| geneid | 219699 |
|---|---|
| ensemblid | ENSG00000107731.12 |
| hgncid | 12568 |
| symbol | UNC5B |
| name | unc-5 netrin receptor B |
| refseq_nuc | NM_170744.5 |
| refseq_prot | NP_734465.2 |
| ensembl_nuc | ENST00000335350.10 |
| ensembl_prot | ENSP00000334329.6 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 71212570 |
| end | 71302864 |
| strand | + |
| ver | v1.2 |
| region | chr10:71212570-71302864 |
| region5000 | chr10:71207570-71307864 |
| regionname0 | UNC5B_chr10_71212570_71302864 |
| regionname5000 | UNC5B_chr10_71207570_71307864 |
| 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 | 945 | 297 | 64 | 49 | 140 | 10 | 32 | 103 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002 | 0/0 | 945 | 20 | 0 | 4 | 12 | 0 | 4 | 10 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0003 | 0/0 | 945 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0004 | 0/0 | 945 | 6 | 2 | 1 | 0 | 2 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0005 | 0/0 | 945 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0006 | 0/0 | 945 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0007 | 0/0 | 945 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0008 | 0/0 | 945 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0009 | 0/0 | 944 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0010 | 0/0 | 942 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0011 | 0/0 | 934 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0012 | 0/0 | 945 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0013 | 0/0 | 945 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0014 | 0/0 | 945 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0015 | 0/0 | 945 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0016 | 0/0 | 945 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0017 | 0/0 | 945 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0018 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0019 | 0/0 | 945 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0020 | 0/0 | 945 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0021 | 0/0 | 945 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0022 | 0/0 | 886 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0023 | 0/0 | 847 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0024 | 0/0 | 935 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0025 | 0/0 | 944 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0026 | 0/0 | 945 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0027 | 0/0 | 945 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0028 | 0/0 | 945 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0029 | 0/0 | 945 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0030 | 0/0 | 945 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0031 | 0/0 | 945 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| 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 | 0/1 | 2838 | 129 | 29 | 25 | 44 | 8 | 22 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0002 | 1/0 | 2838 | 72 | 8 | 14 | 43 | 1 | 5 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0003 | 0/0 | 2838 | 47 | 11 | 6 | 25 | 0 | 5 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0004 | 0/0 | 2838 | 20 | 0 | 0 | 20 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0005 | 0/0 | 2838 | 14 | 0 | 4 | 7 | 0 | 3 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0006 | 0/0 | 2838 | 9 | 8 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0007 | 0/0 | 2838 | 7 | 6 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0008 | 0/0 | 2838 | 5 | 0 | 0 | 5 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0009 | 0/0 | 2838 | 4 | 2 | 2 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0010 | 0/0 | 2838 | 4 | 1 | 1 | 0 | 1 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0011 | 0/0 | 2838 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0012 | 0/0 | 2838 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0013 | 0/0 | 2838 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0014 | 0/0 | 2805 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0015 | 0/0 | 2838 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0016 | 0/0 | 2829 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0017 | 0/0 | 2838 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0018 | 0/0 | 2838 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0019 | 0/0 | 2835 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0020 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0021 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0022 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0023 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0024 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0025 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0026 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0027 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0028 | 0/0 | 2938 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0029 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0030 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0031 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0032 | 0/0 | 2835 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0033 | 0/0 | 2838 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0034 | 0/0 | 2835 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0035 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0036 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0037 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0038 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0039 | 0/0 | 2838 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0040 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0041 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0042 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0043 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0044 | 0/0 | 2808 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0045 | 0/0 | 2888 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0046 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0047 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0048 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0049 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0050 | 0/0 | 2838 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0051 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0052 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0053 | 0/0 | 2838 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0054 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0055 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0056 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| c0057 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4004 | 68 | 4 | 23 | 21 | 5 | 13 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0002 | 0/0 | 4006 | 41 | 0 | 4 | 33 | 0 | 4 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0003 | 0/0 | 4008 | 23 | 0 | 0 | 23 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0004 | 0/0 | 4010 | 23 | 0 | 0 | 21 | 0 | 2 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0005 | 0/0 | 4012 | 13 | 1 | 6 | 0 | 2 | 4 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0006 | 0/0 | 4006 | 12 | 1 | 1 | 10 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0007 | 0/0 | 4011 | 12 | 12 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0008 | 0/0 | 4000 | 10 | 0 | 0 | 8 | 0 | 2 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0009 | 0/0 | 4002 | 9 | 0 | 3 | 1 | 2 | 3 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0010 | 0/0 | 4006 | 9 | 7 | 0 | 0 | 1 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0011 | 0/0 | 4010 | 8 | 6 | 1 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0012 | 0/0 | 4004 | 8 | 7 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0013 | 0/0 | 4010 | 7 | 0 | 0 | 7 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0014 | 0/0 | 4027 | 6 | 0 | 4 | 0 | 0 | 2 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0015 | 0/0 | 3994 | 6 | 5 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0016 | 0/0 | 4008 | 6 | 2 | 0 | 4 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0017 | 0/0 | 4008 | 5 | 0 | 4 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0018 | 0/0 | 4012 | 5 | 5 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0019 | 0/0 | 4008 | 4 | 3 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0020 | 0/0 | 4006 | 4 | 4 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0021 | 0/0 | 4008 | 3 | 0 | 0 | 3 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0022 | 0/0 | 4008 | 3 | 0 | 0 | 3 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0023 | 0/0 | 4012 | 3 | 0 | 0 | 3 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0024 | 0/0 | 4009 | 3 | 2 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0025 | 0/0 | 4008 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0026 | 0/0 | 4012 | 3 | 0 | 0 | 3 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0027 | 0/0 | 4002 | 3 | 0 | 2 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0028 | 0/0 | 4096 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0029 | 0/0 | 4002 | 2 | 1 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0030 | 0/0 | 4000 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0031 | 0/0 | 4002 | 2 | 1 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0032 | 0/0 | 4010 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0033 | 0/0 | 4006 | 2 | 1 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0034 | 0/0 | 4010 | 2 | 1 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0035 | 0/0 | 4007 | 2 | 1 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0036 | 0/0 | 4006 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0037 | 0/0 | 4006 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0038 | 0/0 | 4010 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0039 | 0/0 | 4006 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0040 | 0/0 | 4006 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0041 | 0/0 | 4006 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0042 | 0/0 | 4006 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0043 | 0/0 | 4006 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0044 | 0/0 | 4012 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0045 | 0/0 | 4012 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0046 | 0/0 | 4008 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0047 | 0/0 | 4004 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0048 | 0/0 | 4004 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0049 | 0/0 | 4004 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0050 | 0/0 | 4006 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0051 | 0/0 | 4008 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0052 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0053 | 0/0 | 4010 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0054 | 0/0 | 4027 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0055 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0056 | 0/0 | 4000 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0057 | 0/0 | 4005 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0058 | 0/0 | 4013 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0059 | 0/0 | 4013 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0060 | 0/0 | 4009 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0061 | 0/0 | 4004 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0062 | 0/0 | 4006 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0063 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0064 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0065 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0066 | 0/0 | 4012 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0067 | 0/0 | 4012 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0068 | 0/0 | 4012 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0069 | 0/0 | 4012 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0070 | 0/0 | 4014 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0071 | 0/0 | 4006 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0072 | 0/0 | 4004 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0073 | 0/0 | 4004 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0074 | 0/0 | 4004 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0075 | 0/0 | 4006 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0076 | 0/0 | 4006 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0077 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0078 | 0/0 | 4002 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0079 | 0/0 | 4004 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0080 | 0/0 | 4006 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| t0081 | 0/0 | 4004 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| 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 | 0/1 | 2838 | 129 | 29 | 25 | 44 | 8 | 22 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002 | 1/0 | 2838 | 72 | 8 | 14 | 43 | 1 | 5 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003 | 0/0 | 2838 | 47 | 11 | 6 | 25 | 0 | 5 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0004 | 0/0 | 2838 | 20 | 0 | 0 | 20 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0006 | 0/0 | 2838 | 9 | 8 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0009 | 0/0 | 2838 | 4 | 2 | 2 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0012 | 0/0 | 2838 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0015 | 0/0 | 2838 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0020 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0024 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0026 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0027 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0029 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0030 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0040 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0046 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0051 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0053 | 0/0 | 2838 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0055 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0005 | 0/0 | 2838 | 14 | 0 | 4 | 7 | 0 | 3 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0008 | 0/0 | 2838 | 5 | 0 | 0 | 5 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0049 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0003c0007 | 0/0 | 2838 | 7 | 6 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0003c0038 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0004c0010 | 0/0 | 2838 | 4 | 1 | 1 | 0 | 1 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0004c0042 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0004c0043 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0005c0011 | 0/0 | 2838 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0006c0018 | 0/0 | 2838 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0006c0057 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0007c0017 | 0/0 | 2838 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0008c0041 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0008c0047 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0009c0019 | 0/0 | 2835 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0009c0034 | 0/0 | 2835 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0010c0016 | 0/0 | 2829 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0011c0014 | 0/0 | 2805 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0012c0013 | 0/0 | 2838 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0013c0052 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0014c0050 | 0/0 | 2838 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0015c0036 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0016c0037 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0017c0023 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0018c0022 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0019c0021 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0020c0033 | 0/0 | 2838 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0021c0031 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0022c0045 | 0/0 | 2888 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0023c0028 | 0/0 | 2938 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0024c0044 | 0/0 | 2808 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0025c0032 | 0/0 | 2835 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0026c0054 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0027c0025 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0028c0039 | 0/0 | 2838 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0029c0048 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0030c0035 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0031c0056 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6841 | 36 | 3 | 8 | 12 | 4 | 8 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0002 | 0/0 | 6843 | 12 | 0 | 1 | 8 | 0 | 3 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0004 | 0/0 | 6847 | 9 | 0 | 0 | 9 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0005 | 0/0 | 6849 | 9 | 1 | 3 | 0 | 2 | 3 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0006 | 0/0 | 6843 | 2 | 1 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0007 | 0/0 | 6848 | 6 | 6 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0009 | 0/0 | 6839 | 5 | 0 | 3 | 1 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0010 | 0/0 | 6843 | 4 | 2 | 0 | 0 | 1 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0011 | 0/0 | 6847 | 5 | 4 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0013 | 0/0 | 6847 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0014 | 0/0 | 6864 | 5 | 0 | 4 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0016 | 0/0 | 6845 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0017 | 0/0 | 6845 | 2 | 0 | 1 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0019 | 0/0 | 6845 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0020 | 0/0 | 6843 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0024 | 0/0 | 6846 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0025 | 0/0 | 6845 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0026 | 0/0 | 6849 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0027 | 0/0 | 6839 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0031 | 0/0 | 6839 | 2 | 1 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0034 | 0/0 | 6847 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0042 | 0/0 | 6843 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0045 | 0/0 | 6849 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0047 | 0/0 | 6841 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0048 | 0/0 | 6841 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0055 | 0/0 | 6847 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0057 | 0/0 | 6842 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0061 | 0/0 | 6841 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0062 | 0/0 | 6843 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0063 | 0/0 | 6847 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0064 | 0/0 | 6847 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0068 | 0/0 | 6849 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0069 | 0/0 | 6849 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0070 | 0/0 | 6851 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0071 | 0/0 | 6843 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0073 | 0/0 | 6841 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0074 | 0/0 | 6841 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0001t0080 | 0/0 | 6843 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0001 | 1/0 | 6841 | 15 | 1 | 8 | 4 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0002 | 0/0 | 6843 | 17 | 0 | 2 | 14 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0004 | 0/0 | 6847 | 4 | 0 | 0 | 4 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0005 | 0/0 | 6849 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0006 | 0/0 | 6843 | 10 | 0 | 1 | 9 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0008 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0009 | 0/0 | 6839 | 4 | 0 | 0 | 0 | 1 | 3 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0013 | 0/0 | 6847 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0022 | 0/0 | 6845 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0023 | 0/0 | 6849 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0026 | 0/0 | 6849 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0027 | 0/0 | 6839 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0028 | 0/0 | 6933 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0032 | 0/0 | 6847 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0033 | 0/0 | 6843 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0039 | 0/0 | 6843 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0041 | 0/0 | 6843 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0050 | 0/0 | 6843 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0058 | 0/0 | 6850 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0072 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0077 | 0/0 | 6847 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0002t0078 | 0/0 | 6839 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0001 | 0/0 | 6841 | 6 | 0 | 1 | 2 | 0 | 3 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0002 | 0/0 | 6843 | 6 | 0 | 0 | 6 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0004 | 0/0 | 6847 | 6 | 0 | 0 | 6 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0007 | 0/0 | 6848 | 5 | 5 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0008 | 0/0 | 6837 | 9 | 0 | 0 | 7 | 0 | 2 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0011 | 0/0 | 6847 | 2 | 1 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0013 | 0/0 | 6847 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0017 | 0/0 | 6845 | 3 | 0 | 3 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0019 | 0/0 | 6845 | 2 | 1 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0022 | 0/0 | 6845 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0024 | 0/0 | 6846 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0036 | 0/0 | 6843 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0037 | 0/0 | 6843 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0044 | 0/0 | 6849 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0003t0075 | 0/0 | 6843 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0004t0003 | 0/0 | 6845 | 16 | 0 | 0 | 16 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0004t0021 | 0/0 | 6845 | 3 | 0 | 0 | 3 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0004t0052 | 0/0 | 6847 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0006t0007 | 0/0 | 6848 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0006t0015 | 0/0 | 6831 | 6 | 5 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0006t0033 | 0/0 | 6843 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0006t0081 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0009t0005 | 0/0 | 6849 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0009t0035 | 0/0 | 6844 | 2 | 1 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0009t0076 | 0/0 | 6843 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0012t0016 | 0/0 | 6845 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0012t0038 | 0/0 | 6847 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0015t0018 | 0/0 | 6849 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0015t0056 | 0/0 | 6837 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0020t0065 | 0/0 | 6847 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0024t0002 | 0/0 | 6843 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0026t0001 | 0/0 | 6841 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0027t0003 | 0/0 | 6845 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0029t0002 | 0/0 | 6843 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0030t0067 | 0/0 | 6849 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0040t0043 | 0/0 | 6843 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0046t0016 | 0/0 | 6845 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0051t0001 | 0/0 | 6841 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0053t0001 | 0/0 | 6841 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0001c0055t0024 | 0/0 | 6846 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0005t0001 | 0/0 | 6841 | 5 | 0 | 2 | 2 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0005t0002 | 0/0 | 6843 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0005t0013 | 0/0 | 6847 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0005t0014 | 0/0 | 6864 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0005t0023 | 0/0 | 6849 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0005t0030 | 0/0 | 6837 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0005t0034 | 0/0 | 6847 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0005t0054 | 0/0 | 6864 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0008t0003 | 0/0 | 6845 | 4 | 0 | 0 | 4 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0008t0046 | 0/0 | 6845 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0002c0049t0005 | 0/0 | 6849 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0003c0007t0010 | 0/0 | 6843 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0003c0007t0012 | 0/0 | 6841 | 6 | 5 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0003c0038t0012 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0004c0010t0001 | 0/0 | 6841 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0004c0010t0004 | 0/0 | 6847 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0004c0010t0010 | 0/0 | 6843 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0004c0010t0066 | 0/0 | 6849 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0004c0042t0053 | 0/0 | 6847 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0004c0043t0079 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0005c0011t0010 | 0/0 | 6843 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0006c0018t0040 | 0/0 | 6843 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0006c0057t0036 | 0/0 | 6843 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0007c0017t0011 | 0/0 | 6847 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0007c0017t0016 | 0/0 | 6845 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0008c0041t0012 | 0/0 | 6841 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0008c0047t0029 | 0/0 | 6839 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0009c0019t0004 | 0/0 | 6844 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0009c0034t0004 | 0/0 | 6844 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0010c0016t0002 | 0/0 | 6834 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0010c0016t0049 | 0/0 | 6832 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0011c0014t0018 | 0/0 | 6816 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0012c0013t0003 | 0/0 | 6845 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0013c0052t0002 | 0/0 | 6843 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0014c0050t0029 | 0/0 | 6839 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0015c0036t0039 | 0/0 | 6843 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0016c0037t0013 | 0/0 | 6847 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0017c0023t0020 | 0/0 | 6843 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0018c0022t0018 | 0/0 | 6816 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0019c0021t0020 | 0/0 | 6843 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0020c0033t0001 | 0/0 | 6841 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0021c0031t0002 | 0/0 | 6843 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0022c0045t0004 | 0/0 | 6897 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0023c0028t0005 | 0/0 | 6949 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0024c0044t0001 | 0/0 | 6811 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0025c0032t0023 | 0/0 | 6846 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0026c0054t0051 | 0/0 | 6845 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0027c0025t0059 | 0/0 | 6850 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0028c0039t0060 | 0/0 | 6846 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0029c0048t0016 | 0/0 | 6845 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0030c0035t0018 | 0/0 | 6849 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| a0031c0056t0020 | 0/0 | 6843 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | copy fasta | chr10 | 71207570 | 71307864 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0007g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0009g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0009g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0009g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0009g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0009g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0010g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0010g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0010g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0011g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0011g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0011g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0011g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0013g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0013g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0014g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0014g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0014g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0014g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0016g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0016g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0017g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0017g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0019g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0019g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0020g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0024g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0025g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0025g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0025g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0026g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0027g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0027g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0031g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0031g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0034g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0042g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0045g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0047g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0048g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0055g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0057g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0061g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0062g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0063g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0064g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0068g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0069g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0070g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0071g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0073g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0074g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0001t0080g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0006g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0006g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0008g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0009g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0009g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0009g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0009g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0013g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0022g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0022g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0023g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0026g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0026g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0027g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0028g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0028g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0028g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0032g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0033g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0039g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0041g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0050g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0058g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0072g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0077g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0002t0078g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0007g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0008g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0008g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0008g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0008g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0008g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0008g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0011g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0013g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0017g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0017g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0017g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0019g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0019g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0022g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0024g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0036g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0037g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0037g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0044g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0003t0075g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0021g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0021g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0021g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0004t0052g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0006t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0006t0015g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0006t0015g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0006t0015g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0006t0015g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0006t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0006t0015g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0006t0033g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0006t0081g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0009t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0009t0035g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0009t0035g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0009t0076g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0012t0016g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0012t0038g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0012t0038g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0015t0018g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0015t0056g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0020t0065g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0024t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0026t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0027t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0029t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0030t0067g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0040t0043g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0046t0016g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0051t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0053t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0001c0055t0024g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0013g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0013g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0014g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0023g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0030g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0030g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0034g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0005t0054g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0008t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0008t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0008t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0008t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0008t0046g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0002c0049t0005g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0003c0007t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0003c0007t0012g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0003c0007t0012g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0003c0007t0012g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0003c0007t0012g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0003c0007t0012g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0003c0007t0012g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0003c0038t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0004c0010t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0004c0010t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0004c0010t0010g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0004c0010t0066g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0004c0042t0053g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0004c0043t0079g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0005c0011t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0005c0011t0010g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0005c0011t0010g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0006c0018t0040g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0006c0018t0040g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0006c0057t0036g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0007c0017t0011g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0007c0017t0016g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0008c0041t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0008c0047t0029g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0009c0019t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0009c0034t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0010c0016t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0010c0016t0049g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0011c0014t0018g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0011c0014t0018g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0012c0013t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0012c0013t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0013c0052t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0014c0050t0029g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0015c0036t0039g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0016c0037t0013g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0017c0023t0020g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0018c0022t0018g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0019c0021t0020g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0020c0033t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0021c0031t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0022c0045t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0023c0028t0005g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0024c0044t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0025c0032t0023g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0026c0054t0051g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0027c0025t0059g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0028c0039t0060g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0029c0048t0016g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0030c0035t0018g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| a0031c0056t0020g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | GBR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00099 | hp2 | a0001 | c0051 | t0001 | g0103 | EUR | GBR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0301 | EUR | GBR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00140 | hp2 | a0004 | c0042 | t0053 | g0229 | EUR | GBR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0302 | EUR | FIN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00280 | hp2 | a0001 | c0002 | t0009 | g0304 | EUR | FIN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00408 | hp1 | a0002 | c0005 | t0001 | g0254 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00408 | hp2 | a0001 | c0003 | t0008 | g0223 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00423 | hp1 | a0001 | c0002 | t0006 | g0244 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00423 | hp2 | a0001 | c0003 | t0004 | g0043 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00438 | hp1 | a0001 | c0003 | t0008 | g0190 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00544 | hp1 | a0001 | c0004 | t0003 | g0277 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00544 | hp2 | a0001 | c0002 | t0004 | g0273 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0333 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00597 | hp2 | a0013 | c0052 | t0002 | g0268 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00609 | hp1 | a0029 | c0048 | t0016 | g0035 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00609 | hp2 | a0001 | c0004 | t0003 | g0285 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00639 | hp2 | a0028 | c0039 | t0060 | g0171 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0308 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00673 | hp1 | a0002 | c0008 | t0003 | g0241 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00673 | hp2 | a0001 | c0004 | t0003 | g0279 | EAS | CHS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00733 | hp2 | a0001 | c0001 | t0045 | g0187 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00735 | hp1 | a0001 | c0009 | t0035 | g0360 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00735 | hp2 | a0023 | c0028 | t0005 | g0343 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00738 | hp1 | a0001 | c0001 | t0009 | g0185 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0180 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG00741 | hp2 | a0001 | c0001 | t0014 | g0182 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01069 | hp1 | a0001 | c0001 | t0014 | g0005 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01069 | hp2 | a0001 | c0006 | t0015 | g0011 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01070 | hp1 | a0001 | c0001 | t0014 | g0260 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01070 | hp2 | a0001 | c0001 | t0027 | g0044 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01071 | hp1 | a0001 | c0001 | t0014 | g0005 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01071 | hp2 | a0001 | c0001 | t0027 | g0259 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01081 | hp1 | a0001 | c0002 | t0033 | g0036 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0303 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01106 | hp1 | a0001 | c0003 | t0019 | g0261 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01106 | hp2 | a0003 | c0007 | t0012 | g0227 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0231 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01109 | hp2 | a0004 | c0010 | t0001 | g0151 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01169 | hp2 | a0001 | c0002 | t0078 | g0123 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01243 | hp1 | a0001 | c0001 | t0024 | g0112 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01243 | hp2 | a0014 | c0050 | t0029 | g0352 | AMR | PUR | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01255 | hp1 | a0001 | c0001 | t0009 | g0079 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01255 | hp2 | a0001 | c0009 | t0005 | g0075 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01256 | hp2 | a0001 | c0003 | t0017 | g0209 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01257 | hp1 | a0001 | c0003 | t0017 | g0211 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01258 | hp2 | a0001 | c0003 | t0017 | g0210 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01358 | hp1 | a0001 | c0002 | t0006 | g0119 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01361 | hp1 | a0001 | c0001 | t0074 | g0059 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01361 | hp2 | a0002 | c0005 | t0030 | g0312 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01433 | hp1 | a0001 | c0001 | t0017 | g0173 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01433 | hp2 | a0001 | c0003 | t0011 | g0049 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01496 | hp1 | a0024 | c0044 | t0001 | g0090 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0118 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01515 | hp1 | a0001 | c0001 | t0010 | g0159 | EUR | IBS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | IBS | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01884 | hp1 | a0001 | c0003 | t0007 | g0095 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0361 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01891 | hp2 | a0001 | c0003 | t0007 | g0198 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01943 | hp1 | a0001 | c0001 | t0009 | g0127 | AMR | PEL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01943 | hp2 | a0020 | c0033 | t0001 | g0062 | AMR | PEL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01975 | hp1 | a0001 | c0053 | t0001 | g0113 | AMR | PEL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01975 | hp2 | a0002 | c0005 | t0030 | g0246 | AMR | PEL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | PEL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01981 | hp2 | a0010 | c0016 | t0002 | g0126 | AMR | PEL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02004 | hp1 | a0002 | c0005 | t0001 | g0076 | AMR | PEL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0172 | AMR | PEL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02015 | hp2 | a0025 | c0032 | t0023 | g0084 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02027 | hp1 | a0001 | c0004 | t0021 | g0243 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02027 | hp2 | a0001 | c0002 | t0023 | g0281 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02040 | hp2 | a0001 | c0004 | t0003 | g0236 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02055 | hp2 | a0003 | c0007 | t0012 | g0358 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02056 | hp1 | a0001 | c0001 | t0013 | g0276 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02071 | hp1 | a0001 | c0003 | t0004 | g0213 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02074 | hp1 | a0012 | c0013 | t0003 | g0317 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02074 | hp2 | a0001 | c0001 | t0063 | g0032 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02080 | hp1 | a0001 | c0002 | t0008 | g0033 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02080 | hp2 | a0001 | c0002 | t0041 | g0280 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02083 | hp1 | a0001 | c0001 | t0042 | g0232 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02132 | hp1 | a0001 | c0040 | t0043 | g0214 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02145 | hp1 | a0001 | c0003 | t0019 | g0328 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0326 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CDX | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02155 | hp2 | a0001 | c0002 | t0050 | g0282 | EAS | CDX | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02165 | hp1 | a0009 | c0019 | t0004 | g0208 | EAS | CDX | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02165 | hp2 | a0001 | c0002 | t0006 | g0315 | EAS | CDX | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0101 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02257 | hp2 | a0001 | c0015 | t0018 | g0331 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02273 | hp1 | a0010 | c0016 | t0049 | g0077 | AMR | PEL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02273 | hp2 | a0002 | c0005 | t0001 | g0058 | AMR | PEL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02280 | hp1 | a0001 | c0001 | t0034 | g0230 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02280 | hp2 | a0001 | c0002 | t0058 | g0137 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0344 | AMR | PEL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02451 | hp1 | a0006 | c0018 | t0040 | g0297 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0353 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02523 | hp1 | a0001 | c0003 | t0001 | g0305 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | KHV | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02602 | hp1 | a0002 | c0005 | t0034 | g0150 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0105 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0060 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02615 | hp2 | a0005 | c0011 | t0010 | g0017 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02622 | hp1 | a0030 | c0035 | t0018 | g0048 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0050 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02630 | hp1 | a0001 | c0012 | t0038 | g0196 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02630 | hp2 | a0011 | c0014 | t0018 | g0106 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02647 | hp1 | a0026 | c0054 | t0051 | g0135 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02647 | hp2 | a0003 | c0007 | t0010 | g0027 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02683 | hp1 | a0001 | c0001 | t0062 | g0019 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02717 | hp1 | a0001 | c0001 | t0019 | g0320 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02717 | hp2 | a0007 | c0017 | t0011 | g0354 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02723 | hp1 | a0001 | c0015 | t0056 | g0099 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02723 | hp2 | a0001 | c0003 | t0044 | g0201 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0334 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02735 | hp2 | a0001 | c0002 | t0009 | g0041 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0040 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02738 | hp2 | a0001 | c0003 | t0008 | g0220 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02809 | hp1 | a0001 | c0006 | t0015 | g0167 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02809 | hp2 | a0031 | c0056 | t0020 | g0296 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02818 | hp1 | a0001 | c0006 | t0015 | g0168 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02818 | hp2 | a0001 | c0003 | t0075 | g0329 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02886 | hp1 | a0001 | c0003 | t0036 | g0131 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0335 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02895 | hp1 | a0001 | c0002 | t0032 | g0004 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02895 | hp2 | a0001 | c0003 | t0011 | g0132 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02896 | hp1 | a0001 | c0012 | t0038 | g0096 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02896 | hp2 | a0001 | c0009 | t0035 | g0007 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02897 | hp1 | a0001 | c0009 | t0076 | g0007 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02897 | hp2 | a0001 | c0002 | t0032 | g0004 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02922 | hp1 | a0001 | c0006 | t0033 | g0324 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0139 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02970 | hp1 | a0001 | c0006 | t0007 | g0337 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02970 | hp2 | a0001 | c0002 | t0028 | g0109 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02976 | hp1 | a0008 | c0041 | t0012 | g0197 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02976 | hp2 | a0027 | c0025 | t0059 | g0009 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03041 | hp1 | a0001 | c0001 | t0025 | g0338 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0128 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03098 | hp1 | a0003 | c0007 | t0012 | g0098 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03098 | hp2 | a0001 | c0006 | t0015 | g0169 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03130 | hp1 | a0001 | c0001 | t0020 | g0115 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03130 | hp2 | a0001 | c0001 | t0025 | g0029 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03139 | hp1 | a0001 | c0001 | t0080 | g0130 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03139 | hp2 | a0019 | c0021 | t0020 | g0355 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03195 | hp1 | a0005 | c0011 | t0010 | g0107 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03195 | hp2 | a0001 | c0003 | t0007 | g0258 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03209 | hp1 | a0011 | c0014 | t0018 | g0010 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03209 | hp2 | a0001 | c0001 | t0011 | g0341 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03225 | hp1 | a0018 | c0022 | t0018 | g0186 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03225 | hp2 | a0005 | c0011 | t0010 | g0134 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03239 | hp1 | a0004 | c0010 | t0004 | g0133 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03453 | hp1 | a0001 | c0002 | t0028 | g0110 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03453 | hp2 | a0006 | c0057 | t0036 | g0212 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03486 | hp1 | a0001 | c0012 | t0016 | g0325 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0349 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03490 | hp1 | a0001 | c0002 | t0009 | g0184 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03491 | hp1 | a0001 | c0001 | t0017 | g0202 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0003 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0003 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03492 | hp2 | a0001 | c0002 | t0009 | g0158 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03516 | hp1 | a0003 | c0007 | t0012 | g0122 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03516 | hp2 | a0001 | c0001 | t0025 | g0136 | AFR | ESN | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0323 | AFR | GWD | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03579 | hp1 | a0006 | c0018 | t0040 | g0200 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03579 | hp2 | a0004 | c0043 | t0079 | g0357 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03654 | hp1 | a0002 | c0049 | t0005 | g0300 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03669 | hp1 | a0002 | c0005 | t0001 | g0016 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03669 | hp2 | a0001 | c0001 | t0010 | g0015 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03831 | hp1 | a0001 | c0003 | t0008 | g0100 | SAS | BEB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0188 | SAS | BEB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03834 | hp1 | a0002 | c0005 | t0014 | g0045 | SAS | BEB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0287 | SAS | BEB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03927 | hp1 | a0001 | c0001 | t0014 | g0028 | SAS | BEB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0284 | SAS | BEB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03942 | hp1 | a0001 | c0001 | t0011 | g0272 | SAS | BEB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | STU | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | STU | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG04184 | hp1 | a0001 | c0001 | t0061 | g0140 | SAS | BEB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG04199 | hp1 | a0022 | c0045 | t0004 | g0162 | SAS | STU | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG04199 | hp2 | a0001 | c0001 | t0031 | g0342 | SAS | STU | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18522 | hp1 | a0001 | c0003 | t0007 | g0330 | AFR | YRI | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18522 | hp2 | a0003 | c0007 | t0012 | g0108 | AFR | YRI | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18612 | hp1 | a0001 | c0024 | t0002 | g0235 | EAS | CHB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CHB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | CHB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18906 | hp1 | a0003 | c0007 | t0012 | g0356 | AFR | YRI | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18906 | hp2 | a0004 | c0010 | t0010 | g0092 | AFR | YRI | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18939 | hp1 | a0016 | c0037 | t0013 | g0270 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18939 | hp2 | a0001 | c0003 | t0037 | g0034 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18941 | hp2 | a0001 | c0003 | t0013 | g0225 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18942 | hp1 | a0001 | c0003 | t0022 | g0346 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18942 | hp2 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18944 | hp1 | a0001 | c0003 | t0002 | g0257 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18946 | hp1 | a0001 | c0002 | t0004 | g0071 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18950 | hp1 | a0012 | c0013 | t0003 | g0191 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18950 | hp2 | a0001 | c0020 | t0065 | g0142 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18951 | hp1 | a0001 | c0026 | t0001 | g0310 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18951 | hp2 | a0001 | c0003 | t0004 | g0129 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18952 | hp1 | a0001 | c0001 | t0013 | g0233 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18952 | hp2 | a0001 | c0003 | t0008 | g0042 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18954 | hp1 | a0001 | c0002 | t0004 | g0292 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18954 | hp2 | a0002 | c0005 | t0023 | g0350 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18957 | hp1 | a0001 | c0001 | t0048 | g0290 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18957 | hp2 | a0001 | c0002 | t0004 | g0145 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18960 | hp1 | a0001 | c0002 | t0022 | g0143 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18960 | hp2 | a0001 | c0004 | t0003 | g0289 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18962 | hp1 | a0001 | c0002 | t0006 | g0176 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18962 | hp2 | a0002 | c0005 | t0002 | g0242 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18964 | hp1 | a0002 | c0008 | t0003 | g0065 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18964 | hp2 | a0001 | c0001 | t0055 | g0293 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18966 | hp1 | a0002 | c0008 | t0003 | g0069 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18966 | hp2 | a0001 | c0002 | t0013 | g0052 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18968 | hp1 | a0001 | c0004 | t0021 | g0138 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18968 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18969 | hp1 | a0001 | c0004 | t0021 | g0298 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18969 | hp2 | a0002 | c0008 | t0003 | g0067 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18970 | hp1 | a0015 | c0036 | t0039 | g0347 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18971 | hp2 | a0001 | c0001 | t0047 | g0221 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18973 | hp1 | a0001 | c0002 | t0027 | g0249 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18973 | hp2 | a0001 | c0027 | t0003 | g0262 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18977 | hp1 | a0001 | c0004 | t0003 | g0275 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18977 | hp2 | a0001 | c0030 | t0067 | g0070 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18979 | hp1 | a0001 | c0004 | t0003 | g0207 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18979 | hp2 | a0001 | c0001 | t0064 | g0023 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18981 | hp1 | a0001 | c0004 | t0003 | g0345 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18981 | hp2 | a0001 | c0003 | t0002 | g0291 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18982 | hp2 | a0001 | c0002 | t0039 | g0063 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18984 | hp1 | a0001 | c0003 | t0008 | g0018 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18985 | hp1 | a0001 | c0003 | t0002 | g0181 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18986 | hp1 | a0001 | c0002 | t0006 | g0056 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18986 | hp2 | a0002 | c0005 | t0013 | g0055 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18988 | hp1 | a0001 | c0004 | t0052 | g0089 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18990 | hp1 | a0001 | c0004 | t0003 | g0238 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18990 | hp2 | a0001 | c0001 | t0026 | g0255 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18991 | hp1 | a0001 | c0001 | t0073 | g0026 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18991 | hp2 | a0001 | c0003 | t0004 | g0265 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18995 | hp1 | a0001 | c0001 | t0071 | g0322 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18995 | hp2 | a0001 | c0046 | t0016 | g0179 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18997 | hp1 | a0001 | c0002 | t0006 | g0250 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18997 | hp2 | a0002 | c0005 | t0013 | g0295 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18999 | hp1 | a0001 | c0003 | t0004 | g0351 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18999 | hp2 | a0001 | c0003 | t0008 | g0157 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19000 | hp1 | a0001 | c0001 | t0016 | g0307 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19002 | hp1 | a0001 | c0004 | t0003 | g0030 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19005 | hp1 | a0001 | c0029 | t0002 | g0253 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19005 | hp2 | a0001 | c0004 | t0003 | g0022 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19009 | hp1 | a0001 | c0004 | t0003 | g0247 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19009 | hp2 | a0001 | c0001 | t0016 | g0217 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19010 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19011 | hp1 | a0021 | c0031 | t0002 | g0114 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19011 | hp2 | a0001 | c0004 | t0003 | g0064 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19012 | hp2 | a0001 | c0001 | t0009 | g0177 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19030 | hp1 | a0001 | c0001 | t0069 | g0206 | AFR | LWK | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0263 | AFR | LWK | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19043 | hp1 | a0001 | c0003 | t0007 | g0359 | AFR | LWK | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19043 | hp2 | a0001 | c0006 | t0081 | g0012 | AFR | LWK | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19054 | hp2 | a0009 | c0034 | t0004 | g0286 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19057 | hp1 | a0001 | c0002 | t0026 | g0031 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19057 | hp2 | a0001 | c0002 | t0006 | g0073 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19060 | hp1 | a0001 | c0003 | t0002 | g0152 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19060 | hp2 | a0002 | c0008 | t0046 | g0068 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19064 | hp1 | a0001 | c0004 | t0003 | g0251 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19064 | hp2 | a0001 | c0002 | t0006 | g0311 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19067 | hp2 | a0001 | c0004 | t0003 | g0072 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0321 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19070 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19074 | hp1 | a0001 | c0002 | t0022 | g0192 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19074 | hp2 | a0001 | c0003 | t0037 | g0074 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19077 | hp2 | a0001 | c0003 | t0008 | g0148 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19079 | hp2 | a0001 | c0003 | t0004 | g0266 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19082 | hp1 | a0001 | c0002 | t0026 | g0116 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19082 | hp2 | a0001 | c0002 | t0077 | g0154 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19083 | hp1 | a0002 | c0005 | t0001 | g0278 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19083 | hp2 | a0001 | c0002 | t0006 | g0038 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19087 | hp1 | a0001 | c0004 | t0003 | g0156 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19087 | hp2 | a0001 | c0003 | t0008 | g0057 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19088 | hp1 | a0002 | c0005 | t0054 | g0166 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19240 | hp1 | a0001 | c0002 | t0028 | g0155 | AFR | YRI | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA19240 | hp2 | a0001 | c0001 | t0011 | g0348 | AFR | YRI | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA20129 | hp1 | a0017 | c0023 | t0020 | g0339 | AFR | ASW | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA20129 | hp2 | a0001 | c0002 | t0072 | g0111 | AFR | ASW | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA20752 | hp2 | a0001 | c0001 | t0009 | g0204 | EUR | TSI | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA20805 | hp1 | a0004 | c0010 | t0066 | g0269 | EUR | TSI | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0163 | EUR | TSI | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | GIH | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA20905 | hp2 | a0001 | c0001 | t0070 | g0008 | SAS | GIH | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG01123 | hp2 | a0001 | c0002 | t0005 | g0124 | AMR | CLM | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0161 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02486 | hp2 | a0008 | c0047 | t0029 | g0160 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02559 | hp1 | a0003 | c0038 | t0012 | g0013 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG02559 | hp2 | a0001 | c0055 | t0024 | g0153 | AFR | ACB | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03471 | hp1 | a0007 | c0017 | t0016 | g0327 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG03471 | hp2 | a0001 | c0006 | t0015 | g0021 | AFR | MSL | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG06807 | hp1 | a0001 | c0003 | t0024 | g0097 | AFR | USA | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| HG06807 | hp2 | a0001 | c0001 | t0068 | g0340 | AFR | USA | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18955 | hp1 | a0001 | c0002 | t0006 | g0037 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | USA | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA20300 | hp2 | a0001 | c0006 | t0015 | g0141 | AFR | USA | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA21309 | hp1 | a0001 | c0001 | t0031 | g0336 | AFR | LWK | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| NA21309 | hp2 | a0001 | c0001 | t0057 | g0104 | AFR | LWK | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0086 | REF | REF | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0121 | REF | REF | UNC5B_chr10_71207570_71307864 | UNC5B | chr10 | 71207570 | 71307864 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:71213013
|
G | T | 2 | a0006a0031 | 4 | HG02451.hp1 HG02809.hp2 HG03453.hp2 others(1): Show |
missense_variant | MODERATE | c.28G>T | p.Ala10Ser | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/17 | 444/6841 | 28/2838 | 10/945 | chr10 | 71213013 | ||
| chr10:71213014
|
C | T | 2 | a0006a0031 | 4 | HG02451.hp1 HG02809.hp2 HG03453.hp2 others(1): Show |
missense_variant | MODERATE | c.29C>T | p.Ala10Val | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/17 | 445/6841 | 29/2838 | 10/945 | chr10 | 71213014 | ||
| chr10:71279993
|
G | T | 1 | a0013 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.252G>T | p.Glu84Asp | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/17 | 668/6841 | 252/2838 | 84/945 | chr10 | 71279993 | ||
| chr10:71286755
|
G | A | 1 | a0030 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.619G>A | p.Asp207Asn | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/17 | 1035/6841 | 619/2838 | 207/945 | chr10 | 71286755 | ||
| chr10:71286789
|
C | T | 2 | a0007a0014 | 3 | HG01243.hp2 HG02717.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.653C>T | p.Ser218Leu | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/17 | 1069/6841 | 653/2838 | 218/945 | chr10 | 71286789 | ||
| chr10:71286860
|
A | G | 2 | a0002a0029 | 21 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(18): Show |
missense_variant | MODERATE | c.724A>G | p.Ile242Val | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/17 | 1140/6841 | 724/2838 | 242/945 | chr10 | 71286860 | ||
| chr10:71286869
|
G | A | 1 | a0015 | 1 | NA18970.hp1 | missense_variant&splice_region_variant | MODERATE | c.733G>A | p.Val245Met | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/17 | 1149/6841 | 733/2838 | 245/945 | chr10 | 71286869 | ||
| chr10:71290974
|
G | A | 1 | a0016 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.1159G>A | p.Val387Ile | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 9/17 | 1575/6841 | 1159/2838 | 387/945 | chr10 | 71290974 | ||
| chr10:71291017
|
G | A | 5 | a0003a0017a0018others(2): Show | 12 | HG01106.hp2 HG02055.hp2 HG02559.hp1 others(9): Show |
missense_variant | MODERATE | c.1202G>A | p.Arg401His | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 9/17 | 1618/6841 | 1202/2838 | 401/945 | chr10 | 71291017 | ||
| chr10:71291034
|
G | A | 1 | a0028 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.1219G>A | p.Asp407Asn | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 9/17 | 1635/6841 | 1219/2838 | 407/945 | chr10 | 71291034 | ||
| chr10:71291495
|
G | T | 1 | a0020 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.1358G>T | p.Arg453Leu | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/17 | 1774/6841 | 1358/2838 | 453/945 | chr10 | 71291495 | ||
| chr10:71291677
|
G | A | 1 | a0027 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.1540G>A | p.Asp514Asn | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/17 | 1956/6841 | 1540/2838 | 514/945 | chr10 | 71291677 | ||
| chr10:71291683
|
G | A | 3 | a0004a0019a0026 | 8 | HG00140.hp2 HG01109.hp2 HG02647.hp1 others(5): Show |
missense_variant | MODERATE | c.1546G>A | p.Ala516Thr | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/17 | 1962/6841 | 1546/2838 | 516/945 | chr10 | 71291683 | ||
| chr10:71291761
|
G | T | 1 | a0026 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.1624G>T | p.Gly542Trp | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/17 | 2040/6841 | 1624/2838 | 542/945 | chr10 | 71291761 | ||
| chr10:71291770
|
G | A | 1 | a0029 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.1633G>A | p.Val545Ile | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/17 | 2049/6841 | 1633/2838 | 545/945 | chr10 | 71291770 | ||
| chr10:71291811
|
C | G | 2 | a0012a0025 | 3 | HG02015.hp2 HG02074.hp1 NA18950.hp1 |
missense_variant | MODERATE | c.1674C>G | p.Ile558Met | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/17 | 2090/6841 | 1674/2838 | 558/945 | chr10 | 71291811 | ||
| chr10:71293523
|
C | T | 1 | a0021 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.1891C>T | p.Arg631Cys | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 12/17 | 2307/6841 | 1891/2838 | 631/945 | chr10 | 71293523 | ||
| chr10:71293799
|
G | A | 2 | a0005a0028 | 4 | HG00639.hp2 HG02615.hp2 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.2041G>A | p.Val681Met | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/17 | 2457/6841 | 2041/2838 | 681/945 | chr10 | 71293799 | ||
| chr10:71296630
|
C | G | 3 | a0003a0008a0014 | 11 | HG01106.hp2 HG01243.hp2 HG02055.hp2 others(8): Show |
missense_variant | MODERATE | c.2378C>G | p.Thr793Ser | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/17 | 2794/6841 | 2378/2838 | 793/945 | chr10 | 71296630 | ||
| chr10:71296709
|
CCAGATAT others(143): Show |
C | 2 | a0011a0018 | 3 | HG02630.hp2 HG03209.hp1 HG03225.hp1 |
frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.2475_2490+134del | p.His825fs | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/17 | 2891/6841 | 2475/2838 | 825/945 | INFO_REALIGN_3_PRIME | chr10 | 71296709 | |
| chr10:71296712
|
GATATTCC others(43): Show |
G | 1 | a0024 | 1 | HG01496.hp1 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.2475_2490+34delTAC others(47): Show |
p.His825fs | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/17 | 2891/6841 | 2475/2838 | 825/945 | INFO_REALIGN_3_PRIME | chr10 | 71296712 | |
| chr10:71296733
|
TCTGGCAG others(43): Show |
T | 1 | a0010 | 2 | HG01981.hp2 HG02273.hp1 |
frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.2487_2490+46delAGA others(47): Show |
p.Glu830fs | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/17 | 2903/6841 | 2487/2838 | 829/945 | INFO_REALIGN_3_PRIME | chr10 | 71296733 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:71213045
|
C | T | 1 | a0001c0055 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.60C>T | p.Asp20Asp | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/17 | 476/6841 | 60/2838 | 20/945 | chr10 | 71213045 | ||
| chr10:71279837
|
C | T | 1 | a0026c0054 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.96C>T | p.Ser32Ser | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/17 | 512/6841 | 96/2838 | 32/945 | chr10 | 71279837 | ||
| chr10:71279879
|
G | A | 1 | a0001c0009 | 4 | HG00735.hp1 HG01255.hp2 HG02896.hp2 others(1): Show |
synonymous_variant | LOW | c.138G>A | p.Pro46Pro | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/17 | 554/6841 | 138/2838 | 46/945 | chr10 | 71279879 | ||
| chr10:71279909
|
C | T | 1 | a0001c0053 | 1 | HG01975.hp1 | synonymous_variant | LOW | c.168C>T | p.Asp56Asp | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/17 | 584/6841 | 168/2838 | 56/945 | chr10 | 71279909 | ||
| chr10:71280008
|
C | T | 1 | a0001c0051 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.267C>T | p.Asn89Asn | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/17 | 683/6841 | 267/2838 | 89/945 | chr10 | 71280008 | ||
| chr10:71284754
|
G | A | 1 | a0009c0019 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.339G>A | p.Ser113Ser | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 3/17 | 755/6841 | 339/2838 | 113/945 | chr10 | 71284754 | ||
| chr10:71284823
|
G | A | 21 | a0001c0001a0001c0020a0001c0024others(18): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
synonymous_variant | LOW | c.408G>A | p.Ala136Ala | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 3/17 | 824/6841 | 408/2838 | 136/945 | chr10 | 71284823 | ||
| chr10:71286868
|
C | T | 7 | a0001c0006a0002c0005a0002c0008others(4): Show | 33 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(30): Show |
splice_region_variant&synonymous_variant | LOW | c.732C>T | p.Tyr244Tyr | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/17 | 1148/6841 | 732/2838 | 244/945 | chr10 | 71286868 | ||
| chr10:71287605
|
C | T | 1 | a0008c0047 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.741C>T | p.Gly247Gly | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 6/17 | 1157/6841 | 741/2838 | 247/945 | chr10 | 71287605 | ||
| chr10:71288650
|
G | A | 1 | a0001c0020 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.984G>A | p.Ala328Ala | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 7/17 | 1400/6841 | 984/2838 | 328/945 | chr10 | 71288650 | ||
| chr10:71288974
|
C | T | 1 | a0009c0034 | 1 | NA19054.hp2 | synonymous_variant | LOW | c.1083C>T | p.Ser361Ser | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/17 | 1499/6841 | 1083/2838 | 361/945 | chr10 | 71288974 | ||
| chr10:71291631
|
T | C | 15 | a0001c0003a0001c0015a0001c0024others(12): Show | 81 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
synonymous_variant | LOW | c.1494T>C | p.Asp498Asp | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/17 | 1910/6841 | 1494/2838 | 498/945 | chr10 | 71291631 | ||
| chr10:71293483
|
C | T | 2 | a0001c0046a0016c0037 | 2 | NA18939.hp1 NA18995.hp2 |
synonymous_variant | LOW | c.1851C>T | p.Pro617Pro | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 12/17 | 2267/6841 | 1851/2838 | 617/945 | chr10 | 71293483 | ||
| chr10:71293564
|
C | T | 2 | a0001c0020a0001c0030 | 2 | NA18950.hp2 NA18977.hp2 |
synonymous_variant | LOW | c.1932C>T | p.Gly644Gly | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 12/17 | 2348/6841 | 1932/2838 | 644/945 | chr10 | 71293564 | ||
| chr10:71295861
|
G | A | 1 | a0004c0042 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.2226G>A | p.Pro742Pro | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 14/17 | 2642/6841 | 2226/2838 | 742/945 | chr10 | 71295861 | ||
| chr10:71296727
|
T | C | 8 | a0001c0012a0001c0026a0001c0030others(5): Show | 11 | HG01243.hp2 HG02132.hp1 HG02451.hp1 others(8): Show |
synonymous_variant | LOW | c.2475T>C | p.His825His | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/17 | 2891/6841 | 2475/2838 | 825/945 | chr10 | 71296727 | ||
| chr10:71296733
|
T | A | 1 | a0001c0026 | 1 | NA18951.hp1 | synonymous_variant | LOW | c.2481T>A | p.Thr827Thr | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/17 | 2897/6841 | 2481/2838 | 827/945 | chr10 | 71296733 | ||
| chr10:71296733
|
T | G | 3 | a0001c0015a0001c0030a0004c0043 | 4 | HG02257.hp2 HG02723.hp1 HG03579.hp2 others(1): Show |
synonymous_variant | LOW | c.2481T>G | p.Thr827Thr | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/17 | 2897/6841 | 2481/2838 | 827/945 | chr10 | 71296733 | ||
| chr10:71296739
|
A | G | 4 | a0001c0015a0001c0026a0001c0029others(1): Show | 5 | HG02257.hp2 HG02723.hp1 HG03579.hp2 others(2): Show |
synonymous_variant | LOW | c.2487A>G | p.Ala829Ala | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/17 | 2903/6841 | 2487/2838 | 829/945 | chr10 | 71296739 | ||
| chr10:71297998
|
G | C | 6 | a0001c0004a0001c0027a0001c0040others(3): Show | 29 | HG00140.hp2 HG00544.hp1 HG00609.hp2 others(26): Show |
synonymous_variant | LOW | c.2580G>C | p.Leu860Leu | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 16/17 | 2996/6841 | 2580/2838 | 860/945 | chr10 | 71297998 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:71212596
|
A | G | 1 | a0001c0006t0081 | 1 | NA19043.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-390A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/17 | chr10 | 71212596 | ||||||
| chr10:71212597
|
G | A | 1 | a0001c0002t0041 | 1 | HG02080.hp2 | 5_prime_UTR_variant | MODIFIER | c.-389G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/17 | 389 | chr10 | 71212597 | |||||
| chr10:71212666
|
G | A | 1 | a0001c0001t0042 | 1 | HG02083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-320G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/17 | 320 | chr10 | 71212666 | |||||
| chr10:71212724
|
G | T | 1 | a0001c0001t0080 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-262G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/17 | 262 | chr10 | 71212724 | |||||
| chr10:71212877
|
G | T | 1 | a0004c0043t0079 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-109G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/17 | 109 | chr10 | 71212877 | |||||
| chr10:71299347
|
G | A | 5 | a0001c0002t0008a0001c0003t0008a0001c0040t0043others(2): Show | 13 | HG00408.hp2 HG00438.hp1 HG01243.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*70G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 70 | chr10 | 71299347 | |||||
| chr10:71299407
|
C | A | 1 | a0001c0003t0044 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*130C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 130 | chr10 | 71299407 | |||||
| chr10:71299418
|
C | A | 1 | a0001c0001t0045 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*141C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 141 | chr10 | 71299418 | |||||
| chr10:71299601
|
C | G | 62 | a0001c0001t0002a0001c0001t0010a0001c0001t0016others(59): Show | 128 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*324C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 324 | chr10 | 71299601 | |||||
| chr10:71299629
|
T | C | 1 | a0001c0001t0071 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 352 | chr10 | 71299629 | |||||
| chr10:71299632
|
A | G | 34 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(31): Show | 69 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*355A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 355 | chr10 | 71299632 | |||||
| chr10:71299646
|
C | G | 7 | a0001c0002t0008a0001c0002t0078a0001c0003t0008others(4): Show | 16 | HG00408.hp2 HG00438.hp1 HG01169.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*369C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 369 | chr10 | 71299646 | |||||
| chr10:71299650
|
C | CT | 122 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(119): Show | 240 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*374dupT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 375 | INFO_REALIGN_3_PRIME | chr10 | 71299650 | ||||
| chr10:71299652
|
C | T | 1 | a0001c0001t0061 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*375C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 375 | chr10 | 71299652 | |||||
| chr10:71299664
|
C | A | 1 | a0002c0008t0046 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 387 | chr10 | 71299664 | |||||
| chr10:71299806
|
C | T | 1 | a0028c0039t0060 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*529C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 529 | chr10 | 71299806 | |||||
| chr10:71299894
|
A | G | 2 | a0001c0002t0039a0015c0036t0039 | 2 | NA18970.hp1 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*617A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 617 | chr10 | 71299894 | |||||
| chr10:71299924
|
G | GA | 104 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(101): Show | 209 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*656dupA | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 657 | INFO_REALIGN_3_PRIME | chr10 | 71299924 | ||||
| chr10:71299924
|
G | GAA | 8 | a0001c0001t0019a0001c0003t0019a0001c0003t0044others(5): Show | 12 | HG00735.hp1 HG01106.hp1 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*655_*656dupAA | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 657 | INFO_REALIGN_3_PRIME | chr10 | 71299924 | ||||
| chr10:71300029
|
C | CTG | 15 | a0001c0001t0006a0001c0001t0016a0001c0001t0017others(12): Show | 34 | HG00423.hp1 HG00609.hp1 HG01106.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*784_*785dupGT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 786 | INFO_REALIGN_3_PRIME | chr10 | 71300029 | ||||
| chr10:71300029
|
C | CTGTG | 38 | a0001c0001t0004a0001c0001t0011a0001c0001t0013others(35): Show | 88 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*782_*785dupGTGT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 786 | INFO_REALIGN_3_PRIME | chr10 | 71300029 | ||||
| chr10:71300029
|
C | CTGTGTG | 26 | a0001c0001t0005a0001c0001t0007a0001c0001t0026others(23): Show | 45 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*780_*785dupGTGTGT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 786 | INFO_REALIGN_3_PRIME | chr10 | 71300029 | ||||
| chr10:71300029
|
C | CTGTGTGT others(1): Show |
3 | a0001c0001t0070a0001c0002t0058a0027c0025t0059 | 3 | HG02280.hp2 HG02976.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*778_*785dupGTGTGT others(2): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 786 | INFO_REALIGN_3_PRIME | chr10 | 71300029 | ||||
| chr10:71300029
|
CTG | C | 12 | a0001c0001t0009a0001c0001t0031a0001c0001t0073others(9): Show | 27 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*784_*785delGT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 784 | INFO_REALIGN_3_PRIME | chr10 | 71300029 | ||||
| chr10:71300029
|
CTGTG | C | 6 | a0001c0001t0027a0001c0002t0027a0001c0002t0078others(3): Show | 8 | HG01070.hp2 HG01071.hp2 HG01169.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*782_*785delGTGT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 782 | INFO_REALIGN_3_PRIME | chr10 | 71300029 | ||||
| chr10:71300029
|
CTGTGTG | C | 2 | a0001c0002t0008a0001c0003t0008 | 10 | HG00408.hp2 HG00438.hp1 HG02080.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*780_*785delGTGTGT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 780 | INFO_REALIGN_3_PRIME | chr10 | 71300029 | ||||
| chr10:71300029
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0006t0015 | 6 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*774_*785delGTGTGT others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 774 | INFO_REALIGN_3_PRIME | chr10 | 71300029 | ||||
| chr10:71300070
|
C | G | 36 | a0001c0001t0004a0001c0001t0011a0001c0001t0013others(33): Show | 64 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*793C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 793 | chr10 | 71300070 | |||||
| chr10:71300096
|
T | C | 1 | a0001c0002t0072 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 819 | chr10 | 71300096 | |||||
| chr10:71300308
|
C | T | 54 | a0001c0001t0002a0001c0001t0010a0001c0001t0016others(51): Show | 110 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1031C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 1031 | chr10 | 71300308 | |||||
| chr10:71300346
|
T | A | 1 | a0026c0054t0051 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1069T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 1069 | chr10 | 71300346 | |||||
| chr10:71300390
|
G | A | 1 | a0001c0001t0047 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1113G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 1113 | chr10 | 71300390 | |||||
| chr10:71300520
|
G | A | 15 | a0001c0001t0004a0001c0001t0026a0001c0001t0063others(12): Show | 32 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1243G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 1243 | chr10 | 71300520 | |||||
| chr10:71300585
|
G | A | 1 | a0002c0005t0054 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1308G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 1308 | chr10 | 71300585 | |||||
| chr10:71301117
|
A | G | 1 | a0010c0016t0049 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1840A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 1840 | chr10 | 71301117 | |||||
| chr10:71301303
|
C | T | 1 | a0001c0001t0031 | 2 | HG04199.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2026C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2026 | chr10 | 71301303 | |||||
| chr10:71301325
|
G | A | 2 | a0001c0004t0021a0001c0004t0052 | 4 | HG02027.hp1 NA18968.hp1 NA18969.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2048G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2048 | chr10 | 71301325 | |||||
| chr10:71301473
|
A | C | 2 | a0001c0020t0065a0001c0030t0067 | 2 | NA18950.hp2 NA18977.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2196A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2196 | chr10 | 71301473 | |||||
| chr10:71301581
|
G | A | 1 | a0001c0015t0056 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2304G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2304 | chr10 | 71301581 | |||||
| chr10:71301587
|
G | C | 12 | a0001c0001t0005a0001c0001t0017a0001c0001t0034others(9): Show | 24 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2310G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2310 | chr10 | 71301587 | |||||
| chr10:71301594
|
T | C | 11 | a0001c0001t0007a0001c0001t0024a0001c0001t0057others(8): Show | 20 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2317T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2317 | chr10 | 71301594 | |||||
| chr10:71301745
|
A | G | 27 | a0001c0001t0002a0001c0001t0016a0001c0001t0027others(24): Show | 62 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2468A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2468 | chr10 | 71301745 | |||||
| chr10:71301770
|
GT | G | 7 | a0001c0001t0019a0001c0003t0019a0001c0003t0044others(4): Show | 10 | HG01106.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2494delT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2494 | chr10 | 71301770 | |||||
| chr10:71301797
|
G | A | 1 | a0001c0001t0063 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2520G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2520 | chr10 | 71301797 | |||||
| chr10:71301812
|
G | A | 3 | a0001c0002t0028a0001c0009t0035a0001c0009t0076 | 6 | HG00735.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2535G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2535 | chr10 | 71301812 | |||||
| chr10:71301944
|
C | T | 2 | a0008c0047t0029a0014c0050t0029 | 2 | HG01243.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2667C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2667 | chr10 | 71301944 | |||||
| chr10:71301951
|
A | G | 110 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(107): Show | 219 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*2674A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2674 | chr10 | 71301951 | |||||
| chr10:71302093
|
C | T | 1 | a0001c0001t0074 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2816C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2816 | chr10 | 71302093 | |||||
| chr10:71302108
|
G | GCGGAGGC others(10): Show |
3 | a0001c0001t0014a0002c0005t0014a0002c0005t0054 | 7 | HG00741.hp2 HG01069.hp1 HG01070.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2831_*2832insCGGA others(13): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2832 | chr10 | 71302108 | |||||
| chr10:71302109
|
T | C | 3 | a0001c0001t0014a0002c0005t0014a0002c0005t0054 | 7 | HG00741.hp2 HG01069.hp1 HG01070.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2832T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2832 | chr10 | 71302109 | |||||
| chr10:71302127
|
G | A | 1 | a0001c0001t0048 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2850G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2850 | chr10 | 71302127 | |||||
| chr10:71302270
|
C | T | 1 | a0001c0002t0050 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2993C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 2993 | chr10 | 71302270 | |||||
| chr10:71302272
|
TGTGTGCG others(5): Show |
T | 1 | a0001c0015t0056 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3006_*3017delGCGT others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 3006 | INFO_REALIGN_3_PRIME | chr10 | 71302272 | ||||
| chr10:71302291
|
G | T | 46 | a0001c0001t0004a0001c0001t0010a0001c0001t0011others(43): Show | 93 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*3014G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 3014 | chr10 | 71302291 | |||||
| chr10:71302386
|
C | T | 1 | a0004c0010t0066 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3109C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 3109 | chr10 | 71302386 | |||||
| chr10:71302392
|
A | C | 36 | a0001c0001t0004a0001c0001t0010a0001c0001t0011others(33): Show | 73 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*3115A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 3115 | chr10 | 71302392 | |||||
| chr10:71302505
|
G | A | 1 | a0001c0003t0037 | 2 | NA18939.hp2 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3228G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 3228 | chr10 | 71302505 | |||||
| chr10:71302519
|
G | GGGGTAGG others(85): Show |
1 | a0001c0002t0028 | 3 | HG02970.hp2 HG03453.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3320_*3321insGGCT others(88): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 3321 | INFO_REALIGN_3_PRIME | chr10 | 71302519 | ||||
| chr10:71302731
|
G | A | 26 | a0001c0001t0002a0001c0001t0016a0001c0001t0027others(23): Show | 61 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3454G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 3454 | chr10 | 71302731 | |||||
| chr10:71302777
|
A | G | 5 | a0001c0002t0008a0001c0003t0008a0001c0040t0043others(2): Show | 13 | HG00408.hp2 HG00438.hp1 HG01243.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3500A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 17/17 | 3500 | chr10 | 71302777 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:71213246
|
C | G | 9 | a0001c0001t0011g0361a0001c0001t0019g0353a0001c0003t0007g0359others(6): Show | 9 | HG00735.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+182C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71213246 | ||||||
| chr10:71213331
|
G | T | 5 | a0001c0001t0011g0361a0001c0003t0007g0359a0001c0009t0035g0360others(2): Show | 5 | HG00735.hp1 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+267G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71213331 | ||||||
| chr10:71213389
|
C | T | 37 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0332others(34): Show | 37 | HG00558.hp2 HG00735.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.79+325C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71213389 | ||||||
| chr10:71213457
|
C | T | 1 | a0014c0050t0029g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.79+393C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71213457 | ||||||
| chr10:71213470
|
C | T | 2 | a0001c0001t0004g0316a0012c0013t0003g0317 | 2 | HG02074.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.79+406C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71213470 | ||||||
| chr10:71213474
|
T | C | 1 | a0001c0001t0070g0008 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.79+410T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71213474 | ||||||
| chr10:71213561
|
C | T | 19 | a0001c0001t0001g0299a0001c0001t0001g0301a0001c0001t0002g0313others(16): Show | 20 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.79+497C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71213561 | ||||||
| chr10:71213629
|
G | A | 5 | a0001c0006t0015g0011a0001c0006t0081g0012a0003c0038t0012g0013others(2): Show | 5 | HG01069.hp2 HG02559.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+565G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71213629 | ||||||
| chr10:71213672
|
A | AATTATTA others(8): Show |
1 | a0001c0004t0021g0298 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.79+609_79+610insTT others(13): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213672 | |||||
| chr10:71213674
|
G | T | 1 | a0001c0004t0021g0298 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.79+610G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71213674 | ||||||
| chr10:71213675
|
A | AATT | 70 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(67): Show | 73 | HG00438.hp1 HG00639.hp2 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.79+643_79+645dupTT others(1): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213675 | |||||
| chr10:71213675
|
A | AATTATT | 33 | a0001c0001t0001g0203a0001c0001t0001g0218a0001c0001t0001g0224others(30): Show | 33 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.79+640_79+645dupTT others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213675 | |||||
| chr10:71213675
|
A | AATTATTA others(2): Show |
49 | a0001c0001t0001g0234a0001c0001t0001g0239a0001c0001t0001g0240others(46): Show | 49 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.79+637_79+645dupTT others(7): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213675 | |||||
| chr10:71213675
|
A | AATTATTA others(5): Show |
34 | a0001c0001t0001g0283a0001c0001t0001g0288a0001c0001t0001g0344others(31): Show | 34 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.79+634_79+645dupTT others(10): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213675 | |||||
| chr10:71213675
|
A | AATTATTA others(8): Show |
12 | a0001c0001t0001g0294a0001c0001t0007g0349a0001c0001t0011g0348others(9): Show | 12 | HG02451.hp1 HG02809.hp2 HG03486.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+631_79+645dupTT others(13): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213675 | |||||
| chr10:71213675
|
A | AATTATTT others(3): Show |
1 | a0001c0001t0011g0361 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.79+617_79+618insTA others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213675 | |||||
| chr10:71213675
|
A | T | 1 | a0001c0004t0021g0298 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.79+611A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71213675 | ||||||
| chr10:71213675
|
AATT | A | 28 | a0001c0001t0001g0319a0001c0001t0002g0313a0001c0001t0002g0314others(25): Show | 29 | HG00642.hp1 HG01069.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.79+643_79+645delTT others(1): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213675 | |||||
| chr10:71213675
|
AATTATT | A | 7 | a0001c0001t0001g0299a0001c0001t0001g0301a0001c0001t0005g0302others(4): Show | 7 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+640_79+645delTT others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213675 | |||||
| chr10:71213675
|
AATTATTA others(2): Show |
A | 3 | a0001c0001t0010g0015a0001c0002t0001g0014a0002c0005t0001g0016 | 3 | HG02683.hp2 HG03669.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.79+637_79+645delTT others(7): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213675 | |||||
| chr10:71213680
|
T | TTATTATT others(5): Show |
1 | a0001c0001t0001g0318 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.79+627_79+628insCT others(10): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213680 | |||||
| chr10:71213726
|
A | AGTGTGTG others(1): Show |
3 | a0001c0003t0007g0359a0001c0009t0035g0360a0003c0007t0012g0358 | 3 | HG00735.hp1 HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.79+663_79+664insTG others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213726 | |||||
| chr10:71213728
|
A | AGAGTGTG others(3): Show |
1 | a0003c0007t0012g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.79+665_79+666insAG others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
A | AGAGTGTG others(5): Show |
1 | a0001c0001t0019g0353 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.79+665_79+666insAG others(10): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
A | AGT | 53 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0144others(50): Show | 54 | HG00423.hp2 HG01070.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.79+697_79+698dupGT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
A | AGTGT | 20 | a0001c0001t0004g0316a0001c0001t0005g0040a0001c0001t0006g0039others(17): Show | 21 | HG00609.hp1 HG01081.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+695_79+698dupGT others(2): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
A | AGTGTGT | 54 | a0001c0001t0001g0203a0001c0001t0001g0240a0001c0001t0001g0283others(51): Show | 54 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.79+693_79+698dupGT others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
A | AGTGTGTG others(1): Show |
8 | a0001c0001t0001g0239a0001c0001t0004g0237a0001c0004t0003g0236others(5): Show | 8 | HG01243.hp2 HG02040.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+691_79+698dupGT others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
A | AGTGTGTG others(3): Show |
18 | a0001c0001t0001g0234a0001c0001t0001g0301a0001c0001t0001g0332others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+689_79+698dupGT others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
A | AGTGTGTG others(5): Show |
