 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(7): Show | 10 | HG01175.hp1 HG02257.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1282-9187_1282-917 others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111022421 | |||||
| chr2:111022421
|
T | TCACACAC others(5): Show |
2 | a0002c0002t0001g0114a0002c0002t0001g0132 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1282-9189_1282-917 others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111022421 | |||||
| chr2:111022421
|
T | TCACACAC others(9): Show |
1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1282-9193_1282-917 others(20): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111022421 | |||||
| chr2:111022421
|
TCA | T | 49 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(46): Show | 49 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1282-9179_1282-917 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111022421 | |||||
| chr2:111022421
|
TCACACAC others(3): Show |
T | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1282-9187_1282-917 others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111022421 | |||||
| chr2:111022440
|
C | T | 42 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.1282-9187C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111022440 | ||||||
| chr2:111022506
|
G | T | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1282-9121G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111022506 | ||||||
| chr2:111023069
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1282-8558C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111023069 | ||||||
| chr2:111023142
|
C | T | 30 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(27): Show | 30 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1282-8485C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111023142 | ||||||
| chr2:111023464
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1282-8163T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111023464 | ||||||
| chr2:111023563
|
G | A | 4 | a0001c0001t0001g0039a0001c0001t0002g0123a0002c0002t0002g0014others(1): Show | 4 | HG02257.hp2 HG02723.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-8064G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111023563 | ||||||
| chr2:111023848
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1282-7779G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111023848 | ||||||
| chr2:111023865
|
G | A | 15 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0045others(12): Show | 15 | HG00673.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1282-7762G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111023865 | ||||||
| chr2:111024188
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1282-7439C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111024188 | ||||||
| chr2:111024378
|
G | C | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1282-7249G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111024378 | ||||||
| chr2:111024384
|
T | C | 2 | a0001c0001t0002g0071a0001c0001t0005g0149 | 2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1282-7243T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111024384 | ||||||
| chr2:111024434
|
C | T | 52 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 52 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1282-7193C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111024434 | ||||||
| chr2:111024756
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0002g0123a0002c0002t0002g0014 | 3 | HG02723.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1282-6871A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111024756 | ||||||
| chr2:111024764
|
T | C | 5 | a0001c0001t0001g0049a0001c0001t0001g0085a0001c0001t0001g0110others(2): Show | 5 | HG00438.hp2 HG02027.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-6863T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111024764 | ||||||
| chr2:111024964
|
C | G | 16 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(13): Show | 16 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-6663C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111024964 | ||||||
| chr2:111024968
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1282-6659C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111024968 | ||||||
| chr2:111025064
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1282-6563T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111025064 | ||||||
| chr2:111025076
|
C | T | 51 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(48): Show | 51 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1282-6551C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111025076 | ||||||
| chr2:111025256
|
C | T | 30 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(27): Show | 30 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1282-6371C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111025256 | ||||||
| chr2:111025257
|
G | A | 24 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0063others(21): Show | 24 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.1282-6370G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111025257 | ||||||
| chr2:111025478
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-6149A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111025478 | ||||||
| chr2:111025523
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1282-6104G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111025523 | ||||||
| chr2:111025642
|
G | C | 2 | a0002c0002t0001g0114a0002c0002t0001g0132 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1282-5985G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111025642 | ||||||
| chr2:111026015
|
T | C | 23 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0063others(20): Show | 23 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.1282-5612T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111026015 | ||||||
| chr2:111026355
|
T | C | 2 | a0001c0001t0002g0071a0001c0001t0005g0149 | 2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1282-5272T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111026355 | ||||||
| chr2:111026518
|
T | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-5109T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111026518 | ||||||
| chr2:111026546
|
A | C | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1282-5081A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111026546 | ||||||
| chr2:111026743
|
G | A | 23 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0063others(20): Show | 23 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.1282-4884G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111026743 | ||||||
| chr2:111026744
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1282-4883G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111026744 | ||||||
| chr2:111026859
|
G | T | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1282-4768G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111026859 | ||||||
| chr2:111026863
|
G | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0024others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1282-4764G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111026863 | ||||||
| chr2:111027284
|
A | G | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1282-4343A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111027284 | ||||||
| chr2:111027297
|
C | T | 8 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0088others(5): Show | 8 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282-4330C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111027297 | ||||||
| chr2:111027325
|
CT | C | 46 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 46 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1282-4288delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111027325 | |||||
| chr2:111027391
|
G | A | 30 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(27): Show | 30 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1282-4236G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111027391 | ||||||
| chr2:111027480
|
C | T | 44 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(41): Show | 44 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.1282-4147C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111027480 | ||||||
| chr2:111027555
|
C | T | 16 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(13): Show | 16 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-4072C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111027555 | ||||||
| chr2:111027566
|
C | G | 23 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0063others(20): Show | 23 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.1282-4061C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111027566 | ||||||
| chr2:111027648
|
C | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(28): Show | 31 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.1282-3979C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111027648 | ||||||
| chr2:111027683
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1282-3944C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111027683 | ||||||
| chr2:111028082
|
G | GTCT | 23 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0049others(20): Show | 23 | HG00438.hp1 HG00438.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.1282-3545_1282-354 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111028082 | ||||||
| chr2:111028172
|
G | A | 1 | a0001c0003t0001g0081 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1282-3455G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111028172 | ||||||
| chr2:111028246
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1282-3381C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111028246 | ||||||
| chr2:111028318
|
G | C | 3 | a0001c0001t0001g0044a0001c0001t0002g0111a0013c0011t0001g0130 | 3 | HG01255.hp1 HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1282-3309G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111028318 | ||||||
| chr2:111028419
|
G | A | 1 | a0007c0009t0001g0106 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1282-3208G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111028419 | ||||||
| chr2:111028428
|
T | G | 50 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 50 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1282-3199T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111028428 | ||||||
| chr2:111028553
|
A | AC | 73 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1282-3074_1282-307 others(5): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111028553 | ||||||
| chr2:111029060
|
A | G | 23 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0063others(20): Show | 23 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.1282-2567A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111029060 | ||||||
| chr2:111029260
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1282-2367C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111029260 | ||||||
| chr2:111029450
|
C | T | 120 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.1282-2177C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111029450 | ||||||
| chr2:111029543
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1282-2084G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111029543 | ||||||
| chr2:111029638
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-1989C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111029638 | ||||||
| chr2:111029689
|
C | T | 15 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0002g0052others(12): Show | 15 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.1282-1938C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111029689 | ||||||
| chr2:111029730
|
G | A | 14 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0045others(11): Show | 14 | HG00673.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1282-1897G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111029730 | ||||||
| chr2:111029884
|
T | G | 1 | a0001c0001t0002g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1282-1743T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111029884 | ||||||
| chr2:111029897
|
T | C | 120 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.1282-1730T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111029897 | ||||||
| chr2:111030046
|
T | A | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1282-1581T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111030046 | ||||||
| chr2:111030156
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1282-1471T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111030156 | ||||||
| chr2:111030276
|
C | A | 16 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0096others(13): Show | 16 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-1351C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111030276 | ||||||
| chr2:111030305
|
C | G | 10 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(7): Show | 10 | HG01175.hp1 HG02257.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1282-1322C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111030305 | ||||||
| chr2:111030360
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0002g0101 | 3 | HG00438.hp2 HG02027.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1282-1267G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111030360 | ||||||
| chr2:111030476
|
G | C | 5 | a0002c0002t0001g0114a0002c0002t0001g0132a0006c0006t0001g0136others(2): Show | 5 | HG01243.hp1 HG02258.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-1151G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111030476 | ||||||
| chr2:111030570
|
C | G | 129 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(126): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1282-1057C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111030570 | ||||||
| chr2:111030731
|
C | CA | 63 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1282-885dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 111030731 | |||||
| chr2:111030757
|
G | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0002g0101 | 3 | HG00438.hp2 HG02027.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1282-870G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111030757 | ||||||
| chr2:111030779
|
G | A | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1282-848G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111030779 | ||||||
| chr2:111030883
|
A | G | 2 | a0002c0002t0001g0114a0002c0002t0001g0132 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1282-744A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111030883 | ||||||
| chr2:111031014
|
G | A | 44 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(41): Show | 44 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.1282-613G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111031014 | ||||||
| chr2:111031201
|
T | G | 5 | a0002c0002t0001g0114a0002c0002t0001g0132a0006c0006t0001g0136others(2): Show | 5 | HG01243.hp1 HG02258.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-426T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111031201 | ||||||
| chr2:111031217
|
G | A | 67 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1282-410G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111031217 | ||||||
| chr2:111031272
|
AGATTC | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1282-354_1282-350d others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111031272 | ||||||
| chr2:111031349
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1282-278G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111031349 | ||||||
| chr2:111031364
|
C | T | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1282-263C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111031364 | ||||||
| chr2:111031417
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1282-210G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111031417 | ||||||
| chr2:111031426
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1282-201C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111031426 | ||||||
| chr2:111031515
|
G | A | 49 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(46): Show | 49 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1282-112G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111031515 | ||||||
| chr2:111031555
|
G | A | 1 | a0002c0002t0002g0059 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1282-72G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | 111031555 | ||||||
| chr2:111032094
|
G | C | 2 | a0001c0001t0001g0063a0001c0003t0001g0090 | 2 | HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1369+380G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111032094 | ||||||
| chr2:111032133
|
G | A | 71 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1369+419G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111032133 | ||||||
| chr2:111032139
|
A | G | 1 | a0005c0007t0004g0144 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1369+425A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111032139 | ||||||
| chr2:111032214
|
A | G | 23 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0063others(20): Show | 23 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.1369+500A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111032214 | ||||||
| chr2:111032251
|
CG | C | 5 | a0002c0002t0001g0114a0002c0002t0001g0132a0006c0006t0001g0136others(2): Show | 5 | HG01243.hp1 HG02258.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1369+538delG | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111032251 | ||||||
| chr2:111032293
|
G | A | 2 | a0001c0001t0001g0067a0002c0002t0002g0013 | 2 | HG01081.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1369+579G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111032293 | ||||||
| chr2:111032339
|
G | A | 6 | a0004c0005t0001g0134a0004c0005t0002g0020a0004c0005t0002g0022others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1369+625G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111032339 | ||||||
| chr2:111032680
|
G | T | 1 | a0001c0001t0001g0086 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1369+966G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111032680 | ||||||
| chr2:111033141
|
T | G | 1 | a0001c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1369+1427T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111033141 | ||||||
| chr2:111033227
|
G | C | 23 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0063others(20): Show | 23 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.1369+1513G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111033227 | ||||||
| chr2:111033252
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1369+1538C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111033252 | ||||||
| chr2:111033360
|
T | C | 1 | a0001c0001t0002g0060 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1369+1646T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111033360 | ||||||
| chr2:111033500
|
G | A | 14 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0088others(11): Show | 14 | HG00140.hp2 HG01168.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1369+1786G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111033500 | ||||||
| chr2:111033736
|
C | T | 1 | a0009c0016t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1369+2022C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111033736 | ||||||
| chr2:111033793
|
CAG | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0086a0003c0004t0001g0026others(9): Show | 12 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1369+2080_1369+208 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111033793 | ||||||
| chr2:111033919
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0068others(6): Show | 9 | HG02451.hp2 HG02615.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1369+2205G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111033919 | ||||||
| chr2:111033990
|
C | G | 11 | a0001c0001t0001g0086a0003c0004t0001g0026a0003c0004t0001g0030others(8): Show | 11 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1369+2276C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111033990 | ||||||
| chr2:111034045
|
A | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1369+2331A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111034045 | ||||||
| chr2:111034076
|
C | T | 22 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0063others(19): Show | 22 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.1369+2362C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111034076 | ||||||
| chr2:111034159
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1369+2445C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111034159 | ||||||
| chr2:111034196
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1369+2482C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111034196 | ||||||
| chr2:111034616
|
A | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(12): Show | 15 | HG01175.hp2 HG01243.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.1369+2902A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111034616 | ||||||
| chr2:111034725
|
C | A | 15 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0021others(12): Show | 15 | HG00423.hp2 HG01175.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1369+3011C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111034725 | ||||||
| chr2:111034922
|
C | CT | 21 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0067others(18): Show | 21 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.1369+3223dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 111034922 | |||||
| chr2:111034922
|
CT | C | 29 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0021others(26): Show | 29 | HG00673.hp2 HG01175.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1369+3223delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 111034922 | |||||
| chr2:111034941
|
G | A | 16 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0045others(13): Show | 16 | HG00673.hp2 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1369+3227G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111034941 | ||||||
| chr2:111034952
|
C | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1369+3238C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111034952 | ||||||
| chr2:111034957
|
G | A | 1 | a0001c0017t0002g0073 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1369+3243G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111034957 | ||||||
| chr2:111034972
|
T | C | 49 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0021others(46): Show | 49 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.1369+3258T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111034972 | ||||||
| chr2:111035073
|
T | A | 3 | a0001c0001t0001g0031a0001c0003t0001g0075a0002c0002t0004g0141 | 3 | HG00423.hp1 HG02080.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1369+3359T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111035073 | ||||||
| chr2:111035147
|
T | G | 1 | a0003c0004t0001g0026 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1369+3433T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111035147 | ||||||
| chr2:111035156
|
G | A | 12 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0058others(9): Show | 12 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1369+3442G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111035156 | ||||||
| chr2:111035157
|
T | C | 29 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0029others(26): Show | 29 | HG00673.hp2 HG01175.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1369+3443T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111035157 | ||||||
| chr2:111035410
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1369+3696C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111035410 | ||||||
| chr2:111035412
|
G | T | 1 | a0002c0002t0004g0141 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1369+3698G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111035412 | ||||||
| chr2:111035431
|
G | C | 21 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0067others(18): Show | 21 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.1369+3717G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111035431 | ||||||
| chr2:111035455
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1369+3741A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111035455 | ||||||
| chr2:111035573
|
C | T | 10 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(7): Show | 10 | HG01175.hp1 HG02257.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1369+3859C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111035573 | ||||||
| chr2:111035639
|
T | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(12): Show | 15 | HG01175.hp2 HG01243.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.1369+3925T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111035639 | ||||||
| chr2:111036447
|
G | C | 10 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(7): Show | 10 | HG01175.hp1 HG02257.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1369+4733G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111036447 | ||||||
| chr2:111036760
|
G | A | 20 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0067others(17): Show | 20 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.1369+5046G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111036760 | ||||||
| chr2:111036811
|
A | G | 56 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1369+5097A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111036811 | ||||||
| chr2:111037159
|
T | C | 23 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(20): Show | 23 | HG00140.hp2 HG01168.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1369+5445T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111037159 | ||||||
| chr2:111037448
|
T | C | 17 | a0001c0001t0001g0031a0001c0001t0001g0067a0001c0001t0001g0137others(14): Show | 17 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(14): Show |
intron_variant | MODIFIER | c.1369+5734T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111037448 | ||||||
| chr2:111037742
|
G | A | 23 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(20): Show | 23 | HG00140.hp2 HG01168.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1369+6028G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111037742 | ||||||
| chr2:111037932
|
C | T | 25 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 25 | HG00140.hp1 HG00544.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1369+6218C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111037932 | ||||||
| chr2:111038078
|
G | T | 15 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(12): Show | 15 | HG01175.hp2 HG01243.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.1369+6364G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111038078 | ||||||
| chr2:111038193
|
G | A | 31 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0028others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1369+6479G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111038193 | ||||||
| chr2:111038348
|
CAAAATAA others(5): Show |
C | 15 | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(12): Show | 15 | HG01175.hp2 HG01243.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.1369+6647_1369+665 others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 111038348 | |||||
| chr2:111038462
|
G | A | 16 | a0001c0001t0001g0031a0001c0001t0001g0067a0001c0001t0001g0137others(13): Show | 16 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(13): Show |
intron_variant | MODIFIER | c.1369+6748G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111038462 | ||||||
| chr2:111038607
|
G | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0085others(4): Show | 7 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(4): Show |
intron_variant | MODIFIER | c.1369+6893G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111038607 | ||||||
| chr2:111038618
|
T | C | 23 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(20): Show | 23 | HG00140.hp2 HG01168.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1369+6904T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111038618 | ||||||
| chr2:111038901
|
A | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1369+7187A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111038901 | ||||||
| chr2:111039126
|
A | T | 124 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.1369+7412A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111039126 | ||||||
| chr2:111039256
|
A | G | 70 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(67): Show | 70 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1369+7542A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111039256 | ||||||
| chr2:111039409
|
G | GA | 24 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 24 | HG00140.hp1 HG00544.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.1369+7706dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 111039409 | |||||
| chr2:111039728
|
T | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(33): Show | 36 | HG00140.hp1 HG00544.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1369+8014T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111039728 | ||||||
| chr2:111039736
|
G | A | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1369+8022G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111039736 | ||||||
| chr2:111039818
|
A | G | 102 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1369+8104A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111039818 | ||||||
| chr2:111039881
|
A | G | 12 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0088others(9): Show | 12 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1369+8167A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111039881 | ||||||
| chr2:111039897
|
G | T | 1 | a0009c0016t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1369+8183G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111039897 | ||||||
| chr2:111039950
|
C | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1369+8236C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111039950 | ||||||
| chr2:111039954
|
C | T | 125 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1369+8240C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111039954 | ||||||
| chr2:111039988
|
T | C | 48 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0028others(45): Show | 48 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1369+8274T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111039988 | ||||||
| chr2:111040034
|
T | C | 6 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0003t0001g0090others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1369+8320T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111040034 | ||||||
| chr2:111040069
|
T | C | 1 | a0001c0001t0005g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1369+8355T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111040069 | ||||||
| chr2:111040102
|
T | G | 12 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0058others(9): Show | 12 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1369+8388T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111040102 | ||||||
| chr2:111040179
|
G | A | 22 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0042others(19): Show | 22 | HG00140.hp2 HG01168.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1369+8465G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111040179 | ||||||
| chr2:111040224
|
C | T | 15 | a0001c0001t0001g0031a0001c0001t0001g0067a0001c0001t0002g0032others(12): Show | 15 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(12): Show |
intron_variant | MODIFIER | c.1369+8510C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111040224 | ||||||
| chr2:111040311
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1369+8597G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111040311 | ||||||
| chr2:111040343
|
A | G | 12 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0088others(9): Show | 12 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1369+8629A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111040343 | ||||||
| chr2:111040491
|
T | C | 4 | a0001c0001t0001g0129a0004c0005t0001g0134a0004c0005t0002g0124others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370-8727T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111040491 | ||||||
| chr2:111040593
|
T | C | 1 | a0002c0002t0002g0013 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1370-8625T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111040593 | ||||||
| chr2:111040828
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1370-8390G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111040828 | ||||||
| chr2:111041016
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1370-8202G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111041016 | ||||||
| chr2:111041081
|
G | A | 12 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0088others(9): Show | 12 | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1370-8137G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111041081 | ||||||
| chr2:111041247
|
C | G | 28 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0039others(25): Show | 28 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1370-7971C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111041247 | ||||||
| chr2:111041279
|
C | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1370-7939C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111041279 | ||||||
| chr2:111041324
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1370-7894C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111041324 | ||||||
| chr2:111041697
|
C | T | 4 | a0001c0001t0001g0129a0004c0005t0001g0134a0004c0005t0002g0124others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370-7521C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111041697 | ||||||
| chr2:111041757
|
G | C | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1370-7461G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111041757 | ||||||
| chr2:111041758
|
A | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1370-7460A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111041758 | ||||||
| chr2:111041913
|
C | G | 1 | a0004c0005t0002g0020 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1370-7305C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111041913 | ||||||
| chr2:111042039
|
C | A | 2 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1370-7179C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111042039 | ||||||
| chr2:111042275
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1370-6943C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111042275 | ||||||
| chr2:111042480
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1370-6738C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111042480 | ||||||
| chr2:111042495
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0077others(6): Show | 9 | HG00673.hp2 HG01243.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1370-6723G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111042495 | ||||||
| chr2:111042586
|
T | G | 2 | a0002c0002t0001g0051a0002c0002t0003g0139 | 2 | NA18974.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1370-6632T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111042586 | ||||||
| chr2:111042637
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0002g0076a0001c0001t0002g0078 | 3 | HG02027.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1370-6581T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111042637 | ||||||
| chr2:111042953
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1370-6265T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111042953 | ||||||
| chr2:111042961
|
T | C | 71 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0011others(68): Show | 71 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1370-6257T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111042961 | ||||||
| chr2:111042993
|
T | C | 1 | a0002c0002t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1370-6225T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111042993 | ||||||
| chr2:111043011
|
C | T | 1 | a0001c0003t0001g0075 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1370-6207C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111043011 | ||||||
| chr2:111043103
|
G | A | 23 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0045others(20): Show | 23 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(20): Show |
intron_variant | MODIFIER | c.1370-6115G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111043103 | ||||||
| chr2:111043134
|
A | T | 1 | a0001c0001t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1370-6084A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111043134 | ||||||
| chr2:111043143
|
C | T | 1 | a0003c0004t0003g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1370-6075C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111043143 | ||||||
| chr2:111043491
|
C | T | 28 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(25): Show | 28 | HG00140.hp1 HG00544.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1370-5727C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111043491 | ||||||
| chr2:111043582
|
C | T | 4 | a0001c0001t0001g0145a0002c0002t0001g0019a0002c0002t0001g0135others(1): Show | 4 | HG01167.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370-5636C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111043582 | ||||||
| chr2:111043590
|
G | A | 4 | a0001c0001t0001g0129a0004c0005t0001g0134a0004c0005t0002g0124others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370-5628G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111043590 | ||||||
| chr2:111043799
|
G | T | 4 | a0001c0001t0001g0145a0002c0002t0001g0019a0002c0002t0001g0135others(1): Show | 4 | HG01167.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370-5419G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111043799 | ||||||
| chr2:111043825
|
A | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1370-5393A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111043825 | ||||||
| chr2:111043888
|
C | G | 1 | a0001c0001t0002g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1370-5330C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111043888 | ||||||
| chr2:111043910
|
G | T | 2 | a0007c0009t0001g0092a0007c0009t0001g0106 | 2 | HG00099.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1370-5308G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111043910 | ||||||
| chr2:111043979
|
T | G | 28 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0039others(25): Show | 28 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1370-5239T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111043979 | ||||||
| chr2:111044280
|
A | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1370-4938A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111044280 | ||||||
| chr2:111044356
|
G | C | 3 | a0001c0001t0001g0129a0004c0005t0001g0134a0004c0005t0002g0124 | 3 | HG01243.hp2 HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1370-4862G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111044356 | ||||||
| chr2:111044455
|
G | A | 27 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(24): Show | 27 | HG00140.hp1 HG00544.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1370-4763G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111044455 | ||||||
| chr2:111044528
|
C | T | 36 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(33): Show | 36 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.1370-4690C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111044528 | ||||||
| chr2:111044961
|
A | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1370-4257A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111044961 | ||||||
| chr2:111044976
|
C | G | 1 | a0003c0004t0001g0027 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1370-4242C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111044976 | ||||||
| chr2:111045323
|
G | C | 1 | a0004c0005t0001g0070 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1370-3895G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111045323 | ||||||
| chr2:111045506
|
G | A | 1 | a0006c0006t0001g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1370-3712G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111045506 | ||||||
| chr2:111045605
|
CTCTCAGG others(4): Show |
