Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10048 |
|---|---|
| ensemblid | ENSG00000010017.13 |
| hgncid | 13727 |
| symbol | RANBP9 |
| name | RAN binding protein 9 |
| refseq_nuc | NM_005493.3 |
| refseq_prot | NP_005484.2 |
| ensembl_nuc | ENST00000011619.6 |
| ensembl_prot | ENSP00000011619.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 13621498 |
| end | 13711835 |
| strand | - |
| ver | v1.2 |
| region | chr6:13621498-13711835 |
| region5000 | chr6:13616498-13716835 |
| regionname0 | RANBP9_chr6_13621498_13711835 |
| regionname5000 | RANBP9_chr6_13616498_13716835 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 729 | 342 | 83 | 71 | 138 | 14 | 34 | 103 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0002 | 0/0 | 730 | 15 | 1 | 1 | 13 | 0 | 0 | 11 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0003 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0004 | 0/0 | 729 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0005 | 0/0 | 729 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2190 | 195 | 42 | 38 | 90 | 9 | 14 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0002 | 0/0 | 2190 | 139 | 39 | 31 | 45 | 5 | 19 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0003 | 0/0 | 2193 | 9 | 1 | 1 | 7 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0004 | 0/0 | 2193 | 3 | 0 | 0 | 3 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0005 | 0/0 | 2193 | 3 | 0 | 0 | 3 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0006 | 0/0 | 2190 | 2 | 0 | 2 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0007 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0008 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0009 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0010 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0011 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0012 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0013 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0014 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| c0015 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1195 | 261 | 80 | 51 | 98 | 11 | 20 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| t0002 | 0/1 | 1196 | 78 | 4 | 13 | 47 | 3 | 10 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| t0003 | 0/0 | 1195 | 6 | 0 | 4 | 1 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| t0004 | 0/0 | 1195 | 6 | 1 | 3 | 0 | 0 | 2 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| t0005 | 0/0 | 1195 | 3 | 0 | 0 | 3 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| t0006 | 0/0 | 1195 | 2 | 1 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| t0007 | 0/0 | 1195 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| t0008 | 0/0 | 1195 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| t0009 | 0/0 | 1195 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| t0010 | 0/0 | 1196 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0265 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0297 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2190 | 195 | 42 | 38 | 90 | 9 | 14 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0002 | 0/0 | 2190 | 139 | 39 | 31 | 45 | 5 | 19 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0006 | 0/0 | 2190 | 2 | 0 | 2 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0008 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0009 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0011 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0013 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0014 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0015 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0002c0003 | 0/0 | 2193 | 9 | 1 | 1 | 7 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0002c0004 | 0/0 | 2193 | 3 | 0 | 0 | 3 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0002c0005 | 0/0 | 2193 | 3 | 0 | 0 | 3 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0003c0010 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0004c0007 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0005c0012 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3384 | 121 | 39 | 26 | 45 | 6 | 4 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0001t0002 | 0/1 | 3385 | 68 | 3 | 11 | 41 | 3 | 9 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0001t0003 | 0/0 | 3384 | 3 | 0 | 1 | 1 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0001t0007 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0001t0009 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0001t0010 | 0/0 | 3385 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0002t0001 | 0/0 | 3384 | 119 | 37 | 22 | 40 | 5 | 15 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0002t0002 | 0/0 | 3385 | 6 | 1 | 2 | 2 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0002t0003 | 0/0 | 3384 | 3 | 0 | 3 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0002t0004 | 0/0 | 3384 | 5 | 0 | 3 | 0 | 0 | 2 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0002t0005 | 0/0 | 3384 | 3 | 0 | 0 | 3 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0002t0006 | 0/0 | 3384 | 2 | 1 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0002t0008 | 0/0 | 3384 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0006t0001 | 0/0 | 3384 | 2 | 0 | 2 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0008t0001 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0009t0001 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0011t0001 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0013t0002 | 0/0 | 3385 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0014t0001 | 0/0 | 3384 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0001c0015t0004 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0002c0003t0001 | 0/0 | 3387 | 7 | 1 | 1 | 5 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0002c0003t0002 | 0/0 | 3388 | 2 | 0 | 0 | 2 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0002c0004t0001 | 0/0 | 3387 | 2 | 0 | 0 | 2 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0002c0004t0002 | 0/0 | 3388 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0002c0005t0001 | 0/0 | 3387 | 3 | 0 | 0 | 3 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0003c0010t0001 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0004c0007t0001 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| a0005c0012t0001 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | copy fasta | chr6 | 13616498 | 13716835 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0265 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0297 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0009g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0001t0010g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0004g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0004g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0004g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0004g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0004g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0005g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0005g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0005g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0006g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0006g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0002t0008g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0006t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0006t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0008t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0009t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0011t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0013t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0014t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0001c0015t0004g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0003t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0003t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0003t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0003t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0003t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0003t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0003t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0004t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0004t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0004t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0005t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0005t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0002c0005t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0003c0010t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0004c0007t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| a0005c0012t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0300 | EUR | GBR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0037 | EUR | GBR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0025 | EUR | FIN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0236 | EUR | FIN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00408 | hp2 | a0002 | c0003 | t0001 | g0338 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00544 | hp1 | a0001 | c0002 | t0005 | g0350 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01070 | hp1 | a0001 | c0006 | t0001 | g0221 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0122 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0056 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01071 | hp2 | a0001 | c0006 | t0001 | g0220 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0311 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0108 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0341 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0085 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0120 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01261 | hp2 | a0001 | c0002 | t0004 | g0352 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0030 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01496 | hp2 | a0001 | c0002 | t0006 | g0359 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0040 | EUR | IBS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0199 | EUR | IBS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0203 | EUR | IBS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | IBS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0039 | EUR | IBS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | IBS | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0123 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01978 | hp1 | a0001 | c0002 | t0004 | g0355 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0026 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02004 | hp1 | a0001 | c0002 | t0004 | g0353 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02055 | hp1 | a0001 | c0002 | t0006 | g0358 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02071 | hp1 | a0002 | c0003 | t0002 | g0337 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02074 | hp2 | a0001 | c0002 | t0005 | g0351 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02145 | hp1 | a0005 | c0012 | t0001 | g0328 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | CDX | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | CDX | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | CDX | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0121 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | PEL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02572 | hp2 | a0001 | c0009 | t0001 | g0134 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02647 | hp1 | a0004 | c0007 | t0001 | g0091 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0125 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | ESN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | ESN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | ESN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ESN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | ESN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03239 | hp2 | a0001 | c0002 | t0004 | g0356 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0055 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | ESN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | ESN | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | GWD | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03654 | hp1 | a0001 | c0014 | t0001 | g0333 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0098 | SAS | STU | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0059 | SAS | STU | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03704 | hp2 | a0001 | c0002 | t0004 | g0354 | SAS | PJL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0099 | SAS | BEB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0058 | SAS | BEB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0057 | SAS | BEB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03834 | hp2 | a0001 | c0002 | t0008 | g0079 | SAS | BEB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0307 | SAS | BEB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0118 | SAS | BEB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | BEB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | BEB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | STU | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0275 | SAS | STU | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0325 | SAS | STU | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0019 | SAS | STU | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0095 | SAS | STU | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | STU | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | YRI | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18747 | hp1 | a0003 | c0010 | t0001 | g0248 | EAS | CHB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | CHB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | YRI | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18945 | hp2 | a0002 | c0005 | t0001 | g0343 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18946 | hp1 | a0002 | c0004 | t0001 | g0335 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18952 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18953 | hp1 | a0001 | c0013 | t0002 | g0270 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18953 | hp2 | a0002 | c0003 | t0001 | g0347 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0339 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18959 | hp2 | a0002 | c0003 | t0001 | g0346 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18961 | hp1 | a0002 | c0003 | t0002 | g0348 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18967 | hp1 | a0002 | c0004 | t0001 | g0336 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18970 | hp2 | a0002 | c0005 | t0001 | g0345 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18992 | hp2 | a0001 | c0001 | t0009 | g0278 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18993 | hp1 | a0002 | c0003 | t0001 | g0342 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19012 | hp2 | a0001 | c0002 | t0005 | g0349 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | LWK | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | LWK | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19058 | hp2 | a0002 | c0004 | t0002 | g0334 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19070 | hp1 | a0001 | c0001 | t0010 | g0284 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19080 | hp2 | a0001 | c0008 | t0001 | g0115 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19083 | hp2 | a0001 | c0011 | t0001 | g0240 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19087 | hp2 | a0002 | c0005 | t0001 | g0344 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | YRI | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ASW | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ASW | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0042 | EUR | TSI | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | TSI | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0063 | SAS | GIH | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | GIH | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | CLM | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0340 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | ACB | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | MSL | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | USA | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | USA | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA20300 | hp2 | a0001 | c0015 | t0004 | g0357 | AFR | USA | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0297 | REF | REF | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0265 | REF | REF | RANBP9_chr6_13616498_13716835 | RANBP9 | chr6 | 13616498 | 13716835 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:13622381
|
A | T | 1 | a0003 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.2171T>A | p.Val724Glu | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 14/14 | 2501/3384 | 2171/2190 | 724/729 | chr6 | 13622381 | ||
| chr6:13637841
|
A | G | 1 | a0004 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.1640T>C | p.Met547Thr | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/14 | 1970/3384 | 1640/2190 | 547/729 | chr6 | 13637841 | ||
| chr6:13639595
|
G | A | 1 | a0005 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.1493C>T | p.Ala498Val | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/14 | 1823/3384 | 1493/2190 | 498/729 | chr6 | 13639595 | ||
| chr6:13711474
|
T | TGCG | 1 | a0002 | 15 | HG00408.hp2 HG01243.hp1 HG02071.hp1 others(12): Show |
conservative_inframe_insertion | MODERATE | c.29_31dupCGC | p.Pro10dup | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/14 | 361/3384 | 31/2190 | 11/729 | chr6 | 13711474 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:13625684
|
A | G | 2 | a0001c0008a0002c0005 | 4 | NA18945.hp2 NA18970.hp2 NA19080.hp2 others(1): Show |
synonymous_variant | LOW | c.2028T>C | p.Pro676Pro | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/14 | 2358/3384 | 2028/2190 | 676/729 | chr6 | 13625684 | ||
| chr6:13639576
|
G | A | 1 | a0001c0011 | 1 | NA19083.hp2 | synonymous_variant | LOW | c.1512C>T | p.Thr504Thr | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/14 | 1842/3384 | 1512/2190 | 504/729 | chr6 | 13639576 | ||
| chr6:13641213
|
G | C | 1 | a0001c0013 | 1 | NA18953.hp1 | synonymous_variant | LOW | c.1320C>G | p.Leu440Leu | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/14 | 1650/3384 | 1320/2190 | 440/729 | chr6 | 13641213 | ||
| chr6:13644583
|
G | A | 1 | a0001c0006 | 2 | HG01070.hp1 HG01071.hp2 |
synonymous_variant | LOW | c.1074C>T | p.Ile358Ile | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/14 | 1404/3384 | 1074/2190 | 358/729 | chr6 | 13644583 | ||
| chr6:13711044
|
G | C | 1 | a0001c0009 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.462C>G | p.Leu154Leu | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/14 | 792/3384 | 462/2190 | 154/729 | chr6 | 13711044 | ||
| chr6:13711047
|
A | G | 7 | a0001c0002a0001c0008a0001c0009others(4): Show | 147 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(144): Show |
synonymous_variant | LOW | c.459T>C | p.Arg153Arg | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/14 | 789/3384 | 459/2190 | 153/729 | chr6 | 13711047 | ||
| chr6:13711167
|
G | A | 1 | a0001c0014 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.339C>T | p.Gly113Gly | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/14 | 669/3384 | 339/2190 | 113/729 | chr6 | 13711167 | ||
| chr6:13711173
|
G | A | 1 | a0001c0015 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.333C>T | p.Gly111Gly | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/14 | 663/3384 | 333/2190 | 111/729 | chr6 | 13711173 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:13621737
|
C | T | 1 | a0001c0001t0009 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*625G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 14/14 | 625 | chr6 | 13621737 | |||||
| chr6:13621800
|
G | T | 1 | a0001c0001t0010 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*562C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 14/14 | 562 | chr6 | 13621800 | |||||
| chr6:13621900
|
T | TC | 6 | a0001c0001t0002a0001c0001t0010a0001c0002t0002others(3): Show | 79 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*461dupG | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 14/14 | 461 | chr6 | 13621900 | |||||
| chr6:13622051
|
C | T | 1 | a0001c0002t0008 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*311G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 14/14 | 311 | chr6 | 13622051 | |||||
| chr6:13622335
|
A | G | 2 | a0001c0001t0003a0001c0002t0003 | 6 | HG00609.hp1 HG01074.hp1 HG01496.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*27T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 14/14 | 27 | chr6 | 13622335 | |||||
| chr6:13711549
|
C | T | 1 | a0001c0001t0007 | 1 | NA18952.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/14 | 44 | chr6 | 13711549 | |||||
| chr6:13711639
|
G | A | 1 | a0001c0002t0005 | 3 | HG00544.hp1 HG02074.hp2 NA19012.hp2 |
5_prime_UTR_variant | MODIFIER | c.-134C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/14 | 134 | chr6 | 13711639 | |||||
| chr6:13711789
|
G | A | 2 | a0001c0002t0004a0001c0015t0004 | 6 | HG01261.hp2 HG01978.hp1 HG02004.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-284C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/14 | 284 | chr6 | 13711789 | |||||
| chr6:13711808
|
G | A | 1 | a0001c0002t0006 | 2 | HG01496.hp2 HG02055.hp1 |
5_prime_UTR_variant | MODIFIER | c.-303C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/14 | 303 | chr6 | 13711808 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:13622631
|
A | G | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2060-139T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13622631 | ||||||
| chr6:13622645
|
TGCC | T | 4 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0002t0001g0132others(1): Show | 4 | HG02055.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2060-156_2060-154d others(5): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13622645 | ||||||
| chr6:13622647
|
C | T | 1 | a0001c0001t0002g0290 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2060-155G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13622647 | ||||||
| chr6:13622737
|
T | G | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2060-245A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13622737 | ||||||
| chr6:13622865
|
T | C | 1 | a0001c0001t0002g0298 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2060-373A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13622865 | ||||||
| chr6:13623034
|
C | G | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2060-542G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623034 | ||||||
| chr6:13623092
|
T | C | 155 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(152): Show | 155 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.2060-600A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623092 | ||||||
| chr6:13623140
|
C | T | 6 | a0001c0002t0001g0123a0001c0002t0001g0125a0001c0002t0001g0126others(3): Show | 6 | HG01884.hp1 HG02809.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2060-648G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623140 | ||||||
| chr6:13623315
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2060-823T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623315 | ||||||
| chr6:13623377
|
G | C | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | HG01361.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2060-885C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623377 | ||||||
| chr6:13623488
|
A | C | 1 | a0001c0002t0001g0008 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2060-996T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623488 | ||||||
| chr6:13623489
|
AAAACAGG others(54): Show |
A | 1 | a0001c0002t0001g0008 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2060-1058_2060-998 others(64): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623489 | ||||||
| chr6:13623509
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2060-1017G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623509 | ||||||
| chr6:13623604
|
TA | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0247a0001c0001t0001g0252 | 3 | HG01258.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2060-1113delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623604 | ||||||
| chr6:13623627
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2060-1135G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623627 | ||||||
| chr6:13623698
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0267 | 2 | HG01169.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.2060-1206C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623698 | ||||||
| chr6:13623752
|
G | A | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2060-1260C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623752 | ||||||
| chr6:13623776
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2060-1284A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623776 | ||||||
| chr6:13623891
|
T | C | 1 | a0001c0001t0001g0296 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2060-1399A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13623891 | ||||||
| chr6:13624236
|
G | A | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2059+1417C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13624236 | ||||||
| chr6:13624303
|
G | C | 1 | a0001c0002t0001g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2059+1350C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13624303 | ||||||
| chr6:13624348
|
A | C | 156 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(153): Show | 156 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.2059+1305T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13624348 | ||||||
| chr6:13624513
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2059+1140G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13624513 | ||||||
| chr6:13624677
|
A | C | 1 | a0001c0001t0002g0195 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2059+976T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13624677 | ||||||
| chr6:13624683
|
C | T | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2059+970G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13624683 | ||||||
| chr6:13624689
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2059+964T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13624689 | ||||||
| chr6:13624734
|
G | C | 270 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0143others(267): Show | 270 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.2059+919C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13624734 | ||||||
| chr6:13624776
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0155 | 2 | HG00735.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2059+877G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13624776 | ||||||
| chr6:13624824
|
C | T | 1 | a0001c0001t0001g0309 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2059+829G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13624824 | ||||||
| chr6:13624872
|
C | T | 1 | a0003c0010t0001g0248 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2059+781G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13624872 | ||||||
| chr6:13624873
|
G | A | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2059+780C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13624873 | ||||||
| chr6:13624991
|
T | C | 1 | a0005c0012t0001g0328 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2059+662A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13624991 | ||||||
| chr6:13625181
|
A | G | 55 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0158others(52): Show | 55 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.2059+472T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13625181 | ||||||
| chr6:13625480
|
C | T | 353 | a0001c0001t0001g0001a0001c0001t0001g0135a0001c0001t0001g0136others(350): Show | 354 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(351): Show |
