Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 28981 |
|---|---|
| ensemblid | ENSG00000122970.16 |
| hgncid | 14313 |
| symbol | IFT81 |
| name | intraflagellar transport 81 |
| refseq_nuc | NM_014055.4 |
| refseq_prot | NP_054774.2 |
| ensembl_nuc | ENST00000242591.10 |
| ensembl_prot | ENSP00000242591.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 110124357 |
| end | 110218793 |
| strand | + |
| ver | v1.2 |
| region | chr12:110124357-110218793 |
| region5000 | chr12:110119357-110223793 |
| regionname0 | IFT81_chr12_110124357_110218793 |
| regionname5000 | IFT81_chr12_110119357_110223793 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 676 | 206 | 78 | 49 | 44 | 12 | 21 | 34 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0002 | 0/0 | 676 | 9 | 6 | 3 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0003 | 0/0 | 676 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0004 | 0/0 | 676 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2031 | 204 | 77 | 49 | 44 | 11 | 21 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| c0002 | 0/0 | 2031 | 9 | 6 | 3 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| c0003 | 0/0 | 2031 | 2 | 0 | 0 | 0 | 0 | 2 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| c0004 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| c0005 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| c0006 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1094 | 174 | 74 | 31 | 44 | 7 | 17 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| t0002 | 0/1 | 1094 | 34 | 9 | 16 | 0 | 4 | 4 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| t0003 | 0/0 | 1094 | 5 | 0 | 4 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| t0004 | 0/0 | 1094 | 3 | 0 | 0 | 0 | 0 | 3 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| t0005 | 0/0 | 1094 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| t0006 | 0/0 | 1094 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2031 | 204 | 77 | 49 | 44 | 11 | 21 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0001c0004 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0001c0005 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0002c0002 | 0/0 | 2031 | 9 | 6 | 3 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0003c0003 | 0/0 | 2031 | 2 | 0 | 0 | 0 | 0 | 2 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0004c0006 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3124 | 163 | 67 | 28 | 44 | 6 | 17 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0001c0001t0002 | 0/1 | 3124 | 34 | 9 | 16 | 0 | 4 | 4 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0001c0001t0003 | 0/0 | 3124 | 5 | 0 | 4 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0001c0001t0005 | 0/0 | 3124 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0001c0001t0006 | 0/0 | 3124 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0001c0004t0001 | 0/0 | 3124 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0001c0005t0001 | 0/0 | 3124 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0002c0002t0001 | 0/0 | 3124 | 9 | 6 | 3 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0003c0003t0004 | 0/0 | 3124 | 2 | 0 | 0 | 0 | 0 | 2 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| a0004c0006t0004 | 0/0 | 3124 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | copy fasta | chr12 | 110119357 | 110223793 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0004t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0001c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0003c0003t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0003c0003t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| a0004c0006t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | GBR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0195 | EUR | FIN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | FIN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0214 | EUR | FIN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0176 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0190 | EUR | IBS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01516 | hp2 | a0001 | c0005 | t0001 | g0082 | EUR | IBS | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03654 | hp2 | a0004 | c0006 | t0004 | g0076 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03688 | hp1 | a0003 | c0003 | t0004 | g0077 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04115 | hp2 | a0003 | c0003 | t0004 | g0102 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | BEB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | STU | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0047 | AFR | YRI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | ASW | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | ASW | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0218 | EUR | TSI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | TSI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0210 | EUR | TSI | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0019 | AFR | MSL | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | USA | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | USA | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0198 | REF | REF | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0110 | REF | REF | IFT81_chr12_110119357_110223793 | IFT81 | chr12 | 110119357 | 110223793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110129102
|
A | G | 2 | a0003a0004 | 3 | HG03654.hp2 HG03688.hp1 HG04115.hp2 |
missense_variant | MODERATE | c.401A>G | p.Asp134Gly | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/19 | 927/3124 | 401/2031 | 134/676 | chr12 | 110129102 | ||
| chr12:110135405
|
C | G | 1 | a0002 | 9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
missense_variant | MODERATE | c.664C>G | p.Leu222Val | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/19 | 1190/3124 | 664/2031 | 222/676 | chr12 | 110135405 | ||
| chr12:110136788
|
G | T | 1 | a0004 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.709G>T | p.Val237Leu | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/19 | 1235/3124 | 709/2031 | 237/676 | chr12 | 110136788 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110180430
|
A | G | 1 | a0001c0005 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.1197A>G | p.Arg399Arg | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/19 | 1723/3124 | 1197/2031 | 399/676 | chr12 | 110180430 | ||
| chr12:110180484
|
A | C | 1 | a0001c0004 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.1251A>C | p.Ile417Ile | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/19 | 1777/3124 | 1251/2031 | 417/676 | chr12 | 110180484 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110124404
|
C | T | 1 | a0001c0001t0006 | 1 | HG00735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-479C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/19 | 2977 | chr12 | 110124404 | |||||
| chr12:110124692
|
C | T | 1 | a0001c0001t0002 | 34 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(31): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-191C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/19 | chr12 | 110124692 | ||||||
| chr12:110124714
|