C | 45 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(42): Show | 45 | HG00140.hp1 HG00544.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1370-3609_1370-359 others(15): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 111045605 | |||||
| chr2:111045614
|
A | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1370-3604A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111045614 | ||||||
| chr2:111045733
|
A | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1370-3485A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111045733 | ||||||
| chr2:111045908
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1370-3310C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111045908 | ||||||
| chr2:111046028
|
C | T | 1 | a0006c0006t0001g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1370-3190C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111046028 | ||||||
| chr2:111046059
|
C | T | 6 | a0001c0001t0001g0045a0001c0001t0001g0129a0001c0001t0006g0017others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1370-3159C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111046059 | ||||||
| chr2:111046144
|
A | C | 1 | a0001c0001t0001g0038 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1370-3074A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111046144 | ||||||
| chr2:111046145
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1370-3073C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111046145 | ||||||
| chr2:111046147
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1370-3071G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111046147 | ||||||
| chr2:111046481
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1370-2737C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111046481 | ||||||
| chr2:111046839
|
T | A | 1 | a0001c0001t0002g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1370-2379T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111046839 | ||||||
| chr2:111046840
|
C | A | 1 | a0001c0001t0002g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1370-2378C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111046840 | ||||||
| chr2:111046864
|
CG | C | 6 | a0001c0001t0001g0045a0001c0001t0001g0129a0001c0001t0006g0017others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1370-2350delG | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 111046864 | |||||
| chr2:111046934
|
C | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(25): Show | 28 | HG00140.hp1 HG00544.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1370-2284C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111046934 | ||||||
| chr2:111047017
|
G | C | 2 | a0001c0001t0002g0076a0001c0001t0002g0078 | 2 | NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1370-2201G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111047017 | ||||||
| chr2:111047297
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1370-1921G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111047297 | ||||||
| chr2:111047478
|
T | A | 1 | a0002c0002t0003g0142 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1370-1740T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111047478 | ||||||
| chr2:111047552
|
C | A | 2 | a0001c0001t0005g0149a0012c0018t0001g0053 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1370-1666C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111047552 | ||||||
| chr2:111047678
|
A | T | 10 | a0001c0001t0001g0028a0001c0001t0001g0085a0001c0001t0001g0110others(7): Show | 10 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(7): Show |
intron_variant | MODIFIER | c.1370-1540A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111047678 | ||||||
| chr2:111047684
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1370-1534C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111047684 | ||||||
| chr2:111047802
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1370-1416G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111047802 | ||||||
| chr2:111047881
|
G | T | 6 | a0001c0001t0001g0063a0001c0003t0001g0090a0002c0002t0002g0147others(3): Show | 6 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1370-1337G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111047881 | ||||||
| chr2:111047916
|
A | T | 1 | a0002c0002t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1370-1302A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111047916 | ||||||
| chr2:111047949
|
T | C | 1 | a0006c0006t0001g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1370-1269T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111047949 | ||||||
| chr2:111048118
|
C | T | 3 | a0001c0001t0002g0052a0001c0001t0005g0149a0012c0018t0001g0053 | 3 | HG02615.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1370-1100C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111048118 | ||||||
| chr2:111048198
|
G | A | 9 | a0001c0001t0001g0096a0001c0001t0001g0138a0001c0003t0001g0075others(6): Show | 9 | HG00323.hp1 HG00423.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.1370-1020G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111048198 | ||||||
| chr2:111048276
|
A | G | 41 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(38): Show | 41 | HG00140.hp1 HG00544.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.1370-942A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111048276 | ||||||
| chr2:111048337
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1370-881C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111048337 | ||||||
| chr2:111048499
|
G | C | 5 | a0001c0001t0001g0045a0001c0001t0001g0129a0001c0001t0006g0017others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-719G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111048499 | ||||||
| chr2:111048640
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1370-578A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111048640 | ||||||
| chr2:111048654
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1370-564C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111048654 | ||||||
| chr2:111048672
|
A | G | 2 | a0001c0001t0002g0060a0001c0017t0002g0073 | 2 | HG00140.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1370-546A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111048672 | ||||||
| chr2:111048719
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1370-499G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111048719 | ||||||
| chr2:111048720
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1370-498A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111048720 | ||||||
| chr2:111048765
|
C | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1370-453C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111048765 | ||||||
| chr2:111049048
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1370-170C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | 111049048 | ||||||
| chr2:111049450
|
C | T | 47 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0011others(44): Show | 47 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.1440+162C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111049450 | ||||||
| chr2:111049660
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1440+372G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111049660 | ||||||
| chr2:111049726
|
T | C | 89 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1440+438T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111049726 | ||||||
| chr2:111049969
|
G | C | 4 | a0001c0001t0001g0058a0001c0001t0001g0145a0002c0002t0001g0019others(1): Show | 4 | HG01167.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+681G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111049969 | ||||||
| chr2:111050019
|
C | CACTG | 37 | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0011others(34): Show | 37 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.1440+734_1440+735i others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111050019 | |||||
| chr2:111050100
|
G | A | 41 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0063others(38): Show | 41 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1440+812G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111050100 | ||||||
| chr2:111050115
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1440+827C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111050115 | ||||||
| chr2:111050116
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1440+828G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111050116 | ||||||
| chr2:111050228
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1440+940A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111050228 | ||||||
| chr2:111050262
|
TA | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0108others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1440+986delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111050262 | |||||
| chr2:111050281
|
A | C | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1440+993A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111050281 | ||||||
| chr2:111050459
|
A | G | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1440+1171A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111050459 | ||||||
| chr2:111050479
|
TC | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+1193delC | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111050479 | |||||
| chr2:111050501
|
A | G | 127 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1440+1213A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111050501 | ||||||
| chr2:111050598
|
C | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0002g0040others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+1310C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111050598 | ||||||
| chr2:111050808
|
A | G | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1440+1520A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111050808 | ||||||
| chr2:111050939
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1440+1651G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111050939 | ||||||
| chr2:111050981
|
A | G | 55 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0028others(52): Show | 55 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1440+1693A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111050981 | ||||||
| chr2:111051253
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1440+1965G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111051253 | ||||||
| chr2:111051292
|
A | T | 1 | a0001c0001t0001g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1440+2004A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111051292 | ||||||
| chr2:111051426
|
C | T | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1440+2138C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111051426 | ||||||
| chr2:111051453
|
G | A | 127 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1440+2165G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111051453 | ||||||
| chr2:111051500
|
C | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0122a0002c0002t0001g0114others(1): Show | 4 | HG01243.hp1 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+2212C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111051500 | ||||||
| chr2:111051501
|
T | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0122a0002c0002t0001g0114others(1): Show | 4 | HG01243.hp1 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+2213T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111051501 | ||||||
| chr2:111051753
|
C | A | 127 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1440+2465C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111051753 | ||||||
| chr2:111051823
|
A | G | 6 | a0001c0001t0001g0028a0001c0001t0001g0045a0001c0001t0001g0110others(3): Show | 6 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1440+2535A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111051823 | ||||||
| chr2:111052171
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1440+2883C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111052171 | ||||||
| chr2:111052260
|
T | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0110others(4): Show | 7 | HG00323.hp2 HG00438.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1440+2972T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111052260 | ||||||
| chr2:111052357
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+3069G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111052357 | ||||||
| chr2:111052387
|
C | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+3099C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111052387 | ||||||
| chr2:111052443
|
C | G | 7 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0110others(4): Show | 7 | HG00323.hp2 HG00438.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1440+3155C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111052443 | ||||||
| chr2:111052451
|
C | T | 23 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0039others(20): Show | 23 | HG01081.hp1 HG01175.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1440+3163C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111052451 | ||||||
| chr2:111052539
|
G | A | 90 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1440+3251G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111052539 | ||||||
| chr2:111052704
|
A | G | 90 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1440+3416A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111052704 | ||||||
| chr2:111052765
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+3477C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111052765 | ||||||
| chr2:111052804
|
G | A | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1440+3516G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111052804 | ||||||
| chr2:111052929
|
C | T | 1 | a0010c0015t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1440+3641C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111052929 | ||||||
| chr2:111052937
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0068others(1): Show | 4 | HG02451.hp2 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+3649C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111052937 | ||||||
| chr2:111053056
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+3768A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111053056 | ||||||
| chr2:111053267
|
G | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+3979G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111053267 | ||||||
| chr2:111053375
|
T | TTG | 27 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0018others(24): Show | 27 | HG01081.hp1 HG01175.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1440+4100_1440+410 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111053375 | |||||
| chr2:111053529
|
C | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+4241C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111053529 | ||||||
| chr2:111053548
|
G | A | 1 | a0001c0001t0002g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1440+4260G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111053548 | ||||||
| chr2:111053724
|
A | G | 2 | a0001c0001t0001g0045a0011c0010t0002g0009 | 2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1440+4436A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111053724 | ||||||
| chr2:111053744
|
T | C | 2 | a0001c0001t0001g0056a0001c0001t0002g0071 | 2 | HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1440+4456T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111053744 | ||||||
| chr2:111054088
|
C | T | 46 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0063others(43): Show | 46 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.1440+4800C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111054088 | ||||||
| chr2:111054212
|
T | C | 1 | a0001c0001t0001g0025 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1440+4924T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111054212 | ||||||
| chr2:111054225
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0002g0111a0013c0011t0001g0130 | 3 | HG01255.hp1 HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1440+4937C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111054225 | ||||||
| chr2:111054291
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0006g0017a0002c0002t0001g0099others(1): Show | 4 | HG01081.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+5003C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111054291 | ||||||
| chr2:111054456
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1440+5168G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111054456 | ||||||
| chr2:111054620
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1440+5332C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111054620 | ||||||
| chr2:111054646
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1440+5358C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111054646 | ||||||
| chr2:111055040
|
T | C | 127 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1440+5752T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111055040 | ||||||
| chr2:111055048
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1440+5760C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111055048 | ||||||
| chr2:111055076
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0006g0017a0002c0002t0001g0099others(1): Show | 4 | HG01081.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+5788C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111055076 | ||||||
| chr2:111055156
|
G | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1440+5868G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111055156 | ||||||
| chr2:111055508
|
A | C | 54 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0031others(51): Show | 54 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1440+6220A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111055508 | ||||||
| chr2:111055643
|
C | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+6355C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111055643 | ||||||
| chr2:111055674
|
A | T | 2 | a0001c0001t0001g0028a0001c0001t0002g0040 | 2 | HG00323.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1440+6386A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111055674 | ||||||
| chr2:111055953
|
G | A | 1 | a0000c0013t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1440+6665G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111055953 | ||||||
| chr2:111056146
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1440+6858G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111056146 | ||||||
| chr2:111056176
|
T | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0129a0002c0002t0001g0114others(3): Show | 6 | HG01243.hp1 HG01891.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1440+6888T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111056176 | ||||||
| chr2:111056200
|
T | TA | 83 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0012others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1440+6926dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111056200 | |||||
| chr2:111056200
|
T | TAA | 7 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(4): Show | 7 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1440+6925_1440+692 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111056200 | |||||
| chr2:111056324
|
C | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+7036C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111056324 | ||||||
| chr2:111056516
|
T | C | 126 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.1440+7228T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111056516 | ||||||
| chr2:111056517
|
G | A | 1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1440+7229G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111056517 | ||||||
| chr2:111056520
|
G | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0116others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1440+7232G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111056520 | ||||||
| chr2:111056605
|
G | A | 2 | a0002c0002t0001g0114a0002c0002t0001g0132 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1440+7317G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111056605 | ||||||
| chr2:111056788
|