intron_variant | MODIFIER | c.2059+173G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 13/13 | chr6 | 13625480 | ||||||
| chr6:13625867
|
T | G | 1 | a0001c0002t0001g0025 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1948-103A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13625867 | ||||||
| chr6:13626449
|
T | C | 1 | a0001c0002t0001g0107 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1948-685A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13626449 | ||||||
| chr6:13626675
|
G | A | 6 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0172others(3): Show | 6 | HG01891.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1948-911C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13626675 | ||||||
| chr6:13626686
|
T | G | 6 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0172others(3): Show | 6 | HG01891.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1948-922A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13626686 | ||||||
| chr6:13626695
|
A | T | 1 | a0001c0002t0001g0078 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1948-931T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13626695 | ||||||
| chr6:13626714
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1948-950A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13626714 | ||||||
| chr6:13626828
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1948-1064C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13626828 | ||||||
| chr6:13626919
|
A | G | 56 | a0001c0001t0001g0135a0001c0001t0001g0178a0001c0001t0001g0222others(53): Show | 56 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1948-1155T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13626919 | ||||||
| chr6:13626994
|
C | T | 1 | a0001c0002t0002g0065 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1948-1230G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13626994 | ||||||
| chr6:13627014
|
C | T | 2 | a0001c0001t0001g0154a0001c0002t0001g0132 | 2 | HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1948-1250G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627014 | ||||||
| chr6:13627098
|
T | G | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0173 | 3 | HG02647.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1948-1334A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627098 | ||||||
| chr6:13627104
|
T | A | 1 | a0001c0001t0001g0314 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1948-1340A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627104 | ||||||
| chr6:13627252
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1948-1488C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627252 | ||||||
| chr6:13627257
|
T | C | 2 | a0001c0001t0001g0154a0001c0002t0001g0132 | 2 | HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1948-1493A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627257 | ||||||
| chr6:13627309
|
T | A | 1 | a0001c0001t0002g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1948-1545A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627309 | ||||||
| chr6:13627482
|
TAGTC | T | 4 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0002t0001g0008others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1948-1722_1948-171 others(8): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627482 | ||||||
| chr6:13627567
|
C | T | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0172others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1948-1803G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627567 | ||||||
| chr6:13627630
|
C | CA | 53 | a0001c0001t0001g0136a0001c0001t0001g0153a0001c0001t0001g0167others(50): Show | 53 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1948-1867dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627630 | ||||||
| chr6:13627630
|
C | CAAAAAAA others(3): Show |
1 | a0001c0002t0001g0103 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1948-1876_1948-186 others(14): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627630 | ||||||
| chr6:13627630
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0003g0311 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1948-1878_1948-186 others(16): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627630 | ||||||
| chr6:13627630
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0322a0001c0001t0003g0307a0001c0002t0001g0105others(1): Show | 4 | HG01070.hp1 HG03927.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1948-1879_1948-186 others(17): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627630 | ||||||
| chr6:13627630
|
C | CAAAAAAA others(7): Show |
8 | a0001c0001t0001g0306a0001c0001t0001g0318a0001c0001t0001g0320others(5): Show | 8 | HG00609.hp1 HG01071.hp2 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.1948-1880_1948-186 others(18): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627630 | ||||||
| chr6:13627630
|
C | CAAAAAAA others(8): Show |
12 | a0001c0001t0001g0219a0001c0001t0001g0308a0001c0001t0001g0309others(9): Show | 12 | HG00597.hp2 HG01981.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.1948-1881_1948-186 others(19): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627630 | ||||||
| chr6:13627630
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0313a0001c0001t0001g0317a0002c0003t0001g0346 | 3 | NA18941.hp2 NA18959.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1948-1882_1948-186 others(20): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627630 | ||||||
| chr6:13627630
|
CA | C | 6 | a0001c0001t0001g0247a0001c0001t0002g0253a0001c0001t0002g0298others(3): Show | 6 | HG00558.hp1 HG01517.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1948-1867delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627630 | ||||||
| chr6:13627655
|
T | C | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1948-1891A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627655 | ||||||
| chr6:13627660
|
T | G | 1 | a0001c0001t0002g0206 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1948-1896A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627660 | ||||||
| chr6:13627675
|
G | A | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1948-1911C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627675 | ||||||
| chr6:13627682
|
G | C | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1948-1918C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627682 | ||||||
| chr6:13627827
|
C | T | 143 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(140): Show | 143 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1948-2063G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627827 | ||||||
| chr6:13627844
|
G | A | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1948-2080C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627844 | ||||||
| chr6:13627872
|
CTTAAA | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0173 | 3 | HG02647.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1948-2113_1948-210 others(9): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627872 | ||||||
| chr6:13627928
|
A | G | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1948-2164T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13627928 | ||||||
| chr6:13628065
|
G | A | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1948-2301C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628065 | ||||||
| chr6:13628125
|
A | G | 274 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0143others(271): Show | 274 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.1948-2361T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628125 | ||||||
| chr6:13628128
|
T | G | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1948-2364A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628128 | ||||||
| chr6:13628165
|
C | T | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1948-2401G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628165 | ||||||
| chr6:13628181
|
G | A | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1948-2417C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628181 | ||||||
| chr6:13628203
|
CTAAA | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01891.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1948-2443_1948-244 others(8): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628203 | ||||||
| chr6:13628328
|
A | G | 357 | a0001c0001t0001g0001a0001c0001t0001g0135a0001c0001t0001g0136others(354): Show | 358 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(355): Show |
intron_variant | MODIFIER | c.1948-2564T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628328 | ||||||
| chr6:13628373
|
C | T | 1 | a0001c0002t0001g0013 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1948-2609G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628373 | ||||||
| chr6:13628629
|
T | TA | 4 | a0001c0001t0001g0149a0001c0001t0001g0155a0001c0002t0001g0129others(1): Show | 4 | HG00735.hp2 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1948-2866dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628629 | ||||||
| chr6:13628684
|
T | C | 3 | a0001c0002t0001g0019a0001c0002t0001g0059a0001c0002t0001g0063 | 3 | HG03688.hp2 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1948-2920A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628684 | ||||||
| chr6:13628692
|
C | T | 2 | a0001c0001t0002g0242a0001c0001t0002g0245 | 2 | HG03492.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1948-2928G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628692 | ||||||
| chr6:13628725
|
C | G | 4 | a0001c0001t0001g0279a0001c0002t0001g0004a0001c0002t0001g0005others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1948-2961G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628725 | ||||||
| chr6:13628941
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1948-3177A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628941 | ||||||
| chr6:13628970
|
A | C | 172 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(169): Show | 172 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1948-3206T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628970 | ||||||
| chr6:13628988
|
A | AT | 345 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(342): Show | 345 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(342): Show |
intron_variant | MODIFIER | c.1948-3225dupA | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13628988 | ||||||
| chr6:13629012
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1948-3248A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629012 | ||||||
| chr6:13629109
|
T | C | 1 | a0001c0002t0001g0038 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1947+3261A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629109 | ||||||
| chr6:13629115
|
CTTT | C | 47 | a0001c0001t0001g0156a0001c0001t0001g0168a0001c0002t0001g0011others(44): Show | 47 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1947+3252_1947+325 others(7): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629115 | ||||||
| chr6:13629274
|
C | A | 1 | a0001c0001t0002g0204 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1947+3096G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629274 | ||||||
| chr6:13629277
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1947+3093G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629277 | ||||||
| chr6:13629284
|
T | C | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0002t0001g0133 | 3 | HG02055.hp2 HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1947+3086A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629284 | ||||||
| chr6:13629285
|
T | C | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0002t0001g0133 | 3 | HG02055.hp2 HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1947+3085A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629285 | ||||||
| chr6:13629477
|
C | T | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1947+2893G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629477 | ||||||
| chr6:13629492
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1947+2878A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629492 | ||||||
| chr6:13629793
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1947+2577C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629793 | ||||||
| chr6:13629874
|
ATC | A | 4 | a0001c0001t0001g0279a0001c0002t0001g0004a0001c0002t0001g0005others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1947+2494_1947+249 others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629874 | ||||||
| chr6:13629895
|
GTC | G | 56 | a0001c0001t0001g0136a0001c0001t0001g0149a0001c0001t0001g0152others(53): Show | 56 | HG00323.hp2 HG00408.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1947+2473_1947+247 others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629895 | ||||||
| chr6:13629911
|
C | G | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1947+2459G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629911 | ||||||
| chr6:13629913
|
C | G | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1947+2457G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629913 | ||||||
| chr6:13629915
|
C | G | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1947+2455G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629915 | ||||||
| chr6:13629917
|
C | G | 4 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0002t0001g0004others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1947+2453G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629917 | ||||||
| chr6:13629918
|
T | G | 1 | a0001c0002t0001g0006 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1947+2452A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629918 | ||||||
| chr6:13629919
|
C | G | 2 | a0001c0002t0001g0004a0001c0002t0001g0117 | 2 | HG02109.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1947+2451G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629919 | ||||||
| chr6:13629919
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1947+2451G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629919 | ||||||
| chr6:13629919
|
CTCGT | C | 32 | a0001c0001t0001g0154a0001c0001t0002g0169a0001c0001t0002g0171others(29): Show | 32 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1947+2447_1947+245 others(8): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629919 | ||||||
| chr6:13629919
|
CTCGTGT | C | 3 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0325 | 3 | HG01361.hp1 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1947+2445_1947+245 others(10): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629919 | ||||||
| chr6:13629920
|
T | G | 14 | a0001c0001t0001g0138a0001c0001t0001g0256a0001c0001t0001g0320others(11): Show | 14 | HG00408.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1947+2450A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629920 | ||||||
| chr6:13629921
|
C | CGT | 108 | a0001c0001t0001g0001a0001c0001t0001g0135a0001c0001t0001g0143others(105): Show | 109 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1947+2447_1947+244 others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629921 | ||||||
| chr6:13629921
|
C | CGTGT | 50 | a0001c0001t0001g0231a0001c0001t0001g0243a0001c0001t0001g0282others(47): Show | 50 | HG00558.hp1 HG00741.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1947+2445_1947+244 others(8): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629921 | ||||||
| chr6:13629921
|
C | CGTGTGT | 4 | a0001c0002t0001g0005a0001c0002t0001g0078a0001c0002t0001g0098others(1): Show | 4 | HG02071.hp2 HG03239.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1947+2443_1947+244 others(10): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629921 | ||||||
| chr6:13629921
|
C | CTCGTGT | 12 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0276others(9): Show | 12 | HG02523.hp1 HG03486.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.1947+2448_1947+244 others(10): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629921 | ||||||
| chr6:13629921
|
C | T | 14 | a0001c0001t0001g0138a0001c0001t0001g0256a0001c0001t0001g0320others(11): Show | 14 | HG00408.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1947+2449G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629921 | ||||||
| chr6:13629921
|
CGT | C | 13 | a0001c0001t0002g0170a0001c0001t0002g0213a0001c0001t0002g0217others(10): Show | 13 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1947+2447_1947+244 others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629921 | ||||||
| chr6:13629922
|
G | T | 4 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 4 | HG01099.hp1 HG01891.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1947+2448C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629922 | ||||||
| chr6:13629923
|
T | C | 4 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 4 | HG01099.hp1 HG01891.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1947+2447A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13629923 | ||||||
| chr6:13630062
|
A | T | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1947+2308T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630062 | ||||||
| chr6:13630091
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01891.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1947+2279G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630091 | ||||||
| chr6:13630116
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1947+2254A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630116 | ||||||
| chr6:13630146
|
G | A | 11 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0154others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1947+2224C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630146 | ||||||
| chr6:13630162
|
T | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0154others(1): Show | 4 | HG02647.hp2 HG03579.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1947+2208A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630162 | ||||||
| chr6:13630263
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1947+2107T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630263 | ||||||
| chr6:13630288
|
T | A | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1947+2082A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630288 | ||||||
| chr6:13630518
|
T | TA | 156 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(153): Show | 156 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1947+1851dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630518 | ||||||
| chr6:13630575
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1947+1795C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630575 | ||||||
| chr6:13630632
|
T | G | 160 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(157): Show | 160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1947+1738A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630632 | ||||||
| chr6:13630729
|
C | T | 159 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(156): Show | 159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1947+1641G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630729 | ||||||
| chr6:13630753
|
G | C | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | HG01361.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1947+1617C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630753 | ||||||
| chr6:13630759
|
A | G | 1 | a0001c0002t0001g0095 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1947+1611T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630759 | ||||||
| chr6:13630800
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1947+1570G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13630800 | ||||||
| chr6:13631011
|
G | A | 3 | a0001c0002t0001g0019a0001c0002t0001g0059a0001c0002t0001g0063 | 3 | HG03688.hp2 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1947+1359C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13631011 | ||||||
| chr6:13631076
|
G | T | 1 | a0001c0002t0001g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1947+1294C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13631076 | ||||||
| chr6:13631080
|
A | T | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0002t0001g0133 | 3 | HG02055.hp2 HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1947+1290T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13631080 | ||||||
| chr6:13631099
|
C | T | 2 | a0001c0002t0001g0133a0002c0004t0001g0335 | 2 | HG02055.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1947+1271G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13631099 | ||||||
| chr6:13631323
|
A | C | 23 | a0001c0001t0002g0139a0001c0001t0002g0171a0001c0001t0002g0184others(20): Show | 23 | HG00738.hp1 HG01169.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1947+1047T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13631323 | ||||||
| chr6:13631463
|
T | C | 1 | a0001c0002t0008g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1947+907A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13631463 | ||||||
| chr6:13631477
|
G | A | 7 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0154others(4): Show | 7 | HG01891.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1947+893C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13631477 | ||||||
| chr6:13631517
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0173 | 3 | HG02647.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1947+853G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13631517 | ||||||
| chr6:13631542
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1947+828A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13631542 | ||||||
| chr6:13631554
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0173 | 3 | HG02647.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1947+816G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13631554 | ||||||
| chr6:13631616
|
T | C | 12 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0154others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1947+754A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13631616 | ||||||
| chr6:13631655
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1947+715T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13631655 | ||||||
| chr6:13631832
|
G | A | 1 | a0001c0002t0001g0082 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1947+538C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13631832 | ||||||
| chr6:13632118
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0295 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1947+242_1947+251d others(12): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(1): Show |
C | 13 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(10): Show | 13 | HG02486.hp1 HG02735.hp2 HG03209.hp2 others(10): Show |
intron_variant | MODIFIER | c.1947+244_1947+251d others(10): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(2): Show |
C | 20 | a0001c0001t0001g0219a0001c0001t0001g0246a0001c0001t0001g0277others(17): Show | 20 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.1947+243_1947+251d others(11): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(3): Show |
C | 28 | a0001c0001t0001g0285a0001c0001t0001g0306a0001c0001t0001g0309others(25): Show | 28 | HG00408.hp1 HG00558.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1947+242_1947+251d others(12): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(4): Show |
C | 17 | a0001c0001t0001g0319a0001c0001t0002g0211a0001c0001t0002g0281others(14): Show | 17 | HG01099.hp2 HG02074.hp2 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.1947+241_1947+251d others(13): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0002t0001g0077a0001c0002t0001g0112a0001c0008t0001g0115 | 3 | HG02071.hp2 HG02809.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1947+240_1947+251d others(14): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0251a0001c0006t0001g0220a0001c0006t0001g0221 | 3 | HG01070.hp1 HG01071.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1947+239_1947+251d others(15): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0257a0001c0001t0003g0305a0001c0009t0001g0134 | 3 | HG00558.hp2 HG00609.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1947+238_1947+251d others(16): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(10): Show |
C | 3 | a0001c0001t0001g0279a0001c0001t0001g0331a0001c0002t0001g0006 | 3 | HG01243.hp2 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1947+235_1947+251d others(19): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(11): Show |
C | 5 | a0001c0001t0001g0330a0001c0001t0002g0290a0001c0002t0001g0004others(2): Show | 5 | HG01346.hp2 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1947+234_1947+251d others(20): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(12): Show |
C | 14 | a0001c0001t0001g0256a0001c0001t0002g0180a0001c0001t0002g0184others(11): Show | 14 | HG00423.hp2 HG01192.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1947+233_1947+251d others(21): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(13): Show |
C | 81 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(78): Show | 81 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1947+232_1947+251d others(22): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(14): Show |
C | 82 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0148others(79): Show | 82 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1947+231_1947+251d others(23): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(15): Show |
C | 8 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0249others(5): Show | 8 | HG00544.hp2 NA18961.hp2 NA18992.hp2 others(5): Show |
intron_variant | MODIFIER | c.1947+230_1947+251d others(24): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(16): Show |
C | 7 | a0001c0001t0001g0174a0001c0001t0001g0230a0001c0001t0001g0258others(4): Show | 7 | HG00609.hp2 HG01192.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1947+229_1947+251d others(25): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(17): Show |
C | 8 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0173others(5): Show | 8 | HG01106.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1947+228_1947+251d others(26): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(18): Show |
C | 7 | a0001c0001t0001g0154a0001c0001t0001g0172a0001c0001t0001g0181others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1947+227_1947+251d others(27): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(19): Show |
C | 5 | a0001c0002t0001g0123a0001c0002t0001g0125a0001c0002t0001g0126others(2): Show | 5 | HG01884.hp1 HG02809.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1947+226_1947+251d others(28): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(20): Show |
C | 1 | a0001c0001t0001g0283 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1947+225_1947+251d others(29): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(22): Show |
C | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1947+223_1947+251d others(31): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(23): Show |
C | 1 | a0001c0001t0001g0271 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1947+222_1947+251d others(32): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(24): Show |
C | 4 | a0001c0001t0001g0262a0002c0005t0001g0343a0002c0005t0001g0344others(1): Show | 4 | HG01433.hp2 NA18945.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1947+221_1947+251d others(33): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(25): Show |
C | 7 | a0001c0001t0001g0135a0001c0001t0001g0263a0001c0001t0001g0280others(4): Show | 7 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1947+220_1947+251d others(34): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(26): Show |
C | 10 | a0001c0002t0001g0067a0001c0002t0001g0082a0001c0002t0001g0083others(7): Show | 10 | HG00741.hp2 HG01243.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1947+219_1947+251d others(35): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(27): Show |
C | 1 | a0001c0002t0001g0034 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1947+218_1947+251d others(36): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632118
|
CTTTTTTT others(29): Show |
C | 1 | a0001c0002t0002g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1947+216_1947+251d others(38): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 12/13 | chr6 | 13632118 | ||||||
| chr6:13632560
|