11 | a0001c0001t0002g0313a0001c0001t0002g0314a0001c0001t0007g0349others(8): Show | 11 | HG01361.hp2 HG03209.hp2 HG03486.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+687_79+698dupGT others(10): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
A | AGTGTGTG others(7): Show |
15 | a0001c0001t0001g0299a0001c0001t0001g0318a0001c0001t0011g0361others(12): Show | 16 | HG00642.hp1 HG01123.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.79+685_79+698dupGT others(12): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
A | AGTGTGTG others(9): Show |
6 | a0001c0001t0001g0319a0001c0001t0019g0320a0001c0002t0002g0306others(3): Show | 6 | HG02523.hp1 HG02717.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+683_79+698dupGT others(14): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
A | AGTGTGTG others(11): Show |
3 | a0001c0001t0031g0336a0001c0003t0019g0328a0001c0003t0075g0329 | 3 | HG02145.hp1 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+681_79+698dupGT others(16): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
A | AGTGTGTG others(13): Show |
1 | a0001c0001t0007g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.79+679_79+698dupGT others(18): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
A | AGTGTGTG others(19): Show |
1 | a0007c0017t0016g0327 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.79+673_79+698dupGT others(24): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
A | T | 3 | a0001c0003t0007g0359a0001c0009t0035g0360a0003c0007t0012g0358 | 3 | HG00735.hp1 HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.79+664A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71213728 | ||||||
| chr10:71213728
|
AGT | A | 5 | a0001c0001t0025g0136a0002c0005t0013g0295a0004c0010t0004g0133others(2): Show | 5 | HG02647.hp1 HG03225.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+697_79+698delGT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213728
|
AGTGT | A | 3 | a0006c0018t0040g0200a0006c0018t0040g0297a0031c0056t0020g0296 | 3 | HG02451.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.79+695_79+698delGT others(2): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71213728 | |||||
| chr10:71213960
|
C | T | 3 | a0001c0003t0007g0359a0001c0009t0035g0360a0003c0007t0012g0358 | 3 | HG00735.hp1 HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.79+896C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71213960 | ||||||
| chr10:71213971
|
C | T | 1 | a0001c0003t0011g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.79+907C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71213971 | ||||||
| chr10:71214057
|
A | T | 1 | a0001c0003t0036g0131 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.79+993A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71214057 | ||||||
| chr10:71214068
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.79+1004A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71214068 | ||||||
| chr10:71214075
|
G | C | 4 | a0001c0001t0010g0323a0001c0006t0033g0324a0001c0009t0035g0007others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+1011G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71214075 | ||||||
| chr10:71214096
|
C | A | 1 | a0002c0005t0001g0058 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.79+1032C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71214096 | ||||||
| chr10:71214098
|
G | C | 9 | a0001c0001t0011g0361a0001c0001t0019g0353a0001c0003t0007g0359others(6): Show | 9 | HG00735.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+1034G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71214098 | ||||||
| chr10:71214860
|
T | C | 1 | a0002c0049t0005g0300 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.79+1796T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71214860 | ||||||
| chr10:71214898
|
T | C | 1 | a0001c0001t0074g0059 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.79+1834T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71214898 | ||||||
| chr10:71214914
|
G | T | 29 | a0001c0001t0001g0318a0001c0001t0001g0332a0001c0001t0001g0344others(26): Show | 29 | HG00558.hp2 HG00735.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.79+1850G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71214914 | ||||||
| chr10:71214941
|
G | C | 1 | a0001c0001t0007g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.79+1877G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71214941 | ||||||
| chr10:71215171
|
T | G | 166 | a0001c0001t0001g0203a0001c0001t0001g0218a0001c0001t0001g0224others(163): Show | 167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.79+2107T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71215171 | ||||||
| chr10:71215176
|
T | A | 3 | a0006c0018t0040g0297a0006c0057t0036g0212a0031c0056t0020g0296 | 3 | HG02451.hp1 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.79+2112T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71215176 | ||||||
| chr10:71215270
|
A | G | 9 | a0001c0001t0011g0361a0001c0001t0019g0353a0001c0003t0007g0359others(6): Show | 9 | HG00735.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+2206A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71215270 | ||||||
| chr10:71215291
|
T | C | 4 | a0001c0001t0007g0139a0001c0006t0015g0167a0001c0006t0015g0168others(1): Show | 4 | HG02809.hp1 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+2227T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71215291 | ||||||
| chr10:71215677
|
C | T | 38 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0332others(35): Show | 38 | HG00558.hp2 HG00735.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.79+2613C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71215677 | ||||||
| chr10:71215690
|
T | C | 3 | a0001c0003t0007g0359a0001c0009t0035g0360a0003c0007t0012g0358 | 3 | HG00735.hp1 HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.79+2626T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71215690 | ||||||
| chr10:71215806
|
G | GGT | 3 | a0001c0001t0080g0130a0003c0007t0010g0027a0027c0025t0059g0009 | 3 | HG02647.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.79+2778_79+2779dup others(2): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71215806 | |||||
| chr10:71215806
|
G | GGTGT | 6 | a0001c0001t0005g0040a0001c0001t0014g0028a0001c0002t0009g0041others(3): Show | 7 | HG02735.hp2 HG02738.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+2776_79+2779dup others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71215806 | |||||
| chr10:71215806
|
GGT | G | 100 | a0001c0001t0001g0054a0001c0001t0001g0146a0001c0001t0001g0147others(97): Show | 101 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.79+2778_79+2779del others(2): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71215806 | |||||
| chr10:71215806
|
GGTGT | G | 24 | a0001c0001t0001g0183a0001c0001t0001g0228a0001c0001t0001g0240others(21): Show | 24 | HG00609.hp1 HG00741.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.79+2776_79+2779del others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71215806 | |||||
| chr10:71215806
|
GGTGTGT | G | 66 | a0001c0001t0001g0047a0001c0001t0001g0066a0001c0001t0001g0078others(63): Show | 68 | HG00423.hp2 HG00558.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.79+2774_79+2779del others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71215806 | |||||
| chr10:71215806
|
GGTGTGTG others(1): Show |
G | 23 | a0001c0001t0001g0318a0001c0001t0001g0332a0001c0001t0001g0344others(20): Show | 23 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.79+2772_79+2779del others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71215806 | |||||
| chr10:71215806
|
GGTGTGTG others(3): Show |
G | 77 | a0001c0001t0001g0170a0001c0001t0001g0218a0001c0001t0001g0264others(74): Show | 78 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.79+2770_79+2779del others(10): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71215806 | |||||
| chr10:71215806
|
GGTGTGTG others(7): Show |
G | 9 | a0001c0001t0011g0361a0001c0001t0019g0353a0001c0003t0004g0213others(6): Show | 9 | HG00735.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+2766_79+2779del others(14): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71215806 | |||||
| chr10:71215806
|
GGTGTGTG others(9): Show |
G | 3 | a0001c0003t0044g0201a0007c0017t0011g0354a0019c0021t0020g0355 | 3 | HG02717.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.79+2764_79+2779del others(16): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71215806 | |||||
| chr10:71215846
|
C | T | 1 | a0001c0001t0011g0361 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.79+2782C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71215846 | ||||||
| chr10:71215849
|
G | A | 6 | a0001c0001t0001g0299a0001c0001t0001g0301a0001c0001t0005g0302others(3): Show | 6 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+2785G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71215849 | ||||||
| chr10:71216193
|
C | A | 16 | a0001c0001t0001g0240a0001c0001t0002g0274a0001c0001t0048g0290others(13): Show | 16 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.79+3129C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216193 | ||||||
| chr10:71216306
|
G | A | 36 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0332others(33): Show | 36 | HG00558.hp2 HG00735.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.79+3242G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216306 | ||||||
| chr10:71216368
|
A | G | 160 | a0001c0001t0001g0088a0001c0001t0001g0218a0001c0001t0001g0234others(157): Show | 161 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.79+3304A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216368 | ||||||
| chr10:71216452
|
A | C | 2 | a0001c0001t0007g0128a0001c0001t0080g0130 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.79+3388A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216452 | ||||||
| chr10:71216529
|
C | T | 2 | a0007c0017t0011g0354a0019c0021t0020g0355 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.79+3465C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216529 | ||||||
| chr10:71216603
|
C | G | 1 | a0002c0049t0005g0300 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.79+3539C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216603 | ||||||
| chr10:71216609
|
A | G | 2 | a0007c0017t0011g0354a0019c0021t0020g0355 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.79+3545A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216609 | ||||||
| chr10:71216657
|
C | T | 1 | a0001c0002t0058g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79+3593C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216657 | ||||||
| chr10:71216660
|
C | T | 1 | a0001c0002t0058g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79+3596C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216660 | ||||||
| chr10:71216715
|
G | T | 1 | a0001c0012t0038g0096 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.79+3651G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216715 | ||||||
| chr10:71216747
|
G | A | 1 | a0001c0003t0004g0129 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.79+3683G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216747 | ||||||
| chr10:71216755
|
C | A | 4 | a0001c0001t0063g0032a0001c0004t0003g0207a0001c0020t0065g0142others(1): Show | 4 | HG02074.hp2 HG02165.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+3691C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216755 | ||||||
| chr10:71216761
|
G | A | 2 | a0007c0017t0011g0354a0019c0021t0020g0355 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.79+3697G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216761 | ||||||
| chr10:71216802
|
CTT | C | 5 | a0001c0001t0001g0299a0001c0001t0005g0302a0001c0002t0001g0303others(2): Show | 5 | HG00280.hp1 HG00280.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+3740_79+3741del others(2): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71216802 | |||||
| chr10:71216897
|
C | A | 4 | a0001c0001t0019g0353a0001c0003t0019g0261a0001c0003t0024g0097others(1): Show | 4 | HG01106.hp1 HG02451.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+3833C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216897 | ||||||
| chr10:71216948
|
G | A | 16 | a0001c0001t0004g0316a0001c0001t0006g0039a0001c0001t0064g0023others(13): Show | 16 | HG00609.hp1 HG02074.hp1 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.79+3884G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71216948 | ||||||
| chr10:71217303
|
G | C | 43 | a0001c0001t0001g0299a0001c0001t0002g0313a0001c0001t0002g0314others(40): Show | 45 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.79+4239G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71217303 | ||||||
| chr10:71217399
|
C | G | 15 | a0001c0001t0007g0139a0001c0001t0020g0115a0001c0002t0028g0155others(12): Show | 16 | HG01081.hp1 HG02055.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.79+4335C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71217399 | ||||||
| chr10:71217449
|
C | T | 3 | a0001c0001t0048g0290a0001c0004t0003g0236a0001c0024t0002g0235 | 3 | HG02040.hp2 NA18612.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.79+4385C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71217449 | ||||||
| chr10:71217487
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.79+4423C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71217487 | ||||||
| chr10:71217494
|
C | G | 1 | a0001c0012t0038g0096 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.79+4430C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71217494 | ||||||
| chr10:71217501
|
T | C | 1 | a0001c0003t0004g0043 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.79+4437T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71217501 | ||||||
| chr10:71217607
|
C | T | 1 | a0001c0002t0002g0334 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.79+4543C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71217607 | ||||||
| chr10:71217623
|
G | T | 15 | a0001c0001t0007g0139a0001c0001t0020g0115a0001c0002t0028g0155others(12): Show | 16 | HG01081.hp1 HG02055.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.79+4559G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71217623 | ||||||
| chr10:71217710
|
T | G | 2 | a0006c0018t0040g0297a0031c0056t0020g0296 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.79+4646T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71217710 | ||||||
| chr10:71217713
|
G | A | 2 | a0001c0002t0058g0137a0001c0003t0011g0132 | 2 | HG02280.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.79+4649G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71217713 | ||||||
| chr10:71217774
|
T | A | 24 | a0001c0001t0007g0139a0001c0001t0019g0353a0001c0001t0020g0115others(21): Show | 25 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.79+4710T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71217774 | ||||||
| chr10:71217811
|
G | A | 2 | a0001c0002t0058g0137a0001c0003t0011g0132 | 2 | HG02280.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.79+4747G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71217811 | ||||||
| chr10:71218207
|
A | G | 6 | a0001c0001t0019g0353a0001c0003t0007g0359a0001c0003t0019g0261others(3): Show | 6 | HG00735.hp1 HG01106.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+5143A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71218207 | ||||||
| chr10:71218318
|
TGTG | T | 3 | a0003c0007t0012g0356a0006c0018t0040g0297a0031c0056t0020g0296 | 3 | HG02451.hp1 HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.79+5258_79+5260del others(3): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71218318 | |||||
| chr10:71218467
|
A | G | 1 | a0001c0003t0019g0261 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.79+5403A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71218467 | ||||||
| chr10:71218513
|
A | G | 2 | a0001c0001t0031g0336a0001c0006t0007g0337 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.79+5449A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71218513 | ||||||
| chr10:71218618
|
A | G | 21 | a0001c0001t0007g0139a0001c0001t0019g0353a0001c0001t0020g0115others(18): Show | 22 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.79+5554A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71218618 | ||||||
| chr10:71218658
|
C | T | 2 | a0001c0003t0007g0330a0006c0018t0040g0200 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.79+5594C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71218658 | ||||||
| chr10:71218730
|
C | T | 10 | a0001c0001t0001g0318a0001c0001t0001g0332a0001c0001t0001g0344others(7): Show | 10 | HG00558.hp2 HG00735.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+5666C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71218730 | ||||||
| chr10:71218754
|
T | C | 1 | a0004c0043t0079g0357 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79+5690T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71218754 | ||||||
| chr10:71218759
|
C | G | 21 | a0001c0001t0007g0139a0001c0001t0019g0353a0001c0001t0020g0115others(18): Show | 22 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.79+5695C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71218759 | ||||||
| chr10:71218862
|
C | T | 4 | a0001c0001t0001g0088a0001c0003t0001g0051a0001c0003t0002g0181others(1): Show | 4 | NA18985.hp1 NA18988.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+5798C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71218862 | ||||||
| chr10:71218864
|
G | A | 6 | a0001c0001t0019g0353a0001c0003t0007g0359a0001c0003t0019g0261others(3): Show | 6 | HG00735.hp1 HG01106.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+5800G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71218864 | ||||||
| chr10:71218864
|
G | T | 5 | a0001c0001t0009g0127a0001c0002t0001g0125a0001c0002t0005g0124others(2): Show | 5 | HG01123.hp2 HG01943.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+5800G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71218864 | ||||||
| chr10:71218962
|
A | G | 1 | a0001c0001t0007g0326 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.79+5898A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71218962 | ||||||
| chr10:71218978
|
T | C | 3 | a0001c0001t0001g0189a0001c0001t0005g0188a0001c0001t0045g0187 | 3 | HG00733.hp2 HG03239.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.79+5914T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71218978 | ||||||
| chr10:71219075
|
G | A | 1 | a0001c0001t0070g0008 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.79+6011G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71219075 | ||||||
| chr10:71219113
|
C | T | 1 | a0003c0007t0010g0027 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.79+6049C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71219113 | ||||||
| chr10:71219208
|
A | G | 3 | a0001c0001t0019g0353a0001c0003t0019g0261a0001c0003t0024g0097 | 3 | HG01106.hp1 HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.79+6144A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71219208 | ||||||
| chr10:71219242
|
G | A | 3 | a0003c0007t0012g0356a0006c0018t0040g0297a0031c0056t0020g0296 | 3 | HG02451.hp1 HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.79+6178G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71219242 | ||||||
| chr10:71219378
|
C | T | 3 | a0001c0001t0001g0288a0001c0001t0017g0202a0001c0003t0011g0132 | 3 | HG02895.hp2 HG03490.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.79+6314C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71219378 | ||||||
| chr10:71219483
|
G | A | 22 | a0001c0001t0007g0139a0001c0001t0019g0353a0001c0001t0020g0115others(19): Show | 23 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+6419G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71219483 | ||||||
| chr10:71219566
|
C | T | 1 | a0001c0001t0024g0112 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.79+6502C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71219566 | ||||||
| chr10:71219570
|
C | T | 1 | a0001c0004t0003g0285 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.79+6506C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71219570 | ||||||
| chr10:71219644
|
C | T | 1 | a0001c0002t0002g0002 | 2 | HG02056.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.79+6580C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71219644 | ||||||
| chr10:71219809
|
A | G | 15 | a0001c0001t0007g0139a0001c0001t0020g0115a0001c0002t0028g0155others(12): Show | 16 | HG01081.hp1 HG02055.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.79+6745A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71219809 | ||||||
| chr10:71219869
|
A | G | 74 | a0001c0001t0001g0203a0001c0001t0001g0218a0001c0001t0001g0224others(71): Show | 76 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.79+6805A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71219869 | ||||||
| chr10:71219911
|
C | T | 1 | a0001c0002t0077g0154 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.79+6847C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71219911 | ||||||
| chr10:71219981
|
C | T | 1 | a0001c0004t0003g0345 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.79+6917C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71219981 | ||||||
| chr10:71220105
|
T | C | 1 | a0001c0001t0011g0272 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+7041T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71220105 | ||||||
| chr10:71220187
|
G | A | 1 | a0001c0003t0044g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.79+7123G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71220187 | ||||||
| chr10:71220234
|
G | A | 1 | a0001c0001t0025g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.79+7170G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71220234 | ||||||
| chr10:71220475
|
C | G | 1 | a0001c0002t0058g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79+7411C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71220475 | ||||||
| chr10:71220478
|
C | T | 52 | a0001c0001t0001g0203a0001c0001t0001g0218a0001c0001t0001g0224others(49): Show | 52 | HG00408.hp2 HG00597.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.79+7414C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71220478 | ||||||
| chr10:71220770
|
T | C | 22 | a0001c0001t0007g0139a0001c0001t0019g0353a0001c0001t0020g0115others(19): Show | 23 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+7706T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71220770 | ||||||
| chr10:71220785
|
A | G | 2 | a0007c0017t0011g0354a0019c0021t0020g0355 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.79+7721A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71220785 | ||||||
| chr10:71220925
|
G | A | 1 | a0001c0003t0011g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.79+7861G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71220925 | ||||||
| chr10:71221329
|
C | A | 1 | a0006c0057t0036g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.79+8265C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71221329 | ||||||
| chr10:71221330
|
C | G | 3 | a0001c0001t0019g0353a0001c0003t0019g0261a0001c0003t0024g0097 | 3 | HG01106.hp1 HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.79+8266C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71221330 | ||||||
| chr10:71221404
|
C | G | 1 | a0002c0005t0013g0055 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.79+8340C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71221404 | ||||||
| chr10:71221447
|
A | G | 18 | a0001c0001t0001g0299a0001c0001t0002g0313a0001c0001t0002g0314others(15): Show | 19 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.79+8383A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71221447 | ||||||
| chr10:71221484
|
G | C | 20 | a0001c0001t0001g0299a0001c0001t0002g0313a0001c0001t0002g0314others(17): Show | 21 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+8420G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71221484 | ||||||
| chr10:71221787
|
G | T | 1 | a0001c0001t0007g0139 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.79+8723G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71221787 | ||||||
| chr10:71221846
|
T | A | 1 | a0001c0001t0017g0202 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.79+8782T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71221846 | ||||||
| chr10:71221924
|
G | A | 1 | a0004c0043t0079g0357 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79+8860G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71221924 | ||||||
| chr10:71221971
|
T | A | 1 | a0001c0001t0007g0326 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.79+8907T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71221971 | ||||||
| chr10:71221989
|
G | GTCA | 16 | a0001c0001t0007g0349a0001c0001t0011g0341a0001c0001t0014g0028others(13): Show | 16 | HG00597.hp2 HG01069.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.79+8954_79+8956dup others(3): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71221989 | |||||
| chr10:71221994
|
C | G | 13 | a0001c0001t0001g0086a0001c0001t0002g0313a0001c0001t0002g0314others(10): Show | 13 | HG00558.hp2 HG02896.hp1 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.79+8930C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71221994 | ||||||
| chr10:71222056
|
G | A | 1 | a0002c0005t0013g0055 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.79+8992G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71222056 | ||||||
| chr10:71222201
|
C | T | 1 | a0003c0007t0012g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.79+9137C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71222201 | ||||||
| chr10:71222254
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.79+9190C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71222254 | ||||||
| chr10:71222318
|
T | TAGTAC | 304 | a0001c0001t0001g0047a0001c0001t0001g0066a0001c0001t0001g0078others(301): Show | 308 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.79+9257_79+9258ins others(5): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71222318 | |||||
| chr10:71222370
|
T | C | 324 | a0001c0001t0001g0047a0001c0001t0001g0066a0001c0001t0001g0078others(321): Show | 328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.79+9306T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71222370 | ||||||
| chr10:71222382
|
A | G | 15 | a0001c0001t0007g0349a0001c0001t0011g0341a0001c0001t0025g0029others(12): Show | 15 | HG01069.hp2 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+9318A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71222382 | ||||||
| chr10:71222492
|
A | G | 1 | a0001c0001t0001g0332 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.79+9428A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71222492 | ||||||
| chr10:71222497
|
C | T | 304 | a0001c0001t0001g0047a0001c0001t0001g0066a0001c0001t0001g0078others(301): Show | 308 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.79+9433C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71222497 | ||||||
| chr10:71222524
|
A | AC | 304 | a0001c0001t0001g0047a0001c0001t0001g0066a0001c0001t0001g0078others(301): Show | 308 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.79+9466dupC | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71222524 | |||||
| chr10:71222731
|
G | A | 1 | a0001c0003t0044g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.79+9667G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71222731 | ||||||
| chr10:71222856
|
C | T | 3 | a0001c0002t0058g0137a0014c0050t0029g0352a0028c0039t0060g0171 | 3 | HG00639.hp2 HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.79+9792C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71222856 | ||||||
| chr10:71223228
|
G | T | 219 | a0001c0001t0001g0047a0001c0001t0001g0078a0001c0001t0001g0080others(216): Show | 222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.79+10164G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71223228 | ||||||
| chr10:71223312
|
C | T | 1 | a0001c0015t0056g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.79+10248C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71223312 | ||||||
| chr10:71223313
|
G | A | 20 | a0001c0001t0011g0050a0001c0001t0024g0112a0001c0002t0028g0109others(17): Show | 20 | HG00639.hp2 HG01169.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.79+10249G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71223313 | ||||||
| chr10:71223509
|
A | G | 21 | a0001c0001t0011g0050a0001c0001t0024g0112a0001c0002t0028g0109others(18): Show | 21 | HG00639.hp2 HG01169.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+10445A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71223509 | ||||||
| chr10:71223558
|
C | T | 1 | a0001c0002t0001g0303 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.79+10494C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71223558 | ||||||
| chr10:71223623
|
A | G | 2 | a0001c0001t0071g0322a0001c0002t0002g0321 | 2 | NA18995.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.79+10559A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71223623 | ||||||
| chr10:71223680
|
G | C | 1 | a0001c0002t0001g0303 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.79+10616G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71223680 | ||||||
| chr10:71223681
|
C | T | 1 | a0001c0002t0001g0303 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.79+10617C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71223681 | ||||||
| chr10:71223761
|
C | CCCACCTT others(258): Show |
1 | a0001c0001t0005g0302 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.79+10712_79+10713i others(267): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71223761 | |||||
| chr10:71223761
|
C | CCCACCTT others(259): Show |
1 | a0001c0001t0001g0299 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.79+10712_79+10713i others(268): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71223761 | |||||
| chr10:71223761
|
C | CCCACCTT others(264): Show |
1 | a0001c0002t0001g0303 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.79+10712_79+10713i others(273): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71223761 | |||||
| chr10:71223779
|
G | A | 13 | a0001c0001t0011g0050a0001c0001t0024g0112a0001c0002t0028g0109others(10): Show | 13 | HG01169.hp2 HG01243.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.79+10715G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71223779 | ||||||
| chr10:71223798
|
C | T | 1 | a0001c0001t0007g0326 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.79+10734C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71223798 | ||||||
| chr10:71223804
|
G | A | 13 | a0001c0001t0001g0319a0001c0001t0002g0117a0001c0001t0004g0237others(10): Show | 13 | HG00597.hp1 HG02165.hp1 NA18950.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+10740G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71223804 | ||||||
| chr10:71223987
|
G | A | 1 | a0001c0040t0043g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.79+10923G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71223987 | ||||||
| chr10:71224065
|
A | T | 4 | a0001c0001t0025g0029a0001c0001t0025g0136a0001c0003t0007g0258others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+11001A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224065 | ||||||
| chr10:71224130
|
C | T | 1 | a0001c0001t0007g0326 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.79+11066C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224130 | ||||||
| chr10:71224223
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.79+11159A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224223 | ||||||
| chr10:71224234
|
G | C | 21 | a0001c0001t0011g0050a0001c0001t0024g0112a0001c0002t0028g0109others(18): Show | 21 | HG00639.hp2 HG01169.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+11170G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224234 | ||||||
| chr10:71224234
|
GACACAGA others(7): Show |
G | 1 | a0001c0001t0062g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.79+11190_79+11203d others(16): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224234 | |||||
| chr10:71224244
|
C | T | 1 | a0003c0007t0012g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.79+11180C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224244 | ||||||
| chr10:71224254
|
G | GAC | 21 | a0001c0001t0011g0050a0001c0001t0024g0112a0001c0002t0028g0109others(18): Show | 21 | HG00639.hp2 HG01169.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+11205_79+11206d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224254 | |||||
| chr10:71224301
|
C | T | 270 | a0001c0001t0001g0047a0001c0001t0001g0078a0001c0001t0001g0080others(267): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.79+11237C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224301 | ||||||
| chr10:71224342
|
G | A | 1 | a0001c0001t0007g0326 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.79+11278G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224342 | ||||||
| chr10:71224364
|
G | GAC | 8 | a0001c0001t0001g0299a0001c0001t0010g0323a0001c0002t0002g0308others(5): Show | 8 | HG00642.hp1 HG02615.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+11351_79+11352d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
G | GACAC | 8 | a0001c0001t0001g0066a0001c0001t0005g0302a0001c0001t0025g0136others(5): Show | 8 | HG00280.hp1 HG00558.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+11349_79+11352d others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
G | GACACAC | 5 | a0001c0002t0039g0063a0001c0003t0011g0132a0001c0004t0003g0064others(2): Show | 5 | HG00639.hp2 HG02895.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+11347_79+11352d others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
G | GACACACA others(3): Show |
1 | a0003c0007t0010g0027 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.79+11343_79+11352d others(12): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
G | GACACACA others(7): Show |
1 | a0001c0003t0007g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.79+11339_79+11352d others(16): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
G | GACACACA others(9): Show |
1 | a0001c0001t0025g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.79+11337_79+11352d others(18): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
G | GACGC | 7 | a0001c0001t0001g0194a0001c0001t0006g0060a0001c0002t0001g0172others(4): Show | 7 | HG00733.hp1 HG00735.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+11302_79+11303i others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
G | GACGCAC | 4 | a0001c0002t0002g0195a0001c0003t0004g0351a0001c0012t0038g0096others(1): Show | 4 | HG02486.hp2 HG02896.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+11302_79+11303i others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
G | GACGCACA others(1): Show |
5 | a0001c0001t0002g0117a0001c0001t0025g0338a0001c0001t0074g0059others(2): Show | 5 | HG00597.hp1 HG01361.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+11302_79+11303i others(10): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
G | GACGCACA others(3): Show |
6 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0007g0128others(3): Show | 6 | HG01168.hp1 HG01169.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+11302_79+11303i others(12): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
G | GACGCACA others(5): Show |
9 | a0001c0001t0004g0237a0001c0001t0014g0182a0001c0001t0027g0044others(6): Show | 9 | HG00741.hp2 HG01070.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+11302_79+11303i others(14): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
G | GACGCACA others(7): Show |
2 | a0001c0002t0026g0116a0001c0004t0003g0156 | 2 | NA19082.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.79+11302_79+11303i others(16): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
G | GACGCACA others(9): Show |
2 | a0001c0001t0001g0319a0001c0001t0068g0340 | 2 | HG06807.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.79+11302_79+11303i others(18): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
GAC | G | 56 | a0001c0001t0001g0120a0001c0001t0001g0344a0001c0001t0002g0164others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.79+11351_79+11352d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
GACAC | G | 21 | a0001c0001t0001g0054a0001c0001t0002g0081a0001c0001t0002g0287others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.79+11349_79+11352d others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
GACACAC | G | 33 | a0001c0001t0001g0086a0001c0001t0001g0183a0001c0001t0001g0240others(30): Show | 33 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.79+11347_79+11352d others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
GACACACA others(1): Show |
G | 82 | a0001c0001t0001g0047a0001c0001t0001g0144a0001c0001t0001g0146others(79): Show | 84 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.79+11345_79+11352d others(10): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
GACACACA others(3): Show |
G | 1 | a0001c0001t0011g0272 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+11343_79+11352d others(12): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
GACACACA others(5): Show |
G | 1 | a0006c0057t0036g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.79+11341_79+11352d others(14): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
GACACACA others(9): Show |
G | 1 | a0001c0015t0018g0331 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.79+11337_79+11352d others(18): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
GACACACA others(15): Show |
G | 1 | a0001c0027t0003g0262 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.79+11331_79+11352d others(24): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224364
|
GACACACA others(19): Show |
G | 1 | a0001c0006t0015g0011 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.79+11327_79+11352d others(28): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224364 | |||||
| chr10:71224365
|
A | ACG | 42 | a0001c0001t0001g0189a0001c0001t0001g0199a0001c0001t0001g0224others(39): Show | 44 | HG00642.hp2 HG00733.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.79+11302_79+11303i others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224365 | |||||
| chr10:71224367
|
A | G | 34 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0088others(31): Show | 34 | HG00544.hp2 HG00738.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.79+11303A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224367 | ||||||
| chr10:71224369
|
A | G | 46 | a0001c0001t0001g0120a0001c0001t0002g0164a0001c0001t0004g0316others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.79+11305A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224369 | ||||||
| chr10:71224371
|
A | G | 15 | a0001c0001t0002g0081a0001c0001t0002g0287a0001c0001t0002g0313others(12): Show | 15 | HG00735.hp1 HG01109.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+11307A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224371 | ||||||
| chr10:71224373
|
A | G | 30 | a0001c0001t0001g0086a0001c0001t0001g0183a0001c0001t0001g0240others(27): Show | 30 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+11309A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224373 | ||||||
| chr10:71224375
|
A | G | 70 | a0001c0001t0001g0047a0001c0001t0001g0144a0001c0001t0001g0146others(67): Show | 71 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.79+11311A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224375 | ||||||
| chr10:71224377
|
A | G | 5 | a0001c0001t0001g0239a0001c0001t0011g0272a0001c0001t0026g0255others(2): Show | 5 | HG02155.hp1 HG03098.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+11313A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224377 | ||||||
| chr10:71224383
|
A | G | 1 | a0001c0015t0018g0331 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.79+11319A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224383 | ||||||
| chr10:71224389
|
A | G | 1 | a0001c0027t0003g0262 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.79+11325A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224389 | ||||||
| chr10:71224393
|
A | G | 1 | a0001c0006t0015g0011 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.79+11329A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224393 | ||||||
| chr10:71224415
|
A | ACACACAC others(7): Show |
1 | a0011c0014t0018g0106 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.79+11352_79+11353i others(16): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224415 | |||||
| chr10:71224415
|
A | ACACACAC others(3): Show |
2 | a0001c0003t0011g0049a0001c0003t0036g0131 | 2 | HG01433.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.79+11352_79+11353i others(12): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224415 | |||||
| chr10:71224415
|
A | ACACACG | 3 | a0001c0001t0024g0112a0005c0011t0010g0107a0005c0011t0010g0134 | 3 | HG01243.hp1 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.79+11352_79+11353i others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224415 | |||||
| chr10:71224415
|
A | G | 1 | a0001c0002t0078g0123 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.79+11351A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224415 | ||||||
| chr10:71224416
|
C | T | 1 | a0001c0002t0001g0219 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.79+11352C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224416 | ||||||
| chr10:71224466
|
C | CT | 18 | a0001c0001t0011g0050a0001c0001t0024g0112a0001c0002t0028g0109others(15): Show | 18 | HG00639.hp2 HG01169.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.79+11410dupT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71224466 | |||||
| chr10:71224470
|
T | G | 3 | a0001c0001t0001g0299a0001c0001t0005g0302a0001c0002t0001g0303 | 3 | HG00280.hp1 HG01081.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.79+11406T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224470 | ||||||
| chr10:71224574
|
T | G | 3 | a0001c0001t0025g0029a0001c0003t0007g0258a0001c0006t0015g0021 | 3 | HG03130.hp2 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.79+11510T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224574 | ||||||
| chr10:71224733
|
G | A | 1 | a0003c0007t0012g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.79+11669G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224733 | ||||||
| chr10:71224754
|
A | G | 1 | a0001c0001t0002g0226 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.79+11690A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224754 | ||||||
| chr10:71224939
|
C | T | 3 | a0001c0001t0001g0299a0001c0001t0005g0302a0001c0002t0001g0303 | 3 | HG00280.hp1 HG01081.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.79+11875C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224939 | ||||||
| chr10:71224940
|
G | A | 226 | a0001c0001t0001g0047a0001c0001t0001g0078a0001c0001t0001g0080others(223): Show | 229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.79+11876G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71224940 | ||||||
| chr10:71225011
|
C | T | 2 | a0001c0001t0002g0085a0001c0001t0004g0267 | 2 | HG02083.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.79+11947C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225011 | ||||||
| chr10:71225106
|
G | C | 4 | a0001c0001t0005g0040a0001c0001t0007g0326a0001c0003t0011g0132others(1): Show | 4 | HG02145.hp2 HG02738.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+12042G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225106 | ||||||
| chr10:71225203
|
A | G | 1 | a0001c0003t0001g0284 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.79+12139A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225203 | ||||||
| chr10:71225216
|
C | T | 2 | a0001c0002t0058g0137a0028c0039t0060g0171 | 2 | HG00639.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.79+12152C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225216 | ||||||
| chr10:71225263
|
A | AC | 181 | a0001c0001t0001g0054a0001c0001t0001g0088a0001c0001t0001g0120others(178): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.79+12202dupC | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71225263 | |||||
| chr10:71225269
|
G | A | 342 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(339): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.79+12205G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225269 | ||||||
| chr10:71225451
|
C | T | 10 | a0001c0001t0001g0066a0001c0001t0001g0224a0001c0001t0001g0294others(7): Show | 10 | HG00558.hp1 HG00642.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+12387C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225451 | ||||||
| chr10:71225456
|
A | G | 1 | a0001c0001t0019g0320 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.79+12392A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225456 | ||||||
| chr10:71225527
|
G | A | 1 | a0001c0002t0022g0143 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.79+12463G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225527 | ||||||
| chr10:71225604
|
A | G | 10 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0318others(7): Show | 10 | HG01081.hp2 HG01123.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+12540A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225604 | ||||||
| chr10:71225619
|
C | T | 2 | a0001c0001t0002g0164a0001c0002t0004g0273 | 2 | HG00544.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.79+12555C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225619 | ||||||
| chr10:71225748
|
T | C | 1 | a0001c0001t0011g0361 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.79+12684T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225748 | ||||||
| chr10:71225772
|
C | T | 2 | a0001c0001t0014g0260a0001c0001t0027g0259 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.79+12708C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225772 | ||||||
| chr10:71225777
|
G | A | 314 | a0001c0001t0001g0054a0001c0001t0001g0066a0001c0001t0001g0078others(311): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.79+12713G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225777 | ||||||
| chr10:71225824
|
A | G | 70 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0120others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.79+12760A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225824 | ||||||
| chr10:71225840
|
G | GTGCCACA others(17): Show |
35 | a0001c0001t0001g0066a0001c0001t0001g0203a0001c0001t0001g0224others(32): Show | 36 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.79+12780_79+12803d others(26): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71225840 | |||||
| chr10:71225979
|
A | G | 1 | a0014c0050t0029g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.79+12915A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71225979 | ||||||
| chr10:71226003
|
C | T | 3 | a0001c0001t0001g0224a0002c0005t0034g0150a0004c0010t0001g0151 | 3 | HG00642.hp2 HG01109.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.79+12939C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226003 | ||||||
| chr10:71226041
|
A | G | 6 | a0001c0001t0019g0353a0001c0002t0078g0123a0001c0003t0019g0328others(3): Show | 6 | HG01069.hp2 HG01169.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+12977A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226041 | ||||||
| chr10:71226044
|
A | G | 2 | a0001c0003t0036g0131a0003c0038t0012g0013 | 2 | HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.79+12980A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226044 | ||||||
| chr10:71226055
|
G | A | 360 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(357): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.79+12991G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226055 | ||||||
| chr10:71226092
|
T | G | 8 | a0001c0001t0007g0128a0001c0001t0080g0130a0001c0002t0033g0036others(5): Show | 8 | HG01081.hp1 HG02055.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+13028T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226092 | ||||||
| chr10:71226102
|
T | C | 8 | a0001c0001t0034g0230a0001c0002t0028g0155a0001c0012t0038g0196others(5): Show | 8 | HG00639.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+13038T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226102 | ||||||
| chr10:71226144
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.79+13080G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226144 | ||||||
| chr10:71226185
|
A | C | 10 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(7): Show | 10 | HG00280.hp1 HG00733.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+13121A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226185 | ||||||
| chr10:71226220
|
G | A | 5 | a0001c0006t0015g0141a0001c0006t0015g0167a0001c0006t0015g0168others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+13156G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226220 | ||||||
| chr10:71226224
|
G | A | 2 | a0001c0001t0002g0164a0001c0001t0010g0015 | 2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.79+13160G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226224 | ||||||
| chr10:71226327
|
G | A | 7 | a0001c0002t0058g0137a0001c0002t0072g0111a0003c0007t0010g0027others(4): Show | 7 | HG02280.hp2 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+13263G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226327 | ||||||
| chr10:71226340
|
G | T | 1 | a0001c0003t0008g0220 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.79+13276G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226340 | ||||||
| chr10:71226351
|
G | A | 2 | a0006c0018t0040g0200a0006c0018t0040g0297 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.79+13287G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226351 | ||||||
| chr10:71226412
|
C | T | 31 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(28): Show | 32 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.79+13348C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226412 | ||||||
| chr10:71226527
|
G | A | 1 | a0001c0001t0005g0020 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.79+13463G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226527 | ||||||
| chr10:71226651
|
A | G | 4 | a0001c0003t0007g0198a0001c0003t0007g0258a0001c0003t0007g0330others(1): Show | 4 | HG01891.hp2 HG02723.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+13587A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226651 | ||||||
| chr10:71226709
|
C | T | 7 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(4): Show | 7 | HG00140.hp1 HG00733.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+13645C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226709 | ||||||
