Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55207 |
|---|---|
| ensemblid | ENSG00000134108.14 |
| hgncid | 25564 |
| symbol | ARL8B |
| name | ADP ribosylation factor like GTPase 8B |
| refseq_nuc | NM_018184.3 |
| refseq_prot | NP_060654.1 |
| ensembl_nuc | ENST00000256496.8 |
| ensembl_prot | ENSP00000256496.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 5122292 |
| end | 5180911 |
| strand | + |
| ver | v1.2 |
| region | chr3:5122292-5180911 |
| region5000 | chr3:5117292-5185911 |
| regionname0 | ARL8B_chr3_5122292_5180911 |
| regionname5000 | ARL8B_chr3_5117292_5185911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 186 | 303 | 78 | 56 | 124 | 6 | 37 | 98 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0002 | 0/0 | 186 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| 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 | 1/1 | 561 | 303 | 78 | 56 | 124 | 6 | 37 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| c0002 | 0/0 | 561 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| 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 | 1/0 | 2373 | 137 | 15 | 30 | 69 | 4 | 18 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0002 | 0/1 | 2384 | 131 | 47 | 21 | 43 | 2 | 17 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0003 | 0/0 | 2373 | 7 | 7 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0004 | 0/0 | 2373 | 5 | 0 | 0 | 5 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0005 | 0/0 | 2384 | 3 | 2 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0006 | 0/0 | 2384 | 3 | 0 | 3 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0007 | 0/0 | 2373 | 2 | 0 | 0 | 1 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0008 | 0/0 | 2384 | 2 | 2 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0009 | 0/0 | 2384 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0010 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0011 | 0/0 | 2384 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0012 | 0/0 | 2384 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0013 | 0/0 | 2384 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0014 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0015 | 0/0 | 2384 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0016 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0017 | 0/0 | 2384 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0018 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0019 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0020 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0021 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| t0022 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| 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 | 3 | 0 | 1 | 2 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0242 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 561 | 303 | 78 | 56 | 124 | 6 | 37 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0002c0002 | 0/0 | 561 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2933 | 137 | 15 | 30 | 69 | 4 | 18 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0002 | 0/1 | 2944 | 130 | 47 | 21 | 43 | 2 | 16 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0003 | 0/0 | 2933 | 7 | 7 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0004 | 0/0 | 2933 | 5 | 0 | 0 | 5 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0005 | 0/0 | 2944 | 3 | 2 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0006 | 0/0 | 2944 | 3 | 0 | 3 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0007 | 0/0 | 2933 | 2 | 0 | 0 | 1 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0008 | 0/0 | 2944 | 2 | 2 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0009 | 0/0 | 2944 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0010 | 0/0 | 2933 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0011 | 0/0 | 2944 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0012 | 0/0 | 2944 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0013 | 0/0 | 2944 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0014 | 0/0 | 2933 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0015 | 0/0 | 2944 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0016 | 0/0 | 2933 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0017 | 0/0 | 2944 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0018 | 0/0 | 2933 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0019 | 0/0 | 2933 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0020 | 0/0 | 2933 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0021 | 0/0 | 2933 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0001c0001t0022 | 0/0 | 2933 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| a0002c0002t0002 | 0/0 | 2944 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | copy fasta | chr3 | 5117292 | 5185911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0242 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0005g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0007g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0008g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0010g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0011g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0012g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0013g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0014g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0015g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0016g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0017g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0018g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0019g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0020g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0021g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0001c0001t0022g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00558 | hp2 | a0001 | c0001 | t0021 | g0136 | EAS | CHS | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00738 | hp1 | a0001 | c0001 | t0020 | g0142 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0236 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0235 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0248 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0298 | AMR | PUR | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | CLM | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | CLM | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0063 | EUR | IBS | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | PEL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0123 | EAS | KHV | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CDX | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | CDX | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02257 | hp1 | a0001 | c0001 | t0011 | g0225 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0297 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0296 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0259 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02738 | hp2 | a0001 | c0001 | t0016 | g0006 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02886 | hp2 | a0001 | c0001 | t0012 | g0026 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0216 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0260 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0253 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0214 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | ESN | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | ESN | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ESN | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | MSL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ESN | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | MSL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03225 | hp2 | a0001 | c0001 | t0015 | g0205 | AFR | MSL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | MSL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | MSL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ESN | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ESN | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | MSL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | STU | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0087 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03831 | hp1 | a0001 | c0001 | t0010 | g0268 | SAS | BEB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | BEB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | BEB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | STU | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | STU | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | STU | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0015 | SAS | STU | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | YRI | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | CHB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | YRI | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18941 | hp1 | a0001 | c0001 | t0022 | g0107 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18946 | hp1 | a0001 | c0001 | t0014 | g0196 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18973 | hp2 | a0001 | c0001 | t0019 | g0105 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA18998 | hp2 | a0001 | c0001 | t0017 | g0269 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19012 | hp1 | a0001 | c0001 | t0018 | g0193 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0254 | AFR | LWK | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | LWK | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0286 | AFR | LWK | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | YRI | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ASW | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ASW | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | TSI | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0208 | EUR | TSI | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | GIH | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | GIH | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02109 | hp2 | a0001 | c0001 | t0013 | g0044 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | USA | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | USA | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | LWK | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0242 | REF | REF | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0143 | REF | REF | ARL8B_chr3_5117292_5185911 | ARL8B | chr3 | 5117292 | 5185911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:5174084
|
T | C | 1 | a0002 | 1 | HG04228.hp2 | missense_variant&splice_region_variant | MODERATE | c.440T>C | p.Met147Thr | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 5/7 | 614/2933 | 440/561 | 147/186 | chr3 | 5174084 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:5122314
|
G | T | 1 | a0001c0001t0022 | 1 | NA18941.hp1 | 5_prime_UTR_variant | MODIFIER | c.-152G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/7 | 152 | chr3 | 5122314 | |||||
| chr3:5122331
|
C | G | 1 | a0001c0001t0008 | 2 | HG02895.hp2 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-135C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/7 | 135 | chr3 | 5122331 | |||||
| chr3:5122342
|
C | T | 1 | a0001c0001t0021 | 1 | HG00558.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-124C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/7 | chr3 | 5122342 | ||||||
| chr3:5122368
|
G | T | 1 | a0001c0001t0020 | 1 | HG00738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-98G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/7 | 98 | chr3 | 5122368 | |||||
| chr3:5122450
|
G | C | 4 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(1): Show | 12 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-16G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/7 | 16 | chr3 | 5122450 | |||||
| chr3:5178769
|
G | A | 1 | a0001c0001t0009 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*56G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 56 | chr3 | 5178769 | |||||
| chr3:5179209
|
T | C | 1 | a0001c0001t0011 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*496T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 496 | chr3 | 5179209 | |||||
| chr3:5179326
|
G | C | 1 | a0001c0001t0004 | 5 | NA18962.hp1 NA18964.hp1 NA18983.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*613G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 613 | chr3 | 5179326 | |||||
| chr3:5179383
|
A | G | 1 | a0001c0001t0019 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*670A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 670 | chr3 | 5179383 | |||||
| chr3:5179740
|
G | T | 1 | a0001c0001t0018 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1027G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 1027 | chr3 | 5179740 | |||||
| chr3:5179836
|
C | T | 1 | a0001c0001t0017 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1123C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 1123 | chr3 | 5179836 | |||||
| chr3:5179964
|
G | A | 1 | a0001c0001t0012 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1251G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 1251 | chr3 | 5179964 | |||||
| chr3:5180047
|
T | C | 1 | a0001c0001t0006 | 3 | HG01069.hp1 HG01071.hp1 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1334T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 1334 | chr3 | 5180047 | |||||
| chr3:5180275
|
T | G | 1 | a0001c0001t0013 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1562T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 1562 | chr3 | 5180275 | |||||
| chr3:5180565
|
C | T | 2 | a0001c0001t0010a0001c0001t0016 | 2 | HG02738.hp2 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1852C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 1852 | chr3 | 5180565 | |||||
| chr3:5180649
|
C | T | 1 | a0001c0001t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1936C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 1936 | chr3 | 5180649 | |||||
| chr3:5180651
|
A | G | 1 | a0001c0001t0014 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1938A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 1938 | chr3 | 5180651 | |||||
| chr3:5180747
|
G | T | 1 | a0001c0001t0007 | 2 | HG02080.hp2 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2034G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 2034 | chr3 | 5180747 | |||||
| chr3:5180803
|
G | GAAGGGGA others(4): Show |
11 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(8): Show | 145 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2093_*2094insGGGA others(7): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 7/7 | 2094 | INFO_REALIGN_3_PRIME | chr3 | 5180803 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:5122756
|
G | T | 3 | a0001c0001t0005g0296a0001c0001t0005g0297a0001c0001t0005g0298 | 3 | HG01243.hp2 HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.123+168G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5122756 | ||||||
| chr3:5122915
|
G | A | 1 | a0001c0001t0016g0006 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.123+327G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5122915 | ||||||
| chr3:5123001
|
C | G | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+413C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123001 | ||||||
| chr3:5123084
|
A | G | 47 | a0001c0001t0001g0255a0001c0001t0001g0257a0001c0001t0001g0258others(44): Show | 50 | HG00597.hp2 HG01168.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.123+496A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123084 | ||||||
| chr3:5123170
|
C | G | 92 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(89): Show | 96 | HG00423.hp1 HG00597.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.123+582C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123170 | ||||||
| chr3:5123291
|
G | A | 19 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(16): Show | 20 | HG01109.hp1 HG02135.hp1 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.123+703G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123291 | ||||||
| chr3:5123443
|
G | T | 1 | a0001c0001t0002g0002 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.123+855G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123443 | ||||||
| chr3:5123503
|
G | T | 1 | a0001c0001t0003g0263 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.123+915G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123503 | ||||||
| chr3:5123506
|
T | G | 40 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(37): Show | 43 | HG00597.hp2 HG01106.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.123+918T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123506 | ||||||
| chr3:5123574
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.123+986G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123574 | ||||||
| chr3:5123600
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.123+1012G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123600 | ||||||
| chr3:5123734
|
G | T | 32 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(29): Show | 35 | HG00597.hp2 HG01168.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.123+1146G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123734 | ||||||
| chr3:5123743
|
C | G | 32 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(29): Show | 35 | HG00597.hp2 HG01168.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.123+1155C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123743 | ||||||
| chr3:5123776
|
G | C | 1 | a0001c0001t0001g0025 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.123+1188G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123776 | ||||||
| chr3:5123857
|
C | G | 1 | a0001c0001t0001g0198 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.123+1269C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123857 | ||||||
| chr3:5123865
|
G | A | 33 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0271others(30): Show | 36 | HG00597.hp2 HG01168.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.123+1277G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123865 | ||||||
| chr3:5123868
|
G | T | 33 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0271others(30): Show | 36 | HG00597.hp2 HG01168.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.123+1280G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123868 | ||||||
| chr3:5123883
|
T | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0012g0026 | 3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.123+1295T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123883 | ||||||
| chr3:5123897
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | NA18968.hp1 NA18969.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+1309G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5123897 | ||||||
| chr3:5124139
|
G | A | 30 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0271others(27): Show | 33 | HG00597.hp2 HG01168.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.123+1551G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5124139 | ||||||
| chr3:5124210
|
T | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG00741.hp2 HG01069.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+1622T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5124210 | ||||||
| chr3:5124256
|
A | AT | 24 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0179others(21): Show | 24 | HG01175.hp1 HG01928.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.123+1696dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5124256 | |||||
| chr3:5124256
|