G | A | 1 | a0001c0001t0003 | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-169G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/19 | 2667 | chr12 | 110124714 | |||||
| chr12:110218646
|
C | T | 1 | a0001c0001t0005 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 19/19 | 420 | chr12 | 110218646 | |||||
| chr12:110218708
|
T | G | 2 | a0003c0003t0004a0004c0006t0004 | 3 | HG03654.hp2 HG03688.hp1 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*482T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 19/19 | 482 | chr12 | 110218708 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110125105
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(57): Show | 60 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.-22+244G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110125105 | ||||||
| chr12:110125247
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-22+386G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110125247 | ||||||
| chr12:110125805
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 106 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-22+944C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110125805 | ||||||
| chr12:110126132
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-21-1228G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110126132 | ||||||
| chr12:110126209
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-21-1151C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110126209 | ||||||
| chr12:110126277
|
C | CA | 9 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-1064dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr12 | 110126277 | |||||
| chr12:110126277
|
CA | C | 50 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 50 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.-21-1064delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr12 | 110126277 | |||||
| chr12:110126277
|
CAA | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(56): Show | 59 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-21-1065_-21-1064d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr12 | 110126277 | |||||
| chr12:110126303
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(54): Show | 57 | HG00323.hp2 HG01099.hp1 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.-21-1057G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110126303 | ||||||
| chr12:110126854
|
A | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-21-506A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110126854 | ||||||
| chr12:110126929
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.-21-431C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110126929 | ||||||
| chr12:110126930
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-21-430A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110126930 | ||||||
| chr12:110127073
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-21-287G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110127073 | ||||||
| chr12:110127273
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-21-87C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 1/18 | chr12 | 110127273 | ||||||
| chr12:110128786
|
C | CA | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(8): Show | 11 | HG00099.hp1 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.249-140dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr12 | 110128786 | |||||
| chr12:110128786
|
CA | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 95 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.249-140delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr12 | 110128786 | |||||
| chr12:110128786
|
CAA | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0059a0001c0001t0001g0060others(2): Show | 5 | HG00323.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.249-141_249-140del others(2): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr12 | 110128786 | |||||
| chr12:110129203
|
C | G | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.429+73C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110129203 | ||||||
| chr12:110129490
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.429+360C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110129490 | ||||||
| chr12:110129617
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.429+487A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110129617 | ||||||
| chr12:110129650
|
T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0073 | 2 | NA18953.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.429+520T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110129650 | ||||||
| chr12:110129697
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0014 | 2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.429+567G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110129697 | ||||||
| chr12:110129835
|
AT | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0074a0001c0001t0001g0111others(3): Show | 6 | HG01099.hp2 HG01168.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+720delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr12 | 110129835 | |||||
| chr12:110129850
|
TA | T | 10 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(7): Show | 10 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.429+725delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr12 | 110129850 | |||||
| chr12:110129851
|
A | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0055a0001c0001t0001g0056others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.429+721A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110129851 | ||||||
| chr12:110130365
|
C | CT | 51 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.429+1251dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr12 | 110130365 | |||||
| chr12:110130416
|
A | T | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.429+1286A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110130416 | ||||||
| chr12:110130818
|
A | G | 44 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(41): Show | 44 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.429+1688A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110130818 | ||||||
| chr12:110131118
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.430-1429C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131118 | ||||||
| chr12:110131291
|
C | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 106 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.430-1256C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131291 | ||||||
| chr12:110131317
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.430-1230T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131317 | ||||||
| chr12:110131560
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-987C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131560 | ||||||
| chr12:110131567
|
C | T | 5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-980C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131567 | ||||||
| chr12:110131807
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.430-740A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131807 | ||||||
| chr12:110131855
|
T | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-692T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110131855 | ||||||