| chr10:71226732
|
G | A | 25 | a0001c0001t0001g0224a0001c0001t0004g0024a0001c0001t0004g0316others(22): Show | 26 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.79+13668G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226732 | ||||||
| chr10:71226735
|
A | G | 150 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0144others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.79+13671A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226735 | ||||||
| chr10:71226757
|
A | C | 1 | a0004c0043t0079g0357 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79+13693A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226757 | ||||||
| chr10:71226833
|
G | T | 2 | a0001c0001t0019g0353a0001c0002t0078g0123 | 2 | HG01169.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.79+13769G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226833 | ||||||
| chr10:71226849
|
A | G | 1 | a0001c0001t0019g0320 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.79+13785A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226849 | ||||||
| chr10:71226900
|
A | G | 75 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(72): Show | 76 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.79+13836A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226900 | ||||||
| chr10:71226903
|
C | T | 2 | a0001c0055t0024g0153a0008c0041t0012g0197 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.79+13839C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226903 | ||||||
| chr10:71226983
|
C | CT | 73 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(70): Show | 74 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.79+13934dupT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71226983 | |||||
| chr10:71226983
|
C | CTT | 63 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0144others(60): Show | 65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.79+13933_79+13934d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71226983 | |||||
| chr10:71226983
|
CT | C | 36 | a0001c0001t0001g0088a0001c0001t0005g0040a0001c0001t0009g0177others(33): Show | 36 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.79+13934delT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71226983 | |||||
| chr10:71226987
|
T | C | 3 | a0001c0001t0005g0040a0001c0001t0014g0028a0001c0001t0061g0140 | 3 | HG02738.hp1 HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.79+13923T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71226987 | ||||||
| chr10:71227008
|
G | A | 1 | a0001c0001t0005g0020 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.79+13944G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227008 | ||||||
| chr10:71227021
|
G | T | 140 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0144others(137): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.79+13957G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227021 | ||||||
| chr10:71227038
|
T | G | 144 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0144others(141): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.79+13974T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227038 | ||||||
| chr10:71227075
|
C | G | 1 | a0001c0003t0007g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79+14011C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227075 | ||||||
| chr10:71227154
|
T | G | 75 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(72): Show | 76 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.79+14090T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227154 | ||||||
| chr10:71227405
|
T | C | 1 | a0001c0001t0005g0163 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.79+14341T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227405 | ||||||
| chr10:71227463
|
A | G | 3 | a0001c0001t0031g0336a0001c0001t0068g0340a0004c0043t0079g0357 | 3 | HG03579.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+14399A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227463 | ||||||
| chr10:71227488
|
T | G | 188 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.79+14424T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227488 | ||||||
| chr10:71227504
|
A | C | 75 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(72): Show | 76 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.79+14440A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227504 | ||||||
| chr10:71227599
|
C | CATATATA others(1): Show |
4 | a0001c0003t0019g0328a0001c0012t0016g0325a0001c0015t0018g0331others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+14538_79+14539i others(10): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227599 | |||||
| chr10:71227601
|
TACATATA others(3): Show |
T | 7 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(4): Show | 7 | HG00140.hp1 HG00733.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+14539_79+14548d others(12): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227601 | |||||
| chr10:71227603
|
C | CATATATA others(3): Show |
9 | a0001c0006t0015g0011a0001c0006t0015g0021a0001c0006t0015g0141others(6): Show | 9 | HG01069.hp2 HG01243.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+14555_79+14564d others(12): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227603 | |||||
| chr10:71227603
|
C | T | 48 | a0001c0001t0001g0224a0001c0001t0004g0024a0001c0001t0004g0316others(45): Show | 49 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.79+14539C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227603 | ||||||
| chr10:71227611
|
C | CATATATA others(19): Show |
17 | a0001c0002t0072g0111a0001c0003t0007g0095a0001c0003t0007g0359others(14): Show | 17 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.79+14554_79+14555i others(28): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227611 | |||||
| chr10:71227617
|
T | TACATATA others(43): Show |
1 | a0001c0002t0058g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79+14554_79+14555i others(52): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227617 | |||||
| chr10:71227617
|
T | TACATATA others(47): Show |
1 | a0006c0057t0036g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.79+14554_79+14555i others(56): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227617 | |||||
| chr10:71227619
|
T | C | 26 | a0001c0001t0001g0224a0001c0001t0004g0024a0001c0001t0004g0316others(23): Show | 27 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.79+14555T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227619 | ||||||
| chr10:71227621
|
C | T | 27 | a0001c0001t0001g0224a0001c0001t0004g0024a0001c0001t0004g0316others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.79+14557C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227621 | ||||||
| chr10:71227623
|
T | C | 4 | a0001c0003t0019g0328a0001c0012t0016g0325a0001c0015t0018g0331others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+14559T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227623 | ||||||
| chr10:71227625
|
T | TATACAC | 26 | a0001c0001t0001g0224a0001c0001t0004g0024a0001c0001t0004g0316others(23): Show | 27 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.79+14566_79+14567i others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227625 | |||||
| chr10:71227627
|
T | C | 5 | a0001c0003t0019g0328a0001c0012t0016g0325a0001c0015t0018g0331others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+14563T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227627 | ||||||
| chr10:71227629
|
C | T | 4 | a0001c0003t0019g0328a0001c0012t0016g0325a0001c0015t0018g0331others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+14565C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227629 | ||||||
| chr10:71227631
|
T | C | 2 | a0001c0002t0009g0158a0001c0002t0009g0184 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.79+14567T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227631 | ||||||
| chr10:71227637
|
T | C | 1 | a0006c0057t0036g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.79+14573T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227637 | ||||||
| chr10:71227639
|
C | CAT | 24 | a0001c0001t0001g0224a0001c0001t0004g0024a0001c0001t0004g0316others(21): Show | 25 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.79+14576_79+14577i others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227639 | |||||
| chr10:71227641
|
C | CAT | 3 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0002t0058g0137 | 3 | HG02280.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+14581_79+14582d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227641 | |||||
| chr10:71227641
|
C | T | 29 | a0001c0001t0001g0224a0001c0001t0004g0024a0001c0001t0004g0316others(26): Show | 30 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+14577C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227641 | ||||||
| chr10:71227641
|
CAT | C | 26 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(23): Show | 26 | HG00140.hp1 HG00733.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.79+14581_79+14582d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227641 | |||||
| chr10:71227649
|
T | C | 26 | a0001c0001t0001g0224a0001c0001t0004g0024a0001c0001t0004g0316others(23): Show | 27 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.79+14585T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227649 | ||||||
| chr10:71227649
|
T | TATATATA others(49): Show |
4 | a0001c0003t0019g0328a0001c0012t0016g0325a0001c0015t0018g0331others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+14594_79+14595i others(58): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227649 | |||||
| chr10:71227655
|
T | TACATATA others(25): Show |
1 | a0001c0002t0002g0252 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.79+14607_79+14638d others(34): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227655 | |||||
| chr10:71227659
|
T | C | 4 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0002t0058g0137others(1): Show | 4 | HG02280.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+14595T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227659 | ||||||
| chr10:71227669
|
C | T | 3 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0002t0058g0137 | 3 | HG02280.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+14605C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227669 | ||||||
| chr10:71227677
|
CAT | C | 9 | a0001c0006t0015g0011a0001c0006t0015g0021a0001c0006t0015g0141others(6): Show | 9 | HG01069.hp2 HG01243.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+14621_79+14622d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227677 | |||||
| chr10:71227679
|
T | C | 4 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0002t0058g0137others(1): Show | 4 | HG02280.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+14615T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227679 | ||||||
| chr10:71227687
|
C | CACATATA others(1): Show |
3 | a0001c0001t0010g0323a0004c0043t0079g0357a0027c0025t0059g0009 | 3 | HG02976.hp2 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.79+14625_79+14632d others(10): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227687 | |||||
| chr10:71227687
|
C | CACATATA others(21): Show |
17 | a0001c0002t0072g0111a0001c0003t0007g0095a0001c0003t0007g0359others(14): Show | 17 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.79+14632_79+14633i others(30): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227687 | |||||
| chr10:71227689
|
C | T | 3 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0002t0058g0137 | 3 | HG02280.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+14625C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227689 | ||||||
| chr10:71227697
|
T | C | 4 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0002t0058g0137others(1): Show | 4 | HG02280.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+14633T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227697 | ||||||
| chr10:71227699
|
C | T | 35 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(32): Show | 36 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.79+14635C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227699 | ||||||
| chr10:71227701
|
C | CATAT | 17 | a0001c0002t0072g0111a0001c0003t0007g0095a0001c0003t0007g0359others(14): Show | 17 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.79+14638_79+14639i others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227701 | |||||
| chr10:71227701
|
C | T | 4 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0002t0058g0137others(1): Show | 4 | HG02280.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+14637C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227701 | ||||||
| chr10:71227703
|
C | T | 24 | a0001c0001t0010g0323a0001c0001t0031g0336a0001c0001t0068g0340others(21): Show | 24 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+14639C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227703 | ||||||
| chr10:71227705
|
T | C | 34 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(31): Show | 35 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.79+14641T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227705 | ||||||
| chr10:71227707
|
T | C | 8 | a0001c0001t0006g0039a0001c0001t0007g0349a0001c0001t0025g0029others(5): Show | 8 | HG02559.hp2 HG02976.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+14643T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227707 | ||||||
| chr10:71227707
|
T | TAC | 46 | a0001c0001t0001g0088a0001c0001t0001g0183a0001c0001t0001g0318others(43): Show | 46 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.79+14681_79+14682d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227707 | |||||
| chr10:71227707
|
T | TACAC | 4 | a0001c0002t0004g0292a0001c0004t0003g0275a0001c0004t0003g0279others(1): Show | 4 | HG00673.hp2 NA18906.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+14679_79+14682d others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227707 | |||||
| chr10:71227707
|
T | TACACAC | 3 | a0001c0001t0010g0161a0001c0001t0019g0320a0002c0005t0023g0350 | 3 | HG02486.hp1 HG02717.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.79+14677_79+14682d others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227707 | |||||
| chr10:71227707
|
TAC | T | 34 | a0001c0001t0001g0047a0001c0001t0001g0144a0001c0001t0001g0178others(31): Show | 35 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.79+14681_79+14682d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227707 | |||||
| chr10:71227707
|
TACAC | T | 57 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0146others(54): Show | 59 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.79+14679_79+14682d others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227707 | |||||
| chr10:71227707
|
TACACAC | T | 12 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0117others(9): Show | 12 | HG00597.hp1 HG01256.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+14677_79+14682d others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227707 | |||||
| chr10:71227707
|
TACACACA others(1): Show |
T | 3 | a0001c0001t0002g0274a0001c0001t0063g0032a0001c0002t0002g0083 | 3 | HG02074.hp2 NA19079.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.79+14675_79+14682d others(10): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227707 | |||||
| chr10:71227707
|
TACACACA others(11): Show |
T | 14 | a0001c0001t0002g0094a0001c0001t0013g0233a0001c0002t0001g0001others(11): Show | 15 | HG01123.hp2 HG01257.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+14665_79+14682d others(20): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227707 | |||||
| chr10:71227709
|
C | T | 1 | a0001c0002t0058g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79+14645C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227709 | ||||||
| chr10:71227711
|
C | T | 3 | a0001c0001t0010g0323a0008c0047t0029g0160a0027c0025t0059g0009 | 3 | HG02486.hp2 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.79+14647C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227711 | ||||||
| chr10:71227713
|
C | T | 3 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0003t0011g0132 | 3 | HG02895.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+14649C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227713 | ||||||
| chr10:71227715
|
C | T | 18 | a0001c0002t0072g0111a0001c0003t0007g0095a0001c0003t0007g0359others(15): Show | 18 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+14651C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227715 | ||||||
| chr10:71227717
|
C | T | 1 | a0001c0002t0058g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79+14653C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227717 | ||||||
| chr10:71227739
|
CACACACA others(1): Show |
C | 9 | a0001c0006t0015g0011a0001c0006t0015g0021a0001c0006t0015g0141others(6): Show | 9 | HG01069.hp2 HG01243.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+14679_79+14686d others(10): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227739 | |||||
| chr10:71227741
|
CACACAT | C | 7 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(4): Show | 7 | HG00140.hp1 HG00733.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+14681_79+14686d others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71227741 | |||||
| chr10:71227747
|
T | C | 22 | a0001c0001t0001g0224a0001c0001t0004g0024a0001c0001t0004g0316others(19): Show | 23 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.79+14683T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227747 | ||||||
| chr10:71227790
|
A | T | 59 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(56): Show | 60 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.79+14726A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227790 | ||||||
| chr10:71227918
|
G | C | 1 | a0012c0013t0003g0317 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.79+14854G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227918 | ||||||
| chr10:71227989
|
T | C | 1 | a0001c0002t0002g0308 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.79+14925T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71227989 | ||||||
| chr10:71228234
|
A | G | 2 | a0001c0001t0010g0323a0027c0025t0059g0009 | 2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.79+15170A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71228234 | ||||||
| chr10:71228268
|
A | C | 16 | a0001c0001t0005g0101a0001c0001t0007g0128a0001c0001t0011g0341others(13): Show | 16 | HG01106.hp1 HG01106.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.79+15204A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71228268 | ||||||
| chr10:71228338
|
A | T | 6 | a0001c0001t0007g0263a0001c0001t0007g0335a0001c0001t0010g0161others(3): Show | 6 | HG01243.hp1 HG01433.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+15274A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71228338 | ||||||
| chr10:71228384
|
C | CA | 36 | a0001c0001t0001g0088a0001c0001t0004g0333a0001c0001t0005g0040others(33): Show | 36 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.79+15331dupA | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71228384 | |||||
| chr10:71228384
|
CA | C | 15 | a0001c0001t0001g0299a0001c0003t0036g0131a0001c0006t0015g0011others(12): Show | 15 | HG01069.hp2 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+15331delA | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71228384 | |||||
| chr10:71228539
|
C | A | 67 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(64): Show | 68 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.79+15475C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71228539 | ||||||
| chr10:71228603
|
T | C | 1 | a0008c0047t0029g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.79+15539T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71228603 | ||||||
| chr10:71228679
|
G | T | 28 | a0001c0001t0010g0323a0001c0001t0031g0336a0001c0001t0068g0340others(25): Show | 28 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.79+15615G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71228679 | ||||||
| chr10:71228736
|
G | A | 1 | a0001c0003t0004g0043 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.79+15672G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71228736 | ||||||
| chr10:71228749
|
G | A | 1 | a0001c0003t0011g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.79+15685G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71228749 | ||||||
| chr10:71228749
|
G | C | 1 | a0001c0001t0069g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.79+15685G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71228749 | ||||||
| chr10:71228765
|
C | T | 3 | a0001c0001t0031g0336a0001c0001t0068g0340a0004c0043t0079g0357 | 3 | HG03579.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+15701C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71228765 | ||||||
| chr10:71228881
|
T | C | 1 | a0014c0050t0029g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.79+15817T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71228881 | ||||||
| chr10:71229183
|
C | T | 3 | a0001c0001t0031g0336a0001c0001t0068g0340a0004c0043t0079g0357 | 3 | HG03579.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+16119C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71229183 | ||||||
| chr10:71229273
|
C | T | 1 | a0001c0002t0001g0309 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.79+16209C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71229273 | ||||||
| chr10:71229348
|
T | C | 1 | a0001c0002t0006g0250 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.79+16284T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71229348 | ||||||
| chr10:71229349
|
G | T | 1 | a0001c0002t0006g0250 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.79+16285G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71229349 | ||||||
| chr10:71229388
|
C | G | 33 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(30): Show | 34 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.79+16324C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71229388 | ||||||
| chr10:71229611
|
C | T | 2 | a0001c0001t0014g0260a0001c0001t0027g0259 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.79+16547C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71229611 | ||||||
| chr10:71229637
|
G | C | 1 | a0001c0002t0004g0292 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.79+16573G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71229637 | ||||||
| chr10:71229946
|
A | G | 12 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0006t0015g0011others(9): Show | 12 | HG01069.hp2 HG01243.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+16882A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71229946 | ||||||
| chr10:71230098
|
C | G | 1 | a0004c0010t0066g0269 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.79+17034C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71230098 | ||||||
| chr10:71230200
|
G | T | 1 | a0001c0001t0001g0199 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.79+17136G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71230200 | ||||||
| chr10:71230247
|
G | C | 3 | a0001c0001t0031g0336a0001c0001t0068g0340a0004c0043t0079g0357 | 3 | HG03579.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+17183G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71230247 | ||||||
| chr10:71230555
|
T | C | 12 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0006t0015g0011others(9): Show | 12 | HG01069.hp2 HG01243.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+17491T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71230555 | ||||||
| chr10:71230557
|
C | T | 2 | a0001c0001t0031g0336a0001c0001t0068g0340 | 2 | HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+17493C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71230557 | ||||||
| chr10:71230609
|
T | C | 12 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0006t0015g0011others(9): Show | 12 | HG01069.hp2 HG01243.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+17545T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71230609 | ||||||
| chr10:71230610
|
G | A | 8 | a0001c0006t0015g0011a0001c0006t0015g0021a0001c0006t0015g0141others(5): Show | 8 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+17546G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71230610 | ||||||
| chr10:71230940
|
G | A | 1 | a0001c0001t0011g0361 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.79+17876G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71230940 | ||||||
| chr10:71231056
|
G | T | 25 | a0001c0001t0001g0224a0001c0001t0004g0024a0001c0001t0004g0316others(22): Show | 26 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.79+17992G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231056 | ||||||
| chr10:71231083
|
G | A | 2 | a0001c0001t0010g0323a0027c0025t0059g0009 | 2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.79+18019G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231083 | ||||||
| chr10:71231112
|
C | T | 4 | a0001c0003t0036g0131a0003c0038t0012g0013a0006c0018t0040g0200others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+18048C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231112 | ||||||
| chr10:71231141
|
C | T | 1 | a0001c0003t0008g0190 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.79+18077C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231141 | ||||||
| chr10:71231142
|
G | T | 1 | a0002c0008t0003g0067 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.79+18078G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231142 | ||||||
| chr10:71231209
|
A | G | 137 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0144others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.79+18145A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231209 | ||||||
| chr10:71231277
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0193 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.79+18213G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231277 | ||||||
| chr10:71231289
|
T | G | 4 | a0001c0001t0007g0139a0001c0002t0028g0155a0003c0007t0012g0356others(1): Show | 4 | HG00639.hp2 HG02922.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+18225T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231289 | ||||||
| chr10:71231338
|
G | A | 62 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0144others(59): Show | 63 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.79+18274G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231338 | ||||||
| chr10:71231431
|
C | T | 2 | a0001c0001t0025g0029a0001c0001t0025g0136 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.79+18367C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231431 | ||||||
| chr10:71231500
|
T | C | 25 | a0001c0001t0001g0224a0001c0001t0004g0024a0001c0001t0004g0316others(22): Show | 26 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.79+18436T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231500 | ||||||
| chr10:71231551
|
A | G | 1 | a0001c0001t0055g0293 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.79+18487A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231551 | ||||||
| chr10:71231569
|
G | A | 173 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(170): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.79+18505G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231569 | ||||||
| chr10:71231583
|
G | A | 72 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(69): Show | 73 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.79+18519G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231583 | ||||||
| chr10:71231615
|
G | A | 56 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0144others(53): Show | 57 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.79+18551G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231615 | ||||||
| chr10:71231628
|
C | T | 131 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0144others(128): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.79+18564C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231628 | ||||||
| chr10:71231647
|
A | C | 2 | a0001c0001t0031g0336a0001c0001t0068g0340 | 2 | HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+18583A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231647 | ||||||
| chr10:71231824
|
C | G | 1 | a0001c0001t0025g0338 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.79+18760C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231824 | ||||||
| chr10:71231835
|
G | C | 29 | a0001c0001t0007g0349a0001c0001t0010g0323a0001c0001t0011g0361others(26): Show | 29 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.79+18771G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231835 | ||||||
| chr10:71231960
|
C | T | 1 | a0003c0007t0012g0227 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.79+18896C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71231960 | ||||||
| chr10:71232097
|
C | A | 1 | a0001c0002t0028g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79+19033C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71232097 | ||||||
| chr10:71232100
|
T | A | 1 | a0010c0016t0049g0077 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.79+19036T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71232100 | ||||||
| chr10:71232324
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.79+19260C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71232324 | ||||||
| chr10:71232325
|
G | A | 1 | a0001c0001t0013g0276 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.79+19261G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71232325 | ||||||
| chr10:71232327
|
G | C | 2 | a0001c0001t0001g0288a0001c0001t0011g0272 | 2 | HG03490.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.79+19263G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71232327 | ||||||
| chr10:71232360
|
T | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0147 | 2 | HG01515.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.79+19296T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71232360 | ||||||
| chr10:71232730
|
TA | T | 5 | a0001c0001t0007g0139a0001c0055t0024g0153a0003c0007t0012g0356others(2): Show | 5 | HG00639.hp2 HG02559.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+19667delA | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71232730 | ||||||
| chr10:71232842
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.79+19778C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71232842 | ||||||
| chr10:71232940
|
T | C | 13 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0003t0001g0284others(10): Show | 13 | HG01069.hp2 HG01243.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+19876T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71232940 | ||||||
| chr10:71232997
|
T | G | 1 | a0001c0001t0007g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.79+19933T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71232997 | ||||||
| chr10:71233067
|
C | T | 67 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(64): Show | 69 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.79+20003C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71233067 | ||||||
| chr10:71233228
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.79+20164C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71233228 | ||||||
| chr10:71233323
|
C | T | 66 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(63): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.79+20259C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71233323 | ||||||
| chr10:71233424
|
T | G | 107 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(104): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.79+20360T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71233424 | ||||||
| chr10:71233433
|
G | A | 4 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0003t0001g0284others(1): Show | 4 | HG03579.hp2 HG03927.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+20369G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71233433 | ||||||
| chr10:71233521
|
C | G | 1 | a0001c0001t0011g0361 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.79+20457C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71233521 | ||||||
| chr10:71233846
|
T | C | 4 | a0001c0001t0031g0336a0001c0001t0068g0340a0001c0003t0001g0284others(1): Show | 4 | HG03579.hp2 HG03927.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+20782T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71233846 | ||||||
| chr10:71234017
|
T | C | 92 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0144others(89): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.79+20953T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71234017 | ||||||
| chr10:71234128
|
T | C | 37 | a0001c0001t0007g0139a0001c0001t0007g0349a0001c0001t0011g0361others(34): Show | 37 | HG00639.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.79+21064T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71234128 | ||||||
| chr10:71234300
|
C | T | 2 | a0011c0014t0018g0010a0011c0014t0018g0106 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.79+21236C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71234300 | ||||||
| chr10:71234301
|
G | A | 1 | a0007c0017t0011g0354 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.79+21237G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71234301 | ||||||
| chr10:71234415
|
C | T | 1 | a0001c0001t0011g0050 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.79+21351C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71234415 | ||||||
| chr10:71234462
|
G | A | 1 | a0001c0001t0004g0149 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.79+21398G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71234462 | ||||||
| chr10:71234722
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.79+21658A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71234722 | ||||||
| chr10:71234945
|
C | T | 2 | a0001c0001t0005g0163a0001c0001t0010g0015 | 2 | HG03669.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.79+21881C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71234945 | ||||||
| chr10:71235037
|
C | T | 38 | a0001c0001t0004g0175a0001c0001t0013g0276a0001c0001t0014g0028others(35): Show | 38 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.79+21973C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235037 | ||||||
| chr10:71235050
|
A | G | 28 | a0001c0001t0001g0224a0001c0001t0004g0024a0001c0001t0004g0237others(25): Show | 29 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.79+21986A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235050 | ||||||
| chr10:71235073
|
TC | T | 3 | a0001c0001t0010g0323a0014c0050t0029g0352a0027c0025t0059g0009 | 3 | HG01243.hp2 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.79+22010delC | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235073 | ||||||
| chr10:71235081
|
GCTGCCTC others(5): Show |
G | 91 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(88): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.79+22027_79+22038d others(14): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71235081 | |||||
| chr10:71235121
|
A | C | 1 | a0001c0001t0001g0189 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.79+22057A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235121 | ||||||
| chr10:71235190
|
A | G | 185 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(182): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.79+22126A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235190 | ||||||
| chr10:71235290
|
G | A | 3 | a0001c0001t0010g0323a0014c0050t0029g0352a0027c0025t0059g0009 | 3 | HG01243.hp2 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.79+22226G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235290 | ||||||
| chr10:71235389
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0009g0177 | 2 | NA19002.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.79+22325G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235389 | ||||||
| chr10:71235424
|
C | T | 1 | a0002c0005t0001g0076 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.79+22360C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235424 | ||||||
| chr10:71235425
|
G | A | 1 | a0001c0002t0009g0304 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.79+22361G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235425 | ||||||
| chr10:71235456
|
T | C | 92 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(89): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.79+22392T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235456 | ||||||
| chr10:71235488
|
G | A | 1 | a0008c0047t0029g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.79+22424G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235488 | ||||||
| chr10:71235574
|
G | A | 1 | a0001c0002t0006g0250 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.79+22510G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235574 | ||||||
| chr10:71235645
|
G | A | 4 | a0001c0001t0004g0024a0001c0001t0004g0316a0001c0004t0003g0064others(1): Show | 4 | NA18967.hp1 NA18979.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+22581G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235645 | ||||||
| chr10:71235664
|
G | A | 1 | a0001c0003t0008g0190 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.79+22600G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235664 | ||||||
| chr10:71235816
|
C | T | 10 | a0001c0003t0007g0095a0001c0003t0007g0359a0001c0003t0024g0097others(7): Show | 10 | HG01884.hp1 HG02818.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+22752C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235816 | ||||||
| chr10:71235875
|
A | G | 2 | a0001c0055t0024g0153a0008c0041t0012g0197 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.79+22811A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235875 | ||||||
| chr10:71235902
|
C | T | 1 | a0001c0003t0007g0359 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.79+22838C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71235902 | ||||||
| chr10:71236069
|
G | A | 2 | a0001c0001t0002g0313a0001c0001t0016g0307 | 2 | NA18941.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.79+23005G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71236069 | ||||||
| chr10:71236196
|
C | A | 1 | a0001c0003t0013g0225 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.79+23132C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71236196 | ||||||
| chr10:71236228
|
C | T | 3 | a0001c0001t0007g0128a0001c0001t0080g0130a0004c0010t0010g0092 | 3 | HG03041.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.79+23164C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71236228 | ||||||
| chr10:71236373
|
CAT | C | 3 | a0001c0003t0011g0132a0001c0003t0044g0201a0001c0012t0016g0325 | 3 | HG02723.hp2 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.79+23310_79+23311d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71236373 | ||||||
| chr10:71236402
|
C | A | 1 | a0002c0005t0014g0045 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.79+23338C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71236402 | ||||||
| chr10:71236459
|
C | T | 4 | a0001c0003t0036g0131a0003c0038t0012g0013a0006c0018t0040g0200others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+23395C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71236459 | ||||||
| chr10:71236477
|
C | T | 38 | a0001c0001t0004g0175a0001c0001t0013g0276a0001c0001t0014g0028others(35): Show | 38 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.79+23413C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71236477 | ||||||
| chr10:71236491
|
C | G | 1 | a0001c0002t0002g0306 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.79+23427C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71236491 | ||||||
| chr10:71236567
|
G | A | 1 | a0001c0003t0036g0131 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.79+23503G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71236567 | ||||||
| chr10:71236658
|
C | T | 2 | a0001c0001t0010g0323a0027c0025t0059g0009 | 2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.79+23594C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71236658 | ||||||
| chr10:71236930
|
C | G | 7 | a0001c0002t0001g0001a0001c0002t0001g0087a0001c0002t0001g0091others(4): Show | 8 | HG01123.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+23866C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71236930 | ||||||
| chr10:71237025
|
G | A | 155 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(152): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.79+23961G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71237025 | ||||||
| chr10:71237037
|
T | C | 12 | a0001c0002t0028g0155a0001c0003t0011g0132a0001c0003t0044g0201others(9): Show | 12 | HG01069.hp2 HG02723.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+23973T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71237037 | ||||||
| chr10:71237037
|
T | G | 155 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(152): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.79+23973T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71237037 | ||||||
| chr10:71237098
|
C | T | 2 | a0006c0018t0040g0200a0006c0018t0040g0297 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.79+24034C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71237098 | ||||||
| chr10:71237325
|
C | T | 27 | a0001c0001t0001g0224a0001c0001t0004g0024a0001c0001t0004g0237others(24): Show | 28 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+24261C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71237325 | ||||||
| chr10:71237500
|
C | T | 2 | a0009c0019t0004g0208a0009c0034t0004g0286 | 2 | HG02165.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.79+24436C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71237500 | ||||||
| chr10:71237547
|
GT | G | 149 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(146): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.79+24484delT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71237547 | ||||||
| chr10:71237619
|
A | G | 2 | a0006c0018t0040g0200a0006c0018t0040g0297 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.79+24555A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71237619 | ||||||
| chr10:71237662
|
G | A | 1 | a0001c0003t0001g0284 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.79+24598G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71237662 | ||||||
| chr10:71237937
|
G | T | 6 | a0001c0001t0010g0323a0001c0003t0036g0131a0003c0038t0012g0013others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+24873G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71237937 | ||||||
| chr10:71238103
|
A | G | 1 | a0002c0005t0014g0045 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.79+25039A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71238103 | ||||||
| chr10:71238114
|
G | A | 1 | a0001c0002t0033g0036 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.79+25050G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71238114 | ||||||
| chr10:71238124
|
T | C | 24 | a0001c0002t0028g0155a0001c0003t0011g0132a0001c0003t0019g0328others(21): Show | 24 | HG00735.hp1 HG01069.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.79+25060T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71238124 | ||||||
| chr10:71238142
|
G | A | 2 | a0012c0013t0003g0191a0025c0032t0023g0084 | 2 | HG02015.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.79+25078G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71238142 | ||||||
| chr10:71238297
|
C | T | 4 | a0001c0002t0006g0311a0001c0003t0011g0132a0001c0003t0044g0201others(1): Show | 4 | HG02723.hp2 HG02895.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+25233C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71238297 | ||||||
| chr10:71238362
|
C | A | 94 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(91): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.79+25298C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71238362 | ||||||
| chr10:71238406
|
C | A | 1 | a0016c0037t0013g0270 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.79+25342C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71238406 | ||||||
| chr10:71238416
|
C | T | 2 | a0001c0046t0016g0179a0016c0037t0013g0270 | 2 | NA18939.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+25352C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71238416 | ||||||
| chr10:71238429
|
A | AT | 6 | a0001c0001t0010g0323a0001c0003t0036g0131a0003c0038t0012g0013others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+25367dupT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71238429 | |||||
| chr10:71238464
|
G | A | 36 | a0001c0001t0001g0086a0001c0001t0001g0240a0001c0001t0001g0294others(33): Show | 38 | HG00597.hp2 HG00609.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.79+25400G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71238464 | ||||||
| chr10:71238477
|
C | T | 59 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(56): Show | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.79+25413C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71238477 | ||||||
| chr10:71238724
|
G | A | 2 | a0001c0001t0002g0082a0001c0001t0002g0314 | 2 | NA18612.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.79+25660G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71238724 | ||||||
| chr10:71238844
|
A | G | 3 | a0001c0003t0017g0209a0001c0003t0017g0210a0001c0003t0017g0211 | 3 | HG01256.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.79+25780A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71238844 | ||||||
| chr10:71239055
|
G | T | 1 | a0016c0037t0013g0270 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.79+25991G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71239055 | ||||||
| chr10:71239228
|
G | A | 50 | a0001c0001t0007g0349a0001c0001t0010g0323a0001c0001t0011g0361others(47): Show | 50 | HG00639.hp2 HG00735.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.79+26164G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71239228 | ||||||
| chr10:71239300
|
A | T | 1 | a0001c0001t0002g0046 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.79+26236A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71239300 | ||||||
| chr10:71239314
|
C | T | 1 | a0001c0012t0038g0096 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.79+26250C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71239314 | ||||||
| chr10:71239588
|
G | A | 154 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(151): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.79+26524G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71239588 | ||||||
| chr10:71239806
|
C | T | 1 | a0006c0018t0040g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.79+26742C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71239806 | ||||||
| chr10:71239834
|
G | T | 26 | a0001c0001t0007g0349a0001c0001t0010g0323a0001c0001t0011g0361others(23): Show | 26 | HG00639.hp2 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.79+26770G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71239834 | ||||||
| chr10:71239882
|
T | C | 3 | a0001c0001t0019g0320a0001c0001t0019g0353a0001c0002t0078g0123 | 3 | HG01169.hp2 HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.79+26818T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71239882 | ||||||
| chr10:71239915
|
T | A | 2 | a0001c0001t0031g0336a0001c0001t0068g0340 | 2 | HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+26851T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71239915 | ||||||
| chr10:71240013
|
A | T | 1 | a0001c0001t0002g0046 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.79+26949A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240013 | ||||||
| chr10:71240095
|
G | A | 1 | a0001c0002t0001g0087 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.79+27031G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240095 | ||||||
| chr10:71240130
|
A | C | 1 | a0007c0017t0016g0327 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.79+27066A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240130 | ||||||
| chr10:71240157
|
G | A | 1 | a0003c0007t0012g0227 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.79+27093G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240157 | ||||||
| chr10:71240190
|
C | T | 1 | a0001c0002t0039g0063 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.79+27126C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240190 | ||||||
| chr10:71240259
|
G | C | 22 | a0001c0002t0001g0219a0001c0002t0002g0025a0001c0002t0002g0093others(19): Show | 22 | HG00408.hp2 HG01256.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.79+27195G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240259 | ||||||
| chr10:71240264
|
C | T | 59 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(56): Show | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.79+27200C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240264 | ||||||
| chr10:71240347
|
A | G | 34 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(31): Show | 35 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.79+27283A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240347 | ||||||
| chr10:71240415
|
C | T | 3 | a0001c0055t0024g0153a0003c0007t0012g0356a0008c0041t0012g0197 | 3 | HG02559.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.79+27351C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240415 | ||||||
| chr10:71240574
|
G | A | 58 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(55): Show | 60 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.79+27510G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240574 | ||||||
| chr10:71240683
|
C | G | 1 | a0014c0050t0029g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.79+27619C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240683 | ||||||
| chr10:71240695
|
C | G | 2 | a0006c0018t0040g0200a0006c0018t0040g0297 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.79+27631C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240695 | ||||||
| chr10:71240785
|
G | T | 1 | a0004c0043t0079g0357 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79+27721G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240785 | ||||||
| chr10:71240929
|
T | C | 35 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(32): Show | 36 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.79+27865T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71240929 | ||||||
| chr10:71241083
|