C | CA | 74 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0012others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1440+7520dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111056788 | |||||
| chr2:111056788
|
C | CAA | 7 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0126others(4): Show | 7 | HG02080.hp2 HG02145.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1440+7519_1440+752 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111056788 | |||||
| chr2:111057091
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1440+7803C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111057091 | ||||||
| chr2:111057216
|
C | A | 1 | a0001c0001t0001g0038 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1440+7928C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111057216 | ||||||
| chr2:111057330
|
G | A | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1440+8042G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111057330 | ||||||
| chr2:111057429
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1440+8141G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111057429 | ||||||
| chr2:111057491
|
A | C | 1 | a0001c0001t0002g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1440+8203A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111057491 | ||||||
| chr2:111057565
|
G | A | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1440+8277G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111057565 | ||||||
| chr2:111057740
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+8452A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111057740 | ||||||
| chr2:111057780
|
T | C | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1440+8492T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111057780 | ||||||
| chr2:111057977
|
C | CAG | 126 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.1440+8689_1440+869 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111057977 | ||||||
| chr2:111058015
|
T | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+8727T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111058015 | ||||||
| chr2:111058057
|
T | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(27): Show | 30 | HG00140.hp1 HG00544.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1440+8769T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111058057 | ||||||
| chr2:111058170
|
C | T | 1 | a0006c0006t0001g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1440+8882C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111058170 | ||||||
| chr2:111058286
|
C | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+8998C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111058286 | ||||||
| chr2:111058294
|
C | T | 127 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1440+9006C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111058294 | ||||||
| chr2:111058317
|
T | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+9029T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111058317 | ||||||
| chr2:111058411
|
A | G | 1 | a0003c0004t0004g0140 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1440+9123A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111058411 | ||||||
| chr2:111058415
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1440+9127T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111058415 | ||||||
| chr2:111058558
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+9270G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111058558 | ||||||
| chr2:111058972
|
T | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0077others(8): Show | 11 | HG00673.hp2 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+9684T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111058972 | ||||||
| chr2:111059463
|
T | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+10175T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111059463 | ||||||
| chr2:111059645
|
C | G | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1440+10357C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111059645 | ||||||
| chr2:111059768
|
G | GA | 23 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0039others(20): Show | 23 | HG00140.hp2 HG01081.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1440+10492dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111059768 | |||||
| chr2:111059768
|
G | GAA | 8 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0042others(5): Show | 8 | HG01175.hp1 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1440+10491_1440+10 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111059768 | |||||
| chr2:111059832
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+10544G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111059832 | ||||||
| chr2:111059853
|
AGAG | A | 8 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0042others(5): Show | 8 | HG01175.hp1 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1440+10570_1440+10 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111059853 | |||||
| chr2:111059924
|
A | G | 4 | a0001c0001t0001g0031a0001c0001t0002g0065a0001c0001t0002g0105others(1): Show | 4 | HG00099.hp1 HG02080.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+10636A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111059924 | ||||||
| chr2:111060064
|
G | A | 41 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0063others(38): Show | 41 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1440+10776G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111060064 | ||||||
| chr2:111060211
|
G | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0116others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1440+10923G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111060211 | ||||||
| chr2:111060228
|
T | C | 16 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(13): Show | 16 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.1440+10940T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111060228 | ||||||
| chr2:111060498
|
T | C | 2 | a0001c0001t0001g0056a0001c0001t0002g0071 | 2 | HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1440+11210T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111060498 | ||||||
| chr2:111060582
|
T | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0077others(8): Show | 11 | HG00673.hp2 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+11294T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111060582 | ||||||
| chr2:111060665
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1440+11377G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111060665 | ||||||
| chr2:111060806
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0002g0040 | 3 | HG00323.hp2 HG00438.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1440+11518T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111060806 | ||||||
| chr2:111060909
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1440+11621A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111060909 | ||||||
| chr2:111060928
|
G | A | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1440+11640G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111060928 | ||||||
| chr2:111060930
|
A | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+11642A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111060930 | ||||||
| chr2:111060950
|
A | G | 33 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(30): Show | 33 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1440+11662A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111060950 | ||||||
| chr2:111060976
|
A | G | 1 | a0001c0003t0001g0075 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1440+11688A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111060976 | ||||||
| chr2:111061024
|
G | C | 2 | a0002c0002t0001g0061a0005c0007t0001g0062 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1440+11736G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111061024 | ||||||
| chr2:111061081
|
A | C | 46 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0031others(43): Show | 46 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.1440+11793A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111061081 | ||||||
| chr2:111061102
|
G | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+11814G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111061102 | ||||||
| chr2:111061176
|
T | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+11888T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111061176 | ||||||
| chr2:111061598
|
G | T | 35 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0085others(32): Show | 35 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.1440+12310G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111061598 | ||||||
| chr2:111061600
|
T | C | 1 | a0001c0003t0001g0087 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1440+12312T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111061600 | ||||||
| chr2:111061676
|
T | C | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1440+12388T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111061676 | ||||||
| chr2:111061844
|
C | G | 4 | a0001c0001t0001g0067a0001c0001t0006g0017a0002c0002t0001g0099others(1): Show | 4 | HG01081.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+12556C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111061844 | ||||||
| chr2:111062256
|
A | G | 3 | a0001c0001t0001g0129a0004c0005t0002g0004a0004c0005t0002g0124 | 3 | HG01891.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1440+12968A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111062256 | ||||||
| chr2:111062316
|
T | C | 1 | a0010c0015t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1440+13028T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111062316 | ||||||
| chr2:111062480
|
T | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+13192T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111062480 | ||||||
| chr2:111062613
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+13325G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111062613 | ||||||
| chr2:111062644
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1440+13356G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111062644 | ||||||
| chr2:111062864
|
C | T | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1440+13576C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111062864 | ||||||
| chr2:111062865
|
G | A | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1440+13577G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111062865 | ||||||
| chr2:111063024
|
C | A | 9 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0077others(6): Show | 9 | HG00673.hp2 HG01243.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.1440+13736C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111063024 | ||||||
| chr2:111063338
|
C | T | 7 | a0001c0001t0002g0047a0001c0001t0002g0057a0001c0001t0002g0115others(4): Show | 7 | HG02615.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1440+14050C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111063338 | ||||||
| chr2:111063389
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0108others(2): Show | 5 | HG02258.hp1 HG03831.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+14101G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111063389 | ||||||
| chr2:111063409
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+14121G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111063409 | ||||||
| chr2:111063648
|
CA | C | 4 | a0001c0001t0001g0067a0001c0001t0006g0017a0002c0002t0001g0099others(1): Show | 4 | HG01081.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+14364delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111063648 | |||||
| chr2:111063717
|
A | G | 1 | a0004c0005t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1440+14429A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111063717 | ||||||
| chr2:111063952
|
C | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1440+14664C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111063952 | ||||||
| chr2:111063979
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+14691G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111063979 | ||||||
| chr2:111064023
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+14735A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064023 | ||||||
| chr2:111064151
|
A | T | 1 | a0001c0001t0002g0040 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1440+14863A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064151 | ||||||
| chr2:111064203
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1440+14915A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064203 | ||||||
| chr2:111064252
|
C | G | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1440+14964C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064252 | ||||||
| chr2:111064408
|
A | C | 63 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0024others(60): Show | 63 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1440+15120A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064408 | ||||||
| chr2:111064425
|
C | G | 100 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1440+15137C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064425 | ||||||
| chr2:111064435
|
C | CA | 33 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0035others(30): Show | 33 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1440+15157dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111064435 | |||||
| chr2:111064445
|
AC | A | 4 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132others(1): Show | 4 | HG01243.hp1 HG03195.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+15158delC | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064445 | ||||||
| chr2:111064446
|
C | A | 95 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1440+15158C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064446 | ||||||
| chr2:111064450
|
A | C | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1440+15162A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064450 | ||||||
| chr2:111064457
|
C | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0001g0122others(3): Show | 6 | HG00673.hp2 HG02027.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1440+15169C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064457 | ||||||
| chr2:111064484
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1440+15196C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064484 | ||||||
| chr2:111064615
|
A | G | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1440+15327A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064615 | ||||||
| chr2:111064635
|
G | C | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1440+15347G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064635 | ||||||
| chr2:111064749
|
A | G | 2 | a0001c0001t0001g0034a0002c0002t0001g0103 | 2 | HG01346.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1440+15461A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064749 | ||||||
| chr2:111064760
|
T | C | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1440+15472T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064760 | ||||||
| chr2:111064812
|
G | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0108others(2): Show | 5 | HG02258.hp1 HG03831.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+15524G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064812 | ||||||
| chr2:111064855
|
A | G | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1440+15567A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111064855 | ||||||
| chr2:111065104
|
A | G | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1440+15816A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111065104 | ||||||
| chr2:111065125
|
CTG | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+15839_1440+15 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111065125 | |||||
| chr2:111065188
|
T | G | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1440+15900T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111065188 | ||||||
| chr2:111065291
|
C | T | 1 | a0003c0004t0001g0027 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1440+16003C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111065291 | ||||||
| chr2:111065424
|
A | G | 1 | a0003c0004t0002g0069 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1440+16136A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111065424 | ||||||
| chr2:111065460
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1440+16172G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111065460 | ||||||
| chr2:111065699
|
A | C | 50 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0031others(47): Show | 50 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1440+16411A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111065699 | ||||||
| chr2:111065752
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1440+16464T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111065752 | ||||||
| chr2:111065876
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1440+16588G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111065876 | ||||||
| chr2:111065932
|
A | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0021 | 2 | HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1440+16644A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111065932 | ||||||
| chr2:111066072
|
C | T | 9 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0077others(6): Show | 9 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.1440+16784C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111066072 | ||||||
| chr2:111066085
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+16797A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111066085 | ||||||
| chr2:111066125
|
A | G | 50 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0031others(47): Show | 50 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1440+16837A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111066125 | ||||||
| chr2:111066135
|
C | T | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1440+16847C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111066135 | ||||||
| chr2:111066180
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+16892A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111066180 | ||||||
| chr2:111066258
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0002g0040 | 3 | HG00323.hp2 HG00438.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1440+16970T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111066258 | ||||||
| chr2:111066376
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+17088A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111066376 | ||||||
| chr2:111066378
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1440+17090G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111066378 | ||||||
| chr2:111066516
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1440+17228T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111066516 | ||||||
| chr2:111066884
|
A | C | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1440+17596A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111066884 | ||||||
| chr2:111066959
|
C | T | 6 | a0002c0002t0001g0061a0004c0005t0002g0020a0004c0005t0002g0022others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1440+17671C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111066959 | ||||||
| chr2:111067015
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+17727A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111067015 | ||||||
| chr2:111067479
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0001g0113others(3): Show | 6 | HG00673.hp2 HG02027.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.1440+18191C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111067479 | ||||||
| chr2:111067840
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+18552G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111067840 | ||||||
| chr2:111067882
|
G | T | 33 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0085others(30): Show | 33 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.1440+18594G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111067882 | ||||||
| chr2:111067910
|
A | G | 2 | a0001c0001t0001g0129a0004c0005t0002g0124 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1440+18622A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111067910 | ||||||