AT | A | 20 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(17): Show | 20 | HG00597.hp1 HG00639.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.123+1696delT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5124256 | |||||
| chr3:5124256
|
ATT | A | 39 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0271others(36): Show | 42 | HG00597.hp2 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.123+1695_123+1696d others(4): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5124256 | |||||
| chr3:5124256
|
ATTTTTTT others(1): Show |
A | 29 | a0001c0001t0002g0004a0001c0001t0002g0079a0001c0001t0002g0080others(26): Show | 30 | HG00408.hp1 HG00423.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.123+1689_123+1696d others(10): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5124256 | |||||
| chr3:5124256
|
ATTTTTTT others(2): Show |
A | 40 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0064others(37): Show | 40 | HG00544.hp1 HG00558.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.123+1688_123+1696d others(11): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5124256 | |||||
| chr3:5124256
|
ATTTTTTT others(3): Show |
A | 3 | a0001c0001t0001g0040a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG03239.hp1 HG04199.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.123+1687_123+1696d others(12): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5124256 | |||||
| chr3:5124256
|
ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG01257.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.123+1686_123+1696d others(13): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5124256 | |||||
| chr3:5124284
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+1696T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5124284 | ||||||
| chr3:5124287
|
G | T | 1 | a0001c0001t0002g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123+1699G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5124287 | ||||||
| chr3:5124388
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.123+1800G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5124388 | ||||||
| chr3:5124423
|
A | G | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+1835A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5124423 | ||||||
| chr3:5124584
|
A | G | 1 | a0001c0001t0002g0290 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.123+1996A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5124584 | ||||||
| chr3:5124698
|
G | C | 55 | a0001c0001t0002g0004a0001c0001t0002g0079a0001c0001t0002g0200others(52): Show | 56 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.123+2110G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5124698 | ||||||
| chr3:5124741
|
A | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+2153A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5124741 | ||||||
| chr3:5124907
|
T | A | 3 | a0001c0001t0005g0296a0001c0001t0005g0297a0001c0001t0009g0286 | 3 | HG02258.hp2 HG02622.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.123+2319T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5124907 | ||||||
| chr3:5124914
|
G | A | 3 | a0001c0001t0005g0296a0001c0001t0005g0297a0001c0001t0009g0286 | 3 | HG02258.hp2 HG02622.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.123+2326G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5124914 | ||||||
| chr3:5124963
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.123+2375A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5124963 | ||||||
| chr3:5124998
|
G | C | 3 | a0001c0001t0005g0296a0001c0001t0005g0297a0001c0001t0009g0286 | 3 | HG02258.hp2 HG02622.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.123+2410G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5124998 | ||||||
| chr3:5125077
|
A | C | 2 | a0001c0001t0002g0285a0001c0001t0002g0294 | 2 | NA18966.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.123+2489A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5125077 | ||||||
| chr3:5125089
|
G | C | 5 | a0001c0001t0002g0291a0001c0001t0005g0296a0001c0001t0005g0297others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+2501G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5125089 | ||||||
| chr3:5125104
|
C | A | 5 | a0001c0001t0002g0291a0001c0001t0005g0296a0001c0001t0005g0297others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+2516C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5125104 | ||||||
| chr3:5125231
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.123+2643A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5125231 | ||||||
| chr3:5125231
|
A | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 5 | NA18970.hp2 NA18980.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+2643A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5125231 | ||||||
| chr3:5125371
|
A | G | 1 | a0001c0001t0002g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123+2783A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5125371 | ||||||
| chr3:5125509
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+2921A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5125509 | ||||||
| chr3:5125536
|
C | CT | 137 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(134): Show | 142 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.123+2962dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5125536 | |||||
| chr3:5125555
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.123+2967C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5125555 | ||||||
| chr3:5125556
|
G | A | 17 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0002g0234others(14): Show | 17 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.123+2968G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5125556 | ||||||
| chr3:5125642
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+3054C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5125642 | ||||||
| chr3:5125911
|
A | G | 6 | a0001c0001t0002g0227a0001c0001t0002g0228a0001c0001t0002g0229others(3): Show | 6 | HG02257.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+3323A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5125911 | ||||||
| chr3:5125933
|
G | A | 139 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(136): Show | 144 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.123+3345G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5125933 | ||||||
| chr3:5125963
|
A | G | 1 | a0001c0001t0002g0073 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.123+3375A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5125963 | ||||||
| chr3:5126117
|
CT | C | 70 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0040others(67): Show | 71 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.123+3543delT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5126117 | |||||
| chr3:5126279
|
A | G | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+3691A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5126279 | ||||||
| chr3:5126312
|
G | T | 139 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(136): Show | 144 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.123+3724G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5126312 | ||||||
| chr3:5126338
|
ATGTAT | A | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | HG02976.hp1 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.123+3753_123+3757d others(7): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5126338 | |||||
| chr3:5126350
|
C | T | 2 | a0001c0001t0002g0245a0001c0001t0002g0246 | 2 | HG01243.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.123+3762C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5126350 | ||||||
| chr3:5126834
|
G | A | 140 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(137): Show | 145 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.123+4246G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5126834 | ||||||
| chr3:5126915
|
C | G | 1 | a0001c0001t0015g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.123+4327C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5126915 | ||||||
| chr3:5126977
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.123+4389G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5126977 | ||||||
| chr3:5127018
|
C | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0012g0026 | 3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.123+4430C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5127018 | ||||||
| chr3:5127189
|
G | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+4601G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5127189 | ||||||
| chr3:5127331
|
C | G | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+4743C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5127331 | ||||||
| chr3:5127442
|
G | T | 3 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0265 | 3 | NA18943.hp1 NA18950.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.123+4854G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5127442 | ||||||
| chr3:5127689
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.123+5101C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5127689 | ||||||
| chr3:5127822
|
A | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0012g0026 | 3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.123+5234A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5127822 | ||||||
| chr3:5127827
|
T | A | 17 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0002g0234others(14): Show | 17 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.123+5239T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5127827 | ||||||
| chr3:5127835
|
T | C | 18 | a0001c0001t0002g0096a0001c0001t0002g0232a0001c0001t0002g0233others(15): Show | 18 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.123+5247T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5127835 | ||||||
| chr3:5127872
|
C | CA | 81 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0081others(78): Show | 84 | HG00597.hp1 HG00597.hp2 HG01074.hp1 others(81): Show |
intron_variant | MODIFIER | c.123+5313dupA | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5127872 | |||||
| chr3:5127872
|
C | CAA | 39 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(36): Show | 39 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.123+5312_123+5313d others(4): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5127872 | |||||
| chr3:5127872
|
C | CAAA | 16 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(13): Show | 16 | HG00544.hp1 HG00558.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.123+5311_123+5313d others(5): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5127872 | |||||
| chr3:5127872
|
C | CAAAA | 10 | a0001c0001t0002g0043a0001c0001t0002g0096a0001c0001t0002g0232others(7): Show | 10 | HG01070.hp1 HG01255.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+5310_123+5313d others(6): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5127872 | |||||
| chr3:5127872
|
C | CAAAAA | 9 | a0001c0001t0002g0042a0001c0001t0002g0080a0001c0001t0002g0233others(6): Show | 9 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.123+5309_123+5313d others(7): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5127872 | |||||
| chr3:5127872
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0088 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.123+5304_123+5313d others(12): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5127872 | |||||
| chr3:5127901
|
A | C | 1 | a0001c0001t0001g0267 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.123+5313A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5127901 | ||||||
| chr3:5128003
|
C | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+5415C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5128003 | ||||||
| chr3:5128157
|
C | T | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+5569C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5128157 | ||||||
| chr3:5128162
|
C | CA | 17 | a0001c0001t0001g0040a0001c0001t0001g0082a0001c0001t0001g0100others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.123+5595dupA | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5128162 | |||||
| chr3:5128162
|
CA | C | 16 | a0001c0001t0001g0197a0001c0001t0002g0004a0001c0001t0002g0068others(13): Show | 17 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.123+5595delA | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5128162 | |||||
| chr3:5128317
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.123+5729G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5128317 | ||||||
| chr3:5128362
|
A | G | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0171others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+5774A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5128362 | ||||||
| chr3:5128396
|
T | A | 1 | a0001c0001t0001g0083 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.123+5808T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5128396 | ||||||
| chr3:5128533
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.123+5945C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5128533 | ||||||
| chr3:5128646
|
A | G | 5 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(2): Show | 5 | HG01168.hp1 NA18944.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+6058A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5128646 | ||||||
| chr3:5128647
|
A | C | 143 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(140): Show | 148 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.123+6059A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5128647 | ||||||
| chr3:5128660
|
A | T | 222 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(219): Show | 227 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(224): Show |
intron_variant | MODIFIER | c.123+6072A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5128660 | ||||||
| chr3:5128671
|
GA | G | 18 | a0001c0001t0002g0096a0001c0001t0002g0232a0001c0001t0002g0233others(15): Show | 18 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.123+6086delA | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5128671 | |||||
| chr3:5128691
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.123+6103A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5128691 | ||||||
| chr3:5128828
|
G | A | 1 | a0001c0001t0002g0287 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.123+6240G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5128828 | ||||||
| chr3:5128896
|
T | G | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.123+6308T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5128896 | ||||||
| chr3:5129012
|
ATT | A | 142 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(139): Show | 147 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.123+6428_123+6429d others(4): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5129012 | |||||
| chr3:5129018
|
C | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0170 | 2 | HG00597.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.123+6430C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5129018 | ||||||
| chr3:5129021
|
A | T | 1 | a0001c0001t0005g0297 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123+6433A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5129021 | ||||||
| chr3:5129180
|
T | TTTTTGTG | 144 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(141): Show | 149 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.123+6598_123+6599i others(9): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5129180 | |||||
| chr3:5129221
|
C | T | 144 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(141): Show | 149 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.123+6633C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5129221 | ||||||
| chr3:5129266
|
T | A | 2 | a0001c0001t0002g0291a0001c0001t0005g0298 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.123+6678T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5129266 | ||||||
| chr3:5129594
|
G | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+7006G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5129594 | ||||||
| chr3:5129622
|
C | A | 2 | a0001c0001t0005g0296a0001c0001t0005g0297 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.123+7034C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5129622 | ||||||
| chr3:5129704
|
G | A | 82 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(79): Show | 86 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.123+7116G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5129704 | ||||||
| chr3:5129710
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.123+7122C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5129710 | ||||||
| chr3:5129751
|
C | A | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0127others(2): Show | 5 | HG00423.hp2 HG02080.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+7163C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5129751 | ||||||
| chr3:5129867
|
CTCTT | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | HG02976.hp1 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.123+7281_123+7284d others(6): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5129867 | |||||
| chr3:5129872
|
T | C | 1 | a0001c0001t0012g0026 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.123+7284T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5129872 | ||||||
| chr3:5129945
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0146 | 2 | HG01081.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.123+7357C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5129945 | ||||||
| chr3:5130185
|
A | T | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+7597A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130185 | ||||||
| chr3:5130187
|
A | AT | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0012g0026 | 3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.123+7599_123+7600i others(3): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130187 | ||||||
| chr3:5130187
|
A | T | 149 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(146): Show | 154 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.123+7599A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130187 | ||||||
| chr3:5130192
|
A | AT | 22 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0096others(19): Show | 22 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.123+7605dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5130192 | |||||
| chr3:5130194
|
A | AT | 78 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(75): Show | 79 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.123+7616dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5130194 | |||||
| chr3:5130194
|
A | ATT | 42 | a0001c0001t0001g0067a0001c0001t0001g0265a0001c0001t0002g0001others(39): Show | 45 | HG00597.hp2 HG01109.hp1 HG01257.hp1 others(42): Show |
intron_variant | MODIFIER | c.123+7615_123+7616d others(4): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5130194 | |||||
| chr3:5130194
|
A | T | 22 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0096others(19): Show | 22 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.123+7606A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130194 | ||||||
| chr3:5130195
|
T | TA | 6 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0005g0296others(3): Show | 6 | HG01243.hp2 HG02040.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+7607_123+7608i others(3): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130195 | ||||||
| chr3:5130196
|
T | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG00741.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.123+7608T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130196 | ||||||