T | C | 342 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0086others(339): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.79+28019T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241083 | ||||||
| chr10:71241108
|
C | T | 1 | a0001c0001t0005g0163 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.79+28044C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241108 | ||||||
| chr10:71241120
|
C | T | 17 | a0001c0001t0007g0349a0001c0001t0011g0361a0001c0001t0025g0029others(14): Show | 17 | HG00639.hp2 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.79+28056C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241120 | ||||||
| chr10:71241186
|
A | G | 140 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(137): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.79+28122A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241186 | ||||||
| chr10:71241298
|
G | A | 27 | a0001c0001t0004g0175a0001c0001t0013g0276a0001c0001t0014g0028others(24): Show | 27 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+28234G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241298 | ||||||
| chr10:71241309
|
C | G | 59 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(56): Show | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.79+28245C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241309 | ||||||
| chr10:71241485
|
A | G | 139 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(136): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.79+28421A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241485 | ||||||
| chr10:71241569
|
G | A | 1 | a0001c0002t0058g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79+28505G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241569 | ||||||
| chr10:71241604
|
C | T | 139 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(136): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.79+28540C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241604 | ||||||
| chr10:71241644
|
C | T | 2 | a0001c0009t0035g0007a0001c0009t0076g0007 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.79+28580C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241644 | ||||||
| chr10:71241716
|
G | A | 6 | a0003c0007t0010g0027a0003c0007t0012g0098a0003c0007t0012g0108others(3): Show | 6 | HG02647.hp2 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+28652G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241716 | ||||||
| chr10:71241751
|
G | A | 13 | a0001c0001t0002g0046a0001c0001t0002g0287a0001c0001t0004g0333others(10): Show | 13 | HG00558.hp2 HG01346.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.79+28687G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241751 | ||||||
| chr10:71241787
|
G | A | 27 | a0001c0001t0004g0175a0001c0001t0013g0276a0001c0001t0014g0028others(24): Show | 27 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+28723G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241787 | ||||||
| chr10:71241979
|
A | C | 1 | a0001c0001t0014g0028 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.79+28915A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241979 | ||||||
| chr10:71241999
|
A | C | 1 | a0005c0011t0010g0017 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.79+28935A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71241999 | ||||||
| chr10:71242085
|
C | T | 2 | a0001c0001t0031g0336a0001c0001t0068g0340 | 2 | HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+29021C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71242085 | ||||||
| chr10:71242131
|
G | C | 2 | a0001c0003t0019g0328a0001c0015t0018g0331 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.79+29067G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71242131 | ||||||
| chr10:71242131
|
G | T | 1 | a0001c0002t0028g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79+29067G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71242131 | ||||||
| chr10:71242167
|
C | A | 58 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(55): Show | 60 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.79+29103C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71242167 | ||||||
| chr10:71242176
|
A | G | 1 | a0001c0001t0005g0188 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.79+29112A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71242176 | ||||||
| chr10:71242196
|
C | T | 157 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.79+29132C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71242196 | ||||||
| chr10:71242217
|
CTG | C | 6 | a0001c0001t0011g0341a0001c0001t0011g0348a0001c0001t0020g0115others(3): Show | 6 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+29157_79+29158d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71242217 | |||||
| chr10:71242334
|
G | A | 138 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(135): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.79+29270G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71242334 | ||||||
| chr10:71242497
|
C | G | 31 | a0001c0001t0004g0175a0001c0001t0013g0276a0001c0001t0014g0028others(28): Show | 31 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.79+29433C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71242497 | ||||||
| chr10:71242646
|
G | A | 1 | a0001c0001t0005g0040 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.79+29582G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71242646 | ||||||
| chr10:71242735
|
C | G | 1 | a0001c0002t0004g0145 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.79+29671C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71242735 | ||||||
| chr10:71242921
|
A | T | 34 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(31): Show | 35 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.79+29857A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71242921 | ||||||
| chr10:71243096
|
A | T | 2 | a0005c0011t0010g0107a0005c0011t0010g0134 | 2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.79+30032A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71243096 | ||||||
| chr10:71243105
|
C | T | 1 | a0008c0047t0029g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.79+30041C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71243105 | ||||||
| chr10:71243140
|
C | A | 28 | a0001c0002t0028g0155a0001c0003t0011g0132a0001c0003t0019g0328others(25): Show | 28 | HG00735.hp1 HG01069.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.79+30076C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71243140 | ||||||
| chr10:71243200
|
A | C | 2 | a0001c0001t0005g0101a0001c0001t0034g0230 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.79+30136A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71243200 | ||||||
| chr10:71243632
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.79+30568G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71243632 | ||||||
| chr10:71243643
|
G | A | 1 | a0001c0001t0017g0202 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.79+30579G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71243643 | ||||||
| chr10:71243791
|
A | G | 26 | a0001c0001t0004g0175a0001c0001t0013g0276a0001c0001t0014g0028others(23): Show | 26 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.79+30727A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71243791 | ||||||
| chr10:71243861
|
G | A | 1 | a0001c0002t0001g0014 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.79+30797G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71243861 | ||||||
| chr10:71243906
|
A | G | 3 | a0001c0003t0008g0042a0001c0003t0008g0148a0001c0003t0008g0157 | 3 | NA18952.hp2 NA18999.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.79+30842A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71243906 | ||||||
| chr10:71243984
|
G | A | 1 | a0001c0002t0028g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79+30920G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71243984 | ||||||
| chr10:71244005
|
C | T | 1 | a0001c0002t0032g0004 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.79+30941C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244005 | ||||||
| chr10:71244053
|
G | T | 2 | a0001c0001t0031g0336a0001c0001t0068g0340 | 2 | HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+30989G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244053 | ||||||
| chr10:71244092
|
T | C | 6 | a0001c0001t0010g0323a0001c0003t0036g0131a0003c0038t0012g0013others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+31028T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244092 | ||||||
| chr10:71244186
|
C | A | 1 | a0001c0003t0007g0359 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.79+31122C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244186 | ||||||
| chr10:71244258
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.79+31194G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244258 | ||||||
| chr10:71244293
|
A | G | 138 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(135): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.79+31229A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244293 | ||||||
| chr10:71244473
|
T | A | 1 | a0001c0001t0004g0333 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.79+31409T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244473 | ||||||
| chr10:71244712
|
G | A | 2 | a0003c0007t0012g0098a0003c0007t0012g0122 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.79+31648G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244712 | ||||||
| chr10:71244725
|
C | T | 1 | a0002c0005t0002g0242 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.79+31661C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244725 | ||||||
| chr10:71244728
|
G | A | 3 | a0001c0003t0024g0097a0001c0009t0035g0007a0001c0009t0076g0007 | 3 | HG02896.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.79+31664G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244728 | ||||||
| chr10:71244765
|
A | G | 95 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(92): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.79+31701A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244765 | ||||||
| chr10:71244780
|
G | T | 26 | a0001c0001t0004g0175a0001c0001t0013g0276a0001c0001t0014g0028others(23): Show | 26 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.79+31716G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244780 | ||||||
| chr10:71244817
|
G | C | 36 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(33): Show | 37 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.79+31753G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244817 | ||||||
| chr10:71244826
|
G | A | 1 | a0001c0002t0001g0303 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.79+31762G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244826 | ||||||
| chr10:71244826
|
G | T | 2 | a0001c0001t0006g0039a0001c0002t0002g0252 | 2 | NA18942.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.79+31762G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244826 | ||||||
| chr10:71244996
|
G | A | 1 | a0014c0050t0029g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.79+31932G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71244996 | ||||||
| chr10:71245097
|
C | T | 1 | a0001c0001t0020g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.79+32033C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245097 | ||||||
| chr10:71245117
|
C | T | 6 | a0001c0001t0010g0323a0001c0003t0036g0131a0003c0038t0012g0013others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+32053C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245117 | ||||||
| chr10:71245132
|
T | C | 1 | a0001c0002t0028g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79+32068T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245132 | ||||||
| chr10:71245146
|
G | C | 17 | a0001c0001t0007g0349a0001c0001t0011g0361a0001c0001t0025g0029others(14): Show | 17 | HG00639.hp2 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.79+32082G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245146 | ||||||
| chr10:71245159
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0178 | 2 | HG04184.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.79+32095T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245159 | ||||||
| chr10:71245242
|
G | C | 93 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(90): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.79+32178G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245242 | ||||||
| chr10:71245276
|
C | T | 2 | a0001c0001t0001g0319a0001c0004t0003g0072 | 2 | NA19067.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.79+32212C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245276 | ||||||
| chr10:71245280
|
G | A | 54 | a0001c0001t0001g0078a0001c0001t0001g0183a0001c0001t0005g0020others(51): Show | 55 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.79+32216G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245280 | ||||||
| chr10:71245360
|
G | A | 25 | a0001c0001t0004g0175a0001c0001t0013g0276a0001c0001t0014g0028others(22): Show | 25 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.79+32296G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245360 | ||||||
| chr10:71245410
|
G | C | 8 | a0001c0006t0015g0011a0001c0006t0015g0021a0001c0006t0015g0141others(5): Show | 8 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+32346G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245410 | ||||||
| chr10:71245571
|
G | T | 1 | a0001c0001t0001g0194 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.79+32507G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245571 | ||||||
| chr10:71245796
|
G | T | 1 | a0001c0002t0041g0280 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.79+32732G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245796 | ||||||
| chr10:71245805
|
G | A | 1 | a0002c0005t0054g0166 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.79+32741G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245805 | ||||||
| chr10:71245962
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.79+32898C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245962 | ||||||
| chr10:71245993
|
G | A | 103 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(100): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.79+32929G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71245993 | ||||||
| chr10:71246180
|
G | A | 175 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0086others(172): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.79+33116G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246180 | ||||||
| chr10:71246233
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.79+33169G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246233 | ||||||
| chr10:71246245
|
T | A | 1 | a0001c0001t0073g0026 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.79+33181T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246245 | ||||||
| chr10:71246314
|
G | A | 3 | a0001c0001t0005g0231a0001c0003t0019g0328a0008c0047t0029g0160 | 3 | HG01109.hp1 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.79+33250G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246314 | ||||||
| chr10:71246359
|
C | T | 1 | a0001c0053t0001g0113 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.79+33295C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246359 | ||||||
| chr10:71246373
|
G | A | 2 | a0017c0023t0020g0339a0019c0021t0020g0355 | 2 | HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.79+33309G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246373 | ||||||
| chr10:71246397
|
G | A | 5 | a0001c0003t0036g0131a0002c0005t0014g0045a0003c0038t0012g0013others(2): Show | 5 | HG02451.hp1 HG02559.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+33333G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246397 | ||||||
| chr10:71246570
|
G | A | 30 | a0001c0001t0004g0024a0001c0001t0004g0175a0001c0001t0004g0316others(27): Show | 30 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.80-33251G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246570 | ||||||
| chr10:71246607
|
G | A | 1 | a0001c0002t0001g0061 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.80-33214G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246607 | ||||||
| chr10:71246677
|
A | G | 2 | a0001c0055t0024g0153a0008c0041t0012g0197 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.80-33144A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246677 | ||||||
| chr10:71246697
|
C | T | 59 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(56): Show | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.80-33124C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246697 | ||||||
| chr10:71246786
|
T | C | 1 | a0020c0033t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.80-33035T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246786 | ||||||
| chr10:71246820
|
A | T | 1 | a0001c0002t0009g0041 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.80-33001A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246820 | ||||||
| chr10:71246863
|
C | T | 233 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0086others(230): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.80-32958C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71246863 | ||||||
| chr10:71247000
|
G | A | 1 | a0001c0053t0001g0113 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.80-32821G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71247000 | ||||||
| chr10:71247025
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.80-32796C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71247025 | ||||||
| chr10:71247082
|
A | T | 1 | a0001c0003t0001g0118 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.80-32739A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71247082 | ||||||
| chr10:71247247
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.80-32574G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71247247 | ||||||
| chr10:71247350
|
A | G | 21 | a0001c0001t0001g0224a0001c0001t0004g0237a0001c0001t0013g0276others(18): Show | 22 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.80-32471A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71247350 | ||||||
| chr10:71247458
|
T | A | 236 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0086others(233): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.80-32363T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71247458 | ||||||
| chr10:71247510
|
C | T | 1 | a0022c0045t0004g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.80-32311C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71247510 | ||||||
| chr10:71247651
|
C | T | 1 | a0028c0039t0060g0171 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.80-32170C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71247651 | ||||||
| chr10:71247652
|
A | T | 1 | a0028c0039t0060g0171 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.80-32169A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71247652 | ||||||
| chr10:71247726
|
A | G | 1 | a0002c0005t0054g0166 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.80-32095A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71247726 | ||||||
| chr10:71247795
|
A | AAGACATG others(6): Show |
6 | a0001c0002t0032g0004a0001c0003t0036g0131a0002c0005t0014g0045others(3): Show | 7 | HG02451.hp1 HG02559.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-32025_80-32013d others(15): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71247795 | |||||
| chr10:71247835
|
C | T | 1 | a0001c0001t0055g0293 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.80-31986C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71247835 | ||||||
| chr10:71247852
|
T | C | 2 | a0001c0003t0001g0003a0001c0003t0008g0100 | 3 | HG03491.hp2 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.80-31969T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71247852 | ||||||
| chr10:71248107
|
G | A | 12 | a0001c0002t0058g0137a0001c0002t0072g0111a0001c0003t0007g0095others(9): Show | 12 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-31714G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71248107 | ||||||
| chr10:71248121
|
C | T | 1 | a0001c0002t0028g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.80-31700C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71248121 | ||||||
| chr10:71248167
|
A | G | 85 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(82): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.80-31654A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71248167 | ||||||
| chr10:71248235
|
C | T | 1 | a0002c0005t0014g0045 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.80-31586C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71248235 | ||||||
| chr10:71248277
|
T | C | 1 | a0002c0005t0014g0045 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.80-31544T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71248277 | ||||||
| chr10:71248288
|
G | A | 6 | a0001c0002t0001g0001a0001c0002t0001g0087a0001c0002t0001g0091others(3): Show | 7 | HG01123.hp2 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-31533G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71248288 | ||||||
| chr10:71248324
|
C | T | 3 | a0001c0002t0032g0004a0001c0003t0036g0131a0003c0038t0012g0013 | 4 | HG02559.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-31497C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71248324 | ||||||
| chr10:71248366
|
C | T | 1 | a0014c0050t0029g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.80-31455C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71248366 | ||||||
| chr10:71248371
|
C | G | 1 | a0014c0050t0029g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.80-31450C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71248371 | ||||||
| chr10:71248412
|
AG | A | 104 | a0001c0001t0001g0078a0001c0001t0001g0086a0001c0001t0001g0224others(101): Show | 106 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.80-31403delG | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71248412 | |||||
| chr10:71248465
|
G | A | 1 | a0001c0001t0042g0232 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.80-31356G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71248465 | ||||||
| chr10:71248848
|
GTC | G | 26 | a0001c0001t0001g0224a0001c0001t0004g0237a0001c0001t0006g0039others(23): Show | 26 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.80-30954_80-30953d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71248848 | |||||
| chr10:71248861
|
TCTCTCTC others(5): Show |
T | 2 | a0001c0009t0035g0007a0001c0009t0076g0007 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.80-30958_80-30947d others(14): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71248861 | |||||
| chr10:71248861
|
TCTCTCTC others(7): Show |
T | 7 | a0001c0003t0007g0095a0001c0003t0007g0359a0001c0003t0024g0097others(4): Show | 7 | HG01884.hp1 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-30958_80-30945d others(16): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71248861 | |||||
| chr10:71248863
|
TCTCTCAC others(5): Show |
T | 9 | a0001c0003t0001g0003a0001c0003t0002g0291a0001c0003t0004g0043others(6): Show | 10 | HG00423.hp2 HG02071.hp1 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-30956_80-30945d others(14): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71248863 | |||||
| chr10:71248865
|
T | A | 2 | a0001c0001t0010g0323a0002c0005t0002g0242 | 2 | HG03540.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.80-30956T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71248865 | ||||||
| chr10:71248865
|
TCTCA | T | 9 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(6): Show | 9 | HG00140.hp1 HG00733.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-30954_80-30951d others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71248865 | |||||
| chr10:71248865
|
TCTCACA | T | 95 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(92): Show | 96 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.80-30954_80-30949d others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71248865 | |||||
| chr10:71248865
|
TCTCACAC others(1): Show |
T | 64 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-30954_80-30947d others(10): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71248865 | |||||
| chr10:71248865
|
TCTCACAC others(3): Show |
T | 5 | a0001c0001t0016g0217a0001c0003t0011g0132a0001c0012t0016g0325others(2): Show | 5 | HG00639.hp2 HG02895.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-30954_80-30945d others(12): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71248865 | |||||
| chr10:71248865
|
TCTCACAC others(5): Show |
T | 87 | a0001c0001t0001g0078a0001c0001t0001g0086a0001c0001t0001g0240others(84): Show | 89 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.80-30954_80-30943d others(14): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71248865 | |||||
| chr10:71248867
|
T | A | 26 | a0001c0001t0001g0224a0001c0001t0004g0237a0001c0001t0010g0323others(23): Show | 26 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.80-30954T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71248867 | ||||||
| chr10:71248867
|
TCACA | T | 8 | a0001c0002t0032g0004a0001c0003t0019g0328a0001c0003t0036g0131others(5): Show | 9 | HG02145.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-30926_80-30923d others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71248867 | |||||
| chr10:71248867
|
TCACACAC others(1): Show |
T | 4 | a0001c0001t0005g0040a0001c0001t0009g0127a0001c0002t0058g0137others(1): Show | 4 | HG01943.hp1 HG02280.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-30930_80-30923d others(10): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71248867 | |||||
| chr10:71248867
|
TCACACAC others(5): Show |
T | 1 | a0001c0002t0006g0315 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.80-30934_80-30923d others(14): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71248867 | |||||
| chr10:71249020
|
C | T | 1 | a0001c0003t0002g0181 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.80-30801C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249020 | ||||||
| chr10:71249050
|
A | C | 3 | a0001c0001t0010g0323a0003c0007t0012g0356a0027c0025t0059g0009 | 3 | HG02976.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.80-30771A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249050 | ||||||
| chr10:71249050
|
A | G | 1 | a0004c0043t0079g0357 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.80-30771A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249050 | ||||||
| chr10:71249100
|
A | C | 84 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(81): Show | 85 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.80-30721A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249100 | ||||||
| chr10:71249142
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.80-30679G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249142 | ||||||
| chr10:71249247
|
C | G | 267 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.80-30574C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249247 | ||||||
| chr10:71249258
|
C | T | 1 | a0001c0002t0033g0036 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.80-30563C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249258 | ||||||
| chr10:71249339
|
G | A | 3 | a0001c0002t0032g0004a0001c0003t0036g0131a0003c0038t0012g0013 | 4 | HG02559.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-30482G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249339 | ||||||
| chr10:71249422
|
G | A | 26 | a0001c0001t0004g0024a0001c0001t0004g0175a0001c0001t0004g0316others(23): Show | 27 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.80-30399G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249422 | ||||||
| chr10:71249534
|
G | A | 3 | a0001c0002t0032g0004a0001c0003t0036g0131a0003c0038t0012g0013 | 4 | HG02559.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-30287G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249534 | ||||||
| chr10:71249787
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.80-30034G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249787 | ||||||
| chr10:71249878
|
A | C | 1 | a0001c0001t0001g0240 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.80-29943A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249878 | ||||||
| chr10:71249937
|
T | A | 4 | a0001c0003t0011g0132a0001c0012t0016g0325a0014c0050t0029g0352others(1): Show | 4 | HG00639.hp2 HG01243.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-29884T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249937 | ||||||
| chr10:71249944
|
G | A | 1 | a0028c0039t0060g0171 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.80-29877G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249944 | ||||||
| chr10:71249965
|
A | C | 1 | a0001c0001t0001g0294 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.80-29856A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249965 | ||||||
| chr10:71249993
|
G | T | 1 | a0001c0001t0001g0344 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.80-29828G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71249993 | ||||||
| chr10:71250001
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.80-29820G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250001 | ||||||
| chr10:71250030
|
C | A | 8 | a0001c0006t0015g0011a0001c0006t0015g0021a0001c0006t0015g0141others(5): Show | 8 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-29791C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250030 | ||||||
| chr10:71250055
|
A | G | 11 | a0001c0002t0032g0004a0001c0003t0036g0131a0001c0006t0015g0011others(8): Show | 12 | HG01069.hp2 HG02559.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-29766A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250055 | ||||||
| chr10:71250118
|
C | T | 2 | a0011c0014t0018g0010a0011c0014t0018g0106 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.80-29703C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250118 | ||||||
| chr10:71250237
|
T | C | 4 | a0001c0003t0011g0132a0001c0012t0016g0325a0014c0050t0029g0352others(1): Show | 4 | HG00639.hp2 HG01243.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-29584T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250237 | ||||||
| chr10:71250241
|
C | G | 4 | a0001c0003t0011g0132a0001c0012t0016g0325a0014c0050t0029g0352others(1): Show | 4 | HG00639.hp2 HG01243.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-29580C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250241 | ||||||
| chr10:71250262
|
G | A | 6 | a0001c0009t0005g0075a0001c0009t0035g0360a0001c0055t0024g0153others(3): Show | 6 | HG00735.hp1 HG01255.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-29559G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250262 | ||||||
| chr10:71250267
|
T | C | 188 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0086others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.80-29554T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250267 | ||||||
| chr10:71250269
|
C | T | 1 | a0001c0020t0065g0142 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.80-29552C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250269 | ||||||
| chr10:71250307
|
G | A | 63 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.80-29514G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250307 | ||||||
| chr10:71250352
|
C | T | 81 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.80-29469C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250352 | ||||||
| chr10:71250407
|
A | C | 2 | a0007c0017t0011g0354a0007c0017t0016g0327 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.80-29414A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250407 | ||||||
| chr10:71250446
|
G | T | 3 | a0001c0001t0010g0323a0003c0007t0012g0356a0027c0025t0059g0009 | 3 | HG02976.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.80-29375G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250446 | ||||||
| chr10:71250565
|
T | G | 188 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0086others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.80-29256T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250565 | ||||||
| chr10:71250766
|
A | G | 1 | a0014c0050t0029g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.80-29055A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71250766 | ||||||
| chr10:71251046
|
T | C | 2 | a0001c0001t0031g0336a0001c0001t0068g0340 | 2 | HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.80-28775T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251046 | ||||||
| chr10:71251106
|
T | G | 193 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0086others(190): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.80-28715T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251106 | ||||||
| chr10:71251109
|
T | G | 1 | a0001c0002t0028g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.80-28712T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251109 | ||||||
| chr10:71251253
|
G | A | 93 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(90): Show | 95 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.80-28568G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251253 | ||||||
| chr10:71251311
|
C | T | 2 | a0001c0001t0002g0117a0001c0001t0073g0026 | 2 | HG00597.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.80-28510C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251311 | ||||||
| chr10:71251356
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.80-28465T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251356 | ||||||
| chr10:71251401
|
C | T | 12 | a0001c0001t0005g0040a0001c0002t0058g0137a0001c0002t0072g0111others(9): Show | 12 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-28420C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251401 | ||||||
| chr10:71251402
|
G | A | 56 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.80-28419G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251402 | ||||||
| chr10:71251562
|
A | G | 1 | a0001c0002t0002g0256 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.80-28259A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251562 | ||||||
| chr10:71251623
|
T | G | 1 | a0001c0002t0077g0154 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.80-28198T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251623 | ||||||
| chr10:71251625
|
C | T | 9 | a0001c0001t0001g0047a0001c0001t0005g0020a0001c0001t0006g0060others(6): Show | 10 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-28196C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251625 | ||||||
| chr10:71251660
|
G | C | 3 | a0001c0002t0032g0004a0001c0003t0036g0131a0003c0038t0012g0013 | 4 | HG02559.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-28161G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251660 | ||||||
| chr10:71251669
|
T | C | 3 | a0001c0003t0019g0261a0001c0012t0038g0096a0001c0012t0038g0196 | 3 | HG01106.hp1 HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.80-28152T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251669 | ||||||
| chr10:71251687
|
A | T | 2 | a0001c0055t0024g0153a0008c0041t0012g0197 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.80-28134A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251687 | ||||||
| chr10:71251758
|
C | G | 1 | a0004c0042t0053g0229 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.80-28063C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251758 | ||||||
| chr10:71251952
|
T | G | 29 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(26): Show | 29 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.80-27869T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251952 | ||||||
| chr10:71251980
|
G | A | 188 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(185): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.80-27841G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71251980 | ||||||
| chr10:71252048
|
C | CAT | 29 | a0001c0001t0001g0066a0001c0001t0001g0199a0001c0001t0001g0288others(26): Show | 29 | HG00558.hp1 HG00558.hp2 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.80-27764_80-27763d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71252048 | |||||
| chr10:71252048
|
CAT | C | 57 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.80-27764_80-27763d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71252048 | |||||
| chr10:71252053
|
A | G | 2 | a0001c0003t0036g0131a0014c0050t0029g0352 | 2 | HG01243.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.80-27768A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252053 | ||||||
| chr10:71252223
|
T | C | 12 | a0001c0001t0005g0040a0001c0002t0058g0137a0001c0002t0072g0111others(9): Show | 12 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-27598T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252223 | ||||||
| chr10:71252327
|
G | A | 109 | a0001c0001t0001g0078a0001c0001t0001g0086a0001c0001t0001g0170others(106): Show | 112 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.80-27494G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252327 | ||||||
| chr10:71252372
|
C | T | 1 | a0001c0001t0063g0032 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.80-27449C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252372 | ||||||
| chr10:71252447
|
C | T | 1 | a0001c0001t0006g0039 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.80-27374C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252447 | ||||||
| chr10:71252469
|
C | A | 1 | a0001c0002t0077g0154 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.80-27352C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252469 | ||||||
| chr10:71252480
|
C | T | 1 | a0001c0002t0077g0154 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.80-27341C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252480 | ||||||
| chr10:71252481
|
G | C | 82 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(79): Show | 83 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.80-27340G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252481 | ||||||
| chr10:71252514
|
A | G | 1 | a0001c0002t0077g0154 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.80-27307A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252514 | ||||||
| chr10:71252532
|
A | G | 355 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(352): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.80-27289A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252532 | ||||||
| chr10:71252565
|
A | T | 2 | a0001c0055t0024g0153a0008c0041t0012g0197 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.80-27256A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252565 | ||||||
| chr10:71252584
|
G | A | 57 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.80-27237G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252584 | ||||||
| chr10:71252631
|
C | G | 1 | a0028c0039t0060g0171 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.80-27190C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252631 | ||||||
| chr10:71252801
|
G | C | 8 | a0001c0006t0015g0011a0001c0006t0015g0021a0001c0006t0015g0141others(5): Show | 8 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-27020G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252801 | ||||||
| chr10:71252871
|
C | T | 231 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(228): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.80-26950C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252871 | ||||||
| chr10:71252894
|
G | A | 1 | a0002c0005t0030g0246 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.80-26927G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71252894 | ||||||
| chr10:71253005
|
T | A | 4 | a0001c0009t0005g0075a0001c0009t0035g0360a0018c0022t0018g0186others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-26816T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71253005 | ||||||
| chr10:71253006
|
G | A | 101 | a0001c0001t0001g0078a0001c0001t0001g0086a0001c0001t0001g0240others(98): Show | 104 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.80-26815G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71253006 | ||||||
| chr10:71253099
|
C | T | 3 | a0001c0009t0035g0360a0018c0022t0018g0186a0031c0056t0020g0296 | 3 | HG00735.hp1 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.80-26722C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71253099 | ||||||
| chr10:71253105
|
A | G | 1 | a0001c0003t0008g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.80-26716A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71253105 | ||||||
| chr10:71253146
|
C | T | 1 | a0004c0010t0066g0269 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.80-26675C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71253146 | ||||||
| chr10:71253188
|
C | CA | 232 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(229): Show | 236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.80-26633_80-26632i others(3): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71253188 | ||||||
| chr10:71253219
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.80-26602G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71253219 | ||||||
| chr10:71253714
|
G | T | 7 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(4): Show | 7 | HG00140.hp1 HG00733.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-26107G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71253714 | ||||||
| chr10:71253818
|
G | A | 1 | a0002c0008t0003g0069 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.80-26003G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71253818 | ||||||
| chr10:71254328
|
C | G | 9 | a0001c0001t0001g0047a0001c0001t0005g0020a0001c0001t0006g0060others(6): Show | 10 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-25493C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71254328 | ||||||
| chr10:71254401
|
G | T | 7 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(4): Show | 7 | HG00140.hp1 HG00733.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-25420G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71254401 | ||||||
| chr10:71254412
|
G | C | 4 | a0001c0009t0005g0075a0001c0009t0035g0360a0018c0022t0018g0186others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-25409G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71254412 | ||||||
| chr10:71254506
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.80-25315C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71254506 | ||||||
| chr10:71254546
|
G | C | 2 | a0001c0001t0025g0029a0001c0001t0025g0136 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.80-25275G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71254546 | ||||||
| chr10:71254633
|
C | T | 22 | a0001c0001t0001g0224a0001c0001t0004g0237a0001c0001t0013g0276others(19): Show | 22 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.80-25188C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71254633 | ||||||
| chr10:71254763
|
T | C | 213 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(210): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.80-25058T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71254763 | ||||||
| chr10:71255101
|
G | A | 2 | a0001c0055t0024g0153a0008c0041t0012g0197 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.80-24720G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255101 | ||||||
| chr10:71255226
|
G | A | 2 | a0001c0001t0005g0105a0001c0001t0017g0202 | 2 | HG02602.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.80-24595G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255226 | ||||||
| chr10:71255306
|
G | A | 53 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.80-24515G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255306 | ||||||
| chr10:71255321
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0086 | 2 | HG03710.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.80-24500C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255321 | ||||||
| chr10:71255367
|
T | C | 1 | a0004c0043t0079g0357 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.80-24454T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255367 | ||||||
| chr10:71255378
|
C | A | 11 | a0001c0002t0032g0004a0001c0003t0011g0132a0001c0003t0036g0131others(8): Show | 12 | HG00639.hp2 HG00735.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.80-24443C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255378 | ||||||
| chr10:71255378
|
C | T | 11 | a0001c0002t0058g0137a0001c0002t0072g0111a0001c0003t0007g0095others(8): Show | 11 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-24443C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255378 | ||||||
| chr10:71255475
|
G | T | 1 | a0001c0003t0019g0261 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.80-24346G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255475 | ||||||
| chr10:71255500
|
A | G | 5 | a0001c0002t0002g0271a0001c0002t0002g0321a0001c0002t0027g0249others(2): Show | 5 | NA18973.hp1 NA18985.hp1 NA19070.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-24321A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255500 | ||||||
| chr10:71255578
|
G | A | 1 | a0001c0002t0006g0315 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.80-24243G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255578 | ||||||
| chr10:71255665
|
A | G | 1 | a0001c0002t0001g0303 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.80-24156A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255665 | ||||||
| chr10:71255740
|
C | T | 4 | a0001c0009t0005g0075a0001c0009t0035g0360a0018c0022t0018g0186others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-24081C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255740 | ||||||
| chr10:71255828
|
G | A | 1 | a0028c0039t0060g0171 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.80-23993G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255828 | ||||||
| chr10:71255983
|
T | C | 1 | a0001c0002t0002g0083 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.80-23838T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71255983 | ||||||
| chr10:71256154
|
C | T | 15 | a0001c0001t0005g0040a0001c0001t0069g0206a0001c0002t0058g0137others(12): Show | 15 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-23667C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71256154 | ||||||
| chr10:71256229
|
G | A | 2 | a0001c0001t0005g0163a0001c0001t0010g0015 | 2 | HG03669.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.80-23592G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71256229 | ||||||
| chr10:71256233
|
A | C | 1 | a0001c0001t0005g0040 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.80-23588A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71256233 | ||||||
| chr10:71256317
|
G | A | 1 | a0021c0031t0002g0114 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.80-23504G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71256317 | ||||||
| chr10:71256386
|
G | A | 2 | a0001c0055t0024g0153a0008c0041t0012g0197 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.80-23435G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71256386 | ||||||
| chr10:71256533
|
G | A | 1 | a0004c0042t0053g0229 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.80-23288G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71256533 | ||||||
| chr10:71256553
|
G | A | 49 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(46): Show | 50 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.80-23268G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71256553 | ||||||
| chr10:71256560
|
C | T | 2 | a0001c0055t0024g0153a0008c0041t0012g0197 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.80-23261C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71256560 | ||||||
| chr10:71256613
|
G | C | 3 | a0001c0003t0019g0261a0001c0012t0038g0096a0001c0012t0038g0196 | 3 | HG01106.hp1 HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.80-23208G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71256613 | ||||||
| chr10:71256665
|
A | C | 2 | a0001c0003t0002g0152a0001c0003t0008g0018 | 2 | NA18984.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.80-23156A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71256665 | ||||||
| chr10:71256727
|
C | T | 1 | a0001c0001t0062g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.80-23094C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71256727 | ||||||
| chr10:71256900
|
G | A | 1 | a0020c0033t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.80-22921G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71256900 | ||||||
| chr10:71256951
|
G | A | 2 | a0001c0055t0024g0153a0008c0041t0012g0197 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.80-22870G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71256951 | ||||||
| chr10:71257035
|
C | T | 1 | a0002c0005t0013g0055 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.80-22786C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71257035 | ||||||
| chr10:71257082
|
C | A | 1 | a0001c0001t0009g0079 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.80-22739C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71257082 | ||||||
| chr10:71257102
|
A | G | 1 | a0001c0002t0028g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.80-22719A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71257102 | ||||||
| chr10:71257171
|
G | T | 12 | a0001c0001t0010g0323a0001c0002t0028g0155a0001c0006t0015g0011others(9): Show | 12 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-22650G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71257171 | ||||||
| chr10:71257210
|
G | A | 56 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.80-22611G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71257210 | ||||||
| chr10:71257361
|
G | A | 2 | a0001c0055t0024g0153a0008c0041t0012g0197 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.80-22460G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71257361 | ||||||
| chr10:71257376
|
C | T | 4 | a0001c0009t0005g0075a0001c0009t0035g0360a0018c0022t0018g0186others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-22445C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71257376 | ||||||
| chr10:71257562
|
T | C | 1 | a0001c0003t0008g0190 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.80-22259T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71257562 | ||||||
| chr10:71257753
|
G | A | 1 | a0001c0001t0005g0180 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.80-22068G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71257753 | ||||||
| chr10:71257819
|