A | G | 1 | a0002c0003t0001g0338 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1796-39T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13632560 | ||||||
| chr6:13632838
|
T | TA | 140 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0152others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1796-318dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13632838 | ||||||
| chr6:13632838
|
T | TAA | 7 | a0001c0001t0001g0149a0001c0001t0002g0184a0001c0001t0002g0197others(4): Show | 7 | HG00735.hp2 HG00741.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1796-319_1796-318d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13632838 | ||||||
| chr6:13632838
|
TA | T | 6 | a0001c0001t0001g0225a0001c0002t0001g0078a0001c0002t0001g0093others(3): Show | 6 | HG01346.hp2 HG03239.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1796-318delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13632838 | ||||||
| chr6:13632838
|
TAAAA | T | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0154others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1796-321_1796-318d others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13632838 | ||||||
| chr6:13632882
|
A | T | 1 | a0002c0003t0001g0341 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1796-361T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13632882 | ||||||
| chr6:13632902
|
G | A | 1 | a0001c0002t0002g0065 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1796-381C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13632902 | ||||||
| chr6:13633037
|
A | T | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1796-516T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633037 | ||||||
| chr6:13633119
|
C | T | 1 | a0001c0002t0001g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1796-598G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633119 | ||||||
| chr6:13633145
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1796-624G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633145 | ||||||
| chr6:13633290
|
T | A | 135 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(132): Show | 135 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1796-769A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633290 | ||||||
| chr6:13633297
|
G | C | 1 | a0001c0002t0001g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1796-776C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633297 | ||||||
| chr6:13633324
|
A | G | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1796-803T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633324 | ||||||
| chr6:13633341
|
T | C | 1 | a0001c0002t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1796-820A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633341 | ||||||
| chr6:13633414
|
T | C | 345 | a0001c0001t0001g0001a0001c0001t0001g0135a0001c0001t0001g0136others(342): Show | 346 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(343): Show |
intron_variant | MODIFIER | c.1796-893A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633414 | ||||||
| chr6:13633417
|
C | T | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1796-896G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633417 | ||||||
| chr6:13633505
|
T | A | 1 | a0001c0002t0002g0065 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1795+926A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633505 | ||||||
| chr6:13633589
|
G | C | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1795+842C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633589 | ||||||
| chr6:13633806
|
A | T | 157 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0150others(154): Show | 157 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1795+625T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633806 | ||||||
| chr6:13633834
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1795+597A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633834 | ||||||
| chr6:13633840
|
G | A | 37 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0158others(34): Show | 37 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1795+591C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633840 | ||||||
| chr6:13633928
|
A | T | 1 | a0001c0001t0003g0311 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1795+503T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633928 | ||||||
| chr6:13633948
|
GT | G | 354 | a0001c0001t0001g0001a0001c0001t0001g0135a0001c0001t0001g0136others(351): Show | 355 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(352): Show |
intron_variant | MODIFIER | c.1795+482delA | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633948 | ||||||
| chr6:13633996
|
C | T | 1 | a0001c0001t0002g0202 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1795+435G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13633996 | ||||||
| chr6:13634008
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1795+423A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13634008 | ||||||
| chr6:13634024
|
C | T | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1795+407G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13634024 | ||||||
| chr6:13634059
|
GA | G | 270 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0143others(267): Show | 270 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1795+371delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13634059 | ||||||
| chr6:13634193
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1795+238G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 11/13 | chr6 | 13634193 | ||||||
| chr6:13634750
|
C | T | 157 | a0001c0001t0001g0138a0001c0001t0001g0143a0001c0001t0001g0144others(154): Show | 157 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1674-198G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13634750 | ||||||
| chr6:13634830
|
T | G | 2 | a0001c0002t0001g0073a0001c0002t0001g0103 | 2 | NA19074.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1674-278A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13634830 | ||||||
| chr6:13634879
|
A | AG | 4 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0173others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1674-328_1674-327i others(3): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13634879 | ||||||
| chr6:13635014
|
G | A | 3 | a0001c0001t0002g0171a0001c0001t0002g0281a0001c0001t0002g0287 | 3 | HG02155.hp2 HG02523.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1674-462C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13635014 | ||||||
| chr6:13635072
|
T | G | 43 | a0001c0001t0001g0219a0001c0001t0001g0306a0001c0001t0001g0308others(40): Show | 43 | HG00597.hp2 HG00609.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.1674-520A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13635072 | ||||||
| chr6:13635242
|
C | A | 1 | a0001c0002t0001g0082 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1674-690G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13635242 | ||||||
| chr6:13635485
|
T | C | 6 | a0001c0001t0002g0303a0001c0001t0002g0304a0001c0001t0002g0325others(3): Show | 6 | HG00741.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1674-933A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13635485 | ||||||
| chr6:13635487
|
T | C | 3 | a0001c0002t0001g0019a0001c0002t0001g0059a0001c0002t0001g0063 | 3 | HG03688.hp2 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1674-935A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13635487 | ||||||
| chr6:13635499
|
G | GA | 25 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0152others(22): Show | 25 | HG01069.hp2 HG01175.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1674-948dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13635499 | ||||||
| chr6:13635618
|
T | TA | 10 | a0001c0001t0001g0155a0001c0001t0002g0212a0001c0002t0001g0015others(7): Show | 10 | HG01074.hp2 HG01192.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.1674-1067dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13635618 | ||||||
| chr6:13635618
|
TA | T | 7 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1674-1067delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13635618 | ||||||
| chr6:13635819
|
T | C | 2 | a0001c0001t0002g0304a0001c0002t0002g0122 | 2 | HG00741.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1674-1267A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13635819 | ||||||
| chr6:13635906
|
G | A | 12 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0159others(9): Show | 12 | HG01069.hp2 HG01175.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1674-1354C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13635906 | ||||||
| chr6:13636594
|
AT | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1673+1213delA | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13636594 | ||||||
| chr6:13636711
|
T | C | 26 | a0001c0001t0001g0219a0001c0001t0001g0306a0001c0001t0001g0308others(23): Show | 26 | HG00597.hp2 HG00609.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1673+1097A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13636711 | ||||||
| chr6:13636761
|
C | T | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1673+1047G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13636761 | ||||||
| chr6:13637124
|
G | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0229 | 2 | HG00673.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1673+684C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13637124 | ||||||
| chr6:13637161
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1673+647A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13637161 | ||||||
| chr6:13637331
|
A | G | 1 | a0005c0012t0001g0328 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1673+477T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13637331 | ||||||
| chr6:13637382
|
CA | C | 133 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(130): Show | 133 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1673+425delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13637382 | ||||||
| chr6:13637401
|
G | C | 1 | a0002c0003t0001g0340 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1673+407C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13637401 | ||||||
| chr6:13637584
|
A | G | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1673+224T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13637584 | ||||||
| chr6:13637668
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1673+140G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13637668 | ||||||
| chr6:13637669
|
G | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1673+139C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 10/13 | chr6 | 13637669 | ||||||
| chr6:13637990
|
A | T | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1526-35T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13637990 | ||||||
| chr6:13638011
|
T | C | 125 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(122): Show | 125 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1526-56A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13638011 | ||||||
| chr6:13638219
|
T | G | 42 | a0001c0001t0001g0135a0001c0001t0001g0222a0001c0001t0001g0227others(39): Show | 42 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1526-264A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13638219 | ||||||
| chr6:13638422
|
A | C | 1 | a0001c0001t0001g0174 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1526-467T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13638422 | ||||||
| chr6:13638752
|
A | G | 253 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0143others(250): Show | 253 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.1526-797T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13638752 | ||||||
| chr6:13638829
|
G | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1525+734C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13638829 | ||||||
| chr6:13638860
|
G | T | 6 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1525+703C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13638860 | ||||||
| chr6:13639009
|
C | G | 13 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0157others(10): Show | 13 | HG01069.hp2 HG01175.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1525+554G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13639009 | ||||||
| chr6:13639016
|
T | C | 1 | a0001c0001t0002g0198 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1525+547A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13639016 | ||||||
| chr6:13639089
|
C | G | 3 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0035 | 3 | NA18941.hp1 NA18957.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1525+474G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13639089 | ||||||
| chr6:13639124
|
T | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01891.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1525+439A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13639124 | ||||||
| chr6:13639395
|
G | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1525+168C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13639395 | ||||||
| chr6:13639445
|
T | C | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1525+118A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13639445 | ||||||
| chr6:13639468
|
G | A | 128 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(125): Show | 128 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1525+95C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13639468 | ||||||
| chr6:13639543
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1525+20A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13639543 | ||||||
| chr6:13639544
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1525+19C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 9/13 | chr6 | 13639544 | ||||||
| chr6:13639891
|
A | T | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1335-138T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13639891 | ||||||
| chr6:13639916
|
G | C | 1 | a0001c0001t0007g0002 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1335-163C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13639916 | ||||||
| chr6:13639977
|
C | G | 7 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1335-224G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13639977 | ||||||
| chr6:13640131
|
T | C | 4 | a0001c0001t0002g0213a0001c0001t0002g0217a0001c0001t0002g0218others(1): Show | 4 | HG02027.hp2 HG02080.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1335-378A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13640131 | ||||||
| chr6:13640187
|
C | A | 1 | a0001c0002t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1335-434G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13640187 | ||||||
| chr6:13640213
|
C | T | 5 | a0001c0002t0001g0107a0001c0002t0001g0108a0001c0002t0001g0109others(2): Show | 5 | HG01192.hp2 HG01346.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1335-460G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13640213 | ||||||
| chr6:13640223
|
C | A | 1 | a0005c0012t0001g0328 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1335-470G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13640223 | ||||||
| chr6:13640265
|
G | A | 2 | a0001c0001t0002g0183a0001c0001t0002g0187 | 2 | HG00673.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1335-512C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13640265 | ||||||
| chr6:13640450
|
T | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1335-697A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13640450 | ||||||
| chr6:13640497
|
A | G | 1 | a0001c0002t0001g0075 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1334+702T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13640497 | ||||||
| chr6:13640604
|
A | G | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334+595T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13640604 | ||||||
| chr6:13640689
|
A | C | 1 | a0001c0002t0001g0022 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1334+510T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13640689 | ||||||
| chr6:13640700
|
T | C | 1 | a0001c0002t0008g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1334+499A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13640700 | ||||||
| chr6:13641003
|
A | C | 1 | a0001c0002t0001g0068 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1334+196T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 8/13 | chr6 | 13641003 | ||||||
| chr6:13641507
|
G | T | 135 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(132): Show | 135 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1226-200C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 7/13 | chr6 | 13641507 | ||||||
| chr6:13641515
|
AT | A | 66 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0285others(63): Show | 66 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1226-209delA | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 7/13 | chr6 | 13641515 | ||||||
| chr6:13641600
|
A | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1226-293T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 7/13 | chr6 | 13641600 | ||||||
| chr6:13641796
|
A | C | 2 | a0001c0002t0001g0012a0001c0002t0001g0038 | 2 | NA19000.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1226-489T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 7/13 | chr6 | 13641796 | ||||||
| chr6:13641803
|
G | A | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1226-496C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 7/13 | chr6 | 13641803 | ||||||
| chr6:13642437
|
A | G | 1 | a0001c0002t0001g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1225+42T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 7/13 | chr6 | 13642437 | ||||||
| chr6:13642444
|
A | T | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225+35T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 7/13 | chr6 | 13642444 | ||||||
| chr6:13642690
|
C | T | 64 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0285others(61): Show | 64 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1113-99G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13642690 | ||||||
| chr6:13642746
|
G | A | 1 | a0001c0002t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1113-155C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13642746 | ||||||
| chr6:13642767
|
T | C | 87 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0152others(84): Show | 87 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1113-176A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13642767 | ||||||
| chr6:13642801
|
G | A | 1 | a0001c0002t0001g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1113-210C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13642801 | ||||||
| chr6:13643059
|
G | A | 7 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0243others(4): Show | 7 | HG01123.hp1 HG01346.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113-468C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13643059 | ||||||
| chr6:13643219
|
T | C | 2 | a0001c0002t0001g0034a0001c0002t0001g0036 | 2 | HG00438.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1113-628A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13643219 | ||||||
| chr6:13643372
|
G | A | 66 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(63): Show | 66 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1113-781C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13643372 | ||||||
| chr6:13643513
|
A | G | 1 | a0001c0008t0001g0115 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1113-922T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13643513 | ||||||
| chr6:13643554
|
G | A | 1 | a0001c0002t0003g0026 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1113-963C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13643554 | ||||||
| chr6:13643567
|
A | G | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1113-976T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13643567 | ||||||
| chr6:13643603
|
A | G | 2 | a0001c0002t0001g0016a0001c0002t0001g0042 | 2 | HG01975.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1112+942T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13643603 | ||||||
| chr6:13643769
|
G | A | 6 | a0001c0001t0002g0303a0001c0001t0002g0304a0001c0001t0002g0325others(3): Show | 6 | HG00741.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1112+776C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13643769 | ||||||
| chr6:13643779
|
T | C | 1 | a0001c0002t0001g0107 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1112+766A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13643779 | ||||||
| chr6:13643786
|
T | A | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1112+759A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13643786 | ||||||
| chr6:13643835
|
T | C | 2 | a0001c0001t0001g0282a0001c0002t0001g0078 | 2 | HG01106.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1112+710A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13643835 | ||||||
| chr6:13643928
|
T | C | 125 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(122): Show | 125 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1112+617A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13643928 | ||||||
| chr6:13644039
|
G | T | 2 | a0001c0002t0001g0044a0001c0002t0001g0050 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1112+506C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13644039 | ||||||
| chr6:13644194
|
T | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1112+351A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13644194 | ||||||
| chr6:13644286
|
G | A | 4 | a0002c0003t0001g0340a0002c0005t0001g0343a0002c0005t0001g0344others(1): Show | 4 | HG02486.hp2 NA18945.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1112+259C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13644286 | ||||||
| chr6:13644294
|
A | T | 1 | a0001c0001t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1112+251T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 6/13 | chr6 | 13644294 | ||||||
| chr6:13644998
|
C | T | 64 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0285others(61): Show | 64 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.928-269G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13644998 | ||||||
| chr6:13645105
|
C | T | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.928-376G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13645105 | ||||||
| chr6:13645403
|
C | G | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG03209.hp2 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.928-674G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13645403 | ||||||
| chr6:13645639
|
C | T | 7 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(4): Show | 7 | HG01884.hp1 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.928-910G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13645639 | ||||||
| chr6:13645661
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.928-932C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13645661 | ||||||
| chr6:13645779
|
A | G | 1 | a0001c0014t0001g0333 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.928-1050T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13645779 | ||||||
| chr6:13645827
|
A | G | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.928-1098T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13645827 | ||||||
| chr6:13645850
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.928-1121A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13645850 | ||||||
| chr6:13646301
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.928-1572G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13646301 | ||||||
| chr6:13646761
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.928-2032T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13646761 | ||||||
| chr6:13646798
|
C | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.928-2069G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13646798 | ||||||
| chr6:13646945
|
C | T | 1 | a0001c0002t0001g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.928-2216G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13646945 | ||||||
| chr6:13647132
|
T | C | 24 | a0001c0001t0002g0139a0001c0001t0002g0141a0001c0001t0002g0142others(21): Show | 24 | HG00738.hp1 HG01169.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.928-2403A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13647132 | ||||||
| chr6:13647225
|
A | C | 1 | a0002c0003t0001g0338 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.928-2496T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13647225 | ||||||
| chr6:13647506
|
A | G | 4 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(1): Show | 4 | HG00673.hp1 HG02080.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-2777T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13647506 | ||||||
| chr6:13647522
|
G | A | 7 | a0001c0001t0001g0222a0001c0001t0001g0250a0001c0001t0001g0273others(4): Show | 7 | HG02056.hp1 NA18747.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.928-2793C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13647522 | ||||||
| chr6:13647536
|
T | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.928-2807A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13647536 | ||||||
| chr6:13647603
|
G | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0173 | 3 | HG02647.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.928-2874C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13647603 | ||||||
| chr6:13647731
|
C | T | 1 | a0001c0002t0001g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.928-3002G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13647731 | ||||||
| chr6:13647801
|
C | A | 1 | a0001c0002t0004g0356 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.928-3072G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13647801 | ||||||
| chr6:13647815
|
T | C | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.928-3086A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13647815 | ||||||
| chr6:13648037
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.928-3308G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13648037 | ||||||
| chr6:13648039
|
T | C | 1 | a0002c0003t0001g0338 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.928-3310A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13648039 | ||||||
| chr6:13648141
|
G | GT | 67 | a0001c0001t0001g0157a0001c0001t0001g0166a0001c0001t0001g0167others(64): Show | 67 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.928-3413dupA | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13648141 | ||||||
| chr6:13648141
|
G | GTT | 17 | a0001c0001t0002g0183a0001c0001t0002g0185a0001c0001t0002g0187others(14): Show | 17 | HG00597.hp1 HG00673.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.928-3414_928-3413d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13648141 | ||||||
| chr6:13648141
|
G | GTTTTTTT others(3): Show |
1 | a0001c0002t0001g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.928-3422_928-3413d others(12): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13648141 | ||||||
| chr6:13648141
|
GT | G | 84 | a0001c0001t0001g0138a0001c0001t0001g0143a0001c0001t0001g0144others(81): Show | 84 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.928-3413delA | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13648141 | ||||||
| chr6:13648141
|
GTT | G | 30 | a0001c0001t0001g0136a0001c0001t0001g0150a0001c0001t0001g0151others(27): Show | 30 | HG00738.hp1 HG01169.hp1 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.928-3414_928-3413d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13648141 | ||||||
| chr6:13648333
|
A | G | 1 | a0001c0002t0001g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.928-3604T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13648333 | ||||||
| chr6:13648632
|
A | C | 37 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(34): Show | 37 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.928-3903T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13648632 | ||||||
| chr6:13648712
|
T | G | 1 | a0001c0001t0001g0291 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.927+3947A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13648712 | ||||||
| chr6:13648937
|
T | A | 1 | a0001c0001t0001g0309 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.927+3722A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13648937 | ||||||