| chr12:110132143
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.430-404C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110132143 | ||||||
| chr12:110132255
|
G | C | 2 | a0001c0001t0001g0171a0001c0001t0006g0176 | 2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.430-292G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | chr12 | 110132255 | ||||||
| chr12:110132315
|
CCGGG | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-229_430-226del others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr12 | 110132315 | |||||
| chr12:110132459
|
C | CA | 20 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(17): Show | 20 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.430-72dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr12 | 110132459 | |||||
| chr12:110132825
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.519+189G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110132825 | ||||||
| chr12:110132970
|
C | CT | 18 | a0001c0001t0001g0004a0001c0001t0001g0068a0001c0001t0001g0069others(15): Show | 18 | HG00423.hp2 HG00558.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.519+352dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr12 | 110132970 | |||||
| chr12:110132970
|
CT | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 104 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.519+352delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr12 | 110132970 | |||||
| chr12:110132970
|
CTT | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0213others(2): Show | 5 | HG00323.hp2 HG01074.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+351_519+352del others(2): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr12 | 110132970 | |||||
| chr12:110132997
|
G | T | 1 | a0001c0001t0002g0207 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.519+361G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110132997 | ||||||
| chr12:110133097
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.519+461A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110133097 | ||||||
| chr12:110133120
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.519+484G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110133120 | ||||||
| chr12:110133180
|
C | T | 39 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0114others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.519+544C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110133180 | ||||||
| chr12:110133459
|
GA | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 174 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.519+838delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr12 | 110133459 | |||||
| chr12:110133489
|
ATGG | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0004t0001g0019 | 3 | HG02055.hp1 HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.519+859_519+861del others(3): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr12 | 110133489 | |||||
| chr12:110133569
|
A | G | 23 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0117others(20): Show | 23 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.519+933A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110133569 | ||||||
| chr12:110133829
|
A | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0035 | 2 | HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.520-1119A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110133829 | ||||||
| chr12:110134040
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.520-908A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134040 | ||||||
| chr12:110134158
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.520-790G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134158 | ||||||
| chr12:110134307
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.520-641C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134307 | ||||||
| chr12:110134308
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.520-640G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134308 | ||||||
| chr12:110134335
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 109 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.520-613C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134335 | ||||||
| chr12:110134388
|
T | G | 7 | a0001c0001t0001g0036a0001c0001t0001g0170a0001c0001t0001g0172others(4): Show | 7 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-560T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134388 | ||||||
| chr12:110134424
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.520-524G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134424 | ||||||
| chr12:110134491
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.520-457C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134491 | ||||||
| chr12:110134580
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.520-368T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134580 | ||||||
| chr12:110134732
|
A | C | 2 | a0001c0001t0001g0171a0001c0001t0006g0176 | 2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.520-216A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 5/18 | chr12 | 110134732 | ||||||
| chr12:110135064
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.585+51G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 6/18 | chr12 | 110135064 | ||||||
| chr12:110135108
|
G | A | 19 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.585+95G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 6/18 | chr12 | 110135108 | ||||||
| chr12:110135141
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.585+128G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 6/18 | chr12 | 110135141 | ||||||
| chr12:110135535
|
G | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 106 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.696+98G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135535 | ||||||
| chr12:110135551
|
T | C | 5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+114T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135551 | ||||||
| chr12:110135629
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.696+192G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135629 | ||||||
| chr12:110135640
|
G | A | 9 | a0002c0002t0001g0012a0002c0002t0001g0046a0002c0002t0001g0048others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.696+203G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135640 | ||||||
| chr12:110135721
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+284G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135721 | ||||||
| chr12:110135728
|
A | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.696+291A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135728 | ||||||
| chr12:110135866
|
GA | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 93 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.696+448delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr12 | 110135866 | |||||
| chr12:110135866
|
GAA | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0045others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+447_696+448del others(2): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr12 | 110135866 | |||||
| chr12:110135956