T | A | 12 | a0001c0001t0010g0323a0001c0002t0028g0155a0001c0006t0015g0011others(9): Show | 12 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-22002T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71257819 | ||||||
| chr10:71258012
|
C | T | 2 | a0001c0003t0011g0132a0001c0012t0016g0325 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.80-21809C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258012 | ||||||
| chr10:71258120
|
G | A | 3 | a0001c0002t0032g0004a0001c0003t0036g0131a0003c0038t0012g0013 | 4 | HG02559.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-21701G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258120 | ||||||
| chr10:71258126
|
A | G | 2 | a0001c0001t0005g0105a0001c0001t0017g0202 | 2 | HG02602.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.80-21695A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258126 | ||||||
| chr10:71258197
|
G | A | 1 | a0002c0005t0023g0350 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.80-21624G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258197 | ||||||
| chr10:71258262
|
T | C | 160 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(157): Show | 162 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.80-21559T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258262 | ||||||
| chr10:71258463
|
C | T | 1 | a0001c0003t0008g0148 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.80-21358C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258463 | ||||||
| chr10:71258465
|
T | C | 1 | a0001c0003t0008g0148 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.80-21356T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258465 | ||||||
| chr10:71258466
|
C | T | 1 | a0001c0003t0008g0148 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.80-21355C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258466 | ||||||
| chr10:71258588
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0016g0217a0001c0024t0002g0235others(1): Show | 4 | NA18612.hp1 NA18747.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-21233G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258588 | ||||||
| chr10:71258653
|
C | A | 1 | a0001c0003t0001g0305 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.80-21168C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258653 | ||||||
| chr10:71258678
|
G | A | 1 | a0001c0001t0017g0202 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.80-21143G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258678 | ||||||
| chr10:71258749
|
G | T | 1 | a0001c0003t0008g0148 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.80-21072G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258749 | ||||||
| chr10:71258768
|
T | C | 41 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(38): Show | 41 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.80-21053T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258768 | ||||||
| chr10:71258792
|
T | A | 1 | a0001c0003t0008g0148 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.80-21029T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258792 | ||||||
| chr10:71258894
|
G | A | 99 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0120others(96): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.80-20927G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258894 | ||||||
| chr10:71258975
|
C | T | 2 | a0001c0003t0036g0131a0003c0038t0012g0013 | 2 | HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.80-20846C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258975 | ||||||
| chr10:71258990
|
G | A | 1 | a0001c0003t0001g0118 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.80-20831G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71258990 | ||||||
| chr10:71259357
|
G | A | 1 | a0001c0003t0008g0148 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.80-20464G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71259357 | ||||||
| chr10:71259376
|
A | T | 64 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(61): Show | 65 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.80-20445A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71259376 | ||||||
| chr10:71259385
|
CA | C | 42 | a0001c0001t0001g0240a0001c0001t0002g0274a0001c0001t0010g0323others(39): Show | 43 | HG00639.hp2 HG00735.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.80-20420delA | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71259385 | |||||
| chr10:71259385
|
CAA | C | 29 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(26): Show | 29 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.80-20421_80-20420d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71259385 | |||||
| chr10:71259445
|
C | A | 1 | a0030c0035t0018g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.80-20376C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71259445 | ||||||
| chr10:71259591
|
C | T | 2 | a0001c0001t0001g0239a0001c0026t0001g0310 | 2 | HG02155.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.80-20230C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71259591 | ||||||
| chr10:71259720
|
G | A | 1 | a0014c0050t0029g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.80-20101G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71259720 | ||||||
| chr10:71259795
|
C | T | 29 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(26): Show | 29 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.80-20026C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71259795 | ||||||
| chr10:71259906
|
C | T | 1 | a0001c0002t0004g0071 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.80-19915C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71259906 | ||||||
| chr10:71259936
|
G | T | 2 | a0001c0055t0024g0153a0008c0041t0012g0197 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.80-19885G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71259936 | ||||||
| chr10:71260002
|
G | A | 91 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(88): Show | 92 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.80-19819G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71260002 | ||||||
| chr10:71260006
|
A | G | 2 | a0018c0022t0018g0186a0031c0056t0020g0296 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.80-19815A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71260006 | ||||||
| chr10:71260034
|
A | G | 1 | a0001c0004t0003g0236 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.80-19787A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71260034 | ||||||
| chr10:71260068
|
G | A | 6 | a0001c0002t0001g0001a0001c0002t0001g0087a0001c0002t0001g0091others(3): Show | 7 | HG01123.hp2 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-19753G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71260068 | ||||||
| chr10:71260198
|
A | T | 1 | a0001c0004t0003g0030 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.80-19623A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71260198 | ||||||
| chr10:71260237
|
G | T | 1 | a0001c0004t0003g0285 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.80-19584G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71260237 | ||||||
| chr10:71260461
|
C | G | 2 | a0001c0055t0024g0153a0008c0041t0012g0197 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.80-19360C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71260461 | ||||||
| chr10:71260533
|
G | A | 13 | a0001c0002t0004g0292a0001c0002t0006g0037a0001c0002t0006g0038others(10): Show | 13 | HG00423.hp1 HG02027.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-19288G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71260533 | ||||||
| chr10:71260556
|
C | T | 316 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(313): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.80-19265C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71260556 | ||||||
| chr10:71260684
|
C | T | 1 | a0001c0003t0007g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80-19137C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71260684 | ||||||
| chr10:71260770
|
G | A | 1 | a0001c0003t0002g0291 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.80-19051G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71260770 | ||||||
| chr10:71260813
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.80-19008G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71260813 | ||||||
| chr10:71261011
|
A | G | 279 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(276): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.80-18810A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71261011 | ||||||
| chr10:71261024
|
A | G | 1 | a0001c0004t0003g0251 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.80-18797A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71261024 | ||||||
| chr10:71261310
|
C | T | 12 | a0001c0001t0069g0206a0001c0002t0058g0137a0001c0002t0072g0111others(9): Show | 12 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-18511C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71261310 | ||||||
| chr10:71261352
|
A | T | 1 | a0002c0005t0054g0166 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.80-18469A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71261352 | ||||||
| chr10:71261361
|
A | T | 1 | a0002c0005t0054g0166 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.80-18460A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71261361 | ||||||
| chr10:71261634
|
G | T | 2 | a0001c0002t0006g0176a0001c0002t0006g0311 | 2 | NA18962.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.80-18187G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71261634 | ||||||
| chr10:71261643
|
C | T | 6 | a0001c0003t0004g0043a0001c0003t0004g0129a0001c0003t0004g0265others(3): Show | 6 | HG00423.hp2 NA18951.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-18178C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71261643 | ||||||
| chr10:71261976
|
T | G | 2 | a0014c0050t0029g0352a0028c0039t0060g0171 | 2 | HG00639.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.80-17845T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71261976 | ||||||
| chr10:71262059
|
T | G | 213 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(210): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.80-17762T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262059 | ||||||
| chr10:71262060
|
C | T | 33 | a0001c0001t0001g0078a0001c0001t0001g0086a0001c0001t0001g0240others(30): Show | 35 | HG00597.hp2 HG00609.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.80-17761C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262060 | ||||||
| chr10:71262076
|
G | A | 34 | a0001c0001t0001g0078a0001c0001t0001g0086a0001c0001t0001g0240others(31): Show | 36 | HG00597.hp2 HG00609.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.80-17745G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262076 | ||||||
| chr10:71262296
|
A | T | 1 | a0001c0002t0001g0014 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.80-17525A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262296 | ||||||
| chr10:71262320
|
G | T | 1 | a0001c0003t0017g0210 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.80-17501G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262320 | ||||||
| chr10:71262382
|
G | C | 3 | a0001c0001t0010g0323a0003c0007t0012g0356a0027c0025t0059g0009 | 3 | HG02976.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.80-17439G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262382 | ||||||
| chr10:71262450
|
C | T | 140 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(137): Show | 142 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.80-17371C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262450 | ||||||
| chr10:71262562
|
C | T | 1 | a0001c0001t0002g0046 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.80-17259C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262562 | ||||||
| chr10:71262603
|
G | A | 1 | a0003c0007t0012g0358 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.80-17218G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262603 | ||||||
| chr10:71262708
|
C | A | 2 | a0001c0002t0032g0004a0001c0003t0036g0131 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.80-17113C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262708 | ||||||
| chr10:71262731
|
C | G | 33 | a0001c0001t0001g0078a0001c0001t0001g0086a0001c0001t0001g0240others(30): Show | 35 | HG00597.hp2 HG00609.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.80-17090C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262731 | ||||||
| chr10:71262732
|
T | C | 1 | a0001c0003t0044g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-17089T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262732 | ||||||
| chr10:71262733
|
C | T | 1 | a0001c0003t0044g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-17088C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262733 | ||||||
| chr10:71262853
|
G | A | 2 | a0001c0001t0010g0323a0027c0025t0059g0009 | 2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.80-16968G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262853 | ||||||
| chr10:71262951
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0009g0177a0001c0001t0025g0029others(1): Show | 4 | HG03130.hp2 HG03516.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-16870A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71262951 | ||||||
| chr10:71263258
|
G | T | 72 | a0001c0002t0001g0053a0001c0002t0001g0205a0001c0002t0001g0219others(69): Show | 73 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.80-16563G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71263258 | ||||||
| chr10:71263431
|
C | T | 4 | a0001c0001t0069g0206a0004c0010t0066g0269a0004c0042t0053g0229others(1): Show | 4 | HG00140.hp2 HG02647.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-16390C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71263431 | ||||||
| chr10:71263617
|
G | A | 1 | a0001c0002t0002g0222 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.80-16204G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71263617 | ||||||
| chr10:71263626
|
A | G | 334 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(331): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.80-16195A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71263626 | ||||||
| chr10:71263809
|
G | A | 4 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-16012G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71263809 | ||||||
| chr10:71263842
|
G | T | 197 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.80-15979G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71263842 | ||||||
| chr10:71263857
|
C | T | 14 | a0001c0002t0002g0195a0001c0002t0022g0143a0001c0002t0022g0192others(11): Show | 14 | HG00597.hp2 HG01433.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.80-15964C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71263857 | ||||||
| chr10:71263858
|
A | G | 256 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.80-15963A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71263858 | ||||||
| chr10:71263863
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.80-15958G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71263863 | ||||||
| chr10:71263979
|
A | C | 264 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(261): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.80-15842A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71263979 | ||||||
| chr10:71264113
|
T | C | 4 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-15708T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264113 | ||||||
| chr10:71264217
|
C | G | 1 | a0001c0001t0005g0302 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.80-15604C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264217 | ||||||
| chr10:71264352
|
G | A | 4 | a0001c0001t0019g0320a0001c0001t0019g0353a0001c0001t0068g0340others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-15469G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264352 | ||||||
| chr10:71264684
|
C | T | 3 | a0001c0002t0028g0109a0001c0002t0028g0110a0001c0002t0028g0155 | 3 | HG02970.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.80-15137C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264684 | ||||||
| chr10:71264696
|
G | T | 2 | a0001c0001t0001g0088a0001c0001t0009g0177 | 2 | NA19002.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.80-15125G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264696 | ||||||
| chr10:71264738
|
C | T | 1 | a0001c0001t0062g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.80-15083C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264738 | ||||||
| chr10:71264822
|
A | G | 3 | a0001c0001t0014g0028a0001c0001t0014g0182a0001c0001t0014g0260 | 3 | HG00741.hp2 HG01070.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.80-14999A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264822 | ||||||
| chr10:71264876
|
G | A | 1 | a0004c0010t0004g0133 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.80-14945G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264876 | ||||||
| chr10:71264943
|
G | A | 15 | a0001c0002t0032g0004a0001c0003t0007g0095a0001c0003t0007g0359others(12): Show | 16 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.80-14878G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264943 | ||||||
| chr10:71264970
|
A | C | 1 | a0001c0006t0015g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80-14851A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264970 | ||||||
| chr10:71264971
|
T | TA | 11 | a0001c0003t0001g0284a0001c0003t0002g0291a0001c0003t0004g0043others(8): Show | 11 | HG00423.hp2 HG02071.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-14830dupA | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71264971 | |||||
| chr10:71264971
|
TA | T | 197 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(194): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.80-14830delA | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71264971 | |||||
| chr10:71264971
|
TAA | T | 58 | a0001c0001t0002g0081a0001c0001t0002g0226a0001c0001t0002g0313others(55): Show | 59 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.80-14831_80-14830d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71264971 | |||||
| chr10:71264972
|
A | T | 1 | a0012c0013t0003g0317 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.80-14849A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264972 | ||||||
| chr10:71264973
|
A | C | 1 | a0004c0010t0004g0133 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.80-14848A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264973 | ||||||
| chr10:71264973
|
A | T | 4 | a0001c0001t0001g0264a0001c0002t0004g0071a0012c0013t0003g0191others(1): Show | 4 | HG02015.hp2 HG02040.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-14848A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264973 | ||||||
| chr10:71264974
|
A | T | 8 | a0001c0001t0069g0206a0001c0001t0080g0130a0004c0010t0001g0151others(5): Show | 8 | HG00140.hp2 HG01109.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-14847A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71264974 | ||||||
| chr10:71265024
|
TCAAATG | T | 53 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(50): Show | 55 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.80-14795_80-14790d others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71265024 | |||||
| chr10:71265080
|
C | T | 2 | a0001c0012t0038g0096a0001c0012t0038g0196 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.80-14741C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265080 | ||||||
| chr10:71265126
|
C | T | 4 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-14695C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265126 | ||||||
| chr10:71265235
|
A | G | 2 | a0001c0002t0058g0137a0001c0002t0072g0111 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-14586A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265235 | ||||||
| chr10:71265284
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.80-14537G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265284 | ||||||
| chr10:71265311
|
C | T | 1 | a0001c0001t0063g0032 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.80-14510C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265311 | ||||||
| chr10:71265344
|
G | A | 10 | a0001c0003t0007g0095a0001c0003t0007g0359a0001c0003t0011g0049others(7): Show | 10 | HG01433.hp2 HG01884.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-14477G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265344 | ||||||
| chr10:71265405
|
T | C | 1 | a0001c0001t0007g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.80-14416T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265405 | ||||||
| chr10:71265444
|
C | T | 8 | a0001c0001t0069g0206a0001c0001t0080g0130a0004c0010t0001g0151others(5): Show | 8 | HG00140.hp2 HG01109.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-14377C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265444 | ||||||
| chr10:71265476
|
C | T | 1 | a0004c0043t0079g0357 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.80-14345C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265476 | ||||||
| chr10:71265503
|
G | A | 4 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-14318G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265503 | ||||||
| chr10:71265534
|
C | T | 2 | a0001c0002t0032g0004a0001c0012t0016g0325 | 3 | HG02895.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.80-14287C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265534 | ||||||
| chr10:71265562
|
C | A | 20 | a0001c0001t0013g0276a0002c0005t0001g0058a0002c0005t0001g0076others(17): Show | 20 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.80-14259C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265562 | ||||||
| chr10:71265585
|
T | C | 29 | a0001c0001t0013g0276a0001c0001t0069g0206a0001c0001t0080g0130others(26): Show | 29 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.80-14236T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265585 | ||||||
| chr10:71265610
|
A | G | 4 | a0001c0001t0019g0320a0001c0001t0019g0353a0001c0001t0068g0340others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-14211A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265610 | ||||||
| chr10:71265654
|
A | G | 4 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-14167A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265654 | ||||||
| chr10:71265725
|
G | T | 2 | a0001c0002t0001g0061a0001c0002t0001g0303 | 2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.80-14096G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265725 | ||||||
| chr10:71265730
|
G | A | 4 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-14091G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265730 | ||||||
| chr10:71265831
|
C | G | 4 | a0001c0001t0019g0320a0001c0001t0019g0353a0001c0001t0068g0340others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-13990C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265831 | ||||||
| chr10:71265887
|
C | T | 20 | a0001c0001t0013g0276a0002c0005t0001g0058a0002c0005t0001g0076others(17): Show | 20 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.80-13934C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71265887 | ||||||
| chr10:71266034
|
G | A | 3 | a0005c0011t0010g0017a0005c0011t0010g0107a0005c0011t0010g0134 | 3 | HG02615.hp2 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.80-13787G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71266034 | ||||||
| chr10:71266108
|
C | A | 2 | a0001c0002t0058g0137a0001c0002t0072g0111 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-13713C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71266108 | ||||||
| chr10:71266234
|
A | C | 1 | a0004c0043t0079g0357 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.80-13587A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71266234 | ||||||
| chr10:71266469
|
G | A | 8 | a0001c0006t0015g0011a0001c0006t0015g0021a0001c0006t0015g0141others(5): Show | 8 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-13352G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71266469 | ||||||
| chr10:71266471
|
G | A | 3 | a0001c0002t0002g0102a0001c0002t0002g0308a0010c0016t0002g0126 | 3 | HG00639.hp1 HG00642.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.80-13350G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71266471 | ||||||
| chr10:71266478
|
C | T | 2 | a0001c0002t0058g0137a0001c0002t0072g0111 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-13343C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71266478 | ||||||
| chr10:71266504
|
C | A | 1 | a0001c0006t0007g0337 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.80-13317C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71266504 | ||||||
| chr10:71266521
|
G | A | 4 | a0001c0001t0019g0320a0001c0001t0019g0353a0001c0001t0068g0340others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-13300G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71266521 | ||||||
| chr10:71266556
|
G | A | 2 | a0001c0002t0058g0137a0001c0002t0072g0111 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-13265G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71266556 | ||||||
| chr10:71266664
|
G | C | 201 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(198): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.80-13157G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71266664 | ||||||
| chr10:71266958
|
A | G | 1 | a0001c0001t0014g0028 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.80-12863A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71266958 | ||||||
| chr10:71267063
|
G | A | 1 | a0001c0027t0003g0262 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.80-12758G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71267063 | ||||||
| chr10:71267360
|
C | A | 1 | a0001c0001t0047g0221 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.80-12461C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71267360 | ||||||
| chr10:71267441
|
C | T | 1 | a0001c0003t0013g0225 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.80-12380C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71267441 | ||||||
| chr10:71267586
|
C | T | 1 | a0001c0001t0024g0112 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.80-12235C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71267586 | ||||||
| chr10:71267674
|
A | G | 1 | a0001c0004t0003g0207 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.80-12147A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71267674 | ||||||
| chr10:71267678
|
G | GTGAA | 5 | a0001c0001t0005g0101a0001c0002t0078g0123a0005c0011t0010g0017others(2): Show | 5 | HG01169.hp2 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-12124_80-12121d others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71267678 | |||||
| chr10:71267711
|
C | T | 2 | a0001c0002t0058g0137a0001c0002t0072g0111 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-12110C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71267711 | ||||||
| chr10:71267751
|
C | A | 1 | a0009c0034t0004g0286 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.80-12070C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71267751 | ||||||
| chr10:71267780
|
A | T | 2 | a0001c0012t0038g0096a0001c0012t0038g0196 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.80-12041A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71267780 | ||||||
| chr10:71267932
|
A | T | 1 | a0009c0034t0004g0286 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.80-11889A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71267932 | ||||||
| chr10:71268135
|
G | A | 250 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(247): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.80-11686G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71268135 | ||||||
| chr10:71268263
|
A | G | 2 | a0001c0001t0025g0029a0001c0001t0025g0136 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.80-11558A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71268263 | ||||||
| chr10:71268272
|
C | G | 46 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(43): Show | 48 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.80-11549C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71268272 | ||||||
| chr10:71268389
|
C | T | 176 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(173): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.80-11432C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71268389 | ||||||
| chr10:71268460
|
ATGAAGGG others(14): Show |
A | 1 | a0001c0006t0015g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.80-11348_80-11328d others(23): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71268460 | |||||
| chr10:71268494
|
G | A | 8 | a0001c0001t0019g0320a0001c0001t0019g0353a0001c0001t0068g0340others(5): Show | 8 | HG00735.hp1 HG01255.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-11327G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71268494 | ||||||
| chr10:71268660
|
C | T | 1 | a0002c0005t0002g0242 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.80-11161C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71268660 | ||||||
| chr10:71268669
|
A | G | 3 | a0005c0011t0010g0017a0005c0011t0010g0107a0005c0011t0010g0134 | 3 | HG02615.hp2 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.80-11152A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71268669 | ||||||
| chr10:71268749
|
G | A | 1 | a0001c0003t0075g0329 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.80-11072G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71268749 | ||||||
| chr10:71268759
|
T | C | 1 | a0001c0012t0016g0325 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.80-11062T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71268759 | ||||||
| chr10:71268863
|
C | T | 8 | a0001c0002t0002g0025a0001c0002t0002g0245a0001c0002t0002g0271others(5): Show | 8 | NA18966.hp2 NA18967.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-10958C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71268863 | ||||||
| chr10:71268901
|
G | A | 8 | a0001c0001t0019g0320a0001c0001t0019g0353a0001c0001t0068g0340others(5): Show | 8 | HG00735.hp1 HG01255.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-10920G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71268901 | ||||||
| chr10:71268922
|
G | A | 6 | a0001c0001t0010g0323a0001c0001t0011g0361a0001c0001t0025g0029others(3): Show | 6 | HG01891.hp1 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-10899G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71268922 | ||||||
| chr10:71268964
|
G | A | 1 | a0001c0001t0007g0349 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-10857G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71268964 | ||||||
| chr10:71269061
|
G | T | 1 | a0001c0003t0002g0291 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.80-10760G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71269061 | ||||||
| chr10:71269241
|
C | CT | 8 | a0001c0001t0001g0178a0001c0001t0010g0323a0001c0001t0011g0361others(5): Show | 8 | HG01891.hp1 HG02976.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-10570dupT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71269241 | |||||
| chr10:71269318
|
A | T | 1 | a0002c0005t0034g0150 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.80-10503A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71269318 | ||||||
| chr10:71269343
|
T | TCC | 33 | a0001c0001t0005g0231a0001c0001t0005g0302a0001c0001t0007g0263others(30): Show | 33 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.80-10470_80-10469d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71269343 | |||||
| chr10:71269343
|
T | TCCC | 193 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(190): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.80-10471_80-10469d others(5): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71269343 | |||||
| chr10:71269343
|
T | TCCCC | 19 | a0001c0001t0002g0226a0001c0001t0004g0215a0001c0001t0010g0015others(16): Show | 19 | HG00438.hp2 HG00597.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.80-10472_80-10469d others(6): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71269343 | |||||
| chr10:71269446
|
T | A | 3 | a0003c0007t0010g0027a0003c0007t0012g0098a0003c0007t0012g0122 | 3 | HG02647.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.80-10375T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71269446 | ||||||
| chr10:71269569
|
G | A | 2 | a0001c0002t0058g0137a0001c0002t0072g0111 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-10252G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71269569 | ||||||
| chr10:71269607
|
C | A | 1 | a0001c0001t0010g0159 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.80-10214C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71269607 | ||||||
| chr10:71269634
|
C | T | 2 | a0001c0002t0058g0137a0001c0002t0072g0111 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-10187C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71269634 | ||||||
| chr10:71269796
|
GA | G | 5 | a0001c0003t0007g0198a0001c0003t0007g0258a0001c0003t0007g0330others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-10016delA | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71269796 | |||||
| chr10:71269843
|
T | C | 1 | a0001c0012t0016g0325 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.80-9978T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71269843 | ||||||
| chr10:71269890
|
T | C | 33 | a0001c0001t0010g0323a0001c0001t0011g0361a0001c0001t0025g0029others(30): Show | 33 | HG00140.hp2 HG00408.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.80-9931T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71269890 | ||||||
| chr10:71269988
|
G | A | 1 | a0001c0001t0063g0032 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.80-9833G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71269988 | ||||||
| chr10:71270216
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.80-9605G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71270216 | ||||||
| chr10:71270237
|
A | G | 1 | a0006c0018t0040g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.80-9584A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71270237 | ||||||
| chr10:71270243
|
G | A | 5 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(2): Show | 5 | HG00735.hp1 HG01255.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-9578G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71270243 | ||||||
| chr10:71270259
|
A | G | 209 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(206): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.80-9562A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71270259 | ||||||
| chr10:71270340
|
AAGGG | A | 102 | a0001c0001t0010g0323a0001c0001t0011g0361a0001c0001t0025g0029others(99): Show | 105 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.80-9452_80-9449del others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71270340 | |||||
| chr10:71270340
|
AAGGGAGG others(1): Show |
A | 217 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(214): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.80-9456_80-9449del others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71270340 | |||||
| chr10:71270366
|
G | A | 4 | a0001c0001t0007g0128a0001c0001t0007g0139a0001c0001t0007g0335others(1): Show | 4 | HG02486.hp1 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-9455G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71270366 | ||||||
| chr10:71270372
|
G | A | 2 | a0001c0012t0038g0096a0001c0012t0038g0196 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.80-9449G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71270372 | ||||||
| chr10:71270386
|
G | A | 2 | a0001c0002t0058g0137a0001c0002t0072g0111 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-9435G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71270386 | ||||||
| chr10:71270450
|
C | T | 6 | a0001c0001t0010g0323a0001c0001t0011g0361a0001c0001t0025g0029others(3): Show | 6 | HG01891.hp1 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-9371C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71270450 | ||||||
| chr10:71270593
|
C | T | 67 | a0001c0002t0001g0053a0001c0002t0001g0205a0001c0002t0004g0292others(64): Show | 69 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.80-9228C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71270593 | ||||||
| chr10:71270699
|
G | A | 1 | a0004c0043t0079g0357 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.80-9122G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71270699 | ||||||
| chr10:71270735
|
G | C | 3 | a0001c0001t0014g0028a0001c0001t0014g0182a0001c0001t0014g0260 | 3 | HG00741.hp2 HG01070.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.80-9086G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71270735 | ||||||
| chr10:71270898
|
A | G | 2 | a0001c0012t0038g0096a0001c0012t0038g0196 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.80-8923A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71270898 | ||||||
| chr10:71271018
|
T | C | 252 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(249): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.80-8803T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271018 | ||||||
| chr10:71271306
|
G | A | 251 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.80-8515G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271306 | ||||||
| chr10:71271313
|
C | T | 221 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(218): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.80-8508C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271313 | ||||||
| chr10:71271359
|
T | C | 4 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-8462T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271359 | ||||||
| chr10:71271398
|
C | T | 1 | a0001c0003t0008g0190 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.80-8423C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271398 | ||||||
| chr10:71271471
|
G | A | 6 | a0001c0001t0010g0323a0001c0001t0011g0361a0001c0001t0025g0029others(3): Show | 6 | HG01891.hp1 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-8350G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271471 | ||||||
| chr10:71271479
|
A | T | 2 | a0001c0001t0007g0128a0001c0001t0007g0139 | 2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.80-8342A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271479 | ||||||
| chr10:71271484
|
G | A | 8 | a0001c0001t0001g0178a0001c0001t0001g0218a0001c0001t0001g0283others(5): Show | 8 | HG01943.hp1 HG04184.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-8337G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271484 | ||||||
| chr10:71271557
|
G | A | 1 | a0002c0005t0013g0055 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.80-8264G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271557 | ||||||
| chr10:71271628
|
C | T | 319 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(316): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.80-8193C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271628 | ||||||
| chr10:71271688
|
C | G | 1 | a0005c0011t0010g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.80-8133C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271688 | ||||||
| chr10:71271807
|
A | G | 1 | a0001c0001t0007g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.80-8014A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271807 | ||||||
| chr10:71271819
|
G | A | 9 | a0001c0006t0007g0337a0001c0006t0015g0011a0001c0006t0015g0021others(6): Show | 9 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-8002G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271819 | ||||||
| chr10:71271873
|
G | A | 251 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.80-7948G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271873 | ||||||
| chr10:71271889
|
G | A | 1 | a0001c0001t0069g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.80-7932G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271889 | ||||||
| chr10:71271928
|
G | A | 1 | a0001c0001t0011g0050 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.80-7893G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271928 | ||||||
| chr10:71271949
|
G | A | 9 | a0001c0006t0007g0337a0001c0006t0015g0011a0001c0006t0015g0021others(6): Show | 9 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-7872G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271949 | ||||||
| chr10:71271957
|
C | T | 4 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-7864C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271957 | ||||||
| chr10:71271973
|
G | A | 248 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(245): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.80-7848G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71271973 | ||||||
| chr10:71272003
|
C | T | 3 | a0005c0011t0010g0017a0005c0011t0010g0107a0005c0011t0010g0134 | 3 | HG02615.hp2 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.80-7818C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272003 | ||||||
| chr10:71272030
|
A | G | 251 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.80-7791A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272030 | ||||||
| chr10:71272202
|
C | G | 45 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(42): Show | 47 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.80-7619C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272202 | ||||||
| chr10:71272231
|
A | G | 2 | a0001c0001t0019g0353a0001c0012t0016g0325 | 2 | HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.80-7590A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272231 | ||||||
| chr10:71272392
|
G | A | 1 | a0001c0001t0011g0361 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.80-7429G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272392 | ||||||
| chr10:71272405
|
C | T | 1 | a0015c0036t0039g0347 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.80-7416C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272405 | ||||||
| chr10:71272456
|
G | A | 1 | a0001c0001t0002g0226 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.80-7365G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272456 | ||||||
| chr10:71272532
|
A | G | 1 | a0001c0001t0006g0039 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.80-7289A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272532 | ||||||
| chr10:71272568
|
C | A | 8 | a0001c0001t0010g0323a0001c0001t0011g0361a0001c0001t0025g0029others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-7253C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272568 | ||||||
| chr10:71272572
|
C | G | 1 | a0001c0004t0003g0022 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.80-7249C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272572 | ||||||
| chr10:71272634
|
C | G | 8 | a0001c0001t0010g0323a0001c0001t0011g0361a0001c0001t0025g0029others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-7187C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272634 | ||||||
| chr10:71272698
|
G | A | 58 | a0001c0001t0069g0206a0001c0002t0032g0004a0001c0003t0007g0095others(55): Show | 59 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.80-7123G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272698 | ||||||
| chr10:71272706
|
G | T | 10 | a0001c0001t0001g0146a0001c0003t0008g0042a0001c0003t0008g0148others(7): Show | 10 | HG00408.hp2 HG02071.hp2 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-7115G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272706 | ||||||
| chr10:71272710
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.80-7111G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272710 | ||||||
| chr10:71272848
|
C | G | 1 | a0001c0003t0002g0291 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.80-6973C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71272848 | ||||||
| chr10:71272877
|
C | CTGTT | 130 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(127): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.80-6918_80-6915dup others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71272877 | |||||
| chr10:71272877
|
C | CTGTTGTT others(8): Show |
2 | a0001c0001t0001g0294a0001c0002t0004g0071 | 2 | NA18946.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.80-6940_80-6939ins others(15): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71272877 | |||||
| chr10:71272877
|
C | CTGTTTGT others(1): Show |
62 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0147others(59): Show | 64 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-6922_80-6915dup others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71272877 | |||||
| chr10:71272877
|
C | CTGTTTGT others(5): Show |
11 | a0001c0001t0001g0234a0001c0002t0001g0205a0001c0002t0001g0309others(8): Show | 12 | HG00438.hp2 HG02027.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.80-6926_80-6915dup others(12): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71272877 | |||||
| chr10:71272877
|
C | CTGTTTGT others(9): Show |
8 | a0001c0002t0004g0292a0001c0002t0006g0037a0001c0002t0006g0038others(5): Show | 8 | HG02080.hp2 HG02155.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-6930_80-6915dup others(16): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71272877 | |||||
| chr10:71272877
|
C | CTGTTTGT others(13): Show |
1 | a0001c0002t0006g0244 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.80-6934_80-6915dup others(20): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71272877 | |||||
| chr10:71273099
|
G | C | 3 | a0007c0017t0011g0354a0007c0017t0016g0327a0014c0050t0029g0352 | 3 | HG01243.hp2 HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.80-6722G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71273099 | ||||||
| chr10:71273136
|
G | A | 1 | a0001c0002t0001g0205 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.80-6685G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71273136 | ||||||
| chr10:71273169
|
G | A | 198 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(195): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.80-6652G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71273169 | ||||||
| chr10:71273175
|
C | A | 2 | a0001c0002t0032g0004a0001c0012t0016g0325 | 3 | HG02895.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.80-6646C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71273175 | ||||||
| chr10:71273348
|
T | A | 58 | a0001c0001t0069g0206a0001c0002t0032g0004a0001c0003t0007g0095others(55): Show | 59 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.80-6473T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71273348 | ||||||
| chr10:71273522
|
T | A | 2 | a0001c0002t0032g0004a0001c0012t0016g0325 | 3 | HG02895.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.80-6299T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71273522 | ||||||
| chr10:71273716
|
C | T | 4 | a0001c0001t0007g0128a0001c0001t0007g0139a0001c0001t0007g0335others(1): Show | 4 | HG02486.hp1 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-6105C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71273716 | ||||||
| chr10:71273717
|
G | A | 2 | a0001c0002t0032g0004a0001c0012t0016g0325 | 3 | HG02895.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.80-6104G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71273717 | ||||||
| chr10:71273770
|
C | A | 1 | a0001c0001t0013g0276 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.80-6051C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71273770 | ||||||
| chr10:71273810
|
G | A | 9 | a0001c0006t0007g0337a0001c0006t0015g0011a0001c0006t0015g0021others(6): Show | 9 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-6011G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71273810 | ||||||
| chr10:71274234
|
GC | G | 192 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.80-5585delC | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71274234 | |||||
| chr10:71274331
|
G | A | 2 | a0001c0012t0038g0096a0001c0012t0038g0196 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.80-5490G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71274331 | ||||||
| chr10:71274347
|
A | T | 8 | a0001c0001t0010g0323a0001c0001t0011g0361a0001c0001t0025g0029others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-5474A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71274347 | ||||||
| chr10:71274364
|
A | T | 2 | a0001c0012t0038g0096a0001c0012t0038g0196 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.80-5457A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71274364 | ||||||
| chr10:71274369
|
A | AT | 24 | a0001c0001t0007g0326a0001c0001t0047g0221a0001c0003t0002g0152others(21): Show | 24 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.80-5452_80-5451ins others(1): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71274369 | ||||||
| chr10:71274369
|
A | T | 331 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(328): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.80-5452A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71274369 | ||||||
| chr10:71274829
|
G | A | 9 | a0001c0002t0002g0306a0001c0002t0004g0145a0001c0002t0004g0273others(6): Show | 9 | HG00544.hp2 HG02040.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-4992G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71274829 | ||||||
| chr10:71274847
|
A | T | 28 | a0001c0003t0007g0095a0001c0003t0007g0198a0001c0003t0007g0258others(25): Show | 28 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.80-4974A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71274847 | ||||||
| chr10:71275087
|
C | G | 2 | a0001c0002t0058g0137a0001c0002t0072g0111 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-4734C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71275087 | ||||||
| chr10:71275184
|
G | A | 2 | a0001c0012t0038g0096a0001c0012t0038g0196 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.80-4637G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71275184 | ||||||
| chr10:71275196
|
G | T | 28 | a0001c0001t0069g0206a0002c0005t0001g0016a0002c0005t0001g0058others(25): Show | 28 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.80-4625G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71275196 | ||||||
| chr10:71275214
|
G | A | 9 | a0001c0006t0007g0337a0001c0006t0015g0011a0001c0006t0015g0021others(6): Show | 9 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-4607G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71275214 | ||||||
| chr10:71275392
|
A | C | 1 | a0004c0043t0079g0357 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.80-4429A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71275392 | ||||||