| chr3:5130215
|
C | T | 83 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(80): Show | 87 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.123+7627C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130215 | ||||||
| chr3:5130244
|
G | A | 1 | a0001c0001t0004g0149 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.123+7656G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130244 | ||||||
| chr3:5130244
|
G | T | 1 | a0001c0001t0003g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.123+7656G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130244 | ||||||
| chr3:5130295
|
G | A | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+7707G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130295 | ||||||
| chr3:5130534
|
G | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+7946G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130534 | ||||||
| chr3:5130536
|
T | G | 1 | a0001c0001t0005g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.123+7948T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130536 | ||||||
| chr3:5130628
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.123+8040G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130628 | ||||||
| chr3:5130709
|
T | A | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+8121T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130709 | ||||||
| chr3:5130787
|
C | G | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+8199C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130787 | ||||||
| chr3:5130840
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG00741.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.123+8252G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5130840 | ||||||
| chr3:5131057
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+8469C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5131057 | ||||||
| chr3:5131337
|
A | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0012g0026 | 3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.123+8749A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5131337 | ||||||
| chr3:5131394
|
AT | A | 142 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(139): Show | 147 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.123+8820delT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5131394 | |||||
| chr3:5131395
|
T | A | 8 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0104others(5): Show | 8 | HG01243.hp2 NA18946.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+8807T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5131395 | ||||||
| chr3:5131396
|
T | A | 142 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(139): Show | 147 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.123+8808T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5131396 | ||||||
| chr3:5131397
|
T | A | 61 | a0001c0001t0002g0004a0001c0001t0002g0027a0001c0001t0002g0028others(58): Show | 62 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.123+8809T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5131397 | ||||||
| chr3:5131404
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.123+8816T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5131404 | ||||||
| chr3:5131475
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+8887C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5131475 | ||||||
| chr3:5131503
|
G | A | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+8915G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5131503 | ||||||
| chr3:5131597
|
G | T | 1 | a0001c0001t0005g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.123+9009G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5131597 | ||||||
| chr3:5131669
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.123+9081G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5131669 | ||||||
| chr3:5131716
|
T | A | 18 | a0001c0001t0002g0096a0001c0001t0002g0232a0001c0001t0002g0233others(15): Show | 18 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.123+9128T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5131716 | ||||||
| chr3:5131950
|
C | T | 1 | a0001c0001t0005g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.123+9362C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5131950 | ||||||
| chr3:5132089
|
G | C | 144 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(141): Show | 149 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.123+9501G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5132089 | ||||||
| chr3:5132114
|
A | C | 149 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(146): Show | 154 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.123+9526A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5132114 | ||||||
| chr3:5132146
|
C | T | 83 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(80): Show | 87 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.123+9558C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5132146 | ||||||
| chr3:5132165
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.123+9577G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5132165 | ||||||
| chr3:5132186
|
A | C | 9 | a0001c0001t0001g0054a0001c0001t0001g0064a0001c0001t0001g0065others(6): Show | 9 | NA18970.hp2 NA18973.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.123+9598A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5132186 | ||||||
| chr3:5132406
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.123+9818T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5132406 | ||||||
| chr3:5132449
|
G | A | 18 | a0001c0001t0002g0096a0001c0001t0002g0232a0001c0001t0002g0233others(15): Show | 18 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.123+9861G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5132449 | ||||||
| chr3:5132538
|
T | C | 148 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(145): Show | 153 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.123+9950T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5132538 | ||||||
| chr3:5132605
|
A | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0170 | 2 | HG00597.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.123+10017A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5132605 | ||||||
| chr3:5132638
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0255 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.123+10050T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5132638 | ||||||
| chr3:5132647
|
T | C | 150 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(147): Show | 155 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.123+10059T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5132647 | ||||||
| chr3:5132862
|
G | T | 1 | a0001c0001t0002g0278 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.123+10274G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5132862 | ||||||
| chr3:5132886
|
A | T | 1 | a0001c0001t0002g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123+10298A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5132886 | ||||||
| chr3:5133005
|
A | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 5 | NA18970.hp2 NA18980.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+10417A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133005 | ||||||
| chr3:5133012
|
T | C | 24 | a0001c0001t0001g0025a0001c0001t0001g0082a0001c0001t0001g0089others(21): Show | 24 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.123+10424T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133012 | ||||||
| chr3:5133072
|
C | T | 37 | a0001c0001t0002g0004a0001c0001t0002g0079a0001c0001t0002g0110others(34): Show | 38 | HG00408.hp1 HG00423.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.123+10484C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133072 | ||||||
| chr3:5133087
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.123+10499C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133087 | ||||||
| chr3:5133101
|
G | GA | 148 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(145): Show | 153 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.123+10519dupA | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5133101 | |||||
| chr3:5133223
|
A | AT | 148 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(145): Show | 153 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.123+10636dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5133223 | |||||
| chr3:5133231
|
G | A | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0010g0268 | 3 | HG03239.hp1 HG03831.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.123+10643G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133231 | ||||||
| chr3:5133260
|
A | C | 4 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0071others(1): Show | 4 | HG02976.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+10672A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133260 | ||||||
| chr3:5133353
|
A | G | 1 | a0001c0001t0002g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.123+10765A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133353 | ||||||
| chr3:5133394
|
G | C | 1 | a0001c0001t0001g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.123+10806G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133394 | ||||||
| chr3:5133439
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+10851C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133439 | ||||||
| chr3:5133572
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.123+10984C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133572 | ||||||
| chr3:5133762
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.123+11174C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133762 | ||||||
| chr3:5133845
|
G | A | 148 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(145): Show | 153 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.123+11257G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133845 | ||||||
| chr3:5133873
|
T | C | 1 | a0001c0001t0002g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.123+11285T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133873 | ||||||
| chr3:5133961
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | NA18968.hp1 NA18969.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+11373C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5133961 | ||||||
| chr3:5134107
|
A | AG | 148 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(145): Show | 153 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.123+11519_123+1152 others(5): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5134107 | ||||||
| chr3:5134203
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.123+11615C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5134203 | ||||||
| chr3:5134237
|
C | T | 18 | a0001c0001t0002g0096a0001c0001t0002g0232a0001c0001t0002g0233others(15): Show | 18 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.123+11649C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5134237 | ||||||
| chr3:5134352
|
A | G | 43 | a0001c0001t0001g0265a0001c0001t0002g0001a0001c0001t0002g0002others(40): Show | 47 | HG00597.hp2 HG01109.hp1 HG01257.hp1 others(44): Show |
intron_variant | MODIFIER | c.123+11764A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5134352 | ||||||
| chr3:5134374
|
G | T | 1 | a0001c0001t0005g0297 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123+11786G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5134374 | ||||||
| chr3:5134487
|
A | G | 1 | a0001c0001t0019g0105 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.123+11899A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5134487 | ||||||
| chr3:5134643
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.123+12055A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5134643 | ||||||
| chr3:5134743
|
A | T | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+12155A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5134743 | ||||||
| chr3:5134761
|
A | T | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+12173A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5134761 | ||||||
| chr3:5134802
|
G | A | 1 | a0001c0001t0002g0068 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.123+12214G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5134802 | ||||||
| chr3:5134853
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0169 | 2 | NA18995.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.123+12265C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5134853 | ||||||
| chr3:5134878
|
C | T | 3 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251 | 3 | HG02109.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.123+12290C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5134878 | ||||||
| chr3:5134971
|
C | T | 86 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(83): Show | 90 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.123+12383C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5134971 | ||||||
| chr3:5135005
|
C | T | 1 | a0001c0001t0002g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123+12417C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5135005 | ||||||
| chr3:5135058
|
A | G | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+12470A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5135058 | ||||||
| chr3:5135299
|
A | AT | 144 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(141): Show | 149 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.123+12720dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5135299 | |||||
| chr3:5135302
|
T | TA | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+12714_123+1271 others(5): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5135302 | ||||||
| chr3:5135320
|
A | G | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+12732A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5135320 | ||||||
| chr3:5135339
|
A | AGTGCAGT others(1): Show |
148 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(145): Show | 153 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.123+12758_123+1275 others(12): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5135339 | |||||
| chr3:5135405
|
T | G | 1 | a0001c0001t0002g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.123+12817T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5135405 | ||||||
| chr3:5135497
|
C | T | 1 | a0001c0001t0002g0247 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.123+12909C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5135497 | ||||||
| chr3:5135682
|
C | T | 1 | a0001c0001t0002g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123+13094C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5135682 | ||||||
| chr3:5135732
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.123+13144C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5135732 | ||||||
| chr3:5135737
|
G | A | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+13149G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5135737 | ||||||
| chr3:5135756
|
C | CTAT | 82 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(79): Show | 82 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.123+13212_123+1321 others(7): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5135756 | |||||
| chr3:5135756
|
C | CTATTAT | 25 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0088others(22): Show | 25 | HG00597.hp1 HG00735.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.123+13209_123+1321 others(10): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5135756 | |||||
| chr3:5135756
|
CTAT | C | 7 | a0001c0001t0001g0122a0001c0001t0001g0167a0001c0001t0001g0266others(4): Show | 7 | HG01106.hp2 HG02080.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+13212_123+1321 others(7): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5135756 | |||||
| chr3:5135756
|
CTATTAT | C | 4 | a0001c0001t0001g0124a0001c0001t0001g0189a0001c0001t0001g0270others(1): Show | 4 | HG01109.hp2 HG01934.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+13209_123+1321 others(10): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5135756 | |||||
| chr3:5135756
|
CTATTATT others(2): Show |
C | 9 | a0001c0001t0001g0150a0001c0001t0002g0042a0001c0001t0002g0043others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.123+13206_123+1321 others(13): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5135756 | |||||
| chr3:5135756
|
CTATTATT others(5): Show |
C | 81 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(78): Show | 85 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.123+13203_123+1321 others(16): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5135756 | |||||
| chr3:5135756
|
CTATTATT others(8): Show |
C | 6 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0002g0215others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+13200_123+1321 others(19): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5135756 | |||||
| chr3:5135756
|
CTATTATT others(11): Show |
C | 58 | a0001c0001t0002g0004a0001c0001t0002g0079a0001c0001t0002g0096others(55): Show | 59 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.123+13197_123+1321 others(22): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5135756 | |||||
| chr3:5135756
|
CTATTATT others(14): Show |
C | 1 | a0001c0001t0002g0292 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.123+13194_123+1321 others(25): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5135756 | |||||
| chr3:5135776
|
A | G | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+13188A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5135776 | ||||||
| chr3:5135889
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.123+13301C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5135889 | ||||||
| chr3:5135943
|
C | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+13355C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5135943 | ||||||
| chr3:5136127
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.123+13539G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5136127 | ||||||
| chr3:5136146
|
G | GCA | 145 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(142): Show | 150 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.123+13559_123+1356 others(6): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5136146 | |||||
| chr3:5136288
|
C | T | 1 | a0001c0001t0015g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.123+13700C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5136288 | ||||||
| chr3:5136489
|
T | G | 1 | a0001c0001t0002g0045 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.123+13901T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5136489 | ||||||
| chr3:5136518
|
G | C | 1 | a0001c0001t0015g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.123+13930G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5136518 | ||||||
| chr3:5136663
|
G | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+14075G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5136663 | ||||||
| chr3:5136679
|
G | C | 5 | a0001c0001t0002g0233a0001c0001t0002g0234a0001c0001t0002g0239others(2): Show | 5 | HG00735.hp2 HG01070.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+14091G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5136679 | ||||||
| chr3:5136760
|
GGA | G | 145 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(142): Show | 150 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.123+14177_123+1417 others(6): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5136760 | |||||
| chr3:5136805
|
T | G | 8 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0042others(5): Show | 8 | HG02572.hp1 HG02886.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+14217T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5136805 | ||||||