| chr6:13649055
|
G | A | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.927+3604C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649055 | ||||||
| chr6:13649125
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.927+3534T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649125 | ||||||
| chr6:13649260
|
A | G | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.927+3399T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649260 | ||||||
| chr6:13649461
|
G | GA | 28 | a0001c0001t0001g0145a0001c0001t0001g0219a0001c0001t0001g0306others(25): Show | 28 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.927+3197dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649461 | ||||||
| chr6:13649461
|
GA | G | 136 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.927+3197delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649461 | ||||||
| chr6:13649461
|
GAA | G | 6 | a0001c0001t0001g0155a0001c0001t0001g0179a0001c0002t0001g0004others(3): Show | 6 | HG00639.hp2 HG01069.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+3196_927+3197d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649461 | ||||||
| chr6:13649463
|
A | G | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.927+3196T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649463 | ||||||
| chr6:13649492
|
T | C | 136 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.927+3167A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649492 | ||||||
| chr6:13649513
|
A | C | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.927+3146T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649513 | ||||||
| chr6:13649530
|
C | G | 63 | a0001c0001t0001g0156a0001c0001t0001g0168a0001c0001t0001g0178others(60): Show | 63 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.927+3129G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649530 | ||||||
| chr6:13649737
|
G | A | 4 | a0002c0003t0001g0340a0002c0005t0001g0343a0002c0005t0001g0344others(1): Show | 4 | HG02486.hp2 NA18945.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+2922C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649737 | ||||||
| chr6:13649798
|
C | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.927+2861G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649798 | ||||||
| chr6:13649888
|
A | T | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | NA18993.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.927+2771T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649888 | ||||||
| chr6:13649944
|
C | T | 1 | a0001c0001t0001g0323 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.927+2715G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13649944 | ||||||
| chr6:13650273
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.927+2386A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13650273 | ||||||
| chr6:13650298
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.927+2361C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13650298 | ||||||
| chr6:13650459
|
C | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.927+2200G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13650459 | ||||||
| chr6:13650541
|
G | T | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.927+2118C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13650541 | ||||||
| chr6:13650582
|
G | A | 1 | a0001c0001t0002g0268 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.927+2077C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13650582 | ||||||
| chr6:13650731
|
G | A | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.927+1928C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13650731 | ||||||
| chr6:13650739
|
C | T | 134 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(131): Show | 134 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.927+1920G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13650739 | ||||||
| chr6:13650772
|
C | G | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.927+1887G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13650772 | ||||||
| chr6:13650783
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.927+1876G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13650783 | ||||||
| chr6:13651200
|
T | C | 1 | a0001c0001t0001g0285 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.927+1459A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651200 | ||||||
| chr6:13651245
|
T | C | 1 | a0001c0009t0001g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.927+1414A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651245 | ||||||
| chr6:13651345
|
T | C | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+1314A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651345 | ||||||
| chr6:13651389
|
GTT | G | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.927+1268_927+1269d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651389 | ||||||
| chr6:13651402
|
GT | G | 232 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0143others(229): Show | 232 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.927+1256delA | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651402 | ||||||
| chr6:13651403
|
T | G | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.927+1256A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651403 | ||||||
| chr6:13651505
|
C | T | 1 | a0005c0012t0001g0328 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.927+1154G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651505 | ||||||
| chr6:13651539
|
C | T | 1 | a0001c0001t0002g0215 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.927+1120G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651539 | ||||||
| chr6:13651602
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.927+1057C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651602 | ||||||
| chr6:13651652
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.927+1007C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651652 | ||||||
| chr6:13651774
|
C | T | 129 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(126): Show | 129 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.927+885G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651774 | ||||||
| chr6:13651794
|
C | CA | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.927+864dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651794 | ||||||
| chr6:13651911
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0138 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.927+748G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651911 | ||||||
| chr6:13651931
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.927+728A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651931 | ||||||
| chr6:13651944
|
T | C | 5 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG01891.hp1 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+715A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13651944 | ||||||
| chr6:13652060
|
C | A | 1 | a0001c0001t0001g0292 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.927+599G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13652060 | ||||||
| chr6:13652175
|
A | C | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.927+484T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13652175 | ||||||
| chr6:13652178
|
T | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.927+481A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13652178 | ||||||
| chr6:13652337
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.927+322G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 5/13 | chr6 | 13652337 | ||||||
| chr6:13652863
|
G | A | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.905-182C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13652863 | ||||||
| chr6:13653057
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.905-376C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653057 | ||||||
| chr6:13653100
|
C | G | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-419G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653100 | ||||||
| chr6:13653207
|
G | T | 1 | a0001c0002t0001g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.905-526C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653207 | ||||||
| chr6:13653216
|
G | A | 2 | a0001c0002t0001g0100a0001c0002t0001g0110 | 2 | NA19000.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.905-535C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653216 | ||||||
| chr6:13653276
|
T | C | 29 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0002g0139others(26): Show | 29 | HG00423.hp2 HG00738.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.905-595A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653276 | ||||||
| chr6:13653334
|
G | A | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.905-653C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653334 | ||||||
| chr6:13653337
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0237 | 2 | HG02080.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.905-656T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653337 | ||||||
| chr6:13653388
|
C | T | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-707G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653388 | ||||||
| chr6:13653444
|
A | T | 3 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0106 | 3 | HG02559.hp2 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.905-763T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653444 | ||||||
| chr6:13653467
|
G | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.905-786C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653467 | ||||||
| chr6:13653653
|
G | A | 1 | a0001c0002t0008g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.905-972C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653653 | ||||||
| chr6:13653937
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1256T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653937 | ||||||
| chr6:13653940
|
T | C | 1 | a0001c0002t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-1259A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653940 | ||||||
| chr6:13653964
|
G | T | 1 | a0001c0002t0001g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.905-1283C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13653964 | ||||||
| chr6:13654009
|
T | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.905-1328A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13654009 | ||||||
| chr6:13654420
|
A | G | 9 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-1739T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13654420 | ||||||
| chr6:13654540
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.905-1859C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13654540 | ||||||
| chr6:13654563
|
C | T | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.905-1882G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13654563 | ||||||
| chr6:13654566
|
T | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.905-1885A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13654566 | ||||||
| chr6:13655008
|
G | A | 1 | a0001c0002t0001g0029 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.904+2101C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13655008 | ||||||
| chr6:13655064
|
C | T | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.904+2045G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13655064 | ||||||
| chr6:13655080
|
TA | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.904+2028delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13655080 | ||||||
| chr6:13655107
|
A | G | 34 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(31): Show | 34 | HG00423.hp2 HG00735.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.904+2002T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13655107 | ||||||
| chr6:13655199
|
C | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.904+1910G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13655199 | ||||||
| chr6:13655210
|
G | A | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.904+1899C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13655210 | ||||||
| chr6:13655384
|
T | C | 134 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(131): Show | 134 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.904+1725A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13655384 | ||||||
| chr6:13655415
|
C | T | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.904+1694G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13655415 | ||||||
| chr6:13655564
|
T | C | 2 | a0001c0001t0002g0183a0001c0001t0002g0187 | 2 | HG00673.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.904+1545A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13655564 | ||||||
| chr6:13655602
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.904+1507A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13655602 | ||||||
| chr6:13655679
|
A | G | 1 | a0001c0001t0002g0186 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.904+1430T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13655679 | ||||||
| chr6:13655826
|
A | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.904+1283T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13655826 | ||||||
| chr6:13656263
|
C | T | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.904+846G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13656263 | ||||||
| chr6:13656401
|
T | TA | 8 | a0001c0002t0001g0067a0001c0002t0001g0085a0001c0002t0001g0087others(5): Show | 8 | HG00741.hp2 HG01255.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.904+707dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13656401 | ||||||
| chr6:13656401
|
TA | T | 68 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.904+707delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13656401 | ||||||
| chr6:13656402
|
A | T | 1 | a0001c0001t0001g0230 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.904+707T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13656402 | ||||||
| chr6:13656451
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.904+658A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13656451 | ||||||
| chr6:13656458
|
G | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.904+651C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13656458 | ||||||
| chr6:13656518
|
T | C | 7 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(4): Show | 7 | HG01884.hp1 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.904+591A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13656518 | ||||||
| chr6:13656808
|
G | A | 129 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(126): Show | 129 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.904+301C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13656808 | ||||||
| chr6:13656809
|
T | C | 1 | a0001c0002t0001g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.904+300A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13656809 | ||||||
| chr6:13656896
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.904+213T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 4/13 | chr6 | 13656896 | ||||||
| chr6:13657413
|
A | T | 1 | a0001c0002t0001g0005 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.737-137T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 3/13 | chr6 | 13657413 | ||||||
| chr6:13657418
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.737-142A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 3/13 | chr6 | 13657418 | ||||||
| chr6:13657579
|
C | T | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.737-303G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 3/13 | chr6 | 13657579 | ||||||
| chr6:13657644
|
A | C | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.737-368T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 3/13 | chr6 | 13657644 | ||||||
| chr6:13657722
|
T | C | 1 | a0001c0001t0001g0285 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.737-446A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 3/13 | chr6 | 13657722 | ||||||
| chr6:13657786
|
A | G | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.737-510T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 3/13 | chr6 | 13657786 | ||||||
| chr6:13658275
|
A | G | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(18): Show | 21 | HG01069.hp2 HG01175.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.736+505T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 3/13 | chr6 | 13658275 | ||||||
| chr6:13658277
|
AT | A | 119 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(116): Show | 119 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.736+502delA | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 3/13 | chr6 | 13658277 | ||||||
| chr6:13658566
|
C | T | 129 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(126): Show | 129 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.736+214G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 3/13 | chr6 | 13658566 | ||||||
| chr6:13658570
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.736+210T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 3/13 | chr6 | 13658570 | ||||||
| chr6:13658578
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.736+202G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 3/13 | chr6 | 13658578 | ||||||
| chr6:13658661
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG02451.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.736+119T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 3/13 | chr6 | 13658661 | ||||||
| chr6:13658736
|
A | T | 27 | a0001c0001t0001g0219a0001c0001t0001g0306a0001c0001t0001g0308others(24): Show | 27 | HG00597.hp2 HG00609.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.736+44T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 3/13 | chr6 | 13658736 | ||||||
| chr6:13658847
|
T | G | 256 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(253): Show | 256 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.684-15A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13658847 | ||||||
| chr6:13659062
|
A | G | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.684-230T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659062 | ||||||
| chr6:13659076
|
C | T | 3 | a0002c0005t0001g0343a0002c0005t0001g0344a0002c0005t0001g0345 | 3 | NA18945.hp2 NA18970.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.684-244G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659076 | ||||||
| chr6:13659232
|
A | C | 1 | a0001c0001t0002g0216 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.684-400T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659232 | ||||||
| chr6:13659239
|
ACC | A | 7 | a0001c0001t0001g0257a0001c0001t0001g0259a0001c0001t0001g0260others(4): Show | 7 | HG00558.hp2 HG02486.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.684-409_684-408del others(2): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659239 | ||||||
| chr6:13659240
|
CCCCA | C | 10 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0238others(7): Show | 10 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(7): Show |
intron_variant | MODIFIER | c.684-412_684-409del others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659240 | ||||||
| chr6:13659240
|
CCCCACA | C | 7 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0250others(4): Show | 7 | HG00639.hp1 HG02165.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.684-414_684-409del others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659240 | ||||||
| chr6:13659240
|
CCCCACAC others(1): Show |
C | 10 | a0001c0001t0001g0228a0001c0001t0001g0237a0001c0001t0001g0239others(7): Show | 10 | HG01123.hp1 HG01952.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.684-416_684-409del others(8): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659240 | ||||||
| chr6:13659240
|
CCCCACAC others(3): Show |
C | 4 | a0001c0001t0001g0135a0001c0001t0001g0251a0001c0001t0001g0324others(1): Show | 4 | HG00738.hp2 HG01361.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.684-418_684-409del others(10): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659240 | ||||||
| chr6:13659242
|
C | A | 3 | a0001c0001t0001g0291a0001c0001t0001g0294a0003c0010t0001g0248 | 3 | HG03669.hp1 NA18747.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.684-410G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659242 | ||||||
| chr6:13659244
|
A | C | 4 | a0001c0002t0001g0116a0001c0002t0001g0129a0001c0002t0001g0130others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.684-412T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659244 | ||||||
| chr6:13659246
|
A | C | 2 | a0001c0002t0001g0129a0001c0002t0001g0130 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.684-414T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659246 | ||||||
| chr6:13659251
|
CACACAT | C | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0256 | 3 | NA18522.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.684-425_684-420del others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659251 | ||||||
| chr6:13659257
|
T | C | 42 | a0001c0001t0001g0135a0001c0001t0001g0224a0001c0001t0001g0227others(39): Show | 42 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.684-425A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659257 | ||||||
| chr6:13659257
|
T | TAC | 17 | a0001c0001t0001g0264a0001c0001t0001g0267a0001c0001t0001g0295others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.684-427_684-426dup others(2): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659257 | ||||||
| chr6:13659257
|
T | TACAC | 24 | a0001c0001t0001g0147a0001c0001t0001g0219a0001c0001t0001g0300others(21): Show | 24 | HG00099.hp1 HG00597.hp2 HG01981.hp2 others(21): Show |
intron_variant | MODIFIER | c.684-429_684-426dup others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659257 | ||||||
| chr6:13659257
|
T | TACACAC | 3 | a0001c0001t0001g0148a0001c0002t0001g0123a0002c0003t0001g0347 | 3 | HG01884.hp1 HG03453.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.684-431_684-426dup others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659257 | ||||||
| chr6:13659257
|
T | TACACACA others(1): Show |
3 | a0001c0001t0003g0305a0001c0001t0003g0307a0001c0002t0001g0132 | 3 | HG00609.hp1 HG03927.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.684-433_684-426dup others(8): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659257 | ||||||
| chr6:13659257
|
T | TACACACA others(3): Show |
4 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0127others(1): Show | 4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.684-435_684-426dup others(10): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659257 | ||||||
| chr6:13659257
|
T | TACACACA others(5): Show |
2 | a0001c0002t0001g0124a0001c0002t0001g0128 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.684-437_684-426dup others(12): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659257 | ||||||
| chr6:13659257
|
TAC | T | 85 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(82): Show | 85 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.684-427_684-426del others(2): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659257 | ||||||
| chr6:13659257
|
TACAC | T | 52 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(49): Show | 52 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.684-429_684-426del others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659257 | ||||||
| chr6:13659257
|
TACACAC | T | 17 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0159others(14): Show | 17 | HG01069.hp2 HG01175.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.684-431_684-426del others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659257 | ||||||
| chr6:13659257
|
TACACACA others(1): Show |
T | 4 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.684-433_684-426del others(8): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659257 | ||||||
| chr6:13659257
|
TACACACA others(3): Show |
T | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.684-435_684-426del others(10): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659257 | ||||||
| chr6:13659294
|
A | G | 9 | a0001c0002t0001g0023a0001c0002t0001g0029a0001c0002t0001g0031others(6): Show | 9 | HG00438.hp2 HG02165.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.684-462T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659294 | ||||||
| chr6:13659376
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.684-544A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659376 | ||||||
| chr6:13659455
|
T | C | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.684-623A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659455 | ||||||
| chr6:13659494
|
T | G | 80 | a0001c0001t0001g0222a0001c0001t0001g0282a0001c0001t0001g0283others(77): Show | 80 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.684-662A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659494 | ||||||
| chr6:13659684
|
T | C | 2 | a0001c0001t0002g0199a0001c0001t0002g0203 | 2 | HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.684-852A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659684 | ||||||
| chr6:13659712
|
C | G | 26 | a0001c0001t0002g0139a0001c0001t0002g0141a0001c0001t0002g0142others(23): Show | 26 | HG00423.hp2 HG00738.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.684-880G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659712 | ||||||
| chr6:13659795
|
G | A | 7 | a0001c0001t0001g0249a0001c0001t0001g0259a0001c0001t0001g0260others(4): Show | 7 | HG00544.hp2 NA18952.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.684-963C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13659795 | ||||||
| chr6:13660103
|
T | C | 1 | a0001c0001t0001g0285 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.684-1271A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13660103 | ||||||
| chr6:13660118
|
A | G | 1 | a0001c0001t0003g0311 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.684-1286T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13660118 | ||||||
| chr6:13660399
|
TGTGGGGG others(6): Show |
T | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.684-1580_684-1568d others(15): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13660399 | ||||||
| chr6:13660501
|
G | A | 2 | a0001c0002t0001g0100a0001c0002t0001g0110 | 2 | NA19000.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.684-1669C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13660501 | ||||||
| chr6:13660765
|
G | T | 2 | a0001c0002t0001g0129a0001c0002t0001g0130 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.684-1933C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13660765 | ||||||
| chr6:13660982
|
G | C | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | NA18993.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.684-2150C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13660982 | ||||||
| chr6:13661038
|
T | C | 67 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.684-2206A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13661038 | ||||||
| chr6:13661150
|
T | C | 1 | a0001c0002t0001g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.684-2318A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13661150 | ||||||
| chr6:13661290
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.684-2458G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13661290 | ||||||
| chr6:13661319
|
A | T | 26 | a0001c0001t0002g0139a0001c0001t0002g0141a0001c0001t0002g0142others(23): Show | 26 | HG00423.hp2 HG00738.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.684-2487T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13661319 | ||||||
| chr6:13661731
|
A | C | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.684-2899T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13661731 | ||||||
| chr6:13661802
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0173 | 3 | HG02647.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.684-2970G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13661802 | ||||||
| chr6:13661901
|
C | T | 65 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.684-3069G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13661901 | ||||||
| chr6:13662088
|
G | C | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.684-3256C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13662088 | ||||||
| chr6:13662461
|