| chr2:111067944
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+18656A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111067944 | ||||||
| chr2:111068052
|
A | G | 1 | a0001c0017t0002g0073 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1440+18764A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068052 | ||||||
| chr2:111068303
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+19015C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068303 | ||||||
| chr2:111068583
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+19295G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068583 | ||||||
| chr2:111068593
|
T | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0077others(8): Show | 11 | HG00673.hp2 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+19305T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068593 | ||||||
| chr2:111068644
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1440+19356G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068644 | ||||||
| chr2:111068709
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+19421C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068709 | ||||||
| chr2:111068710
|
G | C | 11 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0116others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1440+19422G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068710 | ||||||
| chr2:111068712
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1440+19424C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068712 | ||||||
| chr2:111068715
|
G | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+19427G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068715 | ||||||
| chr2:111068812
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0110others(4): Show | 7 | HG00323.hp2 HG00438.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1440+19524C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068812 | ||||||
| chr2:111068849
|
A | G | 1 | a0002c0002t0004g0141 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1440+19561A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068849 | ||||||
| chr2:111068890
|
G | C | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1440+19602G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068890 | ||||||
| chr2:111068897
|
A | AATAC | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1440+19622_1440+19 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111068897 | |||||
| chr2:111068905
|
C | T | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1440+19617C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068905 | ||||||
| chr2:111068914
|
G | A | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1440+19626G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111068914 | ||||||
| chr2:111069105
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1440+19817C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111069105 | ||||||
| chr2:111069116
|
C | T | 29 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(26): Show | 29 | HG00140.hp1 HG00544.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1440+19828C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111069116 | ||||||
| chr2:111069145
|
C | CT | 22 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0011others(19): Show | 22 | HG00140.hp2 HG01175.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.1440+19876dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111069145 | |||||
| chr2:111069149
|
T | C | 3 | a0001c0001t0001g0129a0004c0005t0002g0004a0004c0005t0002g0124 | 3 | HG01891.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1440+19861T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111069149 | ||||||
| chr2:111069152
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1440+19864T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111069152 | ||||||
| chr2:111069153
|
T | C | 48 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0031others(45): Show | 48 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.1440+19865T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111069153 | ||||||
| chr2:111069301
|
G | A | 2 | a0004c0005t0002g0004a0004c0005t0002g0124 | 2 | HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1440+20013G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111069301 | ||||||
| chr2:111069377
|
C | T | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1440+20089C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111069377 | ||||||
| chr2:111069409
|
T | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+20121T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111069409 | ||||||
| chr2:111069464
|
T | G | 1 | a0001c0001t0002g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1440+20176T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111069464 | ||||||
| chr2:111069575
|
C | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+20287C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111069575 | ||||||
| chr2:111069901
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+20613A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111069901 | ||||||
| chr2:111070331
|
A | G | 119 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.1440+21043A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111070331 | ||||||
| chr2:111070469
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+21181A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111070469 | ||||||
| chr2:111070489
|
C | A | 1 | a0002c0002t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1440+21201C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111070489 | ||||||
| chr2:111071072
|
C | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+21784C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111071072 | ||||||
| chr2:111071615
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0002g0040 | 2 | HG00323.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1441-21250G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111071615 | ||||||
| chr2:111071633
|
T | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0116others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-21232T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111071633 | ||||||
| chr2:111071844
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-21021A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111071844 | ||||||
| chr2:111071860
|
G | A | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1441-21005G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111071860 | ||||||
| chr2:111072441
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0088 | 2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1441-20424G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111072441 | ||||||
| chr2:111072567
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-20298A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111072567 | ||||||
| chr2:111072696
|
T | G | 29 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(26): Show | 29 | HG00140.hp1 HG00544.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1441-20169T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111072696 | ||||||
| chr2:111072708
|
C | G | 4 | a0001c0001t0001g0067a0001c0001t0006g0017a0002c0002t0001g0099others(1): Show | 4 | HG01081.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441-20157C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111072708 | ||||||
| chr2:111073031
|
T | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 14 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.1441-19834T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111073031 | ||||||
| chr2:111073049
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1441-19816G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111073049 | ||||||
| chr2:111073294
|
G | GATGCCAA others(2): Show |
2 | a0001c0001t0001g0045a0001c0001t0001g0129 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1441-19571_1441-19 others(15): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111073294 | ||||||
| chr2:111073295
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0129 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1441-19570T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111073295 | ||||||
| chr2:111073298
|
T | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0129 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1441-19567T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111073298 | ||||||
| chr2:111073299
|
G | GAA | 2 | a0001c0001t0001g0045a0001c0001t0001g0129 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1441-19566_1441-19 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111073299 | ||||||
| chr2:111073328
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0110others(4): Show | 7 | HG00323.hp2 HG00438.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-19537G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111073328 | ||||||
| chr2:111073497
|
T | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1441-19368T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111073497 | ||||||
| chr2:111073502
|
A | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0108others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1441-19363A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111073502 | ||||||
| chr2:111073601
|
A | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 14 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.1441-19264A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111073601 | ||||||
| chr2:111073738
|
C | G | 2 | a0001c0001t0001g0110a0002c0002t0001g0114 | 2 | HG00438.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1441-19127C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111073738 | ||||||
| chr2:111074061
|
T | A | 4 | a0001c0001t0002g0094a0001c0001t0002g0101a0003c0004t0001g0026others(1): Show | 4 | HG02027.hp1 HG02040.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-18804T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111074061 | ||||||
| chr2:111074124
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0021 | 2 | HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1441-18741T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111074124 | ||||||
| chr2:111074133
|
T | TA | 4 | a0001c0001t0001g0067a0001c0001t0006g0017a0002c0002t0001g0099others(1): Show | 4 | HG01081.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441-18731dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111074133 | |||||
| chr2:111074142
|
T | C | 55 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0031others(52): Show | 55 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1441-18723T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111074142 | ||||||
| chr2:111074144
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0110others(4): Show | 7 | HG00323.hp2 HG00438.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-18721G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111074144 | ||||||
| chr2:111074165
|
GT | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 16 | HG02027.hp2 HG02451.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1441-18687delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111074165 | |||||
| chr2:111074178
|
T | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441-18687T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111074178 | ||||||
| chr2:111074216
|
T | C | 9 | a0000c0013t0001g0046a0001c0001t0001g0044a0001c0001t0002g0111others(6): Show | 9 | HG00140.hp2 HG01255.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1441-18649T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111074216 | ||||||
| chr2:111074488
|
T | A | 43 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0063others(40): Show | 43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.1441-18377T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111074488 | ||||||
| chr2:111074567
|
T | C | 3 | a0001c0001t0001g0085a0002c0002t0001g0051a0002c0002t0003g0139 | 3 | NA18946.hp2 NA18974.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1441-18298T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111074567 | ||||||
| chr2:111074638
|
G | A | 122 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.1441-18227G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111074638 | ||||||
| chr2:111074874
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1441-17991C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111074874 | ||||||
| chr2:111075227
|
C | CT | 54 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0031others(51): Show | 54 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1441-17630dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111075227 | |||||
| chr2:111075275
|
A | G | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1441-17590A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111075275 | ||||||
| chr2:111075465
|
G | GTCTT | 69 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0024others(66): Show | 69 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1441-17397_1441-17 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111075465 | |||||
| chr2:111076067
|
T | G | 1 | a0000c0013t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1441-16798T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111076067 | ||||||
| chr2:111076478
|
T | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-16387T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111076478 | ||||||
| chr2:111076537
|
T | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-16328T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111076537 | ||||||
| chr2:111076628
|
TTTCTC | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-16232_1441-16 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111076628 | |||||
| chr2:111076804
|
G | C | 43 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0063others(40): Show | 43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.1441-16061G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111076804 | ||||||
| chr2:111076809
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0068others(10): Show | 13 | HG02451.hp2 HG02615.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.1441-16056C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111076809 | ||||||
| chr2:111076897
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1441-15968C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111076897 | ||||||
| chr2:111076910
|
C | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0113 | 3 | HG03831.hp1 HG03831.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1441-15955C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111076910 | ||||||
| chr2:111077035
|
A | G | 6 | a0002c0002t0001g0061a0004c0005t0002g0020a0004c0005t0002g0022others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1441-15830A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111077035 | ||||||
| chr2:111077081
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1441-15784A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111077081 | ||||||
| chr2:111077730
|
C | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1441-15135C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111077730 | ||||||
| chr2:111077912
|
T | C | 53 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0031others(50): Show | 53 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1441-14953T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111077912 | ||||||
| chr2:111078020
|
C | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1441-14845C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111078020 | ||||||
| chr2:111078156
|
TCA | T | 43 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0063others(40): Show | 43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.1441-14708_1441-14 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111078156 | ||||||
| chr2:111078304
|
G | A | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1441-14561G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111078304 | ||||||
| chr2:111078343
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1441-14522C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111078343 | ||||||
| chr2:111078361
|
T | G | 4 | a0001c0001t0001g0067a0001c0001t0006g0017a0002c0002t0001g0099others(1): Show | 4 | HG01081.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441-14504T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111078361 | ||||||
| chr2:111078478
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1441-14387G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111078478 | ||||||
| chr2:111078489
|
C | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1441-14376C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111078489 | ||||||
| chr2:111078756
|
A | G | 35 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0085others(32): Show | 35 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.1441-14109A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111078756 | ||||||
| chr2:111078789
|
C | T | 2 | a0004c0005t0002g0004a0004c0005t0002g0124 | 2 | HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1441-14076C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111078789 | ||||||
| chr2:111078932
|
C | T | 4 | a0003c0004t0001g0027a0003c0004t0001g0030a0003c0004t0002g0079others(1): Show | 4 | HG00423.hp2 NA18962.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441-13933C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111078932 | ||||||
| chr2:111078961
|
T | C | 43 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0063others(40): Show | 43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.1441-13904T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111078961 | ||||||
| chr2:111079027
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1441-13838A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111079027 | ||||||
| chr2:111079054
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1441-13811T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111079054 | ||||||
| chr2:111079087
|
A | T | 67 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0024others(64): Show | 67 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1441-13778A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111079087 | ||||||
| chr2:111079394
|
A | T | 1 | a0002c0002t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1441-13471A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111079394 | ||||||
| chr2:111079421
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1441-13444C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111079421 | ||||||
| chr2:111079539
|
A | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1441-13326A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111079539 | ||||||
| chr2:111079823
|
C | CT | 17 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.1441-13030dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111079823 | |||||
| chr2:111079823
|
CT | C | 29 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(26): Show | 29 | HG00140.hp1 HG00544.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1441-13030delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111079823 | |||||
| chr2:111079872
|
C | CA | 36 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0018others(33): Show | 36 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.1441-12978dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111079872 | |||||
| chr2:111079872
|
C | CAA | 19 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0029others(16): Show | 19 | HG00673.hp2 HG02027.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1441-12979_1441-12 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111079872 | |||||
| chr2:111079872
|
CA | C | 6 | a0001c0001t0001g0097a0004c0005t0002g0020a0004c0005t0002g0022others(3): Show | 6 | HG01517.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1441-12978delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111079872 | |||||
| chr2:111080197
|
A | AT | 31 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(28): Show | 31 | HG00140.hp1 HG00544.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1441-12662dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111080197 | |||||