| chr3:5137018
|
C | T | 1 | a0001c0001t0005g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.123+14430C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5137018 | ||||||
| chr3:5137276
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.123+14688G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5137276 | ||||||
| chr3:5137355
|
A | T | 1 | a0001c0001t0002g0231 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.123+14767A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5137355 | ||||||
| chr3:5137437
|
CT | C | 58 | a0001c0001t0001g0085a0001c0001t0001g0157a0001c0001t0002g0004others(55): Show | 59 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.123+14867delT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5137437 | |||||
| chr3:5137437
|
CTTT | C | 86 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(83): Show | 90 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.123+14865_123+1486 others(7): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5137437 | |||||
| chr3:5137442
|
T | C | 1 | a0001c0001t0002g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123+14854T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5137442 | ||||||
| chr3:5137462
|
G | A | 144 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(141): Show | 149 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.123+14874G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5137462 | ||||||
| chr3:5137472
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.123+14884C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5137472 | ||||||
| chr3:5137627
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.123+15039C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5137627 | ||||||
| chr3:5137720
|
G | A | 1 | a0001c0001t0005g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.123+15132G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5137720 | ||||||
| chr3:5138017
|
G | A | 1 | a0001c0001t0002g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123+15429G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5138017 | ||||||
| chr3:5138107
|
G | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0012g0026 | 3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.123+15519G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5138107 | ||||||
| chr3:5138190
|
G | GT | 128 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(125): Show | 133 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.123+15617dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5138190 | |||||
| chr3:5138190
|
G | GTT | 18 | a0001c0001t0002g0096a0001c0001t0002g0232a0001c0001t0002g0233others(15): Show | 18 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.123+15616_123+1561 others(6): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5138190 | |||||
| chr3:5138761
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0151 | 2 | HG01123.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.123+16173G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5138761 | ||||||
| chr3:5138766
|
A | G | 144 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(141): Show | 149 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.123+16178A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5138766 | ||||||
| chr3:5138903
|
G | A | 1 | a0001c0001t0015g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.123+16315G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5138903 | ||||||
| chr3:5138970
|
C | A | 1 | a0001c0001t0001g0170 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.123+16382C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5138970 | ||||||
| chr3:5139065
|
G | A | 1 | a0001c0001t0002g0008 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.123+16477G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5139065 | ||||||
| chr3:5139115
|
AGAAGG | A | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+16531_123+1653 others(9): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5139115 | |||||
| chr3:5139316
|
C | A | 33 | a0001c0001t0002g0004a0001c0001t0002g0079a0001c0001t0002g0204others(30): Show | 34 | HG00408.hp1 HG00423.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.123+16728C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5139316 | ||||||
| chr3:5139324
|
A | G | 1 | a0001c0001t0002g0211 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.123+16736A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5139324 | ||||||
| chr3:5139459
|
A | G | 42 | a0001c0001t0001g0265a0001c0001t0002g0001a0001c0001t0002g0005others(39): Show | 45 | HG00597.hp2 HG01109.hp1 HG01257.hp1 others(42): Show |
intron_variant | MODIFIER | c.123+16871A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5139459 | ||||||
| chr3:5139504
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+16916T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5139504 | ||||||
| chr3:5139718
|
C | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+17130C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5139718 | ||||||
| chr3:5139756
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.123+17168A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5139756 | ||||||
| chr3:5139987
|
G | GT | 96 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(93): Show | 97 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.123+17416dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5139987 | |||||
| chr3:5139988
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.123+17400T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5139988 | ||||||
| chr3:5139991
|
T | TG | 3 | a0001c0001t0002g0046a0001c0001t0002g0058a0001c0001t0002g0068 | 3 | HG02523.hp1 NA18962.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.123+17403_123+1740 others(5): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5139991 | ||||||
| chr3:5140104
|
A | G | 73 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(70): Show | 74 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.123+17516A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5140104 | ||||||
| chr3:5140143
|
T | C | 145 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(142): Show | 150 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.123+17555T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5140143 | ||||||
| chr3:5140326
|
C | G | 4 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+17738C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5140326 | ||||||
| chr3:5140363
|
T | C | 45 | a0001c0001t0001g0032a0001c0001t0002g0007a0001c0001t0002g0009others(42): Show | 45 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.123+17775T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5140363 | ||||||
| chr3:5140395
|
C | G | 118 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0051others(115): Show | 122 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.123+17807C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5140395 | ||||||
| chr3:5140453
|
C | T | 13 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(10): Show | 13 | HG02109.hp1 HG02258.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.123+17865C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5140453 | ||||||
| chr3:5140544
|
C | A | 119 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(116): Show | 123 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.123+17956C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5140544 | ||||||
| chr3:5140558
|
G | GTT | 63 | a0001c0001t0002g0004a0001c0001t0002g0027a0001c0001t0002g0028others(60): Show | 64 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.123+17981_123+1798 others(6): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5140558 | |||||
| chr3:5140596
|
T | C | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+18008T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5140596 | ||||||
| chr3:5140623
|
C | T | 36 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(33): Show | 36 | HG00544.hp1 HG00558.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.123+18035C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5140623 | ||||||
| chr3:5140742
|
C | T | 44 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(41): Show | 44 | HG00544.hp1 HG00558.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.123+18154C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5140742 | ||||||
| chr3:5140797
|
A | G | 131 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(128): Show | 136 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.123+18209A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5140797 | ||||||
| chr3:5140924
|
T | C | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+18336T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5140924 | ||||||
| chr3:5141018
|
A | C | 99 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(96): Show | 103 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.123+18430A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141018 | ||||||
| chr3:5141079
|
C | T | 3 | a0001c0001t0002g0110a0001c0001t0002g0145a0001c0001t0002g0184 | 3 | HG02698.hp1 HG03927.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.123+18491C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141079 | ||||||
| chr3:5141183
|
C | T | 33 | a0001c0001t0002g0004a0001c0001t0002g0079a0001c0001t0002g0204others(30): Show | 34 | HG00408.hp1 HG00423.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.123+18595C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141183 | ||||||
| chr3:5141252
|
C | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0262 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.123+18664C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141252 | ||||||
| chr3:5141280
|
C | T | 2 | a0001c0001t0002g0245a0001c0001t0002g0246 | 2 | HG01243.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.123+18692C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141280 | ||||||
| chr3:5141514
|
A | C | 98 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(95): Show | 102 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.123+18926A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141514 | ||||||
| chr3:5141649
|
A | C | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+19061A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141649 | ||||||
| chr3:5141652
|
G | C | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+19064G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141652 | ||||||
| chr3:5141676
|
G | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+19088G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141676 | ||||||
| chr3:5141699
|
A | G | 51 | a0001c0001t0002g0004a0001c0001t0002g0079a0001c0001t0002g0096others(48): Show | 52 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.123+19111A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141699 | ||||||
| chr3:5141715
|
G | A | 42 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(39): Show | 46 | HG00597.hp2 HG01109.hp1 HG01257.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+19127G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141715 | ||||||
| chr3:5141721
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG00741.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.123+19133C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141721 | ||||||
| chr3:5141768
|
G | A | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+19180G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141768 | ||||||
| chr3:5141773
|
G | A | 99 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(96): Show | 103 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.123+19185G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141773 | ||||||
| chr3:5141816
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG03239.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.123+19228C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141816 | ||||||
| chr3:5141929
|
T | C | 1 | a0001c0001t0015g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.123+19341T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141929 | ||||||
| chr3:5141978
|
G | A | 5 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0070others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+19390G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5141978 | ||||||
| chr3:5142176
|
T | C | 153 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(150): Show | 158 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.123+19588T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5142176 | ||||||
| chr3:5142215
|
G | A | 18 | a0001c0001t0002g0096a0001c0001t0002g0232a0001c0001t0002g0233others(15): Show | 18 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.123+19627G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5142215 | ||||||
| chr3:5142591
|
C | T | 6 | a0001c0001t0002g0004a0001c0001t0002g0222a0001c0001t0002g0223others(3): Show | 7 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+20003C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5142591 | ||||||
| chr3:5142771
|
A | G | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+20183A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5142771 | ||||||
| chr3:5142818
|
T | C | 1 | a0001c0001t0015g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.123+20230T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5142818 | ||||||
| chr3:5142992
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.123+20404T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5142992 | ||||||
| chr3:5143010
|
A | G | 5 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(2): Show | 5 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+20422A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5143010 | ||||||
| chr3:5143094
|
A | G | 150 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(147): Show | 155 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.123+20506A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5143094 | ||||||
| chr3:5143121
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0181 | 2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.123+20533A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5143121 | ||||||
| chr3:5143157
|
G | T | 1 | a0001c0001t0001g0114 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.123+20569G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5143157 | ||||||
| chr3:5143259
|
A | G | 117 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(114): Show | 121 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.123+20671A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5143259 | ||||||
| chr3:5143273
|
A | G | 97 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(94): Show | 101 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.123+20685A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5143273 | ||||||
| chr3:5143434
|
G | A | 98 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(95): Show | 102 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.123+20846G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5143434 | ||||||
| chr3:5143505
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0188 | 2 | NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.123+20917C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5143505 | ||||||
| chr3:5143555
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.123+20967C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5143555 | ||||||
| chr3:5143556
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.123+20968G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5143556 | ||||||
| chr3:5143661
|
C | G | 1 | a0001c0001t0001g0114 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.123+21073C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5143661 | ||||||
| chr3:5143950
|
T | C | 1 | a0001c0001t0010g0268 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.123+21362T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5143950 | ||||||
| chr3:5144003
|
T | G | 43 | a0001c0001t0001g0265a0001c0001t0002g0001a0001c0001t0002g0002others(40): Show | 47 | HG00597.hp2 HG01109.hp1 HG01257.hp1 others(44): Show |
intron_variant | MODIFIER | c.123+21415T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5144003 | ||||||
| chr3:5144146
|
A | T | 1 | a0001c0001t0002g0217 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.123+21558A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5144146 | ||||||
| chr3:5144379
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.123+21791C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5144379 | ||||||
| chr3:5144839
|
C | G | 2 | a0001c0001t0004g0086a0001c0001t0004g0163 | 2 | NA18962.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.123+22251C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5144839 | ||||||
| chr3:5144949
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.123+22361T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5144949 | ||||||
| chr3:5145012
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.123+22424C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5145012 | ||||||
| chr3:5145087
|
CT | C | 150 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(147): Show | 155 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.123+22502delT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5145087 | |||||
| chr3:5145346
|
C | T | 149 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(146): Show | 154 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.123+22758C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5145346 | ||||||
| chr3:5145382
|
G | A | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+22794G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5145382 | ||||||
| chr3:5145516
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.123+22928A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5145516 | ||||||
| chr3:5145567
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.123+22979C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5145567 | ||||||
| chr3:5145627
|
G | A | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+23039G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5145627 | ||||||
| chr3:5145827
|
AC | A | 150 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(147): Show | 155 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.123+23243delC | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5145827 | |||||
| chr3:5146213
|
A | G | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123+23625A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5146213 | ||||||
| chr3:5146358
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG00741.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.123+23770A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5146358 | ||||||
| chr3:5146361
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.123+23773C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5146361 | ||||||
| chr3:5146476
|
T | G | 1 | a0001c0001t0016g0006 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.123+23888T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5146476 | ||||||
| chr3:5146510
|
G | C | 151 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(148): Show | 156 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.123+23922G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5146510 | ||||||
| chr3:5146537
|
G | C | 1 | a0001c0001t0002g0017 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.123+23949G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5146537 | ||||||
| chr3:5146561
|