G | A | 1 | a0001c0002t0001g0007 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.684-3629C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13662461 | ||||||
| chr6:13662631
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.684-3799C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13662631 | ||||||
| chr6:13662689
|
A | T | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.684-3857T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13662689 | ||||||
| chr6:13662871
|
T | C | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.684-4039A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13662871 | ||||||
| chr6:13663012
|
A | C | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.684-4180T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13663012 | ||||||
| chr6:13663023
|
A | G | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.684-4191T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13663023 | ||||||
| chr6:13663081
|
A | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | HG00738.hp2 HG01109.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.684-4249T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13663081 | ||||||
| chr6:13663406
|
C | A | 3 | a0001c0002t0003g0014a0001c0002t0003g0026a0001c0002t0003g0030 | 3 | HG01496.hp1 HG01943.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.684-4574G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13663406 | ||||||
| chr6:13663512
|
T | G | 7 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(4): Show | 7 | HG01884.hp1 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.684-4680A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13663512 | ||||||
| chr6:13663775
|
T | C | 2 | a0001c0006t0001g0220a0001c0006t0001g0221 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.684-4943A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13663775 | ||||||
| chr6:13663896
|
T | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.684-5064A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13663896 | ||||||
| chr6:13663957
|
G | A | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.684-5125C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13663957 | ||||||
| chr6:13663996
|
G | A | 1 | a0001c0002t0004g0353 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.684-5164C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13663996 | ||||||
| chr6:13664374
|
T | C | 27 | a0001c0001t0002g0139a0001c0001t0002g0141a0001c0001t0002g0142others(24): Show | 27 | HG00423.hp2 HG00738.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.684-5542A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13664374 | ||||||
| chr6:13664433
|
A | C | 1 | a0001c0001t0001g0309 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.684-5601T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13664433 | ||||||
| chr6:13664457
|
C | CTTTTCT | 136 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.684-5631_684-5626d others(8): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13664457 | ||||||
| chr6:13664595
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.684-5763A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13664595 | ||||||
| chr6:13664623
|
G | A | 136 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.684-5791C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13664623 | ||||||
| chr6:13664725
|
C | T | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-5893G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13664725 | ||||||
| chr6:13664970
|
T | C | 1 | a0001c0002t0001g0086 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.684-6138A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13664970 | ||||||
| chr6:13665140
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.684-6308A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13665140 | ||||||
| chr6:13665203
|
A | T | 8 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(5): Show | 8 | HG02071.hp2 NA18946.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.684-6371T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13665203 | ||||||
| chr6:13665230
|
G | C | 5 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG01891.hp1 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.684-6398C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13665230 | ||||||
| chr6:13665324
|
A | G | 1 | a0001c0002t0001g0068 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.684-6492T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13665324 | ||||||
| chr6:13665371
|
A | G | 1 | a0001c0002t0002g0122 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.684-6539T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13665371 | ||||||
| chr6:13665550
|
C | G | 1 | a0001c0002t0001g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.684-6718G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13665550 | ||||||
| chr6:13665587
|
T | C | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | NA18993.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.684-6755A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13665587 | ||||||
| chr6:13665692
|
C | G | 3 | a0001c0001t0002g0213a0001c0001t0002g0217a0001c0001t0002g0332 | 3 | HG02080.hp2 NA18983.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.684-6860G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13665692 | ||||||
| chr6:13665991
|
C | T | 1 | a0001c0001t0002g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.684-7159G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13665991 | ||||||
| chr6:13666060
|
A | G | 133 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(130): Show | 133 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.684-7228T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666060 | ||||||
| chr6:13666227
|
G | A | 2 | a0001c0002t0001g0074a0001c0002t0001g0075 | 2 | HG00558.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.684-7395C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666227 | ||||||
| chr6:13666304
|
G | A | 1 | a0001c0002t0001g0006 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.684-7472C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666304 | ||||||
| chr6:13666320
|
C | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.684-7488G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666320 | ||||||
| chr6:13666592
|
C | T | 1 | a0001c0002t0001g0005 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.684-7760G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666592 | ||||||
| chr6:13666593
|
G | A | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.684-7761C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666593 | ||||||
| chr6:13666600
|
C | CA | 11 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0002g0245others(8): Show | 11 | HG01109.hp2 HG01433.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.684-7769dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(3): Show |
8 | a0001c0001t0001g0149a0001c0001t0001g0178a0001c0002t0001g0016others(5): Show | 8 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.684-7778_684-7769d others(12): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(4): Show |
16 | a0001c0001t0001g0156a0001c0002t0001g0015a0001c0002t0001g0022others(13): Show | 16 | HG00438.hp2 HG01074.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.684-7779_684-7769d others(13): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(5): Show |
8 | a0001c0002t0001g0019a0001c0002t0001g0043a0001c0002t0001g0053others(5): Show | 8 | HG01071.hp1 HG01106.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.684-7780_684-7769d others(14): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(6): Show |
3 | a0001c0002t0001g0025a0001c0002t0001g0032a0001c0002t0001g0060 | 3 | HG00323.hp1 HG01361.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.684-7781_684-7769d others(15): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0155a0001c0002t0001g0041a0001c0002t0003g0030others(1): Show | 4 | HG01496.hp1 HG02615.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.684-7782_684-7769d others(16): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(8): Show |
3 | a0001c0002t0001g0021a0001c0002t0001g0061a0001c0002t0002g0058 | 3 | HG00735.hp1 HG01981.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.684-7783_684-7769d others(17): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0002g0180a0001c0002t0001g0024a0001c0002t0004g0352 | 3 | HG00423.hp2 HG00639.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.684-7784_684-7769d others(18): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(10): Show |
1 | a0001c0002t0001g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.684-7785_684-7769d others(19): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(11): Show |
1 | a0001c0015t0004g0357 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.684-7786_684-7769d others(20): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(13): Show |
1 | a0001c0002t0003g0026 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.684-7788_684-7769d others(22): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(14): Show |
2 | a0001c0002t0004g0353a0001c0002t0004g0355 | 2 | HG01978.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.684-7789_684-7769d others(23): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(15): Show |
1 | a0001c0002t0001g0011 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.684-7790_684-7769d others(24): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(18): Show |
1 | a0001c0002t0004g0356 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.684-7793_684-7769d others(27): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(21): Show |
1 | a0001c0001t0001g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.684-7796_684-7769d others(30): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0152 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.684-7769_684-7768i others(31): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
C | CAAAAAAA others(27): Show |
1 | a0001c0002t0001g0029 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.684-7769_684-7768i others(36): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
CA | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0143a0001c0001t0001g0144others(165): Show | 169 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.684-7769delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
CAA | C | 6 | a0001c0001t0001g0231a0001c0002t0001g0004a0001c0002t0001g0067others(3): Show | 6 | HG02109.hp1 HG02735.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.684-7770_684-7769d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
CAAAAA | C | 29 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0159others(26): Show | 29 | HG01069.hp2 HG01175.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.684-7773_684-7769d others(7): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
CAAAAAA | C | 17 | a0001c0001t0002g0141a0001c0001t0002g0171a0001c0001t0002g0188others(14): Show | 17 | HG00738.hp1 HG01169.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.684-7774_684-7769d others(8): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.684-7779_684-7769d others(13): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666600
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.684-7783_684-7769d others(17): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666600 | ||||||
| chr6:13666647
|
T | C | 1 | a0001c0009t0001g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.684-7815A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666647 | ||||||
| chr6:13666669
|
G | C | 33 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(30): Show | 33 | HG00423.hp2 HG00735.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.684-7837C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666669 | ||||||
| chr6:13666688
|
G | C | 1 | a0001c0001t0001g0330 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.684-7856C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666688 | ||||||
| chr6:13666700
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.684-7868G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666700 | ||||||
| chr6:13666775
|
C | A | 1 | a0001c0002t0001g0006 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.684-7943G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13666775 | ||||||
| chr6:13667023
|
C | G | 1 | a0001c0002t0001g0105 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.684-8191G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13667023 | ||||||
| chr6:13667035
|
G | A | 1 | a0001c0001t0002g0293 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.684-8203C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13667035 | ||||||
| chr6:13667123
|
A | C | 1 | a0001c0002t0002g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.684-8291T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13667123 | ||||||
| chr6:13667537
|
A | G | 136 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.684-8705T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13667537 | ||||||
| chr6:13667562
|
G | C | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-8730C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13667562 | ||||||
| chr6:13667733
|
T | G | 1 | a0001c0002t0001g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.684-8901A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13667733 | ||||||
| chr6:13667738
|
T | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.684-8906A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13667738 | ||||||
| chr6:13667741
|
G | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.684-8909C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13667741 | ||||||
| chr6:13667806
|
T | C | 1 | a0001c0002t0001g0062 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.684-8974A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13667806 | ||||||
| chr6:13667852
|
C | A | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.684-9020G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13667852 | ||||||
| chr6:13668113
|
C | A | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.684-9281G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13668113 | ||||||
| chr6:13668194
|
T | G | 1 | a0001c0002t0002g0065 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.684-9362A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13668194 | ||||||
| chr6:13668267
|
C | T | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.684-9435G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13668267 | ||||||
| chr6:13668470
|
C | T | 3 | a0001c0002t0001g0019a0001c0002t0001g0059a0001c0002t0001g0063 | 3 | HG03688.hp2 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.684-9638G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13668470 | ||||||
| chr6:13668578
|
A | G | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.684-9746T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13668578 | ||||||
| chr6:13669051
|
T | A | 1 | a0001c0001t0001g0155 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.684-10219A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13669051 | ||||||
| chr6:13669136
|
T | TA | 121 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(118): Show | 121 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.684-10305dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13669136 | ||||||
| chr6:13669137
|
A | T | 3 | a0001c0001t0002g0281a0001c0001t0002g0287a0001c0001t0002g0290 | 3 | HG02155.hp2 HG02523.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.684-10305T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13669137 | ||||||
| chr6:13669184
|
T | C | 136 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.684-10352A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13669184 | ||||||
| chr6:13669199
|
C | A | 1 | a0001c0001t0003g0305 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.684-10367G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13669199 | ||||||
| chr6:13669441
|
A | G | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.684-10609T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13669441 | ||||||
| chr6:13669462
|
C | T | 1 | a0001c0002t0001g0011 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.684-10630G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13669462 | ||||||
| chr6:13669577
|
G | C | 1 | a0001c0002t0001g0116 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.684-10745C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13669577 | ||||||
| chr6:13669768
|
T | C | 1 | a0001c0002t0001g0005 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.684-10936A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13669768 | ||||||
| chr6:13669947
|
G | GT | 6 | a0001c0001t0002g0245a0001c0002t0001g0004a0001c0002t0001g0006others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-11116dupA | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13669947 | ||||||
| chr6:13669973
|
T | A | 1 | a0001c0002t0001g0064 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.684-11141A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13669973 | ||||||
| chr6:13670028
|
G | C | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.684-11196C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670028 | ||||||
| chr6:13670030
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.684-11198G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670030 | ||||||
| chr6:13670106
|
G | A | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG01109.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.684-11274C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670106 | ||||||
| chr6:13670126
|
G | C | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.684-11294C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670126 | ||||||
| chr6:13670319
|
A | G | 6 | a0001c0001t0001g0156a0001c0002t0001g0016a0001c0002t0001g0025others(3): Show | 6 | HG00323.hp1 HG01361.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-11487T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670319 | ||||||
| chr6:13670424
|
G | A | 2 | a0001c0001t0002g0180a0001c0002t0002g0065 | 2 | HG00423.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.684-11592C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670424 | ||||||
| chr6:13670483
|
C | G | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0173 | 3 | HG02647.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.684-11651G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670483 | ||||||
| chr6:13670579
|
G | A | 2 | a0001c0002t0001g0017a0001c0002t0001g0018 | 2 | NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.684-11747C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670579 | ||||||
| chr6:13670592
|
C | T | 1 | a0001c0001t0002g0298 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.684-11760G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670592 | ||||||
| chr6:13670614
|
G | A | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | NA18993.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.684-11782C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670614 | ||||||
| chr6:13670632
|
C | T | 134 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(131): Show | 134 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.684-11800G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670632 | ||||||
| chr6:13670661
|
G | A | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.684-11829C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670661 | ||||||
| chr6:13670707
|
G | A | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.684-11875C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670707 | ||||||
| chr6:13670724
|
C | T | 1 | a0001c0002t0001g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.684-11892G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670724 | ||||||
| chr6:13670801
|
G | GA | 7 | a0001c0001t0001g0149a0001c0001t0001g0155a0001c0001t0001g0330others(4): Show | 7 | HG00735.hp2 HG02155.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.684-11970dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670801 | ||||||
| chr6:13670801
|
GA | G | 13 | a0001c0001t0001g0136a0001c0001t0001g0146a0001c0001t0002g0142others(10): Show | 13 | HG01517.hp1 HG01975.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.684-11970delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13670801 | ||||||
| chr6:13671003
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.684-12171T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13671003 | ||||||
| chr6:13671359
|
A | G | 1 | a0001c0001t0002g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.684-12527T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13671359 | ||||||
| chr6:13672195
|
T | A | 1 | a0001c0015t0004g0357 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.684-13363A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13672195 | ||||||
| chr6:13672712
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.684-13880A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13672712 | ||||||
| chr6:13672926
|
G | T | 1 | a0001c0002t0001g0103 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.684-14094C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13672926 | ||||||
| chr6:13673473
|
G | C | 1 | a0001c0001t0001g0231 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.684-14641C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13673473 | ||||||
| chr6:13673639
|
T | A | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.684-14807A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13673639 | ||||||
| chr6:13673881
|
A | C | 124 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(121): Show | 124 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.684-15049T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13673881 | ||||||
| chr6:13674035
|
G | A | 1 | a0001c0002t0001g0010 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.684-15203C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13674035 | ||||||
| chr6:13674040
|
C | T | 5 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG01891.hp1 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.684-15208G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13674040 | ||||||
| chr6:13674068
|
A | G | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.684-15236T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13674068 | ||||||
| chr6:13674083
|
C | CA | 13 | a0001c0001t0001g0156a0001c0001t0001g0164a0001c0001t0001g0165others(10): Show | 13 | HG00323.hp1 HG00609.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.684-15252dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13674083 | ||||||
| chr6:13674426
|
T | C | 2 | a0001c0002t0001g0028a0001c0008t0001g0115 | 2 | HG02132.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.684-15594A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13674426 | ||||||
| chr6:13674558
|
C | T | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | NA18993.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.684-15726G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13674558 | ||||||
| chr6:13674625
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.684-15793C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13674625 | ||||||
| chr6:13674710
|
C | A | 1 | a0001c0002t0001g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.684-15878G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13674710 | ||||||
| chr6:13674728
|
A | G | 6 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.684-15896T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13674728 | ||||||
| chr6:13674740
|
T | C | 345 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(342): Show | 345 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(342): Show |
intron_variant | MODIFIER | c.684-15908A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13674740 | ||||||
| chr6:13675127
|
A | G | 6 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(3): Show | 6 | HG01891.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.684-16295T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13675127 | ||||||
| chr6:13675149
|
G | T | 7 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(4): Show | 7 | HG01884.hp1 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.684-16317C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13675149 | ||||||
| chr6:13675164
|
T | C | 12 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0160others(9): Show | 12 | HG01069.hp2 HG01175.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.684-16332A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13675164 | ||||||
| chr6:13675208
|
T | A | 1 | a0001c0001t0001g0149 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.684-16376A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13675208 | ||||||
| chr6:13675299
|
C | T | 7 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(4): Show | 7 | HG01884.hp1 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.684-16467G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13675299 | ||||||
| chr6:13675481
|
T | C | 1 | a0001c0001t0002g0202 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.684-16649A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13675481 | ||||||
| chr6:13675676
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.684-16844T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13675676 | ||||||
| chr6:13675682
|
C | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.684-16850G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13675682 | ||||||
| chr6:13675745
|
A | C | 1 | a0002c0003t0001g0339 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.684-16913T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13675745 | ||||||
| chr6:13675863
|
C | T | 1 | a0001c0002t0001g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.684-17031G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13675863 | ||||||
| chr6:13676050
|
T | C | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.684-17218A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13676050 | ||||||
| chr6:13676121
|
C | T | 1 | a0001c0002t0001g0073 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.684-17289G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13676121 | ||||||
| chr6:13676191
|
A | G | 1 | a0001c0002t0001g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.684-17359T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13676191 | ||||||
| chr6:13676202
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.684-17370G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13676202 | ||||||
| chr6:13676442
|
C | T | 7 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(4): Show | 7 | HG01884.hp1 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.684-17610G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13676442 | ||||||
| chr6:13676582
|
A | T | 1 | a0001c0002t0001g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.684-17750T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13676582 | ||||||
| chr6:13676765
|
C | G | 34 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(31): Show | 34 | HG00597.hp2 HG00609.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.684-17933G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13676765 | ||||||
| chr6:13676784
|
G | A | 1 | a0001c0002t0001g0105 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.684-17952C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13676784 | ||||||
| chr6:13676866
|
A | G | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.684-18034T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13676866 | ||||||
| chr6:13676963
|
T | C | 1 | a0001c0002t0001g0095 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.684-18131A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13676963 | ||||||
| chr6:13677119
|
T | C | 14 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0157others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.684-18287A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13677119 | ||||||
| chr6:13677132
|
C | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.684-18300G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13677132 | ||||||
| chr6:13677364
|
A | G | 1 | a0001c0001t0002g0197 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.684-18532T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13677364 | ||||||
| chr6:13677395
|