| chr2:111080257
|
C | A | 1 | a0002c0002t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1441-12608C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111080257 | ||||||
| chr2:111080486
|
G | A | 5 | a0001c0003t0001g0041a0001c0003t0002g0043a0001c0003t0002g0083others(2): Show | 5 | HG00544.hp1 NA18946.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-12379G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111080486 | ||||||
| chr2:111080611
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1441-12254G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111080611 | ||||||
| chr2:111080866
|
C | T | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1441-11999C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111080866 | ||||||
| chr2:111080980
|
C | T | 1 | a0004c0005t0002g0127 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1441-11885C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111080980 | ||||||
| chr2:111081235
|
C | G | 1 | a0003c0004t0003g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1441-11630C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111081235 | ||||||
| chr2:111081277
|
G | A | 1 | a0002c0002t0003g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1441-11588G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111081277 | ||||||
| chr2:111081294
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1441-11571C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111081294 | ||||||
| chr2:111081444
|
T | C | 102 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1441-11421T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111081444 | ||||||
| chr2:111081559
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0021 | 2 | HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1441-11306A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111081559 | ||||||
| chr2:111081629
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1441-11236C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111081629 | ||||||
| chr2:111081756
|
T | C | 13 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 13 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1441-11109T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111081756 | ||||||
| chr2:111081781
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0108others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1441-11084G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111081781 | ||||||
| chr2:111082041
|
A | G | 4 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0113others(1): Show | 4 | HG02258.hp1 HG03831.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-10824A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111082041 | ||||||
| chr2:111082061
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1441-10804A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111082061 | ||||||
| chr2:111082112
|
A | T | 1 | a0001c0003t0001g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1441-10753A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111082112 | ||||||
| chr2:111082141
|
A | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(12): Show | 15 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.1441-10724A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111082141 | ||||||
| chr2:111082270
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1441-10595G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111082270 | ||||||
| chr2:111082282
|
T | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(12): Show | 15 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.1441-10583T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111082282 | ||||||
| chr2:111082455
|
A | G | 1 | a0004c0005t0002g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1441-10410A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111082455 | ||||||
| chr2:111082611
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0002g0048a0014c0020t0001g0002 | 3 | HG02257.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1441-10254G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111082611 | ||||||
| chr2:111082637
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1441-10228G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111082637 | ||||||
| chr2:111082727
|
A | T | 1 | a0002c0002t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1441-10138A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111082727 | ||||||
| chr2:111082991
|
G | A | 149 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1441-9874G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111082991 | ||||||
| chr2:111083081
|
T | G | 1 | a0006c0006t0002g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1441-9784T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111083081 | ||||||
| chr2:111083188
|
A | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1441-9677A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111083188 | ||||||
| chr2:111083237
|
G | A | 2 | a0001c0001t0001g0126a0012c0018t0001g0053 | 2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1441-9628G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111083237 | ||||||
| chr2:111083437
|
A | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1441-9428A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111083437 | ||||||
| chr2:111083564
|
G | GT | 9 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0080others(6): Show | 9 | HG00099.hp1 HG02027.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1441-9290dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111083564 | |||||
| chr2:111083571
|
T | G | 2 | a0004c0005t0002g0004a0004c0005t0002g0124 | 2 | HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1441-9294T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111083571 | ||||||
| chr2:111083885
|
A | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0110others(4): Show | 7 | HG00323.hp2 HG00438.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-8980A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111083885 | ||||||
| chr2:111084025
|
G | GA | 4 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0113others(1): Show | 4 | HG02258.hp1 HG03831.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-8831dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111084025 | |||||
| chr2:111084026
|
A | G | 3 | a0001c0001t0001g0129a0004c0005t0002g0004a0004c0005t0002g0124 | 3 | HG01891.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1441-8839A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111084026 | ||||||
| chr2:111084056
|
A | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1441-8809A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111084056 | ||||||
| chr2:111084246
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1441-8619A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111084246 | ||||||
| chr2:111084258
|
T | TAC | 13 | a0001c0001t0001g0011a0001c0001t0001g0082a0001c0001t0001g0138others(10): Show | 13 | HG01081.hp2 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1441-8557_1441-855 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111084258 | |||||
| chr2:111084258
|
TAC | T | 24 | a0000c0013t0001g0046a0001c0001t0001g0031a0001c0001t0001g0034others(21): Show | 24 | HG00099.hp1 HG00423.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1441-8557_1441-855 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111084258 | |||||
| chr2:111084258
|
TACAC | T | 24 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0108others(21): Show | 24 | HG00438.hp1 HG00544.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1441-8559_1441-855 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111084258 | |||||
| chr2:111084258
|
TACACAC | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00140.hp1 HG00140.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.1441-8561_1441-855 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111084258 | |||||
| chr2:111084258
|
TACACACA others(1): Show |
T | 10 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0056others(7): Show | 10 | HG01081.hp1 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1441-8563_1441-855 others(12): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111084258 | |||||
| chr2:111084258
|
TACACACA others(3): Show |
T | 6 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0018others(3): Show | 6 | HG01243.hp1 HG01243.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1441-8565_1441-855 others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111084258 | |||||
| chr2:111084258
|
TACACACA others(5): Show |
T | 3 | a0001c0001t0001g0063a0001c0003t0001g0090a0012c0018t0001g0053 | 3 | HG01928.hp1 HG02004.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1441-8567_1441-855 others(16): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111084258 | |||||
| chr2:111084258
|
TACACACA others(7): Show |
T | 4 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(1): Show | 4 | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441-8569_1441-855 others(18): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111084258 | |||||
| chr2:111084258
|
TACACACA others(9): Show |
T | 6 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(3): Show | 6 | HG00673.hp2 HG02027.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1441-8571_1441-855 others(20): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111084258 | |||||
| chr2:111084340
|
G | T | 1 | a0002c0002t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1441-8525G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111084340 | ||||||
| chr2:111084442
|
T | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0110others(4): Show | 7 | HG00323.hp2 HG00438.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-8423T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111084442 | ||||||
| chr2:111084730
|
TA | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-8132delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111084730 | |||||
| chr2:111084784
|
T | C | 1 | a0001c0003t0001g0036 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1441-8081T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111084784 | ||||||
| chr2:111084899
|
G | GA | 15 | a0000c0013t0001g0046a0001c0001t0001g0038a0001c0001t0001g0045others(12): Show | 15 | HG00140.hp2 HG00323.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1441-7950dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111084899 | |||||
| chr2:111084899
|
GA | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 18 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.1441-7950delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111084899 | |||||
| chr2:111084985
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-7880G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111084985 | ||||||
| chr2:111085171
|
C | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 13 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1441-7694C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111085171 | ||||||
| chr2:111085319
|
A | C | 1 | a0002c0002t0001g0023 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1441-7546A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111085319 | ||||||
| chr2:111085373
|
A | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1441-7492A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111085373 | ||||||
| chr2:111085589
|
T | C | 72 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0024others(69): Show | 72 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.1441-7276T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111085589 | ||||||
| chr2:111085666
|
GA | G | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1441-7197delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111085666 | |||||
| chr2:111085973
|
G | A | 4 | a0001c0001t0001g0067a0001c0001t0006g0017a0002c0002t0001g0099others(1): Show | 4 | HG01081.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441-6892G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111085973 | ||||||
| chr2:111086463
|
C | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1441-6402C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111086463 | ||||||
| chr2:111086633
|
C | T | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1441-6232C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111086633 | ||||||
| chr2:111086685
|
A | G | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1441-6180A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111086685 | ||||||
| chr2:111087011
|
A | T | 1 | a0004c0005t0002g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1441-5854A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111087011 | ||||||
| chr2:111087265
|
C | G | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1441-5600C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111087265 | ||||||
| chr2:111087283
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0129 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1441-5582A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111087283 | ||||||
| chr2:111087561
|
G | A | 10 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0037others(7): Show | 10 | HG00140.hp1 HG00544.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1441-5304G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111087561 | ||||||
| chr2:111087606
|
T | C | 7 | a0001c0001t0002g0047a0001c0001t0002g0057a0001c0001t0002g0115others(4): Show | 7 | HG02615.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1441-5259T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111087606 | ||||||
| chr2:111087845
|
A | G | 35 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0085others(32): Show | 35 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.1441-5020A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111087845 | ||||||
| chr2:111087934
|
C | T | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1441-4931C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111087934 | ||||||
| chr2:111088087
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0110others(5): Show | 8 | HG00323.hp2 HG00438.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1441-4778A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111088087 | ||||||
| chr2:111088252
|
A | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0129 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1441-4613A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111088252 | ||||||
| chr2:111088482
|
G | A | 1 | a0003c0004t0002g0069 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1441-4383G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111088482 | ||||||
| chr2:111088491
|
T | C | 48 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0031others(45): Show | 48 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.1441-4374T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111088491 | ||||||
| chr2:111088620
|
G | A | 2 | a0002c0002t0001g0061a0005c0007t0001g0062 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1441-4245G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111088620 | ||||||
| chr2:111088675
|
A | T | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1441-4190A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111088675 | ||||||
| chr2:111088677
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1441-4188C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111088677 | ||||||
| chr2:111088706
|
A | C | 1 | a0002c0002t0001g0066 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1441-4159A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111088706 | ||||||
| chr2:111088713
|
C | T | 1 | a0010c0015t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1441-4152C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111088713 | ||||||
| chr2:111088756
|
C | T | 1 | a0004c0005t0002g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1441-4109C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111088756 | ||||||
| chr2:111088757
|
A | G | 3 | a0001c0001t0001g0129a0004c0005t0002g0004a0004c0005t0002g0124 | 3 | HG01891.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1441-4108A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111088757 | ||||||
| chr2:111088761
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-4104A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111088761 | ||||||
| chr2:111088861
|
G | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(3): Show | 6 | HG00673.hp2 HG01891.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.1441-4004G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111088861 | ||||||
| chr2:111089072
|
A | G | 92 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0018others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1441-3793A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111089072 | ||||||
| chr2:111089292
|
G | A | 3 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1441-3573G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111089292 | ||||||
| chr2:111089298
|
A | AAAAC | 5 | a0001c0001t0001g0049a0001c0001t0002g0048a0004c0005t0002g0004others(2): Show | 5 | HG02257.hp2 HG03579.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-3539_1441-353 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111089298 | |||||
| chr2:111089298
|
AAAAC | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0113others(1): Show | 4 | HG00140.hp2 HG03831.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-3539_1441-353 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 111089298 | |||||
| chr2:111089501
|
A | T | 60 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0024others(57): Show | 60 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1441-3364A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111089501 | ||||||
| chr2:111089523
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0035others(22): Show | 25 | HG00140.hp1 HG00544.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.1441-3342G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111089523 | ||||||
| chr2:111089534
|
G | A | 1 | a0001c0003t0001g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1441-3331G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111089534 | ||||||
| chr2:111089535
|
A | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0113 | 3 | HG03831.hp1 HG03831.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1441-3330A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111089535 | ||||||
| chr2:111089807
|
G | A | 3 | a0001c0001t0002g0033a0002c0002t0003g0142a0009c0016t0001g0112 | 3 | HG03239.hp2 HG04115.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1441-3058G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111089807 | ||||||
| chr2:111089828
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(2): Show | 5 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-3037C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111089828 | ||||||
| chr2:111089967
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0042others(3): Show | 6 | HG01175.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1441-2898G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111089967 | ||||||
| chr2:111090091
|
C | T | 1 | a0005c0007t0001g0062 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1441-2774C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111090091 | ||||||
| chr2:111090161
|
T | C | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1441-2704T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111090161 | ||||||
| chr2:111090294
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1441-2571C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111090294 | ||||||
| chr2:111090719
|
T | C | 8 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0077others(5): Show | 8 | HG00673.hp2 HG02027.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1441-2146T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111090719 | ||||||
| chr2:111090842
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1441-2023G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111090842 | ||||||
| chr2:111090913
|
G | A | 1 | a0004c0005t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1441-1952G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111090913 | ||||||
| chr2:111091135
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1441-1730G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111091135 | ||||||