T | C | 152 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(149): Show | 157 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.124-23942T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5146561 | ||||||
| chr3:5146649
|
C | A | 4 | a0001c0001t0001g0255a0001c0001t0003g0253a0001c0001t0003g0260others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-23854C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5146649 | ||||||
| chr3:5146747
|
C | T | 150 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(147): Show | 155 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.124-23756C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5146747 | ||||||
| chr3:5146812
|
C | G | 1 | a0001c0001t0015g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.124-23691C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5146812 | ||||||
| chr3:5146874
|
G | A | 33 | a0001c0001t0002g0004a0001c0001t0002g0079a0001c0001t0002g0204others(30): Show | 34 | HG00408.hp1 HG00423.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.124-23629G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5146874 | ||||||
| chr3:5147022
|
C | CT | 149 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(146): Show | 154 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.124-23470dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5147022 | |||||
| chr3:5147123
|
C | G | 1 | a0001c0001t0002g0063 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.124-23380C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5147123 | ||||||
| chr3:5147129
|
G | C | 150 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(147): Show | 155 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.124-23374G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5147129 | ||||||
| chr3:5147184
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0158 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.124-23319G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5147184 | ||||||
| chr3:5147184
|
G | C | 6 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0152others(3): Show | 6 | HG00735.hp1 HG01975.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-23319G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5147184 | ||||||
| chr3:5147238
|
C | A | 2 | a0001c0001t0007g0087a0001c0001t0007g0123 | 2 | HG02080.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.124-23265C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5147238 | ||||||
| chr3:5147244
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.124-23259C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5147244 | ||||||
| chr3:5147250
|
A | G | 95 | a0001c0001t0001g0265a0001c0001t0002g0001a0001c0001t0002g0002others(92): Show | 100 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.124-23253A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5147250 | ||||||
| chr3:5147370
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-23133A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5147370 | ||||||
| chr3:5147428
|
C | G | 1 | a0001c0001t0002g0073 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.124-23075C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5147428 | ||||||
| chr3:5147526
|
TC | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(1): Show | 4 | HG00741.hp2 HG01069.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-22975delC | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5147526 | |||||
| chr3:5147549
|
A | G | 150 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(147): Show | 155 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.124-22954A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5147549 | ||||||
| chr3:5147854
|
A | G | 150 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(147): Show | 155 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.124-22649A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5147854 | ||||||
| chr3:5147907
|
A | G | 151 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(148): Show | 156 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.124-22596A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5147907 | ||||||
| chr3:5147991
|
T | G | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-22512T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5147991 | ||||||
| chr3:5148016
|
G | A | 151 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(148): Show | 156 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.124-22487G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5148016 | ||||||
| chr3:5148102
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.124-22401T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5148102 | ||||||
| chr3:5148214
|
C | T | 152 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(149): Show | 157 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.124-22289C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5148214 | ||||||
| chr3:5148217
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-22286T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5148217 | ||||||
| chr3:5148294
|
T | C | 151 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(148): Show | 156 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.124-22209T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5148294 | ||||||
| chr3:5148315
|
T | A | 5 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-22188T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5148315 | ||||||
| chr3:5148315
|
T | G | 145 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(142): Show | 150 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.124-22188T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5148315 | ||||||
| chr3:5148670
|
G | A | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0274 | 3 | NA18944.hp2 NA18974.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.124-21833G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5148670 | ||||||
| chr3:5148839
|
A | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-21664A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5148839 | ||||||
| chr3:5148861
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.124-21642G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5148861 | ||||||
| chr3:5148987
|
G | A | 1 | a0001c0001t0002g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.124-21516G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5148987 | ||||||
| chr3:5148993
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.124-21510C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5148993 | ||||||
| chr3:5149466
|
TGTGGTAG others(5): Show |
T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-21036_124-2102 others(16): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5149466 | ||||||
| chr3:5149480
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-21023A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5149480 | ||||||
| chr3:5149481
|
C | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-21022C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5149481 | ||||||
| chr3:5149483
|
C | A | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-21020C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5149483 | ||||||
| chr3:5149505
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-20998A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5149505 | ||||||
| chr3:5149613
|
T | C | 5 | a0001c0001t0001g0082a0001c0001t0001g0104a0001c0001t0001g0130others(2): Show | 5 | NA18946.hp2 NA18953.hp1 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-20890T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5149613 | ||||||
| chr3:5149688
|
T | A | 3 | a0001c0001t0006g0235a0001c0001t0006g0236a0001c0001t0006g0248 | 3 | HG01069.hp1 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.124-20815T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5149688 | ||||||
| chr3:5149742
|
T | C | 8 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0200others(5): Show | 8 | HG01106.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-20761T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5149742 | ||||||
| chr3:5150071
|
T | G | 153 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(150): Show | 158 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.124-20432T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5150071 | ||||||
| chr3:5150093
|
A | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-20410A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5150093 | ||||||
| chr3:5150145
|
G | A | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-20358G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5150145 | ||||||
| chr3:5150307
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-20196A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5150307 | ||||||
| chr3:5150323
|
C | T | 5 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-20180C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5150323 | ||||||
| chr3:5150355
|
C | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-20148C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5150355 | ||||||
| chr3:5150428
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-20075A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5150428 | ||||||
| chr3:5150454
|
A | C | 154 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(151): Show | 159 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.124-20049A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5150454 | ||||||
| chr3:5150463
|
A | AAAAT | 4 | a0001c0001t0001g0035a0001c0001t0001g0091a0001c0001t0001g0133others(1): Show | 4 | HG01081.hp1 HG01081.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-20012_124-2000 others(8): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5150463 | |||||
| chr3:5150463
|
A | AAAATAAA others(5): Show |
99 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(96): Show | 103 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.124-20020_124-2000 others(16): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5150463 | |||||
| chr3:5150463
|
A | AAAATAAA others(9): Show |
10 | a0001c0001t0002g0017a0001c0001t0002g0019a0001c0001t0002g0020others(7): Show | 10 | HG01928.hp2 HG02040.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.124-20024_124-2000 others(20): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5150463 | |||||
| chr3:5150463
|
A | AAAATAAA others(13): Show |
1 | a0001c0001t0002g0002 | 2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.124-20028_124-2000 others(24): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5150463 | |||||
| chr3:5150463
|
A | AAAGTAAA others(5): Show |
38 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(35): Show | 38 | HG00544.hp1 HG00558.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.124-20038_124-2003 others(16): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5150463 | |||||
| chr3:5150463
|
A | AAAGTAAA others(9): Show |
2 | a0001c0001t0002g0052a0001c0001t0002g0068 | 2 | HG02027.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.124-20038_124-2003 others(20): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5150463 | |||||
| chr3:5150469
|
A | C | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0080 | 3 | HG02976.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.124-20034A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5150469 | ||||||
| chr3:5150509
|
A | G | 153 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(150): Show | 158 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.124-19994A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5150509 | ||||||
| chr3:5150782
|
C | CAAAAT | 9 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0200others(6): Show | 9 | HG01106.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-19699_124-1969 others(9): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5150782 | |||||
| chr3:5150856
|
T | C | 1 | a0001c0001t0015g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.124-19647T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5150856 | ||||||
| chr3:5150867
|
T | G | 154 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(151): Show | 159 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.124-19636T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5150867 | ||||||
| chr3:5150868
|
G | T | 156 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(153): Show | 161 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.124-19635G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5150868 | ||||||
| chr3:5151007
|
C | T | 1 | a0001c0001t0002g0021 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.124-19496C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151007 | ||||||
| chr3:5151029
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG01257.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.124-19474G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151029 | ||||||
| chr3:5151309
|
G | A | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.124-19194G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151309 | ||||||
| chr3:5151367
|
C | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-19136C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151367 | ||||||
| chr3:5151428
|
G | A | 1 | a0001c0001t0013g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.124-19075G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151428 | ||||||
| chr3:5151450
|
T | C | 68 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(65): Show | 72 | HG00597.hp2 HG00639.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.124-19053T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151450 | ||||||
| chr3:5151497
|
C | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-19006C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151497 | ||||||
| chr3:5151721
|
A | AC | 105 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0033others(102): Show | 105 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.124-18773dupC | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5151721 | |||||
| chr3:5151721
|
A | C | 1 | a0001c0001t0001g0065 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.124-18782A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151721 | ||||||
| chr3:5151724
|
C | A | 2 | a0001c0001t0001g0267a0001c0001t0010g0268 | 2 | HG03239.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.124-18779C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151724 | ||||||
| chr3:5151729
|
C | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0012g0026 | 3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.124-18774C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151729 | ||||||
| chr3:5151730
|
C | CCT | 27 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0002g0005others(24): Show | 28 | HG00639.hp2 HG00735.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.124-18773_124-1877 others(6): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151730 | ||||||
| chr3:5151730
|
C | CT | 33 | a0001c0001t0001g0095a0001c0001t0001g0265a0001c0001t0002g0001others(30): Show | 36 | HG00597.hp2 HG01074.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.124-18771dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5151730 | |||||
| chr3:5151730
|
C | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0023 | 3 | HG02818.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.124-18773C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151730 | ||||||
| chr3:5151856
|
C | G | 145 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(142): Show | 150 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.124-18647C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151856 | ||||||
| chr3:5151872
|
A | G | 298 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(295): Show | 303 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(300): Show |
intron_variant | MODIFIER | c.124-18631A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151872 | ||||||
| chr3:5151901
|
T | A | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-18602T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151901 | ||||||
| chr3:5151929
|
G | A | 7 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0154others(4): Show | 7 | HG02155.hp1 NA18747.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-18574G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5151929 | ||||||
| chr3:5152176
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.124-18327A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5152176 | ||||||
| chr3:5152356
|
G | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0181 | 2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.124-18147G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5152356 | ||||||
| chr3:5152632
|
C | T | 7 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0104others(4): Show | 7 | HG01074.hp1 HG01167.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-17871C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5152632 | ||||||
| chr3:5152638
|
G | A | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-17865G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5152638 | ||||||
| chr3:5152724
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.124-17779G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5152724 | ||||||
| chr3:5152725
|
A | T | 1 | a0001c0001t0002g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.124-17778A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5152725 | ||||||
| chr3:5152748
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.124-17755A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5152748 | ||||||
| chr3:5152752
|
C | T | 98 | a0001c0001t0001g0265a0001c0001t0002g0001a0001c0001t0002g0002others(95): Show | 103 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.124-17751C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5152752 | ||||||
| chr3:5152754
|
G | T | 45 | a0001c0001t0001g0265a0001c0001t0002g0001a0001c0001t0002g0002others(42): Show | 49 | HG00597.hp2 HG01109.hp1 HG01257.hp1 others(46): Show |
intron_variant | MODIFIER | c.124-17749G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5152754 | ||||||
| chr3:5152785
|
C | A | 6 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0104others(3): Show | 6 | NA18946.hp2 NA18953.hp1 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-17718C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5152785 | ||||||
| chr3:5152910
|
G | A | 1 | a0001c0001t0002g0293 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.124-17593G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5152910 | ||||||
| chr3:5152911
|
A | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-17592A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5152911 | ||||||
| chr3:5153005
|
A | G | 43 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(40): Show | 43 | HG00544.hp1 HG00558.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.124-17498A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5153005 | ||||||
| chr3:5153198
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.124-17305C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5153198 | ||||||
| chr3:5153327
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.124-17176C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5153327 | ||||||
| chr3:5153395
|
A | G | 146 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(143): Show | 151 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.124-17108A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5153395 | ||||||
| chr3:5153645
|
TC | T | 5 | a0001c0001t0002g0233a0001c0001t0002g0234a0001c0001t0002g0239others(2): Show | 5 | HG00735.hp2 HG01070.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-16856delC | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5153645 | |||||