C | A | 1 | a0001c0001t0002g0203 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.684-18563G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13677395 | ||||||
| chr6:13677614
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0155 | 2 | HG00735.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.684-18782A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13677614 | ||||||
| chr6:13677647
|
T | A | 3 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01891.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.684-18815A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13677647 | ||||||
| chr6:13677648
|
T | A | 3 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01891.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.684-18816A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13677648 | ||||||
| chr6:13677649
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01891.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.684-18817G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13677649 | ||||||
| chr6:13677690
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.684-18858T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13677690 | ||||||
| chr6:13677741
|
A | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.684-18909T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13677741 | ||||||
| chr6:13678379
|
T | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.683+18406A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13678379 | ||||||
| chr6:13678439
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.683+18346T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13678439 | ||||||
| chr6:13678548
|
G | T | 1 | a0001c0002t0001g0053 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.683+18237C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13678548 | ||||||
| chr6:13678647
|
T | C | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | HG01361.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+18138A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13678647 | ||||||
| chr6:13678891
|
T | G | 1 | a0001c0002t0001g0117 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.683+17894A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13678891 | ||||||
| chr6:13678935
|
C | T | 1 | a0001c0001t0002g0298 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.683+17850G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13678935 | ||||||
| chr6:13679154
|
G | A | 4 | a0001c0002t0001g0016a0001c0002t0001g0025a0001c0002t0001g0032others(1): Show | 4 | HG00323.hp1 HG01361.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.683+17631C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13679154 | ||||||
| chr6:13679194
|
C | T | 1 | a0001c0002t0001g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.683+17591G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13679194 | ||||||
| chr6:13679254
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.683+17531A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13679254 | ||||||
| chr6:13679293
|
C | T | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+17492G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13679293 | ||||||
| chr6:13679574
|
T | C | 7 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(4): Show | 7 | HG00735.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.683+17211A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13679574 | ||||||
| chr6:13679603
|
TTGGTTAA others(5): Show |
T | 1 | a0001c0001t0001g0314 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.683+17170_683+1718 others(16): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13679603 | ||||||
| chr6:13679769
|
C | G | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0173 | 3 | HG02647.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.683+17016G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13679769 | ||||||
| chr6:13679832
|
T | C | 135 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(132): Show | 135 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.683+16953A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13679832 | ||||||
| chr6:13679938
|
TTCTTATT others(3): Show |
T | 1 | a0001c0001t0001g0250 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.683+16837_683+1684 others(14): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13679938 | ||||||
| chr6:13680136
|
ACT | A | 3 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01891.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.683+16647_683+1664 others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680136 | ||||||
| chr6:13680153
|
A | C | 1 | a0001c0001t0001g0138 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.683+16632T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680153 | ||||||
| chr6:13680168
|
T | C | 1 | a0001c0002t0001g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.683+16617A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680168 | ||||||
| chr6:13680227
|
A | G | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683+16558T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680227 | ||||||
| chr6:13680303
|
G | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.683+16482C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680303 | ||||||
| chr6:13680341
|
T | A | 1 | a0001c0001t0001g0250 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.683+16444A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680341 | ||||||
| chr6:13680342
|
G | T | 1 | a0001c0001t0001g0250 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.683+16443C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680342 | ||||||
| chr6:13680411
|
T | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+16374A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680411 | ||||||
| chr6:13680436
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.683+16349A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680436 | ||||||
| chr6:13680504
|
G | A | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.683+16281C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680504 | ||||||
| chr6:13680544
|
A | G | 255 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(252): Show | 255 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.683+16241T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680544 | ||||||
| chr6:13680751
|
G | A | 2 | a0001c0001t0002g0293a0001c0013t0002g0270 | 2 | NA18953.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.683+16034C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680751 | ||||||
| chr6:13680827
|
A | G | 1 | a0001c0002t0001g0082 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.683+15958T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680827 | ||||||
| chr6:13680936
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG02004.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.683+15849C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13680936 | ||||||
| chr6:13681067
|
A | C | 1 | a0001c0001t0002g0180 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.683+15718T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681067 | ||||||
| chr6:13681083
|
A | G | 136 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.683+15702T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681083 | ||||||
| chr6:13681111
|
T | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01891.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.683+15674A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681111 | ||||||
| chr6:13681165
|
T | C | 28 | a0001c0001t0001g0219a0001c0001t0001g0306a0001c0001t0001g0308others(25): Show | 28 | HG00597.hp2 HG00609.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.683+15620A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681165 | ||||||
| chr6:13681198
|
T | C | 1 | a0001c0001t0001g0259 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.683+15587A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681198 | ||||||
| chr6:13681293
|
AAG | A | 5 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG01891.hp1 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.683+15490_683+1549 others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681293 | ||||||
| chr6:13681330
|
T | TGTG | 133 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(130): Show | 133 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.683+15452_683+1545 others(7): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681330 | ||||||
| chr6:13681422
|
G | A | 10 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(7): Show | 10 | HG00673.hp1 HG01123.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.683+15363C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681422 | ||||||
| chr6:13681598
|
C | T | 1 | a0001c0002t0001g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.683+15187G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681598 | ||||||
| chr6:13681840
|
G | A | 11 | a0001c0001t0002g0139a0001c0001t0002g0184a0001c0001t0002g0189others(8): Show | 11 | NA18971.hp1 NA18972.hp2 NA18986.hp1 others(8): Show |
intron_variant | MODIFIER | c.683+14945C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681840 | ||||||
| chr6:13681859
|
C | A | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.683+14926G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681859 | ||||||
| chr6:13681886
|
A | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01891.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.683+14899T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681886 | ||||||
| chr6:13681890
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+14895C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681890 | ||||||
| chr6:13681970
|
T | G | 2 | a0001c0001t0002g0293a0001c0013t0002g0270 | 2 | NA18953.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.683+14815A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13681970 | ||||||
| chr6:13682060
|
C | T | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.683+14725G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13682060 | ||||||
| chr6:13682113
|
C | T | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.683+14672G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13682113 | ||||||
| chr6:13682206
|
T | C | 1 | a0001c0002t0001g0095 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.683+14579A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13682206 | ||||||
| chr6:13682395
|
T | TA | 17 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(14): Show | 17 | HG00609.hp2 HG01257.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.683+14389dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13682395 | ||||||
| chr6:13682395
|
TA | T | 16 | a0001c0001t0001g0135a0001c0001t0001g0149a0001c0001t0001g0150others(13): Show | 16 | HG00323.hp2 HG00408.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.683+14389delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13682395 | ||||||
| chr6:13682404
|
AAAAAAAA others(8): Show |
A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+14366_683+1438 others(19): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13682404 | ||||||
| chr6:13683223
|
A | G | 1 | a0001c0002t0001g0008 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.683+13562T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13683223 | ||||||
| chr6:13683244
|
T | A | 1 | a0001c0002t0001g0016 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.683+13541A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13683244 | ||||||
| chr6:13683255
|
A | G | 1 | a0002c0005t0001g0344 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.683+13530T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13683255 | ||||||
| chr6:13683366
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.683+13419T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13683366 | ||||||
| chr6:13683538
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.683+13247G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13683538 | ||||||
| chr6:13683716
|
T | C | 120 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(117): Show | 120 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.683+13069A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13683716 | ||||||
| chr6:13683852
|
A | T | 1 | a0001c0002t0001g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.683+12933T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13683852 | ||||||
| chr6:13683899
|
G | GTAT | 86 | a0001c0001t0001g0222a0001c0001t0001g0282a0001c0001t0001g0283others(83): Show | 86 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.683+12885_683+1288 others(7): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13683899 | ||||||
| chr6:13683900
|
G | A | 86 | a0001c0001t0001g0222a0001c0001t0001g0282a0001c0001t0001g0283others(83): Show | 86 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.683+12885C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13683900 | ||||||
| chr6:13683927
|
A | G | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+12858T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13683927 | ||||||
| chr6:13683978
|
C | G | 2 | a0002c0003t0001g0338a0002c0003t0001g0339 | 2 | HG00408.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.683+12807G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13683978 | ||||||
| chr6:13684196
|
T | C | 6 | a0001c0002t0001g0124a0001c0002t0001g0125a0001c0002t0001g0126others(3): Show | 6 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.683+12589A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13684196 | ||||||
| chr6:13684334
|
A | C | 1 | a0001c0002t0001g0109 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.683+12451T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13684334 | ||||||
| chr6:13684447
|
C | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+12338G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13684447 | ||||||
| chr6:13684509
|
T | A | 1 | a0001c0002t0001g0022 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.683+12276A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13684509 | ||||||
| chr6:13684592
|
T | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+12193A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13684592 | ||||||
| chr6:13684600
|
T | A | 1 | a0002c0003t0001g0346 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.683+12185A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13684600 | ||||||
| chr6:13684714
|
C | T | 2 | a0001c0002t0002g0120a0001c0002t0002g0121 | 2 | HG01255.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.683+12071G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13684714 | ||||||
| chr6:13684909
|
C | T | 1 | a0005c0012t0001g0328 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.683+11876G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13684909 | ||||||
| chr6:13684953
|
A | G | 135 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(132): Show | 135 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.683+11832T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13684953 | ||||||
| chr6:13684978
|
C | T | 1 | a0001c0001t0002g0184 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.683+11807G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13684978 | ||||||
| chr6:13685039
|
C | G | 1 | a0001c0002t0001g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.683+11746G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685039 | ||||||
| chr6:13685081
|
G | C | 1 | a0002c0003t0001g0346 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.683+11704C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685081 | ||||||
| chr6:13685086
|
G | T | 1 | a0002c0003t0001g0346 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.683+11699C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685086 | ||||||
| chr6:13685263
|
A | G | 1 | a0001c0001t0009g0278 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.683+11522T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685263 | ||||||
| chr6:13685263
|
A | T | 1 | a0002c0003t0001g0346 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.683+11522T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685263 | ||||||
| chr6:13685264
|
T | A | 1 | a0002c0003t0001g0346 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.683+11521A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685264 | ||||||
| chr6:13685319
|
A | C | 27 | a0001c0001t0002g0139a0001c0001t0002g0141a0001c0001t0002g0142others(24): Show | 27 | HG00423.hp2 HG00738.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.683+11466T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685319 | ||||||
| chr6:13685355
|
T | A | 1 | a0002c0003t0001g0346 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.683+11430A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685355 | ||||||
| chr6:13685356
|
G | T | 1 | a0002c0003t0001g0346 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.683+11429C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685356 | ||||||
| chr6:13685366
|
T | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+11419A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685366 | ||||||
| chr6:13685370
|
A | G | 6 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(3): Show | 6 | HG02071.hp2 NA18946.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.683+11415T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685370 | ||||||
| chr6:13685397
|
A | T | 1 | a0002c0003t0001g0346 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.683+11388T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685397 | ||||||
| chr6:13685426
|
A | T | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.683+11359T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685426 | ||||||
| chr6:13685457
|
T | A | 1 | a0002c0003t0001g0346 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.683+11328A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685457 | ||||||
| chr6:13685458
|
A | G | 1 | a0002c0003t0001g0346 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.683+11327T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685458 | ||||||
| chr6:13685459
|
G | C | 1 | a0002c0003t0001g0346 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.683+11326C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685459 | ||||||
| chr6:13685524
|
A | G | 78 | a0001c0001t0001g0222a0001c0001t0001g0282a0001c0001t0001g0283others(75): Show | 78 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.683+11261T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685524 | ||||||
| chr6:13685712
|
G | A | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.683+11073C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685712 | ||||||
| chr6:13685720
|
G | C | 2 | a0001c0002t0001g0129a0001c0002t0001g0130 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+11065C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685720 | ||||||
| chr6:13685837
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.683+10948C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685837 | ||||||
| chr6:13685880
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.683+10905C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685880 | ||||||
| chr6:13685917
|
G | A | 121 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(118): Show | 121 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.683+10868C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685917 | ||||||
| chr6:13685929
|
C | A | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.683+10856G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685929 | ||||||
| chr6:13685929
|
C | CA | 7 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0173others(4): Show | 7 | HG02071.hp1 HG02647.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.683+10855dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685929 | ||||||
| chr6:13685929
|
CA | C | 8 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.683+10855delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685929 | ||||||
| chr6:13685994
|
C | T | 2 | a0001c0002t0001g0034a0001c0002t0001g0036 | 2 | HG00438.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.683+10791G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13685994 | ||||||
| chr6:13686013
|
C | T | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+10772G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686013 | ||||||
| chr6:13686064
|
G | A | 1 | a0002c0003t0001g0346 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.683+10721C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686064 | ||||||
| chr6:13686100
|
T | TC | 14 | a0001c0001t0001g0135a0001c0001t0001g0234a0001c0001t0001g0235others(11): Show | 14 | HG00738.hp2 HG01169.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.683+10684dupG | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686100 | ||||||
| chr6:13686100
|
T | TCCCCCCC others(3): Show |
1 | a0001c0001t0001g0269 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.683+10675_683+1068 others(14): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686100 | ||||||
| chr6:13686100
|
T | TCCCCCCC others(4): Show |
2 | a0001c0001t0002g0216a0001c0009t0001g0134 | 2 | HG02074.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.683+10674_683+1068 others(15): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686100 | ||||||
| chr6:13686100
|
T | TCCCCCCC others(7): Show |
1 | a0002c0003t0002g0337 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.683+10671_683+1068 others(18): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686100 | ||||||
| chr6:13686100
|
T | TCCCCCCC others(8): Show |
1 | a0001c0001t0002g0232 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.683+10670_683+1068 others(19): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686100 | ||||||
| chr6:13686100
|
T | TCCCCCCC others(22): Show |
1 | a0001c0001t0001g0292 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.683+10684_683+1068 others(33): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686100 | ||||||
| chr6:13686100
|
T | TCTCCCCC others(3): Show |
1 | a0001c0001t0002g0217 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.683+10684_683+1068 others(14): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686100 | ||||||
| chr6:13686101
|
C | T | 109 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.683+10684G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686101 | ||||||
| chr6:13686103
|
CCCCCCCC others(6): Show |
C | 7 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(4): Show | 7 | HG01891.hp1 HG02818.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.683+10669_683+1068 others(17): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686103 | ||||||
| chr6:13686104
|
CCCCCCCC others(5): Show |
C | 1 | a0001c0002t0001g0066 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.683+10669_683+1068 others(16): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686104 | ||||||
| chr6:13686105
|
C | G | 1 | a0001c0002t0002g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.683+10680G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686105 | ||||||
| chr6:13686105
|
CCCCCCCC others(4): Show |
C | 75 | a0001c0001t0001g0222a0001c0001t0001g0282a0001c0001t0001g0283others(72): Show | 75 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.683+10669_683+1067 others(15): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686105 | ||||||
| chr6:13686106
|
CCCCCCCC others(3): Show |
C | 1 | a0001c0002t0001g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.683+10669_683+1067 others(14): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686106 | ||||||
| chr6:13686107
|
C | T | 2 | a0001c0001t0002g0192a0001c0001t0002g0201 | 2 | HG00738.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.683+10678G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686107 | ||||||
| chr6:13686109
|
CCCCCCCG | C | 46 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0156others(43): Show | 46 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.683+10669_683+1067 others(11): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686109 | ||||||
| chr6:13686110
|
C | A | 1 | a0001c0001t0001g0319 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.683+10675G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686110 | ||||||
| chr6:13686110
|
C | T | 1 | a0001c0002t0001g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.683+10675G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686110 | ||||||
| chr6:13686110
|
CCCCCCG | C | 42 | a0001c0001t0001g0137a0001c0001t0001g0150a0001c0001t0001g0151others(39): Show | 42 | HG00438.hp2 HG00597.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.683+10669_683+1067 others(10): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686110 | ||||||
| chr6:13686111
|
CCCCCG | C | 30 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0312others(27): Show | 30 | HG01123.hp2 HG01169.hp1 HG02683.hp1 others(27): Show |
intron_variant | MODIFIER | c.683+10669_683+1067 others(9): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686111 | ||||||
| chr6:13686112
|
CCCCG | C | 19 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0310others(16): Show | 19 | HG00597.hp2 HG01069.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.683+10669_683+1067 others(8): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686112 | ||||||
| chr6:13686115
|
CG | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0143a0001c0001t0001g0144others(12): Show | 16 | HG01074.hp1 HG02004.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.683+10669delC | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686115 | ||||||
| chr6:13686116
|
G | C | 71 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0145others(68): Show | 71 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.683+10669C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686116 | ||||||
| chr6:13686118
|
C | G | 1 | a0001c0002t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.683+10667G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686118 | ||||||
| chr6:13686121
|
C | A | 1 | a0001c0001t0002g0297 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.683+10664G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686121 | ||||||
| chr6:13686208
|
G | A | 1 | a0001c0001t0002g0275 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.683+10577C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686208 | ||||||
| chr6:13686301
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.683+10484A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686301 | ||||||
| chr6:13686426
|
G | C | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.683+10359C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686426 | ||||||
| chr6:13686449
|
A | AT | 8 | a0001c0001t0001g0250a0001c0001t0001g0273a0001c0001t0001g0274others(5): Show | 8 | HG02056.hp1 HG02056.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.683+10335dupA | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686449 | ||||||
| chr6:13686530
|
C | G | 1 | a0001c0001t0002g0298 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.683+10255G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686530 | ||||||
| chr6:13686649
|
C | T | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.683+10136G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686649 | ||||||
| chr6:13686695
|
C | T | 65 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0007others(62): Show | 65 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.683+10090G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686695 | ||||||
| chr6:13686717
|
T | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+10068A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686717 | ||||||
| chr6:13686840
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.683+9945A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686840 | ||||||
| chr6:13686845
|
C | A | 2 | a0001c0002t0001g0044a0001c0002t0001g0050 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.683+9940G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13686845 | ||||||
| chr6:13687139
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.683+9646C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13687139 | ||||||
| chr6:13687264
|
T | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+9521A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13687264 | ||||||
| chr6:13687266
|
C | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+9519G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13687266 | ||||||