| chr2:111091447
|
C | A | 8 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0077others(5): Show | 8 | HG00673.hp2 HG02027.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1441-1418C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111091447 | ||||||
| chr2:111091453
|
C | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0077others(5): Show | 8 | HG00673.hp2 HG02027.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1441-1412C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111091453 | ||||||
| chr2:111091755
|
A | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0113 | 3 | HG03831.hp1 HG03831.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1441-1110A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111091755 | ||||||
| chr2:111092082
|
A | G | 69 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0024others(66): Show | 69 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1441-783A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111092082 | ||||||
| chr2:111092169
|
G | A | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1441-696G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111092169 | ||||||
| chr2:111092170
|
C | T | 1 | a0002c0002t0001g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1441-695C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111092170 | ||||||
| chr2:111092227
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0110others(4): Show | 7 | HG00323.hp2 HG00438.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-638C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111092227 | ||||||
| chr2:111092336
|
T | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0116others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1441-529T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111092336 | ||||||
| chr2:111092638
|
G | A | 15 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(12): Show | 15 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.1441-227G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111092638 | ||||||
| chr2:111092731
|
T | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0113 | 3 | HG03831.hp1 HG03831.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1441-134T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111092731 | ||||||
| chr2:111092850
|
T | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0113 | 3 | HG03831.hp1 HG03831.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1441-15T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | 111092850 | ||||||
| chr2:111092995
|
T | C | 2 | a0004c0005t0002g0004a0004c0005t0002g0124 | 2 | HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1542+29T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111092995 | ||||||
| chr2:111093226
|
CA | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0077others(6): Show | 9 | HG00140.hp1 HG00673.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.1542+278delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111093226 | |||||
| chr2:111093621
|
A | T | 19 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0038others(16): Show | 19 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.1542+655A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111093621 | ||||||
| chr2:111093622
|
T | C | 2 | a0004c0005t0002g0004a0004c0005t0002g0124 | 2 | HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1542+656T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111093622 | ||||||
| chr2:111093635
|
C | T | 34 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0067others(31): Show | 34 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.1542+669C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111093635 | ||||||
| chr2:111093820
|
C | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0002g0040 | 3 | HG00323.hp2 HG00438.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1542+854C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111093820 | ||||||
| chr2:111093922
|
A | G | 62 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(59): Show | 62 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1542+956A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111093922 | ||||||
| chr2:111093984
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0113 | 2 | HG03831.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1542+1018C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111093984 | ||||||
| chr2:111094039
|
A | G | 19 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0038others(16): Show | 19 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.1542+1073A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111094039 | ||||||
| chr2:111094173
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0129 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1542+1207C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111094173 | ||||||
| chr2:111094267
|
T | C | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1542+1301T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111094267 | ||||||
| chr2:111094323
|
C | T | 11 | a0001c0001t0001g0008a0001c0001t0002g0047a0001c0001t0002g0057others(8): Show | 11 | HG02615.hp1 HG02818.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1542+1357C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111094323 | ||||||
| chr2:111094468
|
C | A | 4 | a0000c0013t0001g0046a0001c0001t0006g0017a0004c0005t0002g0127others(1): Show | 4 | HG02258.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1542+1502C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111094468 | ||||||
| chr2:111094622
|
G | T | 1 | a0002c0002t0001g0061 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1542+1656G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111094622 | ||||||
| chr2:111094789
|
A | G | 11 | a0000c0013t0001g0046a0001c0001t0001g0028a0001c0001t0001g0108others(8): Show | 11 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1542+1823A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111094789 | ||||||
| chr2:111095196
|
G | T | 1 | a0001c0012t0002g0131 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1542+2230G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111095196 | ||||||
| chr2:111095222
|
G | GA | 138 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.1542+2271dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111095222 | |||||
| chr2:111095222
|
G | GAA | 5 | a0001c0001t0001g0080a0001c0001t0001g0113a0003c0004t0001g0064others(2): Show | 5 | HG01496.hp1 HG02145.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542+2270_1542+227 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111095222 | |||||
| chr2:111095385
|
C | A | 1 | a0005c0007t0001g0062 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1542+2419C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111095385 | ||||||
| chr2:111095391
|
C | CT | 62 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1542+2443dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111095391 | |||||
| chr2:111095391
|
CT | C | 8 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0077others(5): Show | 8 | HG00673.hp2 HG01517.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542+2443delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111095391 | |||||
| chr2:111095506
|
T | G | 7 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0077others(4): Show | 7 | HG00673.hp2 HG02027.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542+2540T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111095506 | ||||||
| chr2:111095570
|
T | C | 7 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0077others(4): Show | 7 | HG00673.hp2 HG02027.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542+2604T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111095570 | ||||||
| chr2:111095580
|
AG | A | 7 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0077others(4): Show | 7 | HG00673.hp2 HG02027.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542+2617delG | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111095580 | |||||
| chr2:111095926
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1542+2960T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111095926 | ||||||
| chr2:111095981
|
T | C | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1542+3015T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111095981 | ||||||
| chr2:111096067
|
A | G | 1 | a0000c0013t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1542+3101A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111096067 | ||||||
| chr2:111096224
|
A | AATTATT | 21 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0055others(18): Show | 21 | HG00544.hp2 HG01258.hp1 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.1542+3283_1542+328 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111096224 | |||||
| chr2:111096224
|
A | AATTATTA others(2): Show |
11 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 11 | HG00140.hp1 HG01167.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1542+3280_1542+328 others(13): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111096224 | |||||
| chr2:111096224
|
A | AATTATTA others(11): Show |
1 | a0004c0005t0002g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1542+3271_1542+328 others(22): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111096224 | |||||
| chr2:111096224
|
AATT | A | 55 | a0000c0013t0001g0046a0001c0001t0001g0028a0001c0001t0001g0029others(52): Show | 55 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1542+3286_1542+328 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111096224 | |||||
| chr2:111096765
|
T | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0001g0113 | 3 | HG03831.hp1 HG03831.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1542+3799T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111096765 | ||||||
| chr2:111096947
|
C | T | 32 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0067others(29): Show | 32 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.1542+3981C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111096947 | ||||||
| chr2:111097094
|
A | G | 56 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1542+4128A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111097094 | ||||||
| chr2:111097468
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1542+4502C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111097468 | ||||||
| chr2:111097596
|
T | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1542+4630T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111097596 | ||||||
| chr2:111097681
|
A | C | 125 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1542+4715A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111097681 | ||||||
| chr2:111097940
|
T | C | 4 | a0001c0001t0001g0122a0001c0001t0001g0129a0004c0005t0002g0004others(1): Show | 4 | HG01891.hp1 HG02258.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1542+4974T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111097940 | ||||||
| chr2:111098475
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1542+5509G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111098475 | ||||||
| chr2:111098480
|
G | A | 41 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | HG00140.hp2 HG00673.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.1542+5514G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111098480 | ||||||
| chr2:111098678
|
T | A | 3 | a0001c0001t0001g0129a0004c0005t0002g0004a0004c0005t0002g0124 | 3 | HG01891.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1542+5712T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111098678 | ||||||
| chr2:111098716
|
A | G | 52 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(49): Show | 52 | HG00140.hp2 HG00673.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.1542+5750A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111098716 | ||||||
| chr2:111098856
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1542+5890T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111098856 | ||||||
| chr2:111099196
|
T | C | 57 | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(54): Show | 57 | HG00140.hp2 HG00673.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.1542+6230T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111099196 | ||||||
| chr2:111099884
|
A | T | 1 | a0001c0001t0001g0029 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1542+6918A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111099884 | ||||||
| chr2:111100084
|
C | T | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1542+7118C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111100084 | ||||||
| chr2:111100248
|
A | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0045a0001c0001t0001g0129 | 3 | HG02818.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1542+7282A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111100248 | ||||||
| chr2:111100268
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0002g0048 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1542+7302A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111100268 | ||||||
| chr2:111100531
|
T | C | 1 | a0006c0006t0001g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1542+7565T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111100531 | ||||||
| chr2:111100602
|
C | T | 5 | a0001c0001t0001g0056a0001c0001t0001g0110a0001c0001t0002g0052others(2): Show | 5 | HG00438.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1542+7636C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111100602 | ||||||
| chr2:111100950
|
A | G | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1542+7984A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111100950 | ||||||
| chr2:111101104
|
G | T | 1 | a0001c0001t0001g0097 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1542+8138G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111101104 | ||||||
| chr2:111101400
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1542+8434C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111101400 | ||||||
| chr2:111101602
|
G | A | 1 | a0002c0019t0001g0095 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1542+8636G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111101602 | ||||||
| chr2:111101656
|
G | GA | 19 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0122others(16): Show | 19 | HG00673.hp1 HG01081.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1542+8704dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111101656 | |||||
| chr2:111101710
|
C | A | 19 | a0001c0001t0001g0082a0001c0001t0002g0052a0001c0001t0002g0094others(16): Show | 19 | HG00673.hp1 HG01081.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1542+8744C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111101710 | ||||||
| chr2:111101818
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1542+8852G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111101818 | ||||||
| chr2:111102197
|
A | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0024others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542+9231A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111102197 | ||||||
| chr2:111102626
|
C | T | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1542+9660C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111102626 | ||||||
| chr2:111102646
|
CA | C | 24 | a0001c0001t0001g0082a0001c0001t0002g0052a0001c0001t0002g0094others(21): Show | 24 | HG00673.hp1 HG01081.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.1542+9690delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111102646 | |||||
| chr2:111102777
|
G | A | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1542+9811G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111102777 | ||||||
| chr2:111103026
|
C | A | 1 | a0001c0001t0002g0060 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1542+10060C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111103026 | ||||||
| chr2:111103210
|
A | G | 27 | a0001c0001t0001g0025a0001c0001t0001g0082a0001c0001t0001g0145others(24): Show | 27 | HG00673.hp1 HG01081.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1542+10244A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111103210 | ||||||
| chr2:111103350
|
A | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0049others(6): Show | 9 | HG01167.hp1 HG01175.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1542+10384A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111103350 | ||||||
| chr2:111103469
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1542+10503C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111103469 | ||||||
| chr2:111103495
|
A | T | 1 | a0001c0001t0001g0097 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1542+10529A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111103495 | ||||||
| chr2:111103514
|
T | C | 3 | a0001c0001t0001g0025a0004c0005t0001g0134a0012c0018t0001g0053 | 3 | HG01243.hp2 NA18974.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1542+10548T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111103514 | ||||||
| chr2:111103764
|
AT | A | 19 | a0001c0001t0002g0052a0001c0001t0002g0094a0001c0001t0002g0101others(16): Show | 19 | HG00673.hp1 HG01175.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1542+10808delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111103764 | |||||
| chr2:111103916
|
T | C | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1542+10950T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111103916 | ||||||
| chr2:111104100
|
CT | C | 20 | a0001c0001t0002g0052a0001c0001t0002g0094a0001c0001t0002g0101others(17): Show | 20 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1542+11140delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111104100 | |||||
| chr2:111104261
|
G | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0060a0001c0001t0002g0107others(5): Show | 8 | HG00140.hp2 HG01168.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1542+11295G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111104261 | ||||||
| chr2:111104416
|
T | A | 22 | a0001c0001t0001g0145a0001c0001t0002g0052a0001c0001t0002g0094others(19): Show | 22 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.1542+11450T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111104416 | ||||||
| chr2:111104490
|
A | C | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1542+11524A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111104490 | ||||||
| chr2:111104726
|
T | C | 55 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(52): Show | 55 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1542+11760T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111104726 | ||||||
| chr2:111104878
|
T | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0121 | 3 | HG01891.hp2 HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1542+11912T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111104878 | ||||||
| chr2:111104897
|
A | C | 2 | a0001c0001t0002g0006a0004c0005t0002g0124 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1542+11931A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111104897 | ||||||
| chr2:111104939
|
C | G | 1 | a0005c0007t0001g0062 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1542+11973C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111104939 | ||||||
| chr2:111105244
|
T | C | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1542+12278T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111105244 | ||||||
| chr2:111105273
|
A | G | 1 | a0001c0003t0001g0075 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1542+12307A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111105273 | ||||||
| chr2:111105390
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1543-12226A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111105390 | ||||||
| chr2:111105449
|
C | G | 3 | a0001c0001t0001g0145a0002c0002t0001g0019a0002c0002t0001g0061 | 3 | HG01167.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1543-12167C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111105449 | ||||||
| chr2:111105558
|
T | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0049others(4): Show | 7 | HG01175.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1543-12058T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111105558 | ||||||