| chr3:5153814
|
C | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0262 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.124-16689C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5153814 | ||||||
| chr3:5153815
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.124-16688G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5153815 | ||||||
| chr3:5153841
|
G | A | 5 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(2): Show | 5 | HG01106.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-16662G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5153841 | ||||||
| chr3:5153928
|
CT | C | 145 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(142): Show | 150 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.124-16564delT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5153928 | |||||
| chr3:5153939
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.124-16564T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5153939 | ||||||
| chr3:5153970
|
T | C | 147 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(144): Show | 152 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.124-16533T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5153970 | ||||||
| chr3:5154290
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.124-16213A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154290 | ||||||
| chr3:5154308
|
T | C | 1 | a0001c0001t0002g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.124-16195T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154308 | ||||||
| chr3:5154309
|
A | T | 3 | a0001c0001t0002g0016a0001c0001t0002g0227a0001c0001t0002g0291 | 3 | HG02559.hp1 HG02622.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.124-16194A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154309 | ||||||
| chr3:5154337
|
C | CT | 147 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(144): Show | 152 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.124-16152dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5154337 | |||||
| chr3:5154365
|
G | A | 148 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(145): Show | 153 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.124-16138G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154365 | ||||||
| chr3:5154373
|
GC | G | 148 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(145): Show | 153 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.124-16127delC | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5154373 | |||||
| chr3:5154397
|
C | T | 2 | a0001c0001t0002g0206a0001c0001t0002g0217 | 2 | HG00423.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.124-16106C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154397 | ||||||
| chr3:5154406
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.124-16097C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154406 | ||||||
| chr3:5154540
|
G | T | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-15963G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154540 | ||||||
| chr3:5154576
|
G | A | 6 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0018others(3): Show | 6 | HG02135.hp1 NA18952.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-15927G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154576 | ||||||
| chr3:5154604
|
A | G | 5 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0070others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-15899A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154604 | ||||||
| chr3:5154669
|
A | G | 1 | a0001c0001t0002g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.124-15834A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154669 | ||||||
| chr3:5154721
|
A | G | 147 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(144): Show | 152 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.124-15782A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154721 | ||||||
| chr3:5154791
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.124-15712A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154791 | ||||||
| chr3:5154802
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.124-15701C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154802 | ||||||
| chr3:5154823
|
G | T | 147 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(144): Show | 152 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.124-15680G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154823 | ||||||
| chr3:5154891
|
T | TTTTG | 147 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(144): Show | 152 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.124-15596_124-1559 others(8): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5154891 | |||||
| chr3:5154924
|
G | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.124-15579G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154924 | ||||||
| chr3:5154952
|
C | T | 3 | a0001c0001t0002g0049a0001c0001t0002g0061a0001c0001t0002g0066 | 3 | HG00558.hp1 HG02129.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.124-15551C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154952 | ||||||
| chr3:5154954
|
C | T | 146 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(143): Show | 151 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.124-15549C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5154954 | ||||||
| chr3:5155022
|
C | A | 147 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(144): Show | 152 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.124-15481C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155022 | ||||||
| chr3:5155085
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-15418T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155085 | ||||||
| chr3:5155188
|
C | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-15315C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155188 | ||||||
| chr3:5155427
|
T | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0181 | 2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.124-15076T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155427 | ||||||
| chr3:5155620
|
A | C | 45 | a0001c0001t0001g0265a0001c0001t0002g0001a0001c0001t0002g0002others(42): Show | 49 | HG00597.hp2 HG01109.hp1 HG01257.hp1 others(46): Show |
intron_variant | MODIFIER | c.124-14883A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155620 | ||||||
| chr3:5155633
|
A | G | 149 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(146): Show | 154 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.124-14870A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155633 | ||||||
| chr3:5155664
|
C | T | 1 | a0001c0001t0022g0107 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.124-14839C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155664 | ||||||
| chr3:5155667
|
GC | G | 86 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(83): Show | 87 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.124-14829delC | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5155667 | |||||
| chr3:5155674
|
C | T | 2 | a0001c0001t0005g0296a0001c0001t0005g0297 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.124-14829C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155674 | ||||||
| chr3:5155721
|
G | T | 100 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(97): Show | 105 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.124-14782G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155721 | ||||||
| chr3:5155754
|
A | G | 1 | a0001c0001t0002g0227 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.124-14749A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155754 | ||||||
| chr3:5155843
|
GT | G | 41 | a0001c0001t0001g0054a0001c0001t0001g0064a0001c0001t0001g0065others(38): Show | 41 | HG00544.hp1 HG00558.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.124-14650delT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5155843 | |||||
| chr3:5155853
|
TG | T | 102 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0265others(99): Show | 107 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.124-14649delG | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155853 | ||||||
| chr3:5155854
|
G | T | 9 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(6): Show | 9 | HG01255.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-14649G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155854 | ||||||
| chr3:5155890
|
T | G | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | HG02040.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.124-14613T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155890 | ||||||
| chr3:5155890
|
T | TTG | 143 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(140): Show | 148 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.124-14597_124-1459 others(6): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5155890 | |||||
| chr3:5155912
|
T | G | 2 | a0001c0001t0005g0296a0001c0001t0005g0297 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.124-14591T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155912 | ||||||
| chr3:5155945
|
T | C | 3 | a0001c0001t0005g0296a0001c0001t0005g0297a0001c0001t0005g0298 | 3 | HG01243.hp2 HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.124-14558T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5155945 | ||||||
| chr3:5156191
|
C | A | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.124-14312C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5156191 | ||||||
| chr3:5156192
|
C | T | 1 | a0001c0001t0002g0068 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.124-14311C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5156192 | ||||||
| chr3:5156251
|
AT | A | 5 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(2): Show | 5 | HG01106.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-14244delT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5156251 | |||||
| chr3:5156341
|
A | T | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.124-14162A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5156341 | ||||||
| chr3:5156361
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.124-14142A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5156361 | ||||||
| chr3:5156541
|
A | T | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.124-13962A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5156541 | ||||||
| chr3:5156562
|
C | T | 40 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(37): Show | 40 | HG00544.hp1 HG00558.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.124-13941C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5156562 | ||||||
| chr3:5156662
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.124-13841C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5156662 | ||||||
| chr3:5156839
|
T | C | 152 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(149): Show | 157 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.124-13664T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5156839 | ||||||
| chr3:5156847
|
C | T | 42 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(39): Show | 42 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.124-13656C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5156847 | ||||||
| chr3:5156991
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.124-13512G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5156991 | ||||||
| chr3:5157054
|
T | C | 40 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(37): Show | 40 | HG00544.hp1 HG00558.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.124-13449T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5157054 | ||||||
| chr3:5157195
|
AACCAGGC others(11): Show |
A | 17 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0264others(14): Show | 20 | HG00597.hp2 HG01257.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.124-13307_124-1329 others(22): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5157195 | ||||||
| chr3:5157219
|
A | T | 1 | a0001c0001t0001g0185 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.124-13284A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5157219 | ||||||
| chr3:5157489
|
CA | C | 94 | a0001c0001t0001g0265a0001c0001t0002g0001a0001c0001t0002g0002others(91): Show | 99 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.124-13007delA | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5157489 | |||||
| chr3:5157513
|
G | A | 151 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(148): Show | 156 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.124-12990G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5157513 | ||||||
| chr3:5157666
|
T | G | 145 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(142): Show | 150 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.124-12837T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5157666 | ||||||
| chr3:5157890
|
G | A | 43 | a0001c0001t0001g0265a0001c0001t0002g0001a0001c0001t0002g0002others(40): Show | 47 | HG00597.hp2 HG01109.hp1 HG01257.hp1 others(44): Show |
intron_variant | MODIFIER | c.124-12613G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5157890 | ||||||
| chr3:5157986
|
T | C | 2 | a0001c0001t0002g0204a0001c0001t0002g0218 | 2 | HG02896.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.124-12517T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5157986 | ||||||
| chr3:5158015
|
G | A | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.124-12488G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158015 | ||||||
| chr3:5158056
|
G | A | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-12447G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158056 | ||||||
| chr3:5158071
|
G | A | 4 | a0001c0001t0002g0004a0001c0001t0002g0222a0001c0001t0002g0223others(1): Show | 5 | HG02257.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-12432G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158071 | ||||||
| chr3:5158087
|
T | C | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.124-12416T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158087 | ||||||
| chr3:5158088
|
G | T | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.124-12415G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158088 | ||||||
| chr3:5158089
|
C | G | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.124-12414C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158089 | ||||||
| chr3:5158092
|
C | T | 2 | a0001c0001t0005g0296a0001c0001t0005g0297 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.124-12411C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158092 | ||||||
| chr3:5158133
|
G | T | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.124-12370G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158133 | ||||||
| chr3:5158134
|
C | G | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.124-12369C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158134 | ||||||
| chr3:5158173
|
A | G | 145 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(142): Show | 150 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.124-12330A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158173 | ||||||
| chr3:5158181
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0138 | 2 | HG01074.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.124-12322A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158181 | ||||||
| chr3:5158274
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0133a0001c0001t0001g0146 | 3 | HG01081.hp2 HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.124-12229C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158274 | ||||||
| chr3:5158337
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.124-12166A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158337 | ||||||
| chr3:5158699
|
G | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-11804G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5158699 | ||||||
| chr3:5159158
|
G | A | 294 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(291): Show | 299 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.124-11345G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5159158 | ||||||
| chr3:5159219
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.124-11284G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5159219 | ||||||
| chr3:5159297
|
C | CA | 99 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0030others(96): Show | 104 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.124-11183dupA | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5159297 | |||||
| chr3:5159297
|
C | CAA | 18 | a0001c0001t0002g0011a0001c0001t0002g0013a0001c0001t0002g0017others(15): Show | 18 | HG01175.hp2 HG01891.hp1 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.124-11184_124-1118 others(6): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5159297 | |||||
| chr3:5159297
|
CA | C | 7 | a0001c0001t0001g0089a0001c0001t0001g0103a0001c0001t0001g0114others(4): Show | 7 | HG01243.hp2 HG02698.hp1 NA19003.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-11183delA | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5159297 | |||||
| chr3:5159297
|
CAAAAAAA others(2): Show |
C | 42 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(39): Show | 42 | HG00544.hp1 HG00558.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.124-11191_124-1118 others(13): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5159297 | |||||
| chr3:5159369
|
G | A | 150 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(147): Show | 155 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.124-11134G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5159369 | ||||||
| chr3:5159511
|
A | G | 11 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(8): Show | 11 | NA18964.hp2 NA18970.hp2 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.124-10992A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5159511 | ||||||
| chr3:5159602
|
C | CA | 22 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0127others(19): Show | 22 | HG00544.hp2 HG01891.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.124-10878dupA | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5159602 | |||||
| chr3:5159602
|
CA | C | 13 | a0001c0001t0001g0029a0001c0001t0001g0085a0001c0001t0001g0138others(10): Show | 13 | HG00544.hp1 HG00735.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.124-10878delA | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5159602 | |||||
| chr3:5159602
|
CAA | C | 99 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(96): Show | 100 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.124-10879_124-1087 others(6): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5159602 | |||||
| chr3:5159602
|
CAAA | C | 42 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(39): Show | 46 | HG00597.hp2 HG01069.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.124-10880_124-1087 others(7): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5159602 | |||||
| chr3:5159621
|
A | G | 2 | a0001c0001t0005g0296a0001c0001t0005g0297 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.124-10882A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5159621 | ||||||
| chr3:5159846
|
C | G | 1 | a0001c0001t0001g0024 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.124-10657C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5159846 | ||||||
| chr3:5159868
|
A | G | 1 | a0001c0001t0002g0201 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.124-10635A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5159868 | ||||||
| chr3:5159930
|
A | G | 150 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(147): Show | 155 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.124-10573A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5159930 | ||||||