| chr10:71275480
|
T | A | 235 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.80-4341T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71275480 | ||||||
| chr10:71275563
|
G | A | 3 | a0001c0002t0028g0109a0001c0002t0028g0110a0001c0002t0028g0155 | 3 | HG02970.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.80-4258G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71275563 | ||||||
| chr10:71275608
|
G | A | 8 | a0001c0003t0007g0095a0001c0003t0007g0359a0001c0003t0011g0049others(5): Show | 8 | HG01433.hp2 HG01884.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-4213G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71275608 | ||||||
| chr10:71275712
|
G | T | 1 | a0001c0001t0006g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.80-4109G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71275712 | ||||||
| chr10:71275967
|
C | T | 11 | a0001c0003t0007g0095a0001c0003t0007g0359a0001c0003t0011g0049others(8): Show | 11 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-3854C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71275967 | ||||||
| chr10:71275992
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.80-3829T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71275992 | ||||||
| chr10:71276004
|
C | T | 3 | a0007c0017t0011g0354a0007c0017t0016g0327a0014c0050t0029g0352 | 3 | HG01243.hp2 HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.80-3817C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71276004 | ||||||
| chr10:71276023
|
T | C | 361 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(358): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.80-3798T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71276023 | ||||||
| chr10:71276143
|
T | G | 1 | a0001c0001t0069g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.80-3678T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71276143 | ||||||
| chr10:71276180
|
TA | T | 220 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.80-3633delA | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71276180 | |||||
| chr10:71276213
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.80-3608C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71276213 | ||||||
| chr10:71276234
|
G | A | 3 | a0001c0001t0011g0361a0001c0001t0025g0029a0001c0001t0025g0136 | 3 | HG01891.hp1 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.80-3587G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71276234 | ||||||
| chr10:71276235
|
G | A | 5 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0194others(2): Show | 5 | HG00140.hp1 HG00733.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-3586G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71276235 | ||||||
| chr10:71276240
|
T | C | 2 | a0004c0010t0066g0269a0004c0042t0053g0229 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.80-3581T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71276240 | ||||||
| chr10:71276270
|
T | C | 14 | a0001c0001t0010g0323a0001c0001t0057g0104a0003c0007t0010g0027others(11): Show | 14 | HG01106.hp2 HG02055.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-3551T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71276270 | ||||||
| chr10:71276634
|
G | A | 322 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.80-3187G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71276634 | ||||||
| chr10:71276737
|
T | C | 3 | a0005c0011t0010g0017a0005c0011t0010g0107a0005c0011t0010g0134 | 3 | HG02615.hp2 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.80-3084T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71276737 | ||||||
| chr10:71276886
|
G | GAC | 258 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.80-2933_80-2932dup others(2): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71276886 | |||||
| chr10:71276923
|
G | A | 9 | a0001c0006t0007g0337a0001c0006t0015g0011a0001c0006t0015g0021others(6): Show | 9 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-2898G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71276923 | ||||||
| chr10:71276923
|
G | C | 220 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.80-2898G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71276923 | ||||||
| chr10:71276967
|
G | A | 3 | a0001c0001t0011g0361a0001c0001t0025g0029a0001c0001t0025g0136 | 3 | HG01891.hp1 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.80-2854G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71276967 | ||||||
| chr10:71277055
|
C | T | 1 | a0016c0037t0013g0270 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.80-2766C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71277055 | ||||||
| chr10:71277142
|
T | C | 38 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(35): Show | 41 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.80-2679T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71277142 | ||||||
| chr10:71277189
|
G | A | 11 | a0001c0002t0032g0004a0001c0006t0007g0337a0001c0006t0015g0011others(8): Show | 12 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-2632G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71277189 | ||||||
| chr10:71277213
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.80-2608G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71277213 | ||||||
| chr10:71277281
|
G | A | 34 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(31): Show | 36 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.80-2540G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71277281 | ||||||
| chr10:71277557
|
C | T | 2 | a0001c0001t0014g0182a0001c0001t0014g0260 | 2 | HG00741.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.80-2264C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71277557 | ||||||
| chr10:71277581
|
C | T | 2 | a0001c0012t0038g0096a0001c0012t0038g0196 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.80-2240C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71277581 | ||||||
| chr10:71277609
|
G | T | 2 | a0004c0010t0001g0151a0004c0010t0004g0133 | 2 | HG01109.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.80-2212G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71277609 | ||||||
| chr10:71277708
|
G | A | 2 | a0001c0002t0004g0145a0001c0002t0004g0273 | 2 | HG00544.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.80-2113G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71277708 | ||||||
| chr10:71278009
|
C | T | 1 | a0001c0002t0032g0004 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.80-1812C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71278009 | ||||||
| chr10:71278094
|
C | T | 4 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-1727C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71278094 | ||||||
| chr10:71278258
|
A | G | 1 | a0002c0005t0030g0312 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.80-1563A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71278258 | ||||||
| chr10:71278276
|
A | C | 323 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.80-1545A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71278276 | ||||||
| chr10:71278278
|
C | T | 1 | a0002c0005t0014g0045 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.80-1543C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71278278 | ||||||
| chr10:71278301
|
G | A | 4 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-1520G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71278301 | ||||||
| chr10:71278402
|
C | CAGAACAT others(1): Show |
6 | a0001c0003t0007g0198a0001c0003t0007g0258a0001c0003t0007g0330others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-1418_80-1411dup others(8): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr10 | 71278402 | |||||
| chr10:71278462
|
G | A | 2 | a0001c0002t0032g0004a0001c0012t0016g0325 | 3 | HG02895.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.80-1359G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71278462 | ||||||
| chr10:71278473
|
C | T | 1 | a0001c0001t0005g0188 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.80-1348C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71278473 | ||||||
| chr10:71278552
|
T | C | 1 | a0001c0002t0001g0219 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.80-1269T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71278552 | ||||||
| chr10:71278617
|
C | T | 34 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(31): Show | 36 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.80-1204C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71278617 | ||||||
| chr10:71278643
|
A | G | 325 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.80-1178A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71278643 | ||||||
| chr10:71278719
|
G | T | 219 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.80-1102G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71278719 | ||||||
| chr10:71278868
|
G | T | 26 | a0001c0001t0001g0199a0001c0001t0001g0203a0001c0001t0001g0234others(23): Show | 26 | HG00558.hp2 HG01358.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.80-953G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71278868 | ||||||
| chr10:71279259
|
A | T | 27 | a0001c0003t0007g0095a0001c0003t0007g0198a0001c0003t0007g0258others(24): Show | 27 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.80-562A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71279259 | ||||||
| chr10:71279318
|
T | C | 255 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(252): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.80-503T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71279318 | ||||||
| chr10:71279421
|
C | G | 220 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.80-400C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71279421 | ||||||
| chr10:71279427
|
G | C | 3 | a0001c0001t0010g0323a0001c0001t0057g0104a0027c0025t0059g0009 | 3 | HG02976.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.80-394G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71279427 | ||||||
| chr10:71279477
|
T | C | 221 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(218): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.80-344T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71279477 | ||||||
| chr10:71279537
|
C | T | 1 | a0001c0002t0009g0041 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.80-284C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71279537 | ||||||
| chr10:71279683
|
C | T | 11 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0147others(8): Show | 11 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-138C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71279683 | ||||||
| chr10:71279734
|
G | A | 21 | a0002c0005t0001g0016a0002c0005t0001g0058a0002c0005t0001g0076others(18): Show | 21 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.80-87G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71279734 | ||||||
| chr10:71279745
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.80-76G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71279745 | ||||||
| chr10:71279750
|
C | T | 16 | a0001c0003t0007g0198a0001c0003t0007g0258a0001c0003t0007g0330others(13): Show | 16 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.80-71C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 1/16 | chr10 | 71279750 | ||||||
| chr10:71280103
|
C | T | 215 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.304+58C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71280103 | ||||||
| chr10:71280221
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.304+176C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71280221 | ||||||
| chr10:71280292
|
G | A | 1 | a0001c0015t0056g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.304+247G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71280292 | ||||||
| chr10:71280387
|
G | A | 214 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(211): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.304+342G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71280387 | ||||||
| chr10:71280391
|
C | T | 18 | a0001c0001t0010g0323a0001c0001t0011g0361a0001c0001t0025g0029others(15): Show | 18 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.304+346C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71280391 | ||||||
| chr10:71280405
|
A | G | 1 | a0001c0001t0045g0187 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.304+360A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71280405 | ||||||
| chr10:71280410
|
A | G | 2 | a0001c0012t0038g0096a0001c0012t0038g0196 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.304+365A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71280410 | ||||||
| chr10:71280481
|
A | G | 1 | a0001c0001t0057g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.304+436A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71280481 | ||||||
| chr10:71280804
|
G | A | 9 | a0001c0006t0007g0337a0001c0006t0015g0011a0001c0006t0015g0021others(6): Show | 9 | HG01069.hp2 HG02809.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.304+759G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71280804 | ||||||
| chr10:71280814
|
G | A | 4 | a0001c0003t0019g0328a0001c0003t0044g0201a0006c0018t0040g0200others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.304+769G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71280814 | ||||||
| chr10:71280846
|
A | AC | 13 | a0003c0007t0010g0027a0003c0007t0012g0098a0003c0007t0012g0108others(10): Show | 13 | HG00140.hp2 HG01106.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.304+808dupC | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr10 | 71280846 | |||||
| chr10:71280935
|
G | A | 322 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.304+890G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71280935 | ||||||
| chr10:71281053
|
C | T | 1 | a0001c0001t0034g0230 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.304+1008C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281053 | ||||||
| chr10:71281065
|
C | G | 1 | a0001c0003t0008g0057 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.304+1020C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281065 | ||||||
| chr10:71281070
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1025T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281070 | ||||||
| chr10:71281071
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1026G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281071 | ||||||
| chr10:71281072
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1027T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281072 | ||||||
| chr10:71281081
|
C | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1036C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281081 | ||||||
| chr10:71281082
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1037T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281082 | ||||||
| chr10:71281085
|
C | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1040C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281085 | ||||||
| chr10:71281086
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1041T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281086 | ||||||
| chr10:71281104
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1059A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281104 | ||||||
| chr10:71281108
|
T | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1063T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281108 | ||||||
| chr10:71281110
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1065C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281110 | ||||||
| chr10:71281111
|
T | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1066T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281111 | ||||||
| chr10:71281113
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1068C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281113 | ||||||
| chr10:71281118
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1073C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281118 | ||||||
| chr10:71281121
|
C | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1076C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281121 | ||||||
| chr10:71281122
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1077T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281122 | ||||||
| chr10:71281126
|
T | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1081T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281126 | ||||||
| chr10:71281129
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1084G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281129 | ||||||
| chr10:71281130
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1085T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281130 | ||||||
| chr10:71281133
|
C | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1088C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281133 | ||||||
| chr10:71281133
|
C | T | 1 | a0001c0002t0002g0334 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.304+1088C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281133 | ||||||
| chr10:71281134
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1089T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281134 | ||||||
| chr10:71281135
|
G | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1090G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281135 | ||||||
| chr10:71281137
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1092T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281137 | ||||||
| chr10:71281139
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1094T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281139 | ||||||
| chr10:71281141
|
T | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1096T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281141 | ||||||
| chr10:71281142
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1097C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281142 | ||||||
| chr10:71281143
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1098A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281143 | ||||||
| chr10:71281145
|
G | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1100G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281145 | ||||||
| chr10:71281146
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1101T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281146 | ||||||
| chr10:71281149
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1104A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281149 | ||||||
| chr10:71281151
|
C | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1106C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281151 | ||||||
| chr10:71281153
|
C | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1108C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281153 | ||||||
| chr10:71281154
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1109A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281154 | ||||||
| chr10:71281155
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1110C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281155 | ||||||
| chr10:71281158
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1113A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281158 | ||||||
| chr10:71281160
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1115T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281160 | ||||||
| chr10:71281163
|
A | T | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1118A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281163 | ||||||
| chr10:71281165
|
A | T | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1120A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281165 | ||||||
| chr10:71281167
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1122A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281167 | ||||||
| chr10:71281169
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1124A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281169 | ||||||
| chr10:71281170
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1125G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281170 | ||||||
| chr10:71281179
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1134A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281179 | ||||||
| chr10:71281180
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1135A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281180 | ||||||
| chr10:71281181
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1136A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281181 | ||||||
| chr10:71281185
|
A | T | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1140A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281185 | ||||||
| chr10:71281186
|
T | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1141T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281186 | ||||||
| chr10:71281194
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1149A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281194 | ||||||
| chr10:71281196
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1151T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281196 | ||||||
| chr10:71281199
|
A | T | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1154A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281199 | ||||||
| chr10:71281202
|
CGAGGTCA others(3): Show |
C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1158_304+1167d others(12): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281202 | ||||||
| chr10:71281214
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1169A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281214 | ||||||
| chr10:71281218
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1173T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281218 | ||||||
| chr10:71281219
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1174A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281219 | ||||||
| chr10:71281220
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1175T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281220 | ||||||
| chr10:71281230
|
T | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1185T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281230 | ||||||
| chr10:71281232
|
G | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1187G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281232 | ||||||
| chr10:71281233
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1188T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281233 | ||||||
| chr10:71281235
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1190A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281235 | ||||||
| chr10:71281238
|
A | T | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1193A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281238 | ||||||
| chr10:71281239
|
T | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1194T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281239 | ||||||
| chr10:71281242
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1197T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281242 | ||||||
| chr10:71281243
|
A | T | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1198A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281243 | ||||||
| chr10:71281244
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1199A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281244 | ||||||
| chr10:71281248
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1203T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281248 | ||||||
| chr10:71281249
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1204T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281249 | ||||||
| chr10:71281250
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1205A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281250 | ||||||
| chr10:71281251
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1206T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281251 | ||||||
| chr10:71281253
|
G | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1208G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281253 | ||||||
| chr10:71281254
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1209A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281254 | ||||||
| chr10:71281259
|
G | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1214G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281259 | ||||||
| chr10:71281260
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1215T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281260 | ||||||
| chr10:71281262
|
T | TGAGCCCC others(3): Show |
1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1217_304+1218i others(12): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281262 | ||||||
| chr10:71281263
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1218T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281263 | ||||||
| chr10:71281264
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1219T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281264 | ||||||
| chr10:71281265
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1220T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281265 | ||||||
| chr10:71281267
|
C | A | 1 | a0001c0001t0002g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.304+1222C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281267 | ||||||
| chr10:71281322
|
A | C | 21 | a0002c0005t0001g0016a0002c0005t0001g0058a0002c0005t0001g0076others(18): Show | 21 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.304+1277A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281322 | ||||||
| chr10:71281327
|
A | G | 1 | a0001c0020t0065g0142 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.304+1282A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281327 | ||||||
| chr10:71281336
|
A | G | 78 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(75): Show | 81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.304+1291A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281336 | ||||||
| chr10:71281342
|
AT | A | 105 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(102): Show | 108 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.304+1312delT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr10 | 71281342 | |||||
| chr10:71281375
|
C | T | 11 | a0003c0007t0010g0027a0003c0007t0012g0098a0003c0007t0012g0108others(8): Show | 11 | HG01106.hp2 HG02055.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.304+1330C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281375 | ||||||
| chr10:71281410
|
G | A | 107 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(104): Show | 110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.304+1365G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281410 | ||||||
| chr10:71281415
|
A | C | 1 | a0002c0005t0002g0242 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.304+1370A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281415 | ||||||
| chr10:71281431
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.304+1386C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281431 | ||||||
| chr10:71281487
|
C | T | 106 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(103): Show | 109 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.304+1442C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281487 | ||||||
| chr10:71281515
|
T | G | 1 | a0001c0001t0014g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.304+1470T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281515 | ||||||
| chr10:71281682
|
T | C | 2 | a0001c0012t0038g0096a0001c0012t0038g0196 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.304+1637T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281682 | ||||||
| chr10:71281688
|
T | A | 2 | a0001c0012t0038g0096a0001c0012t0038g0196 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.304+1643T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281688 | ||||||
| chr10:71281696
|
C | T | 107 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(104): Show | 110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.304+1651C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281696 | ||||||
| chr10:71281702
|
T | G | 322 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.304+1657T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281702 | ||||||
| chr10:71281703
|
T | G | 322 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.304+1658T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281703 | ||||||
| chr10:71281726
|
C | G | 107 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(104): Show | 110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.304+1681C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281726 | ||||||
| chr10:71281784
|
C | T | 1 | a0004c0043t0079g0357 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.304+1739C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281784 | ||||||
| chr10:71281911
|
C | T | 2 | a0001c0012t0038g0096a0001c0012t0038g0196 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.304+1866C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281911 | ||||||
| chr10:71281912
|
G | A | 1 | a0001c0002t0001g0309 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.304+1867G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281912 | ||||||
| chr10:71281968
|
G | A | 107 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(104): Show | 110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.304+1923G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71281968 | ||||||
| chr10:71282079
|
CAA | C | 107 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(104): Show | 110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.304+2037_304+2038d others(4): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr10 | 71282079 | |||||
| chr10:71282112
|
A | G | 109 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(106): Show | 112 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.304+2067A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71282112 | ||||||
| chr10:71282240
|
CAGAAG | C | 8 | a0001c0003t0007g0095a0001c0003t0007g0359a0001c0003t0011g0049others(5): Show | 8 | HG01433.hp2 HG01884.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.304+2198_304+2202d others(7): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr10 | 71282240 | |||||
| chr10:71282275
|
C | T | 3 | a0001c0001t0010g0323a0001c0001t0057g0104a0027c0025t0059g0009 | 3 | HG02976.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.304+2230C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71282275 | ||||||
| chr10:71282544
|
T | G | 1 | a0001c0001t0055g0293 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.305-2176T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71282544 | ||||||
| chr10:71282624
|
T | C | 322 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.305-2096T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71282624 | ||||||
| chr10:71282665
|
G | A | 213 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(210): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.305-2055G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71282665 | ||||||
| chr10:71282882
|
C | T | 1 | a0014c0050t0029g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.305-1838C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71282882 | ||||||
| chr10:71282912
|
C | T | 1 | a0001c0001t0004g0175 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.305-1808C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71282912 | ||||||
| chr10:71282961
|
C | CA | 106 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(103): Show | 109 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.305-1750dupA | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr10 | 71282961 | |||||
| chr10:71283076
|
C | T | 3 | a0001c0002t0058g0137a0001c0002t0072g0111a0028c0039t0060g0171 | 3 | HG00639.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.305-1644C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71283076 | ||||||
| chr10:71283119
|
CA | C | 106 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(103): Show | 109 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.305-1590delA | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr10 | 71283119 | |||||
| chr10:71283259
|
T | C | 107 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(104): Show | 110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.305-1461T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71283259 | ||||||
| chr10:71283333
|
C | T | 107 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(104): Show | 110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.305-1387C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71283333 | ||||||
| chr10:71283515
|
C | A | 1 | a0001c0001t0042g0232 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.305-1205C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71283515 | ||||||
| chr10:71283515
|
C | T | 3 | a0001c0001t0010g0323a0001c0001t0057g0104a0027c0025t0059g0009 | 3 | HG02976.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.305-1205C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71283515 | ||||||
| chr10:71283575
|
G | T | 21 | a0002c0005t0001g0016a0002c0005t0001g0058a0002c0005t0001g0076others(18): Show | 21 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.305-1145G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71283575 | ||||||
| chr10:71283686
|
T | A | 107 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(104): Show | 110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.305-1034T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71283686 | ||||||
| chr10:71284054
|
G | A | 34 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(31): Show | 36 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.305-666G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71284054 | ||||||
| chr10:71284179
|
G | A | 1 | a0001c0012t0016g0325 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.305-541G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71284179 | ||||||
| chr10:71284206
|
G | A | 4 | a0001c0001t0001g0234a0001c0003t0008g0042a0001c0003t0008g0148others(1): Show | 4 | NA18952.hp2 NA18999.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.305-514G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71284206 | ||||||
| chr10:71284403
|
G | A | 109 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(106): Show | 112 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.305-317G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71284403 | ||||||
| chr10:71284443
|
C | T | 21 | a0002c0005t0001g0016a0002c0005t0001g0058a0002c0005t0001g0076others(18): Show | 21 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.305-277C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71284443 | ||||||
| chr10:71284491
|
C | T | 1 | a0002c0005t0013g0295 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.305-229C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71284491 | ||||||
| chr10:71284511
|
T | A | 109 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(106): Show | 112 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.305-209T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71284511 | ||||||
| chr10:71284548
|
G | A | 5 | a0001c0001t0011g0341a0001c0001t0011g0348a0001c0001t0020g0115others(2): Show | 5 | HG03041.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-172G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71284548 | ||||||
| chr10:71284625
|
T | A | 322 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.305-95T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71284625 | ||||||
| chr10:71284656
|
G | C | 199 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(196): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.305-64G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 2/16 | chr10 | 71284656 | ||||||
| chr10:71284867
|
C | T | 1 | a0001c0002t0002g0002 | 2 | HG02056.hp2 HG02132.hp2 |
splice_region_variant&intron_variant | LOW | c.448+4C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 3/16 | chr10 | 71284867 | ||||||
| chr10:71284917
|
G | A | 213 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(210): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.448+54G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 3/16 | chr10 | 71284917 | ||||||
| chr10:71284935
|
T | C | 1 | a0001c0040t0043g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.448+72T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 3/16 | chr10 | 71284935 | ||||||
| chr10:71284982
|
C | T | 6 | a0004c0010t0001g0151a0004c0010t0004g0133a0004c0010t0010g0092others(3): Show | 6 | HG00140.hp2 HG01109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.448+119C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 3/16 | chr10 | 71284982 | ||||||
| chr10:71284983
|
G | A | 34 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(31): Show | 36 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.448+120G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 3/16 | chr10 | 71284983 | ||||||
| chr10:71285016
|
A | T | 4 | a0001c0003t0019g0328a0001c0003t0044g0201a0001c0015t0018g0331others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+153A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 3/16 | chr10 | 71285016 | ||||||
| chr10:71285167
|
A | G | 322 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.449-159A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 3/16 | chr10 | 71285167 | ||||||
| chr10:71285173
|
C | T | 322 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.449-153C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 3/16 | chr10 | 71285173 | ||||||
| chr10:71285197
|
A | G | 322 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.449-129A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 3/16 | chr10 | 71285197 | ||||||
| chr10:71285436
|
G | A | 1 | a0001c0002t0033g0036 | 1 | HG01081.hp1 | splice_region_variant&intron_variant | LOW | c.552+7G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71285436 | ||||||
| chr10:71285527
|
C | G | 253 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(250): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.552+98C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71285527 | ||||||
| chr10:71285535
|
C | T | 3 | a0001c0001t0010g0323a0001c0001t0057g0104a0027c0025t0059g0009 | 3 | HG02976.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.552+106C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71285535 | ||||||
| chr10:71285581
|
A | C | 41 | a0001c0002t0001g0053a0001c0002t0006g0119a0001c0002t0009g0304others(38): Show | 43 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.552+152A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71285581 | ||||||
| chr10:71285640
|
A | AC | 65 | a0001c0003t0007g0095a0001c0003t0007g0198a0001c0003t0007g0258others(62): Show | 65 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.552+215dupC | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr10 | 71285640 | |||||
| chr10:71285716
|
C | G | 1 | a0001c0001t0063g0032 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.552+287C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71285716 | ||||||
| chr10:71285758
|
G | T | 21 | a0002c0005t0001g0016a0002c0005t0001g0058a0002c0005t0001g0076others(18): Show | 21 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.552+329G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71285758 | ||||||
| chr10:71285780
|
C | T | 212 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(209): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.552+351C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71285780 | ||||||
| chr10:71285815
|
C | T | 1 | a0001c0051t0001g0103 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.552+386C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71285815 | ||||||
| chr10:71285857
|
T | G | 1 | a0004c0043t0079g0357 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.552+428T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71285857 | ||||||
| chr10:71286341
|
C | T | 3 | a0007c0017t0011g0354a0007c0017t0016g0327a0014c0050t0029g0352 | 3 | HG01243.hp2 HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.553-348C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71286341 | ||||||
| chr10:71286342
|
A | G | 321 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(318): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.553-347A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71286342 | ||||||
| chr10:71286420
|
G | T | 85 | a0001c0001t0001g0054a0001c0001t0001g0066a0001c0001t0001g0078others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.553-269G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71286420 | ||||||
| chr10:71286604
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.553-85G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71286604 | ||||||
| chr10:71286664
|
T | C | 1 | a0001c0001t0005g0180 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.553-25T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 4/16 | chr10 | 71286664 | ||||||
| chr10:71286874
|
G | A | 2 | a0001c0001t0047g0221a0001c0001t0048g0290 | 2 | NA18957.hp1 NA18971.hp2 |
splice_region_variant&intron_variant | LOW | c.733+5G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/16 | chr10 | 71286874 | ||||||
| chr10:71287011
|
A | G | 1 | a0004c0010t0066g0269 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.733+142A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/16 | chr10 | 71287011 | ||||||
| chr10:71287254
|
G | T | 33 | a0001c0006t0007g0337a0001c0006t0015g0011a0001c0006t0015g0021others(30): Show | 33 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.734-344G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/16 | chr10 | 71287254 | ||||||
| chr10:71287256
|
C | T | 33 | a0001c0006t0007g0337a0001c0006t0015g0011a0001c0006t0015g0021others(30): Show | 33 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.734-342C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/16 | chr10 | 71287256 | ||||||
| chr10:71287275
|
T | C | 33 | a0001c0006t0007g0337a0001c0006t0015g0011a0001c0006t0015g0021others(30): Show | 33 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.734-323T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/16 | chr10 | 71287275 | ||||||
| chr10:71287288
|
C | T | 1 | a0001c0001t0047g0221 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.734-310C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/16 | chr10 | 71287288 | ||||||
| chr10:71287310
|
C | T | 6 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(3): Show | 6 | HG00735.hp1 HG01255.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-288C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/16 | chr10 | 71287310 | ||||||
| chr10:71287330
|
C | A | 33 | a0001c0006t0007g0337a0001c0006t0015g0011a0001c0006t0015g0021others(30): Show | 33 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.734-268C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/16 | chr10 | 71287330 | ||||||
| chr10:71287346
|
C | G | 1 | a0001c0001t0019g0353 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.734-252C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/16 | chr10 | 71287346 | ||||||
| chr10:71287368
|
G | A | 33 | a0001c0006t0007g0337a0001c0006t0015g0011a0001c0006t0015g0021others(30): Show | 33 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.734-230G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/16 | chr10 | 71287368 | ||||||
| chr10:71287394
|
A | T | 21 | a0002c0005t0001g0016a0002c0005t0001g0058a0002c0005t0001g0076others(18): Show | 21 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.734-204A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/16 | chr10 | 71287394 | ||||||
| chr10:71287424
|
C | T | 1 | a0001c0002t0001g0053 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.734-174C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/16 | chr10 | 71287424 | ||||||
| chr10:71287425
|
G | A | 33 | a0001c0006t0007g0337a0001c0006t0015g0011a0001c0006t0015g0021others(30): Show | 33 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.734-173G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 5/16 | chr10 | 71287425 | ||||||
| chr10:71287798
|
C | T | 57 | a0001c0003t0007g0095a0001c0003t0007g0198a0001c0003t0007g0258others(54): Show | 57 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.901+33C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 6/16 | chr10 | 71287798 | ||||||
| chr10:71287836
|
G | A | 356 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(353): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.901+71G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 6/16 | chr10 | 71287836 | ||||||
| chr10:71287864
|
G | T | 1 | a0001c0001t0001g0288 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.901+99G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 6/16 | chr10 | 71287864 | ||||||
| chr10:71287896
|
G | A | 2 | a0001c0001t0014g0182a0001c0001t0014g0260 | 2 | HG00741.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.901+131G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 6/16 | chr10 | 71287896 | ||||||
| chr10:71287933
|
C | T | 260 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(257): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.901+168C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 6/16 | chr10 | 71287933 | ||||||
| chr10:71287984
|
T | C | 1 | a0001c0002t0001g0303 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.901+219T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 6/16 | chr10 | 71287984 | ||||||
| chr10:71288140
|
A | G | 263 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(260): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.901+375A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 6/16 | chr10 | 71288140 | ||||||
| chr10:71288193
|
C | G | 53 | a0001c0002t0032g0004a0001c0003t0001g0003a0001c0003t0001g0118others(50): Show | 56 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.902-375C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 6/16 | chr10 | 71288193 | ||||||
| chr10:71288255
|
G | A | 43 | a0001c0003t0001g0003a0001c0003t0001g0118a0001c0003t0001g0284others(40): Show | 45 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.902-313G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 6/16 | chr10 | 71288255 | ||||||
| chr10:71288297
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.902-271C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 6/16 | chr10 | 71288297 | ||||||
| chr10:71288535
|
G | A | 2 | a0001c0002t0058g0137a0001c0002t0072g0111 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.902-33G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 6/16 | chr10 | 71288535 | ||||||
| chr10:71288564
|
A | G | 1 | a0001c0003t0019g0261 | 1 | HG01106.hp1 | splice_region_variant&intron_variant | LOW | c.902-4A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 6/16 | chr10 | 71288564 | ||||||
| chr10:71288875
|
T | C | 43 | a0001c0003t0001g0003a0001c0003t0001g0118a0001c0003t0001g0284others(40): Show | 45 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1067-83T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 7/16 | chr10 | 71288875 | ||||||
| chr10:71289060
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1099+70G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289060 | ||||||
| chr10:71289154
|
A | G | 1 | a0014c0050t0029g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1099+164A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289154 | ||||||
| chr10:71289197
|
T | C | 254 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1099+207T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289197 | ||||||
| chr10:71289250
|
A | C | 1 | a0001c0002t0078g0123 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1099+260A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289250 | ||||||
| chr10:71289275
|
C | G | 2 | a0001c0002t0001g0309a0001c0002t0026g0116 | 2 | NA19065.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1099+285C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289275 | ||||||
| chr10:71289298
|
G | A | 3 | a0001c0001t0010g0323a0001c0001t0057g0104a0027c0025t0059g0009 | 3 | HG02976.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1099+308G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289298 | ||||||
| chr10:71289350
|
C | T | 31 | a0001c0003t0001g0003a0001c0003t0001g0118a0001c0003t0001g0284others(28): Show | 33 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.1099+360C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289350 | ||||||
| chr10:71289378
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1099+388G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289378 | ||||||
| chr10:71289465
|
T | A | 254 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1099+475T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289465 | ||||||
| chr10:71289521
|
G | A | 1 | a0001c0002t0005g0124 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1099+531G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289521 | ||||||
| chr10:71289565
|
G | A | 55 | a0001c0001t0010g0323a0001c0001t0011g0361a0001c0001t0025g0029others(52): Show | 55 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1099+575G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289565 | ||||||
| chr10:71289620
|
A | C | 1 | a0001c0001t0063g0032 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1099+630A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289620 | ||||||
| chr10:71289651
|
C | A | 1 | a0004c0010t0010g0092 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1099+661C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289651 | ||||||
| chr10:71289651
|
C | T | 1 | a0001c0003t0011g0049 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1099+661C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289651 | ||||||
| chr10:71289707
|
A | G | 254 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1099+717A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289707 | ||||||
| chr10:71289758
|
GGAGCCCA others(5): Show |
G | 254 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1099+772_1099+783d others(14): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr10 | 71289758 | |||||
| chr10:71289972
|
T | C | 45 | a0001c0003t0007g0095a0001c0003t0007g0198a0001c0003t0007g0258others(42): Show | 45 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1100-943T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289972 | ||||||
| chr10:71289973
|