| chr6:13687300
|
A | ACACTGTT others(6): Show |
1 | a0001c0001t0002g0232 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.683+9472_683+9484d others(15): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13687300 | ||||||
| chr6:13687489
|
T | TA | 6 | a0001c0001t0001g0250a0001c0001t0001g0271a0001c0001t0001g0294others(3): Show | 6 | HG00438.hp1 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.683+9295dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13687489 | ||||||
| chr6:13687552
|
A | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+9233T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13687552 | ||||||
| chr6:13687610
|
C | T | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683+9175G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13687610 | ||||||
| chr6:13688057
|
C | G | 1 | a0001c0001t0002g0297 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.683+8728G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688057 | ||||||
| chr6:13688120
|
T | G | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.683+8665A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688120 | ||||||
| chr6:13688157
|
G | A | 2 | a0001c0002t0001g0074a0001c0002t0001g0075 | 2 | HG00558.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.683+8628C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688157 | ||||||
| chr6:13688167
|
G | T | 1 | a0001c0001t0001g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.683+8618C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688167 | ||||||
| chr6:13688169
|
C | A | 1 | a0001c0001t0001g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.683+8616G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688169 | ||||||
| chr6:13688241
|
A | G | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683+8544T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688241 | ||||||
| chr6:13688385
|
C | T | 4 | a0001c0001t0002g0213a0001c0001t0002g0217a0001c0001t0002g0218others(1): Show | 4 | HG02027.hp2 HG02080.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.683+8400G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688385 | ||||||
| chr6:13688470
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.683+8315G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688470 | ||||||
| chr6:13688593
|
C | T | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+8192G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688593 | ||||||
| chr6:13688693
|
A | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0247a0001c0001t0001g0252 | 3 | HG01258.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.683+8092T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688693 | ||||||
| chr6:13688740
|
T | C | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.683+8045A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688740 | ||||||
| chr6:13688915
|
G | A | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683+7870C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688915 | ||||||
| chr6:13688982
|
C | CA | 38 | a0001c0001t0001g0135a0001c0001t0001g0230a0001c0001t0001g0251others(35): Show | 38 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.683+7802dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688982 | ||||||
| chr6:13688982
|
C | CAAAAAAA others(9): Show |
2 | a0001c0002t0001g0129a0001c0002t0001g0130 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+7787_683+7802d others(18): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688982 | ||||||
| chr6:13688982
|
C | CAAAAAAA others(31): Show |
1 | a0005c0012t0001g0328 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.683+7802_683+7803i others(40): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688982 | ||||||
| chr6:13688982
|
CAAAAAAA others(5): Show |
C | 8 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0225others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.683+7791_683+7802d others(14): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688982 | ||||||
| chr6:13688982
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.683+7790_683+7802d others(15): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13688982 | ||||||
| chr6:13689004
|
A | AAAAAAAA others(4): Show |
9 | a0001c0001t0001g0154a0001c0001t0001g0330a0001c0001t0001g0331others(6): Show | 9 | HG00735.hp1 HG01361.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.683+7780_683+7781i others(13): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13689004 | ||||||
| chr6:13689004
|
A | AAAAAAAA others(3): Show |
47 | a0001c0001t0001g0136a0001c0001t0001g0149a0001c0001t0001g0152others(44): Show | 47 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.683+7780_683+7781i others(12): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13689004 | ||||||
| chr6:13689004
|
A | AAAAAAAA others(2): Show |
69 | a0001c0001t0001g0138a0001c0001t0001g0150a0001c0001t0001g0151others(66): Show | 69 | HG00323.hp1 HG00438.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.683+7780_683+7781i others(11): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13689004 | ||||||
| chr6:13689004
|
A | G | 1 | a0001c0001t0002g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.683+7781T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13689004 | ||||||
| chr6:13689005
|
T | G | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+7780A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13689005 | ||||||
| chr6:13689123
|
C | T | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683+7662G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13689123 | ||||||
| chr6:13689262
|
C | T | 134 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(131): Show | 134 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.683+7523G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13689262 | ||||||
| chr6:13689438
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.683+7347A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13689438 | ||||||
| chr6:13689921
|
C | A | 2 | a0001c0002t0001g0129a0001c0002t0001g0130 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+6864G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13689921 | ||||||
| chr6:13690003
|
A | C | 2 | a0001c0002t0001g0129a0001c0002t0001g0130 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+6782T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13690003 | ||||||
| chr6:13690065
|
C | A | 5 | a0001c0002t0001g0072a0001c0002t0001g0076a0001c0002t0001g0077others(2): Show | 5 | HG01099.hp2 HG02559.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.683+6720G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13690065 | ||||||
| chr6:13690242
|
C | G | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+6543G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13690242 | ||||||
| chr6:13690521
|
T | G | 1 | a0001c0002t0001g0103 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.683+6264A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13690521 | ||||||
| chr6:13690580
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.683+6205A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13690580 | ||||||
| chr6:13690663
|
A | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+6122T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13690663 | ||||||
| chr6:13690707
|
A | T | 345 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(342): Show | 345 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(342): Show |
intron_variant | MODIFIER | c.683+6078T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13690707 | ||||||
| chr6:13690932
|
G | A | 1 | a0001c0001t0002g0286 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.683+5853C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13690932 | ||||||
| chr6:13690940
|
T | G | 39 | a0001c0001t0001g0222a0001c0001t0001g0243a0001c0001t0001g0285others(36): Show | 39 | HG00423.hp1 HG00741.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.683+5845A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13690940 | ||||||
| chr6:13691065
|
G | A | 1 | a0001c0002t0001g0116 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.683+5720C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13691065 | ||||||
| chr6:13691163
|
C | CA | 27 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0177others(24): Show | 27 | HG00423.hp2 HG00597.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.683+5621dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13691163 | ||||||
| chr6:13691163
|
CA | C | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0173others(6): Show | 9 | HG00423.hp1 HG01069.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.683+5621delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13691163 | ||||||
| chr6:13691163
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0294 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.683+5612_683+5621d others(12): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13691163 | ||||||
| chr6:13691194
|
A | T | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683+5591T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13691194 | ||||||
| chr6:13691294
|
A | G | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.683+5491T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13691294 | ||||||
| chr6:13691370
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.683+5415G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13691370 | ||||||
| chr6:13691592
|
A | T | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.683+5193T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13691592 | ||||||
| chr6:13691598
|
T | C | 1 | a0004c0007t0001g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.683+5187A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13691598 | ||||||
| chr6:13691658
|
G | T | 1 | a0001c0001t0001g0261 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.683+5127C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13691658 | ||||||
| chr6:13691760
|
T | G | 1 | a0001c0001t0001g0309 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.683+5025A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13691760 | ||||||
| chr6:13691856
|
G | A | 1 | a0001c0001t0002g0287 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.683+4929C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13691856 | ||||||
| chr6:13692225
|
T | C | 1 | a0001c0002t0001g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.683+4560A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692225 | ||||||
| chr6:13692263
|
C | T | 1 | a0001c0002t0003g0014 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.683+4522G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692263 | ||||||
| chr6:13692267
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+4518C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692267 | ||||||
| chr6:13692333
|
C | T | 65 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0002t0001g0007others(62): Show | 65 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.683+4452G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692333 | ||||||
| chr6:13692343
|
T | C | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.683+4442A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692343 | ||||||
| chr6:13692468
|
AG | A | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683+4316delC | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692468 | ||||||
| chr6:13692500
|
C | T | 1 | a0001c0002t0001g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.683+4285G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692500 | ||||||
| chr6:13692527
|
C | CA | 189 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.683+4257dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692527 | ||||||
| chr6:13692527
|
C | CAA | 66 | a0001c0001t0001g0135a0001c0001t0001g0145a0001c0001t0001g0149others(63): Show | 66 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.683+4256_683+4257d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692527 | ||||||
| chr6:13692527
|
C | CAAA | 15 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0170others(12): Show | 15 | HG00423.hp2 HG01099.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.683+4255_683+4257d others(5): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692527 | ||||||
| chr6:13692542
|
A | C | 7 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(4): Show | 7 | HG01884.hp1 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.683+4243T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692542 | ||||||
| chr6:13692553
|
A | AC | 4 | a0001c0002t0001g0114a0001c0008t0001g0115a0002c0004t0001g0335others(1): Show | 4 | NA18946.hp1 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.683+4231_683+4232i others(3): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692553 | ||||||
| chr6:13692553
|
A | C | 4 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0133others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.683+4232T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692553 | ||||||
| chr6:13692555
|
C | A | 1 | a0001c0002t0001g0004 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.683+4230G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692555 | ||||||
| chr6:13692559
|
A | C | 1 | a0001c0002t0001g0114 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.683+4226T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692559 | ||||||
| chr6:13692569
|
A | C | 1 | a0001c0001t0002g0232 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.683+4216T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692569 | ||||||
| chr6:13692598
|
T | C | 1 | a0001c0002t0002g0065 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.683+4187A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692598 | ||||||
| chr6:13692813
|
A | G | 1 | a0001c0001t0001g0260 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.683+3972T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692813 | ||||||
| chr6:13692980
|
A | C | 1 | a0001c0002t0001g0022 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.683+3805T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13692980 | ||||||
| chr6:13693014
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+3771C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693014 | ||||||
| chr6:13693389
|
T | A | 6 | a0001c0002t0001g0067a0001c0002t0001g0088a0001c0002t0001g0089others(3): Show | 6 | HG02647.hp1 HG02976.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.683+3396A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693389 | ||||||
| chr6:13693390
|
A | T | 5 | a0001c0002t0001g0100a0001c0002t0001g0110a0002c0005t0001g0343others(2): Show | 5 | NA18945.hp2 NA18970.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.683+3395T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693390 | ||||||
| chr6:13693436
|
T | A | 1 | a0001c0002t0001g0097 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.683+3349A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693436 | ||||||
| chr6:13693453
|
T | C | 4 | a0001c0001t0001g0230a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.683+3332A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693453 | ||||||
| chr6:13693472
|
C | A | 1 | a0001c0002t0008g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.683+3313G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693472 | ||||||
| chr6:13693565
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+3220C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693565 | ||||||
| chr6:13693605
|
G | A | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+3180C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693605 | ||||||
| chr6:13693609
|
G | T | 1 | a0001c0002t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.683+3176C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693609 | ||||||
| chr6:13693610
|
T | C | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683+3175A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693610 | ||||||
| chr6:13693639
|
A | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+3146T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693639 | ||||||
| chr6:13693669
|
T | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+3116A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693669 | ||||||
| chr6:13693678
|
A | C | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.683+3107T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693678 | ||||||
| chr6:13693682
|
C | G | 351 | a0001c0001t0001g0001a0001c0001t0001g0135a0001c0001t0001g0136others(348): Show | 352 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(349): Show |
intron_variant | MODIFIER | c.683+3103G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693682 | ||||||
| chr6:13693765
|
G | A | 1 | a0001c0001t0003g0311 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.683+3020C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693765 | ||||||
| chr6:13693840
|
C | T | 2 | a0002c0004t0001g0335a0002c0004t0001g0336 | 2 | NA18946.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.683+2945G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693840 | ||||||
| chr6:13693856
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.683+2929T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13693856 | ||||||
| chr6:13694012
|
C | T | 66 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(63): Show | 66 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.683+2773G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13694012 | ||||||
| chr6:13694077
|
A | G | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.683+2708T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13694077 | ||||||
| chr6:13694135
|
A | G | 1 | a0001c0001t0002g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.683+2650T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13694135 | ||||||
| chr6:13694169
|
C | T | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+2616G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13694169 | ||||||
| chr6:13694220
|
T | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+2565A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13694220 | ||||||
| chr6:13694294
|
T | C | 10 | a0001c0001t0001g0219a0001c0001t0001g0312a0001c0001t0001g0313others(7): Show | 10 | NA18941.hp2 NA18945.hp1 NA18971.hp2 others(7): Show |
intron_variant | MODIFIER | c.683+2491A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13694294 | ||||||
| chr6:13694344
|
T | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.683+2441A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13694344 | ||||||
| chr6:13694368
|
T | C | 1 | a0001c0002t0001g0007 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.683+2417A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13694368 | ||||||
| chr6:13694746
|
A | G | 1 | a0005c0012t0001g0328 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.683+2039T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13694746 | ||||||
| chr6:13694902
|
C | G | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.683+1883G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13694902 | ||||||
| chr6:13694991
|
A | T | 142 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(139): Show | 142 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.683+1794T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13694991 | ||||||
| chr6:13695020
|
G | A | 142 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(139): Show | 142 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.683+1765C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13695020 | ||||||
| chr6:13695043
|
A | T | 3 | a0001c0001t0001g0178a0001c0002t0001g0012a0001c0002t0001g0038 | 3 | NA18998.hp2 NA19000.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.683+1742T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13695043 | ||||||
| chr6:13695130
|
G | C | 1 | a0001c0001t0002g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.683+1655C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13695130 | ||||||
| chr6:13695134
|
C | T | 34 | a0001c0001t0002g0139a0001c0001t0002g0141a0001c0001t0002g0142others(31): Show | 34 | HG00423.hp2 HG00597.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.683+1651G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13695134 | ||||||
| chr6:13695400
|
TG | T | 8 | a0001c0001t0001g0222a0001c0001t0001g0285a0001c0001t0001g0291others(5): Show | 8 | HG02155.hp2 NA18949.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.683+1384delC | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13695400 | ||||||
| chr6:13695401
|
G | GT | 130 | a0001c0001t0001g0143a0001c0001t0001g0146a0001c0001t0001g0147others(127): Show | 130 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.683+1383dupA | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13695401 | ||||||
| chr6:13695401
|
G | GTT | 19 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0145others(16): Show | 19 | HG00609.hp1 HG01109.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.683+1382_683+1383d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13695401 | ||||||
| chr6:13695401
|
G | T | 6 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0060others(3): Show | 6 | HG00735.hp1 HG01928.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.683+1384C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13695401 | ||||||
| chr6:13695401
|
GT | G | 14 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(11): Show | 14 | HG01069.hp2 HG01175.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.683+1383delA | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13695401 | ||||||
| chr6:13695608
|
G | C | 1 | a0001c0001t0002g0197 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.683+1177C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13695608 | ||||||
| chr6:13695781
|
A | G | 10 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0160others(7): Show | 10 | HG01069.hp2 HG01175.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.683+1004T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13695781 | ||||||
| chr6:13695949
|
T | C | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.683+836A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13695949 | ||||||
| chr6:13695982
|
A | ACCCTATG others(49): Show |
3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683+802_683+803ins others(56): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13695982 | ||||||
| chr6:13696299
|
A | G | 6 | a0001c0001t0002g0303a0001c0001t0002g0304a0001c0001t0002g0325others(3): Show | 6 | HG00741.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.683+486T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13696299 | ||||||
| chr6:13696333
|
A | C | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(18): Show | 21 | HG01069.hp2 HG01175.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.683+452T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13696333 | ||||||
| chr6:13696411
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.683+374G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13696411 | ||||||
| chr6:13696455
|
T | A | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683+330A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13696455 | ||||||
| chr6:13696492
|
G | A | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+293C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13696492 | ||||||
| chr6:13696517
|
T | C | 1 | a0001c0001t0001g0319 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.683+268A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13696517 | ||||||
| chr6:13696758
|
C | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+27G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | 13696758 | ||||||
| chr6:13696959
|
T | C | 1 | a0001c0001t0002g0299 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.572-63A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13696959 | ||||||
| chr6:13697007
|
C | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.572-111G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13697007 | ||||||
| chr6:13697029
|
A | G | 1 | a0001c0001t0001g0283 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.572-133T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13697029 | ||||||
| chr6:13697064
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.572-168T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13697064 | ||||||
| chr6:13697215
|
G | T | 1 | a0001c0001t0002g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.572-319C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13697215 | ||||||
| chr6:13697244
|
C | A | 34 | a0001c0001t0002g0139a0001c0001t0002g0141a0001c0001t0002g0142others(31): Show | 34 | HG00423.hp2 HG00597.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.572-348G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13697244 | ||||||
| chr6:13697244
|
C | T | 182 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(179): Show | 182 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.572-348G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13697244 | ||||||
| chr6:13697252
|
T | C | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | NA18952.hp2 NA18955.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.572-356A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13697252 | ||||||
| chr6:13697264
|
T | C | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.572-368A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13697264 | ||||||
| chr6:13697309
|
G | A | 1 | a0001c0002t0001g0005 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.572-413C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13697309 | ||||||
| chr6:13697893
|
A | C | 6 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.572-997T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13697893 | ||||||
| chr6:13697930
|
A | G | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.572-1034T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13697930 | ||||||
| chr6:13697980
|
G | A | 1 | a0001c0001t0002g0205 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.572-1084C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13697980 | ||||||
| chr6:13698007
|
T | C | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG01109.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.572-1111A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13698007 | ||||||
| chr6:13698036
|
T | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.572-1140A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13698036 | ||||||
| chr6:13698126
|
A | G | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.572-1230T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13698126 | ||||||
| chr6:13698144
|
C | T | 1 | a0002c0003t0001g0340 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.572-1248G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13698144 | ||||||
| chr6:13698192
|
C | T | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.572-1296G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13698192 | ||||||
| chr6:13698215
|
T | C | 1 | a0001c0002t0001g0012 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.572-1319A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13698215 | ||||||
| chr6:13698289
|
A | G | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.572-1393T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13698289 | ||||||
| chr6:13698439
|
T | C | 6 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.572-1543A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13698439 | ||||||
| chr6:13698603
|
T | C | 1 | a0001c0002t0001g0109 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.572-1707A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13698603 | ||||||
| chr6:13698625
|
G | A | 2 | a0001c0002t0001g0044a0001c0002t0001g0050 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.572-1729C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13698625 | ||||||
| chr6:13698916
|
C | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.572-2020G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13698916 | ||||||
| chr6:13698930
|
C | T | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.572-2034G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13698930 | ||||||
| chr6:13698940
|
T | C | 1 | a0001c0002t0001g0004 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.572-2044A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13698940 | ||||||
| chr6:13699208