| chr3:5159948
|
C | T | 1 | a0001c0001t0002g0045 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.124-10555C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5159948 | ||||||
| chr3:5159980
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-10523T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5159980 | ||||||
| chr3:5159983
|
A | G | 1 | a0001c0001t0002g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.124-10520A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5159983 | ||||||
| chr3:5160038
|
A | T | 150 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(147): Show | 155 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.124-10465A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5160038 | ||||||
| chr3:5160092
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.124-10411C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5160092 | ||||||
| chr3:5160121
|
T | C | 1 | a0001c0001t0002g0218 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124-10382T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5160121 | ||||||
| chr3:5160130
|
C | A | 145 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(142): Show | 150 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.124-10373C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5160130 | ||||||
| chr3:5160185
|
A | G | 25 | a0001c0001t0002g0079a0001c0001t0002g0096a0001c0001t0002g0206others(22): Show | 25 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.124-10318A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5160185 | ||||||
| chr3:5160271
|
G | A | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | HG02976.hp1 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.124-10232G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5160271 | ||||||
| chr3:5160378
|
G | A | 1 | a0001c0001t0002g0247 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124-10125G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5160378 | ||||||
| chr3:5160461
|
G | A | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-10042G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5160461 | ||||||
| chr3:5160496
|
A | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0169 | 2 | NA18995.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.124-10007A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5160496 | ||||||
| chr3:5160686
|
T | C | 1 | a0001c0001t0013g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.124-9817T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5160686 | ||||||
| chr3:5160760
|
G | A | 146 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(143): Show | 151 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.124-9743G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5160760 | ||||||
| chr3:5161088
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.124-9415G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5161088 | ||||||
| chr3:5161108
|
T | C | 151 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(148): Show | 156 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.124-9395T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5161108 | ||||||
| chr3:5161150
|
C | T | 1 | a0001c0001t0015g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.124-9353C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5161150 | ||||||
| chr3:5161200
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-9303A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5161200 | ||||||
| chr3:5161251
|
A | C | 294 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(291): Show | 299 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.124-9252A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5161251 | ||||||
| chr3:5161273
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.124-9230C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5161273 | ||||||
| chr3:5161299
|
C | CA | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-9197dupA | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5161299 | |||||
| chr3:5161307
|
G | A | 145 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(142): Show | 150 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.124-9196G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5161307 | ||||||
| chr3:5161413
|
A | T | 1 | a0001c0001t0002g0240 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.124-9090A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5161413 | ||||||
| chr3:5161492
|
T | C | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0012g0026 | 3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.124-9011T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5161492 | ||||||
| chr3:5161512
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-8991T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5161512 | ||||||
| chr3:5161752
|
T | A | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.124-8751T>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5161752 | ||||||
| chr3:5161968
|
A | G | 1 | a0001c0001t0022g0107 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.124-8535A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5161968 | ||||||
| chr3:5162091
|
T | C | 149 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(146): Show | 154 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.124-8412T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5162091 | ||||||
| chr3:5162480
|
A | G | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0291others(1): Show | 4 | HG02559.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-8023A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5162480 | ||||||
| chr3:5162801
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | NA18968.hp1 NA18969.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-7702C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5162801 | ||||||
| chr3:5162987
|
C | CTT | 44 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(41): Show | 44 | HG00544.hp1 HG00558.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.124-7499_124-7498d others(4): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5162987 | |||||
| chr3:5162987
|
C | CTTT | 94 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(91): Show | 99 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.124-7500_124-7498d others(5): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5162987 | |||||
| chr3:5162987
|
C | CTTTT | 6 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0096others(3): Show | 6 | HG02257.hp1 HG02630.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-7501_124-7498d others(6): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5162987 | |||||
| chr3:5162987
|
C | CTTTTT | 6 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(3): Show | 6 | HG01106.hp1 HG01243.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-7502_124-7498d others(7): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5162987 | |||||
| chr3:5163466
|
AT | A | 46 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0265others(43): Show | 50 | HG00597.hp2 HG01109.hp1 HG01257.hp1 others(47): Show |
intron_variant | MODIFIER | c.124-7034delT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5163466 | |||||
| chr3:5163617
|
C | T | 1 | a0001c0001t0005g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.124-6886C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5163617 | ||||||
| chr3:5163635
|
C | T | 11 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(8): Show | 11 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.124-6868C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5163635 | ||||||
| chr3:5163762
|
C | T | 1 | a0001c0001t0002g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.124-6741C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5163762 | ||||||
| chr3:5163907
|
C | A | 1 | a0001c0001t0002g0284 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.124-6596C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5163907 | ||||||
| chr3:5164060
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.124-6443G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5164060 | ||||||
| chr3:5164135
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.124-6368A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5164135 | ||||||
| chr3:5164201
|
T | C | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.124-6302T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5164201 | ||||||
| chr3:5164381
|
A | C | 1 | a0001c0001t0001g0150 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.124-6122A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5164381 | ||||||
| chr3:5164488
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.124-6015C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5164488 | ||||||
| chr3:5164721
|
G | A | 2 | a0001c0001t0002g0295a0001c0001t0009g0286 | 2 | HG02280.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.124-5782G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5164721 | ||||||
| chr3:5164727
|
C | A | 1 | a0001c0001t0002g0023 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.124-5776C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5164727 | ||||||
| chr3:5164973
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.124-5530T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5164973 | ||||||
| chr3:5165131
|
C | T | 5 | a0001c0001t0002g0279a0001c0001t0002g0281a0001c0001t0002g0288others(2): Show | 5 | NA18943.hp2 NA18969.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-5372C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5165131 | ||||||
| chr3:5165252
|
CA | C | 45 | a0001c0001t0001g0065a0001c0001t0001g0078a0001c0001t0002g0001others(42): Show | 49 | HG00597.hp2 HG01109.hp1 HG01257.hp1 others(46): Show |
intron_variant | MODIFIER | c.124-5241delA | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5165252 | |||||
| chr3:5165277
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.124-5226T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5165277 | ||||||
| chr3:5165319
|
A | G | 1 | a0001c0001t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.124-5184A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5165319 | ||||||
| chr3:5165386
|
G | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-5117G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5165386 | ||||||
| chr3:5165448
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.124-5055C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5165448 | ||||||
| chr3:5165461
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-5042T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5165461 | ||||||
| chr3:5165539
|
G | A | 1 | a0001c0001t0002g0168 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.124-4964G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5165539 | ||||||
| chr3:5165552
|
T | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-4951T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5165552 | ||||||
| chr3:5165668
|
G | A | 2 | a0001c0001t0002g0295a0001c0001t0009g0286 | 2 | HG02280.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.124-4835G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5165668 | ||||||
| chr3:5165841
|
T | G | 1 | a0001c0001t0002g0073 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.124-4662T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5165841 | ||||||
| chr3:5165984
|
C | G | 1 | a0001c0001t0005g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.124-4519C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5165984 | ||||||
| chr3:5166020
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0014g0196 | 2 | NA18946.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.124-4483C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5166020 | ||||||
| chr3:5166171
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-4332T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5166171 | ||||||
| chr3:5166185
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-4318A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5166185 | ||||||
| chr3:5166197
|
C | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-4306C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5166197 | ||||||
| chr3:5166250
|
A | G | 1 | a0001c0001t0013g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.124-4253A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5166250 | ||||||
| chr3:5166273
|
C | T | 1 | a0001c0001t0002g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.124-4230C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5166273 | ||||||
| chr3:5166327
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-4176T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5166327 | ||||||
| chr3:5166348
|
G | GT | 22 | a0001c0001t0001g0030a0001c0001t0001g0091a0001c0001t0001g0100others(19): Show | 22 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.124-4136dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5166348 | |||||
| chr3:5166348
|
GT | G | 16 | a0001c0001t0001g0078a0001c0001t0001g0102a0001c0001t0001g0127others(13): Show | 16 | HG00735.hp2 HG00738.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.124-4136delT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5166348 | |||||
| chr3:5166348
|
GTT | G | 126 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(123): Show | 131 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.124-4137_124-4136d others(4): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5166348 | |||||
| chr3:5166352
|
T | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-4151T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5166352 | ||||||
| chr3:5166423
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-4080A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5166423 | ||||||
| chr3:5166445
|
C | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-4058C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5166445 | ||||||
| chr3:5166629
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.124-3874C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5166629 | ||||||
| chr3:5167005
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.124-3498A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5167005 | ||||||
| chr3:5167051
|
T | G | 1 | a0001c0001t0001g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.124-3452T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5167051 | ||||||
| chr3:5167108
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-3395A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5167108 | ||||||
| chr3:5167244
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-3259A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5167244 | ||||||
| chr3:5167358
|
A | C | 2 | a0001c0001t0005g0296a0001c0001t0005g0297 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.124-3145A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5167358 | ||||||
| chr3:5167426
|
T | C | 3 | a0001c0001t0002g0049a0001c0001t0002g0061a0001c0001t0002g0066 | 3 | HG00558.hp1 HG02129.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.124-3077T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5167426 | ||||||
| chr3:5167612
|
G | A | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0010g0268 | 3 | HG03239.hp1 HG03831.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.124-2891G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5167612 | ||||||
| chr3:5167718
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.124-2785G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5167718 | ||||||
| chr3:5167770
|
A | T | 1 | a0001c0001t0002g0215 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.124-2733A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5167770 | ||||||
| chr3:5167787
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.124-2716A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5167787 | ||||||
| chr3:5168348
|
A | G | 56 | a0001c0001t0002g0004a0001c0001t0002g0079a0001c0001t0002g0096others(53): Show | 57 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.124-2155A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5168348 | ||||||
| chr3:5168493
|
G | A | 151 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(148): Show | 156 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.124-2010G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5168493 | ||||||
| chr3:5168517
|
G | T | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-1986G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5168517 | ||||||
| chr3:5168672
|
G | T | 2 | a0001c0001t0005g0296a0001c0001t0005g0297 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.124-1831G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5168672 | ||||||
| chr3:5168710
|
C | A | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-1793C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5168710 | ||||||
| chr3:5168785
|
G | A | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-1718G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5168785 | ||||||
| chr3:5168827
|
G | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0262 | 3 | HG03579.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.124-1676G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5168827 | ||||||
| chr3:5169165
|
T | C | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0127others(2): Show | 5 | HG00423.hp2 HG02080.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-1338T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5169165 | ||||||
| chr3:5169305
|
T | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0162a0001c0001t0004g0086 | 3 | NA19002.hp1 NA19087.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.124-1198T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5169305 | ||||||
| chr3:5169305
|
T | TTG | 20 | a0001c0001t0001g0100a0001c0001t0001g0115a0001c0001t0001g0135others(17): Show | 20 | HG00408.hp2 HG01106.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.124-1161_124-1160d others(4): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5169305 | |||||
| chr3:5169305
|
T | TTGTG | 4 | a0001c0001t0001g0083a0001c0001t0001g0106a0001c0001t0002g0295others(1): Show | 4 | HG02280.hp2 NA18941.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-1163_124-1160d others(6): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5169305 | |||||
| chr3:5169305
|
T | TTGTGTG | 3 | a0001c0001t0001g0088a0001c0001t0001g0122a0001c0001t0001g0188 | 3 | HG01106.hp2 NA18747.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.124-1165_124-1160d others(8): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5169305 | |||||
| chr3:5169305
|
TTG | T | 36 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(33): Show | 36 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.124-1161_124-1160d others(4): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5169305 | |||||
| chr3:5169305
|
TTGTG | T | 30 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0016others(27): Show | 31 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.124-1163_124-1160d others(6): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5169305 | |||||
| chr3:5169305
|
TTGTGTG | T | 9 | a0001c0001t0001g0109a0001c0001t0001g0120a0001c0001t0002g0110others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-1165_124-1160d others(8): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5169305 | |||||
| chr3:5169305
|
TTGTGTGT others(1): Show |
T | 80 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(77): Show | 84 | HG00558.hp1 HG00597.hp2 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.124-1167_124-1160d others(10): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5169305 | |||||