| chr2:111105861
|
T | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1543-11755T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111105861 | ||||||
| chr2:111106062
|
C | T | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1543-11554C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111106062 | ||||||
| chr2:111106083
|
T | C | 13 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0024others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1543-11533T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111106083 | ||||||
| chr2:111106181
|
C | G | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1543-11435C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111106181 | ||||||
| chr2:111106223
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0150a0001c0001t0005g0149 | 3 | HG02922.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1543-11393T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111106223 | ||||||
| chr2:111106417
|
CT | C | 5 | a0001c0001t0002g0060a0001c0001t0002g0107a0001c0001t0002g0125others(2): Show | 5 | HG00140.hp2 HG01168.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1543-11189delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111106417 | |||||
| chr2:111106684
|
C | G | 1 | a0000c0014t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1543-10932C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111106684 | ||||||
| chr2:111106883
|
G | A | 1 | a0002c0002t0001g0023 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1543-10733G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111106883 | ||||||
| chr2:111106928
|
C | T | 2 | a0001c0001t0002g0125a0002c0002t0002g0014 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1543-10688C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111106928 | ||||||
| chr2:111107084
|
G | A | 2 | a0001c0001t0001g0096a0002c0002t0001g0135 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1543-10532G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111107084 | ||||||
| chr2:111107133
|
G | C | 1 | a0001c0001t0001g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1543-10483G>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111107133 | ||||||
| chr2:111107239
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0117others(2): Show | 5 | HG01167.hp1 HG01175.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1543-10377A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111107239 | ||||||
| chr2:111107338
|
C | T | 20 | a0001c0001t0002g0052a0001c0001t0002g0094a0001c0001t0002g0101others(17): Show | 20 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1543-10278C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111107338 | ||||||
| chr2:111107433
|
A | C | 1 | a0001c0001t0001g0085 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1543-10183A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111107433 | ||||||
| chr2:111107458
|
G | T | 2 | a0001c0001t0002g0125a0002c0002t0002g0014 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1543-10158G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111107458 | ||||||
| chr2:111107724
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0045others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1543-9892G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111107724 | ||||||
| chr2:111108067
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1543-9549C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111108067 | ||||||
| chr2:111108118
|
T | C | 2 | a0001c0001t0002g0076a0001c0001t0002g0078 | 2 | NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1543-9498T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111108118 | ||||||
| chr2:111108371
|
C | CTTTTT | 22 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0024others(19): Show | 22 | HG00323.hp1 HG01168.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1543-9226_1543-922 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111108371 | |||||
| chr2:111108371
|
C | CTTTTTT | 35 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0021others(32): Show | 35 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.1543-9227_1543-922 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111108371 | |||||
| chr2:111108371
|
C | CTTTTTTT | 30 | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0011others(27): Show | 30 | HG00544.hp2 HG01175.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1543-9228_1543-922 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111108371 | |||||
| chr2:111108371
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0097 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1543-9231_1543-922 others(14): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111108371 | |||||
| chr2:111108371
|
CT | C | 20 | a0001c0001t0001g0145a0001c0001t0002g0052a0001c0001t0002g0094others(17): Show | 20 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.1543-9222delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111108371 | |||||
| chr2:111108371
|
CTTTTTTT others(4): Show |
C | 1 | a0013c0011t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1543-9232_1543-922 others(15): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111108371 | |||||
| chr2:111108558
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1543-9058T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111108558 | ||||||
| chr2:111108817
|
T | A | 1 | a0014c0020t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1543-8799T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111108817 | ||||||
| chr2:111108998
|
G | A | 2 | a0001c0001t0001g0096a0002c0002t0001g0135 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1543-8618G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111108998 | ||||||
| chr2:111109148
|
A | G | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1543-8468A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111109148 | ||||||
| chr2:111109315
|
C | G | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1543-8301C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111109315 | ||||||
| chr2:111109444
|
AT | A | 49 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(46): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1543-8163delT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111109444 | |||||
| chr2:111109671
|
A | AT | 22 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(19): Show | 22 | HG00673.hp2 HG01243.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.1543-7920dupT | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111109671 | |||||
| chr2:111109671
|
A | ATT | 18 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0047others(15): Show | 18 | HG00544.hp1 HG01255.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1543-7921_1543-792 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111109671 | |||||
| chr2:111109671
|
A | ATTT | 11 | a0001c0001t0001g0021a0001c0001t0001g0096a0001c0001t0001g0121others(8): Show | 11 | HG00099.hp1 HG01258.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.1543-7922_1543-792 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111109671 | |||||
| chr2:111109671
|
A | ATTTT | 19 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(16): Show | 19 | HG00323.hp1 HG00438.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.1543-7923_1543-792 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111109671 | |||||
| chr2:111109671
|
ATTT | A | 18 | a0001c0001t0002g0094a0001c0001t0002g0101a0001c0001t0002g0105others(15): Show | 18 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1543-7922_1543-792 others(7): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111109671 | |||||
| chr2:111109710
|
G | A | 2 | a0001c0001t0001g0096a0002c0002t0001g0135 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1543-7906G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111109710 | ||||||
| chr2:111109899
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0117others(2): Show | 5 | HG01167.hp1 HG01175.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1543-7717G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111109899 | ||||||
| chr2:111110315
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1543-7301C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111110315 | ||||||
| chr2:111110402
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0006g0017a0002c0002t0001g0061others(1): Show | 4 | HG02280.hp1 NA18974.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543-7214G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111110402 | ||||||
| chr2:111110433
|
C | A | 23 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0040others(20): Show | 23 | HG00099.hp1 HG00544.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1543-7183C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111110433 | ||||||
| chr2:111110518
|
G | T | 1 | a0001c0001t0001g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1543-7098G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111110518 | ||||||
| chr2:111110730
|
G | A | 8 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0057others(5): Show | 8 | HG02615.hp1 HG02622.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1543-6886G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111110730 | ||||||
| chr2:111110949
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0058 | 2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1543-6667C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111110949 | ||||||
| chr2:111110970
|
G | A | 2 | a0000c0013t0001g0046a0000c0014t0001g0072 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1543-6646G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111110970 | ||||||
| chr2:111111024
|
TTGAG | T | 5 | a0001c0001t0002g0060a0001c0001t0002g0107a0001c0001t0002g0125others(2): Show | 5 | HG00140.hp2 HG01168.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1543-6590_1543-658 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111111024 | |||||
| chr2:111111027
|
A | C | 25 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1543-6589A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111111027 | ||||||
| chr2:111111114
|
T | A | 3 | a0001c0001t0002g0060a0001c0001t0002g0107a0001c0017t0002g0073 | 3 | HG00140.hp2 HG01168.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1543-6502T>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111111114 | ||||||
| chr2:111111172
|
T | C | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1543-6444T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111111172 | ||||||
| chr2:111111659
|
T | G | 1 | a0001c0001t0001g0025 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1543-5957T>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111111659 | ||||||
| chr2:111111740
|
C | A | 2 | a0001c0001t0001g0039a0006c0006t0001g0136 | 2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1543-5876C>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111111740 | ||||||
| chr2:111111859
|
A | G | 1 | a0004c0005t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1543-5757A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111111859 | ||||||
| chr2:111111925
|
T | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0117others(2): Show | 5 | HG01167.hp1 HG01175.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1543-5691T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111111925 | ||||||
| chr2:111112086
|
A | T | 2 | a0001c0001t0001g0096a0002c0002t0001g0135 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1543-5530A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111112086 | ||||||
| chr2:111112155
|
T | C | 1 | a0002c0002t0001g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1543-5461T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111112155 | ||||||
| chr2:111112272
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1543-5344C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111112272 | ||||||
| chr2:111112368
|
A | G | 4 | a0001c0003t0002g0043a0001c0003t0002g0104a0003c0004t0002g0069others(1): Show | 4 | HG00673.hp1 HG02080.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-5248A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111112368 | ||||||
| chr2:111112630
|
C | CA | 5 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0117others(2): Show | 5 | HG01167.hp1 HG01175.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1543-4981dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111112630 | |||||
| chr2:111112643
|
T | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.1543-4973T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111112643 | ||||||
| chr2:111112779
|
A | G | 4 | a0001c0003t0002g0043a0001c0003t0002g0104a0003c0004t0002g0069others(1): Show | 4 | HG00673.hp1 HG02080.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-4837A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111112779 | ||||||
| chr2:111113086
|
G | A | 1 | a0012c0018t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1543-4530G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111113086 | ||||||
| chr2:111113565
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1543-4051A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111113565 | ||||||
| chr2:111113922
|
G | A | 2 | a0001c0001t0006g0017a0002c0002t0001g0061 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1543-3694G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111113922 | ||||||
| chr2:111114038
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1543-3578T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111114038 | ||||||
| chr2:111114137
|
A | C | 1 | a0011c0010t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1543-3479A>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111114137 | ||||||
| chr2:111114299
|
C | T | 2 | a0001c0001t0001g0122a0006c0006t0001g0001 | 2 | HG02258.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1543-3317C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111114299 | ||||||
| chr2:111114320
|
G | A | 49 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0040others(46): Show | 49 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.1543-3296G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111114320 | ||||||
| chr2:111114571
|
A | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1543-3045A>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111114571 | ||||||
| chr2:111114584
|
G | A | 1 | a0001c0003t0001g0090 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1543-3032G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111114584 | ||||||
| chr2:111115029
|
G | A | 1 | a0010c0015t0001g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1543-2587G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111115029 | ||||||
| chr2:111115414
|
A | T | 1 | a0001c0001t0002g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1543-2202A>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111115414 | ||||||
| chr2:111115679
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1543-1937G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111115679 | ||||||
| chr2:111115801
|
T | C | 55 | a0001c0001t0001g0129a0001c0001t0001g0145a0001c0001t0002g0006others(52): Show | 55 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1543-1815T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111115801 | ||||||
| chr2:111115875
|
T | C | 1 | a0001c0001t0001g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1543-1741T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111115875 | ||||||
| chr2:111116090
|
T | C | 2 | a0001c0001t0002g0125a0002c0002t0002g0014 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1543-1526T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111116090 | ||||||
| chr2:111116121
|
G | T | 8 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0057others(5): Show | 8 | HG02615.hp1 HG02622.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1543-1495G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111116121 | ||||||
| chr2:111116173
|
G | T | 1 | a0002c0002t0002g0119 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1543-1443G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111116173 | ||||||
| chr2:111116198
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0117 | 3 | HG01175.hp1 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1543-1418G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111116198 | ||||||
| chr2:111116355
|
G | A | 53 | a0001c0001t0001g0129a0001c0001t0002g0006a0001c0001t0002g0032others(50): Show | 53 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1543-1261G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111116355 | ||||||
| chr2:111116460
|
T | C | 53 | a0001c0001t0001g0129a0001c0001t0002g0006a0001c0001t0002g0032others(50): Show | 53 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1543-1156T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111116460 | ||||||
| chr2:111116483
|
ACTGAAAA others(11): Show |
A | 18 | a0001c0001t0002g0052a0001c0001t0002g0094a0001c0001t0002g0101others(15): Show | 18 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1543-1116_1543-109 others(22): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111116483 | |||||
| chr2:111116586
|
T | C | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1543-1030T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111116586 | ||||||
| chr2:111116617
|
ATGT | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(16): Show | 19 | HG00323.hp1 HG00438.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1543-994_1543-992d others(5): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111116617 | |||||
| chr2:111116699
|
C | T | 51 | a0001c0001t0001g0012a0001c0001t0001g0121a0001c0001t0002g0032others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1543-917C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111116699 | ||||||
| chr2:111116792
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0117others(2): Show | 5 | HG01167.hp1 HG01175.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1543-824G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111116792 | ||||||
| chr2:111116817
|
T | TA | 33 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0024others(30): Show | 33 | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1543-788dupA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111116817 | |||||
| chr2:111116817
|
TA | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(17): Show | 20 | HG00323.hp1 HG00438.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1543-788delA | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 111116817 | |||||
| chr2:111116905
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1543-711C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111116905 | ||||||
| chr2:111116931
|
T | C | 53 | a0001c0001t0001g0129a0001c0001t0002g0006a0001c0001t0002g0032others(50): Show | 53 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1543-685T>C | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111116931 | ||||||
| chr2:111116974
|
G | A | 49 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0040others(46): Show | 49 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.1543-642G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111116974 | ||||||
| chr2:111117022
|
G | A | 1 | a0001c0003t0002g0084 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1543-594G>A | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111117022 | ||||||
| chr2:111117052
|
C | T | 50 | a0001c0001t0001g0129a0001c0001t0002g0006a0001c0001t0002g0032others(47): Show | 50 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1543-564C>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111117052 | ||||||
| chr2:111117117
|
C | G | 2 | a0001c0001t0006g0017a0002c0002t0001g0061 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1543-499C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111117117 | ||||||
| chr2:111117122
|
G | T | 3 | a0001c0001t0002g0060a0001c0001t0002g0107a0001c0017t0002g0073 | 3 | HG00140.hp2 HG01168.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1543-494G>T | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111117122 | ||||||
| chr2:111117132
|
C | G | 1 | a0005c0007t0001g0062 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1543-484C>G | ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | chr2 | 111117132 |