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.572-2312G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13699208 | ||||||
| chr6:13699279
|
G | T | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.572-2383C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13699279 | ||||||
| chr6:13699589
|
G | A | 3 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209 | 3 | NA18949.hp2 NA18957.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.572-2693C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13699589 | ||||||
| chr6:13699902
|
A | G | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.572-3006T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13699902 | ||||||
| chr6:13699915
|
G | A | 1 | a0002c0003t0001g0341 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.572-3019C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13699915 | ||||||
| chr6:13699945
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.572-3049G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13699945 | ||||||
| chr6:13700187
|
C | T | 63 | a0001c0001t0001g0156a0001c0001t0001g0168a0001c0001t0001g0178others(60): Show | 63 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.572-3291G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13700187 | ||||||
| chr6:13700207
|
T | G | 1 | a0001c0002t0001g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.572-3311A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13700207 | ||||||
| chr6:13700271
|
C | G | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.572-3375G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13700271 | ||||||
| chr6:13700400
|
C | T | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.572-3504G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13700400 | ||||||
| chr6:13700403
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.572-3507G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13700403 | ||||||
| chr6:13700487
|
AGTAG | A | 141 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0149others(138): Show | 141 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.572-3595_572-3592d others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13700487 | ||||||
| chr6:13700747
|
C | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.572-3851G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13700747 | ||||||
| chr6:13700758
|
G | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.572-3862C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13700758 | ||||||
| chr6:13700908
|
A | T | 5 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG01891.hp1 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.572-4012T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13700908 | ||||||
| chr6:13700993
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.572-4097C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13700993 | ||||||
| chr6:13701048
|
G | A | 1 | a0001c0002t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.572-4152C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13701048 | ||||||
| chr6:13701066
|
T | C | 5 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG01891.hp1 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.572-4170A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13701066 | ||||||
| chr6:13701235
|
C | T | 1 | a0001c0002t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.572-4339G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13701235 | ||||||
| chr6:13701463
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.572-4567A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13701463 | ||||||
| chr6:13701465
|
A | G | 8 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.572-4569T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13701465 | ||||||
| chr6:13701865
|
C | T | 5 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0132others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.572-4969G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13701865 | ||||||
| chr6:13701866
|
G | A | 5 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG01891.hp1 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.572-4970C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13701866 | ||||||
| chr6:13702375
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.572-5479C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13702375 | ||||||
| chr6:13702483
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.572-5587G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13702483 | ||||||
| chr6:13702680
|
A | C | 10 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(7): Show | 10 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.572-5784T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13702680 | ||||||
| chr6:13702890
|
C | G | 1 | a0001c0002t0001g0004 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.572-5994G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13702890 | ||||||
| chr6:13703179
|
T | C | 10 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(7): Show | 10 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.572-6283A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13703179 | ||||||
| chr6:13703318
|
T | G | 2 | a0001c0002t0001g0044a0001c0002t0001g0050 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.572-6422A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13703318 | ||||||
| chr6:13703374
|
C | T | 6 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.572-6478G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13703374 | ||||||
| chr6:13703568
|
G | C | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.572-6672C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13703568 | ||||||
| chr6:13703598
|
T | A | 8 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.572-6702A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13703598 | ||||||
| chr6:13703777
|
A | G | 8 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.572-6881T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13703777 | ||||||
| chr6:13704044
|
T | C | 6 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.571+6891A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13704044 | ||||||
| chr6:13704109
|
G | T | 350 | a0001c0001t0001g0001a0001c0001t0001g0135a0001c0001t0001g0136others(347): Show | 351 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(348): Show |
intron_variant | MODIFIER | c.571+6826C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13704109 | ||||||
| chr6:13704128
|
T | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571+6807A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13704128 | ||||||
| chr6:13704215
|
A | C | 2 | a0001c0006t0001g0220a0001c0006t0001g0221 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.571+6720T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13704215 | ||||||
| chr6:13704513
|
T | A | 6 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.571+6422A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13704513 | ||||||
| chr6:13704903
|
G | A | 6 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.571+6032C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13704903 | ||||||
| chr6:13704931
|
A | G | 6 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.571+6004T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13704931 | ||||||
| chr6:13704945
|
A | G | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.571+5990T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13704945 | ||||||
| chr6:13704951
|
C | T | 19 | a0001c0001t0001g0282a0001c0002t0001g0072a0001c0002t0001g0073others(16): Show | 19 | HG00558.hp1 HG01099.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.571+5984G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13704951 | ||||||
| chr6:13705269
|
T | G | 1 | a0001c0001t0001g0001 | 2 | HG02004.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.571+5666A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705269 | ||||||
| chr6:13705277
|
G | A | 2 | a0001c0006t0001g0220a0001c0006t0001g0221 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.571+5658C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705277 | ||||||
| chr6:13705291
|
C | T | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.571+5644G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705291 | ||||||
| chr6:13705356
|
A | G | 5 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG01891.hp1 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.571+5579T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705356 | ||||||
| chr6:13705378
|
G | A | 1 | a0001c0001t0002g0268 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.571+5557C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705378 | ||||||
| chr6:13705406
|
C | CA | 125 | a0001c0001t0001g0136a0001c0001t0001g0143a0001c0001t0001g0144others(122): Show | 125 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.571+5528dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705406 | ||||||
| chr6:13705406
|
C | CAA | 25 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0154others(22): Show | 25 | HG01099.hp1 HG01106.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.571+5527_571+5528d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705406 | ||||||
| chr6:13705406
|
C | CAAA | 8 | a0001c0001t0001g0168a0001c0001t0001g0172a0001c0001t0001g0182others(5): Show | 8 | HG02145.hp2 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.571+5526_571+5528d others(5): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705406 | ||||||
| chr6:13705406
|
CA | C | 37 | a0001c0001t0001g0150a0001c0001t0001g0173a0001c0001t0001g0219others(34): Show | 37 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.571+5528delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705406 | ||||||
| chr6:13705406
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0002t0001g0013a0001c0002t0006g0358a0001c0002t0006g0359 | 3 | HG01496.hp2 HG02055.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.571+5519_571+5528d others(12): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705406 | ||||||
| chr6:13705406
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.571+5517_571+5528d others(14): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705406 | ||||||
| chr6:13705636
|
C | G | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.571+5299G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705636 | ||||||
| chr6:13705654
|
G | A | 1 | a0001c0002t0001g0105 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.571+5281C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705654 | ||||||
| chr6:13705717
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0155 | 2 | HG00735.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.571+5218C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705717 | ||||||
| chr6:13705773
|
G | C | 1 | a0001c0002t0001g0006 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.571+5162C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705773 | ||||||
| chr6:13705868
|
C | CAAAA | 77 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0152others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.571+5063_571+5066d others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705868 | ||||||
| chr6:13705868
|
C | CAAAAA | 8 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0173others(5): Show | 8 | HG01175.hp2 HG02145.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.571+5062_571+5066d others(7): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705868 | ||||||
| chr6:13705868
|
C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(7): Show | 10 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.571+5059_571+5066d others(10): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705868 | ||||||
| chr6:13705868
|
C | CAAAAAAA others(9): Show |
5 | a0001c0001t0002g0169a0001c0001t0002g0185a0001c0001t0002g0207others(2): Show | 5 | HG00597.hp1 HG01981.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.571+5051_571+5066d others(18): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705868 | ||||||
| chr6:13705868
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0002g0209 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.571+5050_571+5066d others(19): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705868 | ||||||
| chr6:13705868
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0002g0170a0001c0001t0002g0186a0001c0002t0006g0359 | 3 | HG01496.hp2 HG02132.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.571+5066_571+5067i others(21): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705868 | ||||||
| chr6:13705868
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0002g0187 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.571+5066_571+5067i others(22): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705868 | ||||||
| chr6:13705868
|
C | CAAAAAAA others(14): Show |
14 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(11): Show | 14 | HG00735.hp2 HG00738.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.571+5066_571+5067i others(23): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705868 | ||||||
| chr6:13705868
|
C | CAAAAAAA others(15): Show |
11 | a0001c0001t0001g0155a0001c0001t0002g0139a0001c0001t0002g0141others(8): Show | 11 | HG00673.hp2 HG01169.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.571+5066_571+5067i others(24): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705868 | ||||||
| chr6:13705868
|
C | CAAAAAAA others(16): Show |
6 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(3): Show | 6 | HG01516.hp1 HG02109.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.571+5066_571+5067i others(25): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705868 | ||||||
| chr6:13705868
|
C | CAAAAAAA others(17): Show |
2 | a0001c0001t0002g0180a0001c0002t0001g0006 | 2 | HG00423.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.571+5066_571+5067i others(26): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705868 | ||||||
| chr6:13705868
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0002g0206 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.571+5066_571+5067i others(29): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705868 | ||||||
| chr6:13705875
|
A | AAAAAAAA others(39): Show |
1 | a0001c0001t0001g0331 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.571+5059_571+5060i others(48): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705875 | ||||||
| chr6:13705875
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0330 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.571+5059_571+5060i others(23): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705875 | ||||||
| chr6:13705980
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571+4955C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705980 | ||||||
| chr6:13705993
|
C | A | 1 | a0001c0002t0001g0005 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.571+4942G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13705993 | ||||||
| chr6:13706018
|
C | G | 263 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(260): Show | 263 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.571+4917G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13706018 | ||||||
| chr6:13706131
|
CAG | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01891.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.571+4802_571+4803d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13706131 | ||||||
| chr6:13706211
|
G | A | 1 | a0001c0002t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.571+4724C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13706211 | ||||||
| chr6:13706773
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571+4162C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13706773 | ||||||
| chr6:13706905
|
G | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0173 | 3 | HG02647.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.571+4030C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13706905 | ||||||
| chr6:13706936
|
G | A | 7 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+3999C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13706936 | ||||||
| chr6:13706985
|
G | A | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0294 | 3 | HG00639.hp1 HG01243.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.571+3950C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13706985 | ||||||
| chr6:13707005
|
C | CA | 63 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0285others(60): Show | 63 | HG00544.hp1 HG00558.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.571+3929dupT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707005 | ||||||
| chr6:13707005
|
C | CAA | 13 | a0001c0002t0001g0107a0001c0002t0001g0108a0001c0002t0001g0109others(10): Show | 13 | HG01192.hp2 HG01346.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.571+3928_571+3929d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707005 | ||||||
| chr6:13707005
|
CA | C | 8 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0002t0001g0133others(5): Show | 8 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.571+3929delT | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707005 | ||||||
| chr6:13707005
|
CAA | C | 134 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(131): Show | 134 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.571+3928_571+3929d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707005 | ||||||
| chr6:13707111
|
C | T | 1 | a0001c0014t0001g0333 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.571+3824G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707111 | ||||||
| chr6:13707251
|
T | G | 1 | a0001c0002t0001g0116 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.571+3684A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707251 | ||||||
| chr6:13707527
|
T | TAAA | 3 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209 | 3 | NA18949.hp2 NA18957.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.571+3407_571+3408i others(5): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707527 | ||||||
| chr6:13707536
|
C | T | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.571+3399G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707536 | ||||||
| chr6:13707665
|
A | G | 1 | a0001c0001t0002g0183 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.571+3270T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707665 | ||||||
| chr6:13707705
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.571+3230G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707705 | ||||||
| chr6:13707760
|
A | G | 7 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(4): Show | 7 | HG01884.hp1 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.571+3175T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707760 | ||||||
| chr6:13707782
|
T | C | 1 | a0002c0003t0001g0342 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.571+3153A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707782 | ||||||
| chr6:13707802
|
TAA | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.571+3131_571+3132d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707802 | ||||||
| chr6:13707837
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.571+3098G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707837 | ||||||
| chr6:13707875
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.571+3060A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707875 | ||||||
| chr6:13707878
|
T | G | 2 | a0001c0002t0001g0118a0001c0002t0001g0119 | 2 | HG01358.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.571+3057A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707878 | ||||||
| chr6:13707891
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.571+3044T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707891 | ||||||
| chr6:13707917
|
T | C | 6 | a0001c0001t0002g0303a0001c0001t0002g0304a0001c0001t0002g0325others(3): Show | 6 | HG00741.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.571+3018A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13707917 | ||||||
| chr6:13708092
|
C | T | 1 | a0001c0002t0004g0352 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.571+2843G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708092 | ||||||
| chr6:13708208
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571+2727C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708208 | ||||||
| chr6:13708430
|
A | G | 8 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0002t0001g0004others(5): Show | 8 | HG01361.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.571+2505T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708430 | ||||||
| chr6:13708433
|
T | C | 10 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(7): Show | 10 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.571+2502A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708433 | ||||||
| chr6:13708504
|
T | C | 1 | a0001c0002t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.571+2431A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708504 | ||||||
| chr6:13708527
|
G | T | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571+2408C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708527 | ||||||
| chr6:13708686
|
T | C | 144 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(141): Show | 144 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.571+2249A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708686 | ||||||
| chr6:13708753
|
T | G | 1 | a0001c0001t0001g0326 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.571+2182A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708753 | ||||||
| chr6:13708812
|
G | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.571+2123C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708812 | ||||||
| chr6:13708819
|
T | TCA | 35 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(32): Show | 35 | HG00099.hp1 HG00423.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.571+2114_571+2115d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708819 | ||||||
| chr6:13708819
|
T | TCACA | 58 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0309others(55): Show | 58 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.571+2112_571+2115d others(6): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708819 | ||||||
| chr6:13708819
|
T | TCACACA | 3 | a0001c0001t0001g0327a0001c0001t0002g0210a0001c0002t0001g0132 | 3 | HG01981.hp2 NA18965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571+2110_571+2115d others(8): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708819 | ||||||
| chr6:13708819
|
TCA | T | 11 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0002g0213others(8): Show | 11 | HG00423.hp1 HG02027.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.571+2114_571+2115d others(4): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708819 | ||||||
| chr6:13708844
|
C | G | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | NA18993.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.571+2091G>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708844 | ||||||
| chr6:13708871
|
A | G | 1 | a0001c0002t0001g0123 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.571+2064T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708871 | ||||||
| chr6:13708908
|
G | A | 7 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(4): Show | 7 | HG01884.hp1 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.571+2027C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708908 | ||||||
| chr6:13708933
|
T | C | 1 | a0005c0012t0001g0328 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.571+2002A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708933 | ||||||
| chr6:13708938
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571+1997C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708938 | ||||||
| chr6:13708942
|
G | T | 2 | a0001c0002t0001g0003a0001c0002t0001g0010 | 2 | HG01099.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.571+1993C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708942 | ||||||
| chr6:13708948
|
A | G | 144 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(141): Show | 144 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.571+1987T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13708948 | ||||||
| chr6:13709007
|
G | A | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.571+1928C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709007 | ||||||
| chr6:13709081
|
A | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.571+1854T>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709081 | ||||||
| chr6:13709171
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.571+1764T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709171 | ||||||
| chr6:13709282
|
A | C | 9 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.571+1653T>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709282 | ||||||
| chr6:13709321
|
A | G | 3 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009 | 3 | HG02970.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.571+1614T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709321 | ||||||
| chr6:13709342
|
A | G | 12 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0002t0001g0004others(9): Show | 12 | HG01361.hp1 HG01496.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.571+1593T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709342 | ||||||
| chr6:13709424
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.571+1511T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709424 | ||||||
| chr6:13709627
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.571+1308A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709627 | ||||||
| chr6:13709631
|
G | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0005c0012t0001g0328 | 3 | HG02145.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.571+1304C>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709631 | ||||||
| chr6:13709646
|
G | T | 1 | a0001c0001t0002g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.571+1289C>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709646 | ||||||
| chr6:13709652
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.571+1283G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709652 | ||||||
| chr6:13709669
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG02451.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.571+1266G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709669 | ||||||
| chr6:13709706
|
T | C | 1 | a0001c0001t0001g0329 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571+1229A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709706 | ||||||
| chr6:13709789
|
C | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571+1146G>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709789 | ||||||
| chr6:13709894
|
A | G | 1 | a0001c0002t0001g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.571+1041T>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709894 | ||||||
| chr6:13709940
|
T | C | 1 | a0001c0002t0001g0131 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.571+995A>G | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13709940 | ||||||
| chr6:13710091
|
T | A | 3 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0009t0001g0134 | 3 | HG02055.hp2 HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571+844A>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13710091 | ||||||
| chr6:13710170
|
T | G | 2 | a0001c0002t0006g0358a0001c0002t0006g0359 | 2 | HG01496.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.571+765A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13710170 | ||||||
| chr6:13710305
|
G | A | 3 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0009t0001g0134 | 3 | HG02055.hp2 HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571+630C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13710305 | ||||||
| chr6:13710403
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.571+532G>A | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13710403 | ||||||
| chr6:13710609
|
G | A | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.571+326C>T | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13710609 | ||||||
| chr6:13710679
|
T | G | 1 | a0001c0001t0002g0332 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.571+256A>C | RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 1/13 | chr6 | 13710679 |