G | A | 6 | a0001c0003t0007g0198a0001c0003t0007g0258a0001c0003t0007g0330others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100-942G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71289973 | ||||||
| chr10:71290009
|
C | G | 45 | a0001c0003t0007g0095a0001c0003t0007g0198a0001c0003t0007g0258others(42): Show | 45 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1100-906C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290009 | ||||||
| chr10:71290074
|
G | A | 6 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(3): Show | 6 | HG00735.hp1 HG01255.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100-841G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290074 | ||||||
| chr10:71290109
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0301 | 2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1100-806A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290109 | ||||||
| chr10:71290143
|
T | C | 45 | a0001c0003t0007g0095a0001c0003t0007g0198a0001c0003t0007g0258others(42): Show | 45 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1100-772T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290143 | ||||||
| chr10:71290214
|
T | C | 45 | a0001c0003t0007g0095a0001c0003t0007g0198a0001c0003t0007g0258others(42): Show | 45 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1100-701T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290214 | ||||||
| chr10:71290284
|
C | T | 1 | a0001c0001t0004g0333 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1100-631C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290284 | ||||||
| chr10:71290311
|
G | A | 1 | a0001c0001t0004g0267 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1100-604G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290311 | ||||||
| chr10:71290319
|
G | A | 306 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(303): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1100-596G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290319 | ||||||
| chr10:71290321
|
G | A | 4 | a0001c0001t0009g0185a0001c0001t0010g0015a0001c0001t0014g0005others(1): Show | 5 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1100-594G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290321 | ||||||
| chr10:71290374
|
G | A | 32 | a0001c0003t0001g0003a0001c0003t0001g0118a0001c0003t0001g0284others(29): Show | 34 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.1100-541G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290374 | ||||||
| chr10:71290398
|
T | G | 3 | a0007c0017t0011g0354a0007c0017t0016g0327a0014c0050t0029g0352 | 3 | HG01243.hp2 HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1100-517T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290398 | ||||||
| chr10:71290467
|
A | G | 5 | a0001c0001t0001g0264a0001c0001t0001g0294a0012c0013t0003g0191others(2): Show | 5 | HG02015.hp2 HG02040.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1100-448A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290467 | ||||||
| chr10:71290505
|
T | C | 4 | a0001c0009t0005g0075a0001c0009t0035g0007a0001c0009t0035g0360others(1): Show | 4 | HG00735.hp1 HG01255.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1100-410T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290505 | ||||||
| chr10:71290598
|
C | A | 3 | a0001c0001t0010g0323a0001c0001t0057g0104a0027c0025t0059g0009 | 3 | HG02976.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1100-317C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290598 | ||||||
| chr10:71290619
|
G | T | 1 | a0001c0020t0065g0142 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1100-296G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290619 | ||||||
| chr10:71290724
|
G | A | 10 | a0001c0003t0019g0261a0001c0003t0019g0328a0001c0003t0044g0201others(7): Show | 10 | HG01106.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1100-191G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | chr10 | 71290724 | ||||||
| chr10:71290880
|
C | CTG | 45 | a0001c0003t0007g0095a0001c0003t0007g0198a0001c0003t0007g0258others(42): Show | 45 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1100-34_1100-33dup others(2): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr10 | 71290880 | |||||
| chr10:71291120
|
G | A | 3 | a0001c0001t0009g0204a0001c0002t0032g0004a0001c0012t0016g0325 | 4 | HG02895.hp1 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1294+11G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 9/16 | chr10 | 71291120 | ||||||
| chr10:71291226
|
C | T | 210 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(207): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1294+117C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 9/16 | chr10 | 71291226 | ||||||
| chr10:71291281
|
G | C | 260 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(257): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1295-151G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 9/16 | chr10 | 71291281 | ||||||
| chr10:71291296
|
C | T | 2 | a0001c0002t0032g0004a0001c0012t0016g0325 | 3 | HG02895.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1295-136C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 9/16 | chr10 | 71291296 | ||||||
| chr10:71291939
|
G | A | 2 | a0001c0003t0036g0131a0006c0057t0036g0212 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1684+118G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/16 | chr10 | 71291939 | ||||||
| chr10:71292009
|
C | A | 1 | a0001c0001t0006g0039 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1684+188C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/16 | chr10 | 71292009 | ||||||
| chr10:71292017
|
C | A | 1 | a0001c0001t0031g0342 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1684+196C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/16 | chr10 | 71292017 | ||||||
| chr10:71292096
|
G | C | 1 | a0001c0001t0011g0361 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1684+275G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/16 | chr10 | 71292096 | ||||||
| chr10:71292153
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1685-314G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/16 | chr10 | 71292153 | ||||||
| chr10:71292330
|
C | A | 1 | a0003c0007t0012g0227 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1685-137C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/16 | chr10 | 71292330 | ||||||
| chr10:71292355
|
T | G | 2 | a0001c0002t0032g0004a0001c0012t0016g0325 | 3 | HG02895.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1685-112T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/16 | chr10 | 71292355 | ||||||
| chr10:71292357
|
C | T | 2 | a0001c0012t0038g0096a0001c0012t0038g0196 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1685-110C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/16 | chr10 | 71292357 | ||||||
| chr10:71292375
|
T | C | 20 | a0001c0001t0001g0047a0001c0001t0001g0086a0003c0007t0010g0027others(17): Show | 20 | HG01106.hp2 HG01109.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1685-92T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/16 | chr10 | 71292375 | ||||||
| chr10:71292391
|
C | G | 11 | a0001c0002t0078g0123a0001c0006t0015g0011a0001c0006t0015g0021others(8): Show | 11 | HG01069.hp2 HG01169.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1685-76C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 10/16 | chr10 | 71292391 | ||||||
| chr10:71292592
|
C | G | 1 | a0001c0002t0078g0123 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1772+38C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 11/16 | chr10 | 71292592 | ||||||
| chr10:71292691
|
T | C | 7 | a0001c0024t0002g0235a0002c0005t0001g0278a0002c0005t0013g0055others(4): Show | 7 | HG00609.hp1 HG00673.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1772+137T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 11/16 | chr10 | 71292691 | ||||||
| chr10:71292875
|
G | A | 235 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1772+321G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 11/16 | chr10 | 71292875 | ||||||
| chr10:71292921
|
T | G | 1 | a0001c0001t0004g0149 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1772+367T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 11/16 | chr10 | 71292921 | ||||||
| chr10:71292934
|
G | T | 8 | a0001c0001t0024g0112a0001c0001t0062g0019a0001c0003t0019g0261others(5): Show | 8 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1772+380G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 11/16 | chr10 | 71292934 | ||||||
| chr10:71293028
|
T | G | 14 | a0001c0001t0010g0161a0003c0007t0010g0027a0003c0007t0012g0098others(11): Show | 14 | HG01106.hp2 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1773-377T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 11/16 | chr10 | 71293028 | ||||||
| chr10:71293161
|
A | T | 335 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(332): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1773-244A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 11/16 | chr10 | 71293161 | ||||||
| chr10:71293585
|
C | T | 7 | a0001c0001t0007g0128a0001c0001t0007g0139a0001c0001t0007g0335others(4): Show | 7 | HG02280.hp2 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1941+12C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 12/16 | chr10 | 71293585 | ||||||
| chr10:71293673
|
C | G | 1 | a0001c0001t0010g0015 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1942-27C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 12/16 | chr10 | 71293673 | ||||||
| chr10:71293679
|
C | T | 8 | a0001c0003t0007g0359a0001c0003t0011g0049a0001c0003t0019g0261others(5): Show | 8 | HG01106.hp1 HG01433.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1942-21C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 12/16 | chr10 | 71293679 | ||||||
| chr10:71293691
|
C | A | 1 | a0001c0001t0009g0185 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1942-9C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 12/16 | chr10 | 71293691 | ||||||
| chr10:71293963
|
C | T | 1 | a0001c0003t0036g0131 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2175+30C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71293963 | ||||||
| chr10:71294066
|
C | T | 1 | a0001c0001t0068g0340 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2175+133C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294066 | ||||||
| chr10:71294068
|
A | G | 348 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(345): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.2175+135A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294068 | ||||||
| chr10:71294071
|
C | T | 8 | a0001c0003t0007g0359a0001c0003t0011g0049a0001c0003t0019g0261others(5): Show | 8 | HG01106.hp1 HG01433.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2175+138C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294071 | ||||||
| chr10:71294073
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2175+140C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294073 | ||||||
| chr10:71294087
|
GC | G | 9 | a0001c0002t0078g0123a0001c0006t0015g0011a0001c0006t0015g0021others(6): Show | 9 | HG01069.hp2 HG01169.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2175+156delC | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr10 | 71294087 | |||||
| chr10:71294125
|
A | G | 1 | a0001c0003t0007g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2175+192A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294125 | ||||||
| chr10:71294145
|
G | A | 3 | a0001c0002t0028g0109a0001c0002t0028g0110a0001c0002t0028g0155 | 3 | HG02970.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2175+212G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294145 | ||||||
| chr10:71294176
|
C | T | 1 | a0001c0001t0045g0187 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2175+243C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294176 | ||||||
| chr10:71294286
|
G | A | 1 | a0001c0002t0001g0303 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2175+353G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294286 | ||||||
| chr10:71294325
|
C | A | 300 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(297): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.2175+392C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294325 | ||||||
| chr10:71294388
|
C | T | 1 | a0016c0037t0013g0270 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2175+455C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294388 | ||||||
| chr10:71294389
|
C | G | 71 | a0001c0001t0001g0088a0001c0001t0001g0170a0001c0001t0001g0189others(68): Show | 72 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.2175+456C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294389 | ||||||
| chr10:71294548
|
T | C | 324 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(321): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.2175+615T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294548 | ||||||
| chr10:71294675
|
C | A | 2 | a0007c0017t0011g0354a0007c0017t0016g0327 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2175+742C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294675 | ||||||
| chr10:71294794
|
T | C | 20 | a0001c0001t0011g0341a0001c0001t0011g0348a0001c0001t0020g0115others(17): Show | 20 | HG00140.hp2 HG01069.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.2175+861T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294794 | ||||||
| chr10:71294867
|
T | C | 2 | a0007c0017t0011g0354a0007c0017t0016g0327 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2175+934T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294867 | ||||||
| chr10:71294874
|
T | C | 15 | a0001c0001t0024g0112a0001c0001t0062g0019a0001c0003t0007g0359others(12): Show | 15 | HG01106.hp1 HG01243.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.2176-937T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71294874 | ||||||
| chr10:71295014
|
C | T | 2 | a0007c0017t0011g0354a0007c0017t0016g0327 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2176-797C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71295014 | ||||||
| chr10:71295207
|
G | A | 31 | a0001c0001t0010g0161a0001c0001t0045g0187a0001c0001t0070g0008others(28): Show | 32 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.2176-604G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71295207 | ||||||
| chr10:71295244
|
C | T | 2 | a0007c0017t0011g0354a0007c0017t0016g0327 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2176-567C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71295244 | ||||||
| chr10:71295245
|
G | A | 18 | a0001c0001t0011g0341a0001c0001t0011g0348a0001c0001t0020g0115others(15): Show | 18 | HG00140.hp2 HG01069.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2176-566G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71295245 | ||||||
| chr10:71295268
|
C | A | 1 | a0001c0001t0004g0215 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2176-543C>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71295268 | ||||||
| chr10:71295342
|
CCATCCAT others(17): Show |
C | 8 | a0001c0001t0011g0341a0001c0001t0011g0348a0001c0001t0020g0115others(5): Show | 8 | HG00140.hp2 HG02647.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2176-452_2176-429d others(26): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr10 | 71295342 | |||||
| chr10:71295676
|
A | T | 1 | a0001c0001t0004g0215 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2176-135A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71295676 | ||||||
| chr10:71295698
|
A | C | 8 | a0001c0001t0011g0341a0001c0001t0011g0348a0001c0001t0020g0115others(5): Show | 8 | HG00140.hp2 HG02647.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2176-113A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71295698 | ||||||
| chr10:71295727
|
T | A | 1 | a0001c0001t0004g0215 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2176-84T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71295727 | ||||||
| chr10:71295739
|
C | T | 1 | a0001c0002t0032g0004 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2176-72C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 13/16 | chr10 | 71295739 | ||||||
| chr10:71296019
|
A | G | 9 | a0001c0002t0078g0123a0001c0006t0015g0011a0001c0006t0015g0021others(6): Show | 9 | HG01069.hp2 HG01169.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2325+59A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 14/16 | chr10 | 71296019 | ||||||
| chr10:71296037
|
G | A | 1 | a0001c0004t0003g0251 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2325+77G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 14/16 | chr10 | 71296037 | ||||||
| chr10:71296092
|
T | C | 262 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(259): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.2325+132T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 14/16 | chr10 | 71296092 | ||||||
| chr10:71296096
|
C | T | 1 | a0001c0001t0019g0353 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2325+136C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 14/16 | chr10 | 71296096 | ||||||
| chr10:71296208
|
A | C | 257 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.2325+248A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 14/16 | chr10 | 71296208 | ||||||
| chr10:71296315
|
G | A | 303 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2326-263G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 14/16 | chr10 | 71296315 | ||||||
| chr10:71296464
|
G | A | 1 | a0001c0002t0033g0036 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2326-114G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 14/16 | chr10 | 71296464 | ||||||
| chr10:71296520
|
C | T | 7 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0147others(4): Show | 7 | HG00099.hp1 HG00738.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.2326-58C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 14/16 | chr10 | 71296520 | ||||||
| chr10:71296709
|
C | CCAGATAT others(93): Show |
1 | a0023c0028t0005g0343 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2490+40_2490+41ins others(100): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296709 | |||||
| chr10:71296727
|
T | TACCACTC others(43): Show |
1 | a0022c0045t0004g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2481_2490+40dupTCT others(47): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296727 | |||||
| chr10:71296739
|
AGAGGTGA others(43): Show |
A | 2 | a0009c0034t0004g0286a0025c0032t0023g0084 | 2 | HG02015.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2490+11_2490+60del others(50): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296739 | |||||
| chr10:71296739
|
AGAGGTGA others(93): Show |
A | 1 | a0009c0019t0004g0208 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2490+11_2490+110de others(101): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296739 | |||||
| chr10:71296753
|
T | C | 10 | a0001c0002t0028g0109a0001c0002t0028g0110a0001c0002t0028g0155others(7): Show | 10 | HG01243.hp2 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2490+11T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296753 | ||||||
| chr10:71296753
|
T | G | 1 | a0001c0029t0002g0253 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2490+11T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296753 | ||||||
| chr10:71296754
|
C | G | 1 | a0001c0029t0002g0253 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2490+12C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296754 | ||||||
| chr10:71296755
|
G | A | 1 | a0001c0001t0001g0344 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2490+13G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296755 | ||||||
| chr10:71296755
|
G | T | 1 | a0001c0029t0002g0253 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2490+13G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296755 | ||||||
| chr10:71296759
|
C | G | 1 | a0001c0029t0002g0253 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2490+17C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296759 | ||||||
| chr10:71296762
|
C | CATATTCC others(143): Show |
1 | a0001c0001t0026g0255 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2490+28_2490+29ins others(150): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296762 | |||||
| chr10:71296762
|
C | CATATTCC others(143): Show |
1 | a0001c0001t0006g0039 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2490+90_2490+91ins others(150): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296762 | |||||
| chr10:71296762
|
C | CATATTCC others(143): Show |
1 | a0001c0027t0003g0262 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2490+140_2490+141i others(152): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296762 | |||||
| chr10:71296762
|
C | CATATTCC others(493): Show |
1 | a0002c0005t0014g0045 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2490+90_2490+91ins others(500): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296762 | |||||
| chr10:71296762
|
C | CATATTCC others(43): Show |
2 | a0001c0001t0017g0173a0001c0001t0074g0059 | 2 | HG01361.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2490+40_2490+41ins others(50): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296762 | |||||
| chr10:71296762
|
C | CATATTCC others(93): Show |
1 | a0001c0002t0026g0031 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2490+40_2490+41ins others(100): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296762 | |||||
| chr10:71296762
|
C | CATATTCC others(293): Show |
1 | a0001c0001t0002g0046 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2490+40_2490+41ins others(300): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296762 | |||||
| chr10:71296762
|
C | G | 3 | a0001c0012t0016g0325a0001c0012t0038g0196a0001c0029t0002g0253 | 3 | HG02630.hp1 HG03486.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2490+20C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296762 | ||||||
| chr10:71296762
|
CATATTCC others(43): Show |
C | 8 | a0001c0001t0013g0233a0001c0001t0014g0028a0001c0002t0002g0093others(5): Show | 8 | HG01106.hp2 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2490+41_2490+90del others(50): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296762 | |||||
| chr10:71296762
|
CATATTCC others(93): Show |
C | 7 | a0001c0001t0016g0217a0001c0002t0002g0248a0001c0003t0037g0074others(4): Show | 7 | HG02523.hp2 HG02647.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2490+41_2490+140de others(101): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296762 | |||||
| chr10:71296777
|
C | T | 2 | a0001c0001t0014g0182a0001c0001t0014g0260 | 2 | HG00741.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.2490+35C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296777 | ||||||
| chr10:71296783
|
A | ACTGGCGG others(93): Show |
1 | a0001c0001t0002g0274 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2490+90_2490+91ins others(100): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296783 | |||||
| chr10:71296783
|
A | ACTGGCGG others(43): Show |
13 | a0001c0001t0001g0174a0001c0001t0002g0082a0001c0001t0002g0314others(10): Show | 13 | HG00408.hp1 HG01081.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2490+163_2490+212d others(52): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296783 | |||||
| chr10:71296783
|
A | ACTGGCGG others(93): Show |
6 | a0001c0001t0001g0224a0001c0001t0017g0202a0001c0001t0020g0115others(3): Show | 6 | HG00642.hp2 HG02602.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2490+113_2490+212d others(102): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296783 | |||||
| chr10:71296783
|
A | ACTGGCGG others(143): Show |
3 | a0001c0001t0001g0294a0001c0004t0003g0022a0001c0024t0002g0235 | 3 | NA18612.hp1 NA18946.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2490+63_2490+212du others(151): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296783 | |||||
| chr10:71296783
|
A | ACTGGCGG others(193): Show |
1 | a0001c0003t0004g0351 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2490+212_2490+213i others(202): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296783 | |||||
| chr10:71296783
|
A | ACTGGCGG others(243): Show |
1 | a0001c0003t0002g0291 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2490+212_2490+213i others(252): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296783 | |||||
| chr10:71296783
|
A | ACTGGCGG others(1043): Show |
1 | a0001c0001t0068g0340 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2490+212_2490+213i others(1052): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296783 | |||||
| chr10:71296783
|
A | ACTGGCGG others(143): Show |
1 | a0002c0005t0001g0016 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2490+90_2490+91ins others(150): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296783 | |||||
| chr10:71296783
|
A | ACTGGCGG others(93): Show |
1 | a0002c0005t0054g0166 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2490+90_2490+91ins others(100): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296783 | |||||
| chr10:71296783
|
A | G | 6 | a0001c0001t0007g0326a0001c0001t0010g0161a0001c0001t0014g0005others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2490+41A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296783 | ||||||
| chr10:71296783
|
A | T | 4 | a0001c0001t0014g0182a0001c0001t0014g0260a0022c0045t0004g0162others(1): Show | 4 | HG00741.hp2 HG01070.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.2490+41A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296783 | ||||||
| chr10:71296783
|
ACTGGCGG others(43): Show |
A | 78 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0066others(75): Show | 80 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.2490+163_2490+212d others(52): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296783 | |||||
| chr10:71296783
|
ACTGGCGG others(93): Show |
A | 11 | a0001c0001t0004g0149a0001c0001t0019g0353a0001c0002t0001g0205others(8): Show | 12 | HG00438.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2490+113_2490+212d others(102): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296783 | |||||
| chr10:71296789
|
G | A | 3 | a0001c0001t0014g0182a0001c0001t0014g0260a0022c0045t0004g0162 | 3 | HG00741.hp2 HG01070.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2490+47G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296789 | ||||||
| chr10:71296802
|
G | GTCGGGGC others(142): Show |
1 | a0001c0003t0011g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2490+60_2490+61ins others(149): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296802 | ||||||
| chr10:71296802
|
G | GTCGGGGC others(42): Show |
2 | a0001c0001t0014g0182a0001c0001t0014g0260 | 2 | HG00741.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.2490+60_2490+61ins others(49): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296802 | ||||||
| chr10:71296803
|
G | T | 2 | a0001c0001t0061g0140a0001c0040t0043g0214 | 2 | HG02132.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2490+61G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296803 | ||||||
| chr10:71296804
|
G | C | 2 | a0001c0001t0061g0140a0001c0040t0043g0214 | 2 | HG02132.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2490+62G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296804 | ||||||
| chr10:71296804
|
G | T | 3 | a0001c0001t0014g0182a0001c0001t0014g0260a0001c0003t0011g0132 | 3 | HG00741.hp2 HG01070.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2490+62G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296804 | ||||||
| chr10:71296805
|
T | C | 3 | a0001c0001t0014g0182a0001c0001t0014g0260a0001c0003t0011g0132 | 3 | HG00741.hp2 HG01070.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2490+63T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296805 | ||||||
| chr10:71296805
|
T | G | 2 | a0001c0001t0061g0140a0001c0040t0043g0214 | 2 | HG02132.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2490+63T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296805 | ||||||
| chr10:71296809
|
G | C | 2 | a0001c0001t0061g0140a0001c0040t0043g0214 | 2 | HG02132.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2490+67G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296809 | ||||||
| chr10:71296809
|
G | GC | 3 | a0001c0001t0014g0182a0001c0001t0014g0260a0001c0003t0011g0132 | 3 | HG00741.hp2 HG01070.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2490+68dupC | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296809 | |||||
| chr10:71296812
|
G | C | 5 | a0001c0001t0014g0182a0001c0001t0014g0260a0001c0001t0061g0140others(2): Show | 5 | HG00741.hp2 HG01070.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.2490+70G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296812 | ||||||
| chr10:71296812
|
G | GATATTCC others(43): Show |
2 | a0001c0001t0010g0161a0001c0003t0008g0100 | 2 | HG02486.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2490+90_2490+91ins others(50): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296812 | |||||
| chr10:71296812
|
G | GATATTCC others(43): Show |
1 | a0015c0036t0039g0347 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2490+84_2490+85ins others(50): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296812 | |||||
| chr10:71296827
|
C | T | 1 | a0010c0016t0049g0077 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2490+85C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296827 | ||||||
| chr10:71296833
|
G | A | 20 | a0001c0001t0002g0081a0001c0001t0004g0216a0001c0001t0010g0161others(17): Show | 20 | HG00423.hp1 HG02132.hp1 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.2490+91G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296833 | ||||||
| chr10:71296833
|
G | GCTGGCGG others(43): Show |
2 | a0001c0001t0007g0326a0001c0001t0007g0349 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2490+140_2490+141i others(52): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296833 | |||||
| chr10:71296833
|
G | GCTGGCGG others(93): Show |
2 | a0001c0003t0007g0095a0001c0006t0007g0337 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2490+140_2490+141i others(102): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296833 | |||||
| chr10:71296833
|
G | GCTGGCGG others(293): Show |
1 | a0001c0001t0007g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2490+140_2490+141i others(302): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296833 | |||||
| chr10:71296833
|
G | T | 4 | a0001c0004t0003g0251a0008c0047t0029g0160a0010c0016t0049g0077others(1): Show | 4 | HG01243.hp2 HG02273.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490+91G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296833 | ||||||
| chr10:71296838
|
CGGAGGTG others(142): Show |
C | 1 | a0001c0001t0013g0276 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2490+113_2490+261d others(2): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296838 | |||||
| chr10:71296839
|
G | A | 2 | a0001c0004t0003g0251a0010c0016t0002g0126 | 2 | HG01981.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2490+97G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296839 | ||||||
| chr10:71296853
|
G | T | 3 | a0001c0004t0003g0251a0003c0007t0012g0356a0010c0016t0002g0126 | 3 | HG01981.hp2 NA18906.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2490+111G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296853 | ||||||
| chr10:71296854
|
G | C | 3 | a0001c0004t0003g0251a0003c0007t0012g0356a0010c0016t0002g0126 | 3 | HG01981.hp2 NA18906.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2490+112G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296854 | ||||||
| chr10:71296854
|
GTGGGGCA others(44): Show |
G | 3 | a0001c0003t0022g0346a0008c0047t0029g0160a0016c0037t0013g0270 | 3 | HG02486.hp2 NA18939.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.2490+113_2490+163d others(53): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296854 | ||||||
| chr10:71296855
|
T | G | 3 | a0001c0004t0003g0251a0003c0007t0012g0356a0010c0016t0002g0126 | 3 | HG01981.hp2 NA18906.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2490+113T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296855 | ||||||
| chr10:71296856
|
G | C | 2 | a0001c0001t0001g0299a0014c0050t0029g0352 | 2 | HG01243.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2490+114G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296856 | ||||||
| chr10:71296859
|
G | C | 5 | a0001c0001t0001g0299a0001c0004t0003g0251a0003c0007t0012g0356others(2): Show | 5 | HG01243.hp2 HG01981.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2490+117G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296859 | ||||||
| chr10:71296859
|
G | GCAGATAT others(140): Show |
1 | a0001c0002t0004g0292 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2490+162_2490+163i others(149): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296859 | |||||
| chr10:71296859
|
G | GCAGATAT others(337): Show |
1 | a0001c0002t0004g0273 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2490+162_2490+163i others(346): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296859 | |||||
| chr10:71296859
|
GCAGATAT others(92): Show |
G | 2 | a0001c0001t0010g0159a0001c0001t0062g0019 | 2 | HG01515.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2490+128_2490+226d others(101): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296859 | |||||
| chr10:71296862
|
G | C | 5 | a0001c0001t0027g0044a0001c0001t0027g0259a0001c0004t0003g0251others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.2490+120G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296862 | ||||||
| chr10:71296862
|
G | GATATTCC others(43): Show |
1 | a0007c0017t0011g0354 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2490+140_2490+141i others(52): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296862 | |||||
| chr10:71296883
|
G | A | 28 | a0001c0001t0001g0283a0001c0001t0007g0326a0001c0001t0007g0349others(25): Show | 28 | HG00639.hp2 HG01069.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.2490+141G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296883 | ||||||
| chr10:71296883
|
G | GCTGGCGG others(93): Show |
1 | a0001c0015t0056g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2490+190_2490+191i others(102): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296883 | |||||
| chr10:71296888
|
CGGAGGTG others(92): Show |
C | 6 | a0001c0001t0005g0020a0001c0001t0005g0231a0001c0001t0005g0302others(3): Show | 6 | HG00280.hp1 HG01109.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.2490+163_2490+261d others(101): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296888 | |||||
| chr10:71296904
|
GT | G | 25 | a0001c0001t0004g0267a0001c0001t0004g0333a0001c0001t0005g0105others(22): Show | 25 | HG00558.hp2 HG01243.hp2 HG01975.hp2 others(22): Show |
intron_variant | MODIFIER | c.2490+163delT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296904 | ||||||
| chr10:71296906
|
G | C | 28 | a0001c0001t0004g0267a0001c0001t0004g0333a0001c0001t0005g0105others(25): Show | 28 | HG00558.hp2 HG01243.hp2 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.2490+164G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296906 | ||||||
| chr10:71296909
|
G | C | 28 | a0001c0001t0004g0267a0001c0001t0004g0333a0001c0001t0005g0105others(25): Show | 28 | HG00558.hp2 HG01243.hp2 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.2490+167G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296909 | ||||||
| chr10:71296909
|
G | GCAGATAT others(42): Show |
3 | a0001c0001t0002g0081a0001c0001t0027g0044a0001c0001t0027g0259 | 3 | HG01070.hp2 HG01071.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2490+178_2490+226d others(51): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296909 | |||||
| chr10:71296909
|
G | GCAGATAT others(42): Show |
1 | a0001c0003t0001g0051 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2490+177_2490+178i others(51): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296909 | |||||
| chr10:71296909
|
GCAGATAT others(42): Show |
G | 6 | a0001c0001t0019g0320a0001c0001t0069g0206a0001c0003t0019g0261others(3): Show | 6 | HG00735.hp1 HG01106.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2490+178_2490+226d others(51): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296909 | |||||
| chr10:71296920
|
A | AGCTGCAC others(42): Show |
2 | a0001c0001t0001g0199a0001c0004t0003g0156 | 2 | HG01358.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2490+191_2490+239d others(51): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296920 | |||||
| chr10:71296920
|
A | AGCTGCAC others(43): Show |
9 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0001g0193others(6): Show | 9 | HG00140.hp1 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.2490+212_2490+213i others(52): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296920 | |||||
| chr10:71296920
|
A | AGCTGCAC others(143): Show |
1 | a0001c0001t0004g0175 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2490+212_2490+213i others(152): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296920 | |||||
| chr10:71296920
|
A | G | 47 | a0001c0001t0001g0078a0001c0001t0001g0088a0001c0001t0001g0183others(44): Show | 49 | HG00558.hp2 HG00733.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.2490+178A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296920 | ||||||
| chr10:71296933
|
G | A | 12 | a0001c0001t0010g0323a0001c0003t0011g0049a0001c0003t0036g0131others(9): Show | 12 | HG01069.hp2 HG01433.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.2490+191G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296933 | ||||||
| chr10:71296933
|
G | T | 10 | a0001c0001t0004g0267a0001c0001t0004g0333a0001c0001t0005g0105others(7): Show | 10 | HG00558.hp2 HG01243.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.2490+191G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296933 | ||||||
| chr10:71296933
|
GCTGGCGG others(42): Show |
G | 3 | a0001c0004t0003g0064a0001c0004t0003g0207a0001c0004t0003g0236 | 3 | HG02040.hp2 NA18979.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2490+196_2490+244d others(51): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296933 | |||||
| chr10:71296938
|
C | CGGAGGTG others(91): Show |
1 | a0001c0002t0028g0109 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2490+226_2490+227i others(100): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296938 | |||||
| chr10:71296938
|
C | CGGAGGTG others(42): Show |
4 | a0001c0001t0001g0147a0001c0001t0002g0274a0001c0002t0028g0155others(1): Show | 4 | HG01169.hp2 HG01515.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.2490+236_2490+284d others(51): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296938 | |||||
| chr10:71296938
|
C | CGGAGGTG others(242): Show |
5 | a0001c0006t0015g0011a0001c0006t0015g0141a0001c0006t0015g0167others(2): Show | 5 | HG01069.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2490+212_2490+213i others(251): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296938 | |||||
| chr10:71296938
|
C | CGGAGGTG others(192): Show |
2 | a0001c0006t0081g0012a0028c0039t0060g0171 | 2 | HG00639.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2490+212_2490+213i others(201): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296938 | |||||
| chr10:71296938
|
C | CGGAGGTG others(142): Show |
1 | a0001c0006t0015g0168 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2490+212_2490+213i others(151): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296938 | |||||
| chr10:71296938
|
C | CGGAGGTG others(92): Show |
1 | a0001c0006t0015g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2490+212_2490+213i others(101): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296938 | |||||
| chr10:71296938
|
C | T | 9 | a0001c0001t0004g0267a0001c0001t0005g0105a0001c0002t0009g0041others(6): Show | 9 | HG01243.hp2 HG01975.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.2490+196C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296938 | ||||||
| chr10:71296938
|
CGGAGGTG others(42): Show |
C | 3 | a0001c0001t0031g0336a0001c0002t0072g0111a0013c0052t0002g0268 | 3 | HG00597.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2490+236_2490+284d others(51): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296938 | |||||
| chr10:71296940
|
GAGGTGAG others(91): Show |
G | 1 | a0001c0002t0002g0083 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2490+214_2490+311d others(100): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296940 | |||||
| chr10:71296954
|
G | GT | 7 | a0001c0001t0014g0182a0001c0001t0014g0260a0001c0001t0034g0230others(4): Show | 7 | HG00741.hp2 HG01070.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2490+212_2490+213i others(3): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296954 | ||||||
| chr10:71296954
|
G | GTGGGGCA others(144): Show |
4 | a0001c0001t0024g0112a0001c0003t0007g0359a0001c0003t0075g0329others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490+212_2490+213i others(153): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296954 | ||||||
| chr10:71296954
|
G | GTGGGGCA others(44): Show |
2 | a0001c0002t0058g0137a0001c0003t0008g0190 | 2 | HG00438.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2490+212_2490+213i others(53): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296954 | ||||||
| chr10:71296954
|
G | GTGGGGCA others(94): Show |
4 | a0001c0001t0010g0323a0001c0003t0011g0049a0001c0003t0036g0131others(1): Show | 4 | HG01433.hp2 HG02886.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490+212_2490+213i others(103): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296954 | ||||||
| chr10:71296954
|
G | GTGGGGCA others(144): Show |
1 | a0001c0003t0024g0097 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2490+212_2490+213i others(153): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296954 | ||||||
| chr10:71296955
|
C | G | 18 | a0001c0001t0010g0323a0001c0001t0014g0182a0001c0001t0014g0260others(15): Show | 18 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.2490+213C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296955 | ||||||
| chr10:71296958
|
C | G | 18 | a0001c0001t0010g0323a0001c0001t0014g0182a0001c0001t0014g0260others(15): Show | 18 | HG00438.hp1 HG00741.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.2490+216C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296958 | ||||||
| chr10:71296966
|
T | G | 1 | a0001c0001t0005g0180 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2490+224T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296966 | ||||||
| chr10:71296968
|
C | T | 1 | a0001c0002t0004g0273 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2490+226C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296968 | ||||||
| chr10:71296969
|
G | A | 6 | a0001c0001t0034g0230a0001c0002t0002g0306a0001c0003t0008g0190others(3): Show | 6 | HG00438.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2490+227G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296969 | ||||||
| chr10:71296969
|
GGCTGCAC others(91): Show |
G | 4 | a0001c0001t0011g0341a0001c0001t0011g0348a0001c0001t0025g0338others(1): Show | 4 | HG02647.hp1 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490+240_2490+337d others(100): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71296969 | |||||
| chr10:71296982
|
T | G | 20 | a0001c0001t0001g0066a0001c0001t0001g0240a0001c0001t0010g0161others(17): Show | 21 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.2490+240T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296982 | ||||||
| chr10:71296987
|
T | C | 18 | a0001c0001t0001g0066a0001c0001t0001g0240a0001c0001t0010g0161others(15): Show | 19 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(16): Show |
intron_variant | MODIFIER | c.2490+245T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71296987 | ||||||
| chr10:71297003
|
G | GTGGGGCA others(44): Show |
1 | a0004c0042t0053g0229 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2490+261_2490+262i others(53): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297003 | ||||||
| chr10:71297004
|
C | G | 2 | a0001c0002t0002g0306a0004c0042t0053g0229 | 2 | HG00140.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2490+262C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297004 | ||||||
| chr10:71297007
|
C | G | 2 | a0001c0002t0002g0306a0004c0042t0053g0229 | 2 | HG00140.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2490+265C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297007 | ||||||
| chr10:71297018
|
G | A | 2 | a0001c0002t0002g0306a0004c0042t0053g0229 | 2 | HG00140.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2490+276G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297018 | ||||||
| chr10:71297018
|
GGCTGCAC others(42): Show |
G | 3 | a0001c0002t0013g0052a0001c0003t0008g0223a0001c0003t0013g0225 | 3 | HG00408.hp2 NA18941.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2490+285_2490+333d others(51): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr10 | 71297018 | |||||
| chr10:71297027
|
G | C | 4 | a0001c0002t0002g0306a0001c0003t0008g0190a0002c0005t0054g0166others(1): Show | 4 | HG00140.hp2 HG00438.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490+285G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297027 | ||||||
| chr10:71297031
|
T | G | 4 | a0001c0002t0002g0306a0001c0003t0008g0190a0002c0005t0054g0166others(1): Show | 4 | HG00140.hp2 HG00438.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490+289T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297031 | ||||||
| chr10:71297032
|
G | C | 4 | a0001c0002t0002g0306a0001c0003t0008g0190a0002c0005t0054g0166others(1): Show | 4 | HG00140.hp2 HG00438.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490+290G>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297032 | ||||||
| chr10:71297037
|
A | G | 4 | a0001c0002t0002g0306a0001c0003t0008g0190a0002c0005t0054g0166others(1): Show | 4 | HG00140.hp2 HG00438.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490+295A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297037 | ||||||
| chr10:71297038
|
T | G | 4 | a0001c0002t0002g0306a0001c0003t0008g0190a0002c0005t0054g0166others(1): Show | 4 | HG00140.hp2 HG00438.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490+296T>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297038 | ||||||
| chr10:71297054
|
C | G | 3 | a0001c0003t0008g0190a0002c0005t0054g0166a0004c0042t0053g0229 | 3 | HG00140.hp2 HG00438.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2490+312C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297054 | ||||||
| chr10:71297067
|
A | G | 3 | a0001c0003t0008g0190a0002c0005t0054g0166a0004c0042t0053g0229 | 3 | HG00140.hp2 HG00438.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2490+325A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297067 | ||||||
| chr10:71297085
|
T | C | 7 | a0001c0001t0011g0341a0001c0001t0011g0348a0001c0001t0025g0338others(4): Show | 7 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(4): Show |
intron_variant | MODIFIER | c.2490+343T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297085 | ||||||
| chr10:71297142
|
A | C | 9 | a0001c0001t0010g0161a0001c0001t0011g0341a0001c0001t0011g0348others(6): Show | 9 | HG00140.hp2 HG01243.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.2490+400A>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297142 | ||||||
| chr10:71297177
|
G | A | 7 | a0001c0002t0022g0143a0001c0002t0022g0192a0001c0002t0026g0116others(4): Show | 7 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.2490+435G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297177 | ||||||
| chr10:71297236
|
C | G | 1 | a0007c0017t0016g0327 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2490+494C>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297236 | ||||||
| chr10:71297279
|
G | A | 10 | a0001c0001t0010g0015a0001c0001t0010g0159a0001c0001t0010g0323others(7): Show | 10 | HG01515.hp1 HG02683.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2490+537G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297279 | ||||||
| chr10:71297300
|
C | T | 9 | a0001c0001t0010g0015a0001c0001t0010g0159a0001c0001t0010g0323others(6): Show | 9 | HG01515.hp1 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2490+558C>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297300 | ||||||
| chr10:71297337
|
G | A | 1 | a0001c0015t0018g0331 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2491-572G>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297337 | ||||||
| chr10:71297603
|
A | T | 336 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0080others(333): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.2491-306A>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297603 | ||||||
| chr10:71297606
|
G | T | 5 | a0001c0001t0020g0115a0001c0001t0080g0130a0017c0023t0020g0339others(2): Show | 5 | HG02809.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2491-303G>T | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297606 | ||||||
| chr10:71297793
|
T | C | 7 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0001g0193others(4): Show | 7 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.2491-116T>C | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 15/16 | chr10 | 71297793 | ||||||
| chr10:71298536
|
G | GGATAAAT others(14): Show |
3 | a0001c0009t0035g0007a0001c0009t0035g0360a0001c0009t0076g0007 | 3 | HG00735.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2672+447_2672+467d others(23): Show |
UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr10 | 71298536 | |||||
| chr10:71298614
|
AT | A | 3 | a0001c0002t0078g0123a0006c0018t0040g0200a0006c0018t0040g0297 | 3 | HG01169.hp2 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2673-497delT | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 16/16 | chr10 | 71298614 | ||||||
| chr10:71298615
|
T | A | 118 | a0001c0001t0004g0024a0001c0001t0004g0149a0001c0001t0004g0175others(115): Show | 119 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.2673-497T>A | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 16/16 | chr10 | 71298615 | ||||||
| chr10:71298712
|
A | G | 97 | a0001c0001t0001g0178a0001c0001t0004g0024a0001c0001t0004g0149others(94): Show | 98 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2673-400A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 16/16 | chr10 | 71298712 | ||||||
| chr10:71298801
|
A | G | 95 | a0001c0001t0004g0024a0001c0001t0004g0149a0001c0001t0004g0175others(92): Show | 96 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.2673-311A>G | UNC5B | ENSG00000107731.12 | transcript | ENST00000335350.10 | protein_coding | 16/16 | chr10 | 71298801 |