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG00558.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.696+519C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110135956 | ||||||
| chr12:110136172
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.697-604C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110136172 | ||||||
| chr12:110136480
|
T | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.697-296T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110136480 | ||||||
| chr12:110136583
|
A | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.697-193A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 7/18 | chr12 | 110136583 | ||||||
| chr12:110136870
|
AATT | A | 23 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(20): Show | 23 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.781+16_781+18delTA others(1): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110136870 | |||||
| chr12:110136942
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.781+82G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110136942 | ||||||
| chr12:110136947
|
A | T | 1 | a0001c0001t0001g0034 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.781+87A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110136947 | ||||||
| chr12:110137003
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.781+143G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137003 | ||||||
| chr12:110137121
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0033 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.781+261C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137121 | ||||||
| chr12:110137148
|
T | G | 1 | a0001c0001t0002g0181 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.781+288T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137148 | ||||||
| chr12:110137300
|
A | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0113 | 3 | HG02615.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.781+440A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137300 | ||||||
| chr12:110137639
|
G | A | 44 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(41): Show | 44 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.781+779G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137639 | ||||||
| chr12:110137691
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.781+831G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137691 | ||||||
| chr12:110137740
|
A | AAAAT | 4 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0002g0206others(1): Show | 4 | HG00642.hp2 HG02258.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+904_781+907dup others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110137740 | |||||
| chr12:110137787
|
T | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0020 | 3 | HG01099.hp1 HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.781+927T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110137787 | ||||||
| chr12:110137926
|
T | TCTCTGGC others(354): Show |
1 | a0001c0001t0001g0035 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.781+1082_781+1083i others(363): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110137926 | |||||
| chr12:110138057
|
G | T | 1 | a0001c0001t0001g0034 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.781+1197G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138057 | ||||||
| chr12:110138130
|
A | ATCTTTC | 2 | a0001c0001t0001g0171a0001c0001t0006g0176 | 2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.781+1272_781+1277d others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110138130 | |||||
| chr12:110138196
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.781+1336C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138196 | ||||||
| chr12:110138200
|
G | T | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.781+1340G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138200 | ||||||
| chr12:110138290
|
A | G | 19 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.781+1430A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138290 | ||||||
| chr12:110138481
|
G | A | 11 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0116others(8): Show | 11 | HG00423.hp2 HG00558.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.781+1621G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138481 | ||||||
| chr12:110138553
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.781+1693C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138553 | ||||||
| chr12:110138668
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.781+1808G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110138668 | ||||||
| chr12:110139203
|
G | T | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(40): Show | 43 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.781+2343G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139203 | ||||||
| chr12:110139239
|
A | C | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(40): Show | 43 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.781+2379A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139239 | ||||||
| chr12:110139336
|
C | CA | 19 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0017others(16): Show | 19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.781+2495dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139336 | |||||
| chr12:110139439
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.781+2579C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139439 | ||||||
| chr12:110139626
|
T | A | 1 | a0001c0001t0002g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.781+2766T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139626 | ||||||
| chr12:110139643
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG01099.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.781+2783G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139643 | ||||||
| chr12:110139664
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0006g0176 | 2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.781+2804C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139664 | ||||||
| chr12:110139707
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.781+2847G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139707 | ||||||
| chr12:110139782
|
CACAT | C | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.781+2938_781+2941d others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139782 | |||||
| chr12:110139797
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.781+2937A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139797 | ||||||
| chr12:110139800
|
C | A | 1 | a0001c0001t0002g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.781+2940C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139800 | ||||||
| chr12:110139817
|
A | T | 1 | a0001c0001t0002g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.781+2957A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139817 | ||||||
| chr12:110139818
|
T | A | 1 | a0001c0001t0002g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.781+2958T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139818 | ||||||
| chr12:110139818
|
T | TAAATA | 23 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(20): Show | 23 | HG00323.hp2 HG01099.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.781+2986_781+2990d others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139818 | |||||
| chr12:110139818
|
T | TAAATAAA others(3): Show |
15 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0033others(12): Show | 15 | HG00735.hp2 HG01167.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.781+2981_781+2990d others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139818 | |||||
| chr12:110139818
|
T | TAAATAAA others(8): Show |
10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0055others(7): Show | 10 | HG01243.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.781+2976_781+2990d others(17): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139818 | |||||
| chr12:110139846
|
A | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.781+2986A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139846 | ||||||
| chr12:110139847
|
T | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.781+2987T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139847 | ||||||
| chr12:110139847
|
T | TA | 6 | a0001c0001t0001g0008a0002c0002t0001g0012a0002c0002t0001g0048others(3): Show | 6 | HG02109.hp2 HG02818.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.781+2990dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139847 | |||||
| chr12:110139849
|
A | AAATAAAA others(20): Show |
1 | a0001c0001t0001g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.781+2990_781+2991i others(29): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139849 | |||||
| chr12:110139849
|
A | AATAAAAT others(5): Show |
3 | a0001c0001t0002g0178a0001c0001t0002g0204a0001c0001t0002g0214 | 3 | HG00323.hp1 HG01928.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.781+2991_781+3002d others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139849 | |||||
| chr12:110139851
|
T | A | 2 | a0001c0001t0002g0207a0001c0004t0001g0019 | 2 | HG01109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.781+2991T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139851 | ||||||
| chr12:110139852
|
A | T | 2 | a0001c0001t0002g0207a0001c0004t0001g0019 | 2 | HG01109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.781+2992A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139852 | ||||||
| chr12:110139854
|
A | AATAAAAT | 18 | a0001c0001t0002g0179a0001c0001t0002g0192a0001c0001t0002g0193others(15): Show | 18 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.781+2996_781+3002d others(9): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139854 | |||||
| chr12:110139859
|
A | AAT | 6 | a0001c0001t0002g0177a0001c0001t0002g0182a0001c0001t0002g0186others(3): Show | 6 | HG01123.hp1 HG01516.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+3001_781+3002d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139859 | |||||
| chr12:110139863
|
A | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0002g0181others(2): Show | 5 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+3003A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139863 | ||||||
| chr12:110139866
|
T | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0002g0181others(2): Show | 5 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+3006T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139866 | ||||||
| chr12:110139866
|
T | TAAA | 28 | a0001c0001t0001g0042a0001c0001t0002g0177a0001c0001t0002g0178others(25): Show | 28 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.781+3007_781+3008i others(5): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | |||||
| chr12:110139866
|
T | TAAAATAA others(18): Show |
1 | a0002c0002t0001g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.781+3007_781+3008i others(27): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | |||||
| chr12:110139866
|
T | TAAATAAA others(22): Show |
4 | a0002c0002t0001g0012a0002c0002t0001g0049a0002c0002t0001g0050others(1): Show | 4 | HG02109.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+3007_781+3008i others(31): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | |||||
| chr12:110139866
|
T | TATAAA | 45 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(42): Show | 45 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.781+3043_781+3047d others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | |||||
| chr12:110139866
|
T | TATAAAAT others(3): Show |
23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(20): Show | 23 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.781+3038_781+3047d others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | |||||
| chr12:110139866
|
T | TATAAAAT others(8): Show |
5 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0040others(2): Show | 5 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+3033_781+3047d others(17): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | |||||
| chr12:110139866
|
TATAAA | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0075 | 2 | HG03710.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.781+3043_781+3047d others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139866 | |||||
| chr12:110139868
|
T | A | 2 | a0001c0001t0001g0008a0001c0004t0001g0019 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.781+3008T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139868 | ||||||
| chr12:110139871
|
A | T | 2 | a0001c0001t0001g0008a0001c0004t0001g0019 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.781+3011A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139871 | ||||||
| chr12:110139873
|
T | A | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.781+3013T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139873 | ||||||
| chr12:110139876
|
A | T | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.781+3016A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139876 | ||||||
| chr12:110139903
|
T | TAAAATAA others(18): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.781+3047_781+3048i others(27): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110139903 | |||||
| chr12:110139955
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.781+3095G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110139955 | ||||||
| chr12:110140035
|
C | A | 1 | a0001c0001t0001g0135 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.781+3175C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140035 | ||||||
| chr12:110140105
|
T | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(56): Show | 59 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.781+3245T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140105 | ||||||
| chr12:110140106
|
T | A | 9 | a0002c0002t0001g0012a0002c0002t0001g0046a0002c0002t0001g0048others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.781+3246T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140106 | ||||||
| chr12:110140288
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.782-3094G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140288 | ||||||
| chr12:110140372
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.782-3010G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140372 | ||||||
| chr12:110140387
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 109 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.782-2995C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140387 | ||||||
| chr12:110140466
|
T | G | 9 | a0002c0002t0001g0012a0002c0002t0001g0046a0002c0002t0001g0048others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.782-2916T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110140466 | ||||||
| chr12:110141018
|
C | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.782-2364C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110141018 | ||||||
| chr12:110141198
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.782-2184G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110141198 | ||||||
| chr12:110141360
|
TTTCTC | T | 4 | a0001c0001t0001g0061a0003c0003t0004g0077a0003c0003t0004g0102others(1): Show | 4 | HG03654.hp2 HG03688.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.782-2013_782-2009d others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr12 | 110141360 | |||||
| chr12:110141474
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.782-1908G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110141474 | ||||||
| chr12:110141612
|
G | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.782-1770G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110141612 | ||||||
| chr12:110141823
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.782-1559G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110141823 | ||||||
| chr12:110142272
|
A | G | 1 | a0001c0001t0005g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.782-1110A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110142272 | ||||||
| chr12:110142329
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.782-1053G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110142329 | ||||||
| chr12:110142356
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.782-1026C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110142356 | ||||||
| chr12:110142418
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.782-964C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110142418 | ||||||
| chr12:110142533
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0060 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.782-849A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110142533 | ||||||
| chr12:110142949
|
C | G | 10 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(7): Show | 10 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.782-433C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110142949 | ||||||
| chr12:110143081
|
A | G | 1 | a0001c0001t0002g0177 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.782-301A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110143081 | ||||||
| chr12:110143099
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.782-283G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110143099 | ||||||
| chr12:110143215
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.782-167T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 8/18 | chr12 | 110143215 | ||||||
| chr12:110143926
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0034 | 3 | HG00323.hp2 HG01175.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.945+381A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110143926 | ||||||
| chr12:110144007
|
C | CT | 11 | a0001c0001t0001g0067a0001c0001t0001g0099a0001c0001t0001g0100others(8): Show | 11 | HG01071.hp1 HG01081.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.945+483dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144007 | |||||
| chr12:110144007
|
C | CTT | 25 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0024others(22): Show | 25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.945+482_945+483dup others(2): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144007 | |||||
| chr12:110144007
|
C | CTTT | 17 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(14): Show | 17 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.945+481_945+483dup others(3): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144007 | |||||
| chr12:110144007
|
CT | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0111others(6): Show | 9 | HG00735.hp2 HG00738.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.945+483delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144007 | |||||
| chr12:110144302
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0004t0001g0019 | 3 | HG02055.hp1 HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.945+757C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144302 | ||||||
| chr12:110144363
|
C | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG00621.hp2 NA18968.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.945+818C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144363 | ||||||
| chr12:110144430
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0060 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.945+885T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144430 | ||||||
| chr12:110144533
|
C | T | 5 | a0001c0001t0001g0067a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 5 | HG00423.hp1 NA18944.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.945+988C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144533 | ||||||
| chr12:110144577
|
C | G | 1 | a0001c0001t0002g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.945+1032C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144577 | ||||||
| chr12:110144711
|
A | AT | 36 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0098others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.945+1169dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144711 | |||||
| chr12:110144756
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.945+1211C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144756 | ||||||
| chr12:110144863
|
C | CT | 6 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0134others(3): Show | 6 | HG00735.hp1 HG01081.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.945+1341dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144863 | |||||
| chr12:110144863
|
CT | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(80): Show | 83 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.945+1341delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110144863 | |||||
| chr12:110144898
|
C | G | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.945+1353C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110144898 | ||||||
| chr12:110145028
|
A | AT | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(65): Show | 68 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.945+1506dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110145028 | |||||
| chr12:110145028
|
A | ATT | 27 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(24): Show | 27 | HG00738.hp1 HG01069.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.945+1505_945+1506d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110145028 | |||||
| chr12:110145140
|
C | T | 9 | a0002c0002t0001g0012a0002c0002t0001g0046a0002c0002t0001g0048others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.945+1595C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110145140 | ||||||
| chr12:110145308
|
G | T | 13 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(10): Show | 