| chr3:5169305
|
TTGTGTGT others(3): Show |
T | 3 | a0001c0001t0002g0053a0001c0001t0002g0080a0001c0001t0002g0250 | 3 | HG00544.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.124-1169_124-1160d others(12): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5169305 | |||||
| chr3:5169305
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0002g0008 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.124-1171_124-1160d others(14): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5169305 | |||||
| chr3:5169305
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0015g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.124-1173_124-1160d others(16): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5169305 | |||||
| chr3:5169315
|
G | T | 6 | a0001c0001t0002g0004a0001c0001t0002g0222a0001c0001t0002g0223others(3): Show | 7 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-1188G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5169315 | ||||||
| chr3:5169353
|
G | C | 1 | a0001c0001t0013g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.124-1150G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5169353 | ||||||
| chr3:5169354
|
A | ACTTCTGG others(2723): Show |
1 | a0001c0001t0001g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.124-1134_124-1133i others(2732): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5169354 | |||||
| chr3:5169354
|
A | ACTTCTGG others(2734): Show |
1 | a0001c0001t0001g0157 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.124-1134_124-1133i others(2743): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5169354 | |||||
| chr3:5169566
|
TC | T | 101 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(98): Show | 106 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.124-936delC | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5169566 | ||||||
| chr3:5169567
|
C | T | 196 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(193): Show | 196 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(193): Show |
intron_variant | MODIFIER | c.124-936C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5169567 | ||||||
| chr3:5169572
|
C | T | 147 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(144): Show | 152 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.124-931C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5169572 | ||||||
| chr3:5169705
|
C | G | 151 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(148): Show | 156 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.124-798C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5169705 | ||||||
| chr3:5169809
|
T | TA | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-693dupA | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 5169809 | |||||
| chr3:5169887
|
T | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-616T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5169887 | ||||||
| chr3:5170186
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.124-317A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5170186 | ||||||
| chr3:5170452
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.124-51C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 1/6 | chr3 | 5170452 | ||||||
| chr3:5170600
|
C | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0012g0026 | 3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.204+17C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5170600 | ||||||
| chr3:5170733
|
T | G | 1 | a0001c0001t0002g0201 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.204+150T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5170733 | ||||||
| chr3:5170738
|
G | GT | 12 | a0001c0001t0001g0093a0001c0001t0001g0114a0001c0001t0001g0140others(9): Show | 12 | HG00741.hp1 HG02027.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.204+165dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 5170738 | |||||
| chr3:5170764
|
C | T | 1 | a0001c0001t0002g0242 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.204+181C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5170764 | ||||||
| chr3:5170795
|
G | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.204+212G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5170795 | ||||||
| chr3:5170825
|
G | A | 2 | a0001c0001t0002g0285a0001c0001t0002g0294 | 2 | NA18966.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.204+242G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5170825 | ||||||
| chr3:5170868
|
T | C | 1 | a0001c0001t0003g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.204+285T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5170868 | ||||||
| chr3:5171012
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.204+429G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5171012 | ||||||
| chr3:5171031
|
C | G | 52 | a0001c0001t0002g0004a0001c0001t0002g0079a0001c0001t0002g0096others(49): Show | 53 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.204+448C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5171031 | ||||||
| chr3:5171107
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.204+524A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5171107 | ||||||
| chr3:5171218
|
C | T | 152 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(149): Show | 157 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.204+635C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5171218 | ||||||
| chr3:5171397
|
C | G | 1 | a0001c0001t0001g0169 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.205-753C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5171397 | ||||||
| chr3:5171588
|
T | G | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.205-562T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5171588 | ||||||
| chr3:5171597
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.205-553C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5171597 | ||||||
| chr3:5171693
|
A | C | 1 | a0001c0001t0015g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-457A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5171693 | ||||||
| chr3:5171981
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.205-169G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5171981 | ||||||
| chr3:5172043
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.205-107T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 2/6 | chr3 | 5172043 | ||||||
| chr3:5172303
|
G | C | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.278+80G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 3/6 | chr3 | 5172303 | ||||||
| chr3:5172349
|
C | G | 3 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0211 | 3 | HG01123.hp1 HG04199.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.278+126C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 3/6 | chr3 | 5172349 | ||||||
| chr3:5172434
|
A | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+211A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 3/6 | chr3 | 5172434 | ||||||
| chr3:5172441
|
G | A | 147 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0054others(144): Show | 152 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.279-206G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 3/6 | chr3 | 5172441 | ||||||
| chr3:5172607
|
A | G | 1 | a0001c0001t0021g0136 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.279-40A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 3/6 | chr3 | 5172607 | ||||||
| chr3:5172925
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.372+185C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5172925 | ||||||
| chr3:5172944
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.372+204T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5172944 | ||||||
| chr3:5172955
|
C | A | 2 | a0001c0001t0005g0296a0001c0001t0005g0297 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.372+215C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5172955 | ||||||
| chr3:5173084
|
G | A | 1 | a0001c0001t0002g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.372+344G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173084 | ||||||
| chr3:5173235
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.372+495G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173235 | ||||||
| chr3:5173277
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.372+537T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173277 | ||||||
| chr3:5173331
|
A | G | 52 | a0001c0001t0002g0004a0001c0001t0002g0079a0001c0001t0002g0096others(49): Show | 53 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.372+591A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173331 | ||||||
| chr3:5173422
|
G | A | 44 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(41): Show | 48 | HG00597.hp2 HG01109.hp1 HG01257.hp1 others(45): Show |
intron_variant | MODIFIER | c.373-595G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173422 | ||||||
| chr3:5173431
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.373-586C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173431 | ||||||
| chr3:5173551
|
G | A | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.373-466G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173551 | ||||||
| chr3:5173552
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.373-465C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173552 | ||||||
| chr3:5173561
|
C | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.373-456C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173561 | ||||||
| chr3:5173563
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.373-454C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173563 | ||||||
| chr3:5173713
|
T | TCAAA | 26 | a0001c0001t0001g0118a0001c0001t0001g0154a0001c0001t0001g0177others(23): Show | 26 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.373-275_373-272dup others(4): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 5173713 | |||||
| chr3:5173713
|
TCAAA | T | 32 | a0001c0001t0001g0091a0001c0001t0002g0004a0001c0001t0002g0013others(29): Show | 33 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(30): Show |
intron_variant | MODIFIER | c.373-275_373-272del others(4): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 5173713 | |||||
| chr3:5173772
|
C | T | 4 | a0001c0001t0002g0050a0001c0001t0002g0052a0001c0001t0002g0056others(1): Show | 4 | HG02027.hp2 HG02040.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-245C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173772 | ||||||
| chr3:5173792
|
A | T | 1 | a0001c0001t0002g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.373-225A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173792 | ||||||
| chr3:5173920
|
T | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0151 | 2 | HG01123.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.373-97T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173920 | ||||||
| chr3:5173955
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.373-62G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4/6 | chr3 | 5173955 | ||||||
| chr3:5174122
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.440+38A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 5/6 | chr3 | 5174122 | ||||||
| chr3:5174222
|
A | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0012g0026 | 3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.441-122A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 5/6 | chr3 | 5174222 | ||||||
| chr3:5174230
|
A | G | 1 | a0001c0001t0005g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.441-114A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 5/6 | chr3 | 5174230 | ||||||
| chr3:5174615
|
G | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01891.hp2 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.511+201G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5174615 | ||||||
| chr3:5174665
|
AATATATG others(27): Show |
A | 138 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(135): Show | 143 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.511+299_511+332del others(34): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 5174665 | |||||
| chr3:5174682
|
TTATATAT others(29): Show |
T | 2 | a0001c0001t0002g0041a0001c0001t0002g0060 | 2 | NA19056.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.511+274_511+309del others(36): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 5174682 | |||||
| chr3:5174749
|
A | T | 1 | a0001c0001t0001g0116 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.511+335A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5174749 | ||||||
| chr3:5174754
|
A | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511+340A>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5174754 | ||||||
| chr3:5174781
|
A | AAT | 3 | a0001c0001t0005g0296a0001c0001t0005g0297a0001c0001t0007g0123 | 3 | HG02080.hp2 HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.511+379_511+380dup others(2): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 5174781 | |||||
| chr3:5174959
|
C | T | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | HG02040.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.511+545C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5174959 | ||||||
| chr3:5174963
|
C | T | 1 | a0001c0001t0002g0251 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.511+549C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5174963 | ||||||
| chr3:5175033
|
T | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511+619T>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5175033 | ||||||
| chr3:5175165
|
A | G | 1 | a0001c0001t0003g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.511+751A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5175165 | ||||||
| chr3:5175216
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0158 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.511+802T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5175216 | ||||||
| chr3:5175314
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511+900T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5175314 | ||||||
| chr3:5175441
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.511+1027A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5175441 | ||||||
| chr3:5175694
|
G | A | 2 | a0001c0001t0008g0214a0001c0001t0008g0216 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.511+1280G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5175694 | ||||||
| chr3:5175786
|
T | C | 1 | a0001c0001t0005g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511+1372T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5175786 | ||||||
| chr3:5175920
|
C | G | 1 | a0001c0001t0002g0023 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511+1506C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5175920 | ||||||
| chr3:5176139
|
A | G | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.511+1725A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5176139 | ||||||
| chr3:5176208
|
A | G | 5 | a0001c0001t0002g0279a0001c0001t0002g0281a0001c0001t0002g0288others(2): Show | 5 | NA18943.hp2 NA18969.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.511+1794A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5176208 | ||||||
| chr3:5176323
|
C | T | 17 | a0001c0001t0002g0096a0001c0001t0002g0232a0001c0001t0002g0233others(14): Show | 17 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.511+1909C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5176323 | ||||||
| chr3:5176362
|
C | T | 1 | a0001c0001t0005g0296 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.511+1948C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5176362 | ||||||
| chr3:5176537
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511+2123T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5176537 | ||||||
| chr3:5176568
|
C | T | 1 | a0001c0001t0002g0008 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.512-2096C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5176568 | ||||||
| chr3:5176666
|
A | G | 1 | a0001c0001t0005g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.512-1998A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5176666 | ||||||
| chr3:5176953
|
A | G | 18 | a0001c0001t0002g0096a0001c0001t0002g0232a0001c0001t0002g0233others(15): Show | 18 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.512-1711A>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5176953 | ||||||
| chr3:5177070
|
C | G | 42 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(39): Show | 46 | HG00597.hp2 HG01109.hp1 HG01257.hp1 others(43): Show |
intron_variant | MODIFIER | c.512-1594C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5177070 | ||||||
| chr3:5177076
|
A | T | 3 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251 | 3 | HG02109.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.512-1588A>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5177076 | ||||||
| chr3:5177139
|
C | A | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.512-1525C>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5177139 | ||||||
| chr3:5177459
|
C | CT | 12 | a0001c0001t0001g0054a0001c0001t0001g0064a0001c0001t0001g0065others(9): Show | 12 | HG01175.hp2 NA18943.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.512-1190dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 5177459 | |||||
| chr3:5177513
|
G | A | 137 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(134): Show | 142 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.512-1151G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5177513 | ||||||
| chr3:5177543
|
G | A | 4 | a0001c0001t0002g0079a0001c0001t0002g0206a0001c0001t0002g0217others(1): Show | 4 | HG00408.hp1 HG00423.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-1121G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5177543 | ||||||
| chr3:5177605
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.512-1059G>A | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5177605 | ||||||
| chr3:5177706
|
C | T | 4 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 4 | HG01106.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-958C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5177706 | ||||||
| chr3:5177733
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.512-931T>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5177733 | ||||||
| chr3:5177794
|
G | C | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.512-870G>C | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5177794 | ||||||
| chr3:5177801
|
C | T | 2 | a0001c0001t0005g0296a0001c0001t0005g0297 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.512-863C>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5177801 | ||||||
| chr3:5178117
|
C | G | 1 | a0001c0001t0009g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.512-547C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5178117 | ||||||
| chr3:5178326
|
C | G | 1 | a0001c0001t0001g0179 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.512-338C>G | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5178326 | ||||||
| chr3:5178338
|
CAG | C | 3 | a0001c0001t0002g0215a0001c0001t0008g0214a0001c0001t0008g0216 | 3 | HG02630.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.512-325_512-324del others(2): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5178338 | ||||||
| chr3:5178350
|
C | CT | 18 | a0001c0001t0001g0034a0001c0001t0001g0065a0001c0001t0001g0111others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.512-293dupT | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 5178350 | |||||
| chr3:5178372
|
G | T | 1 | a0001c0001t0001g0272 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.512-292G>T | ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | chr3 | 5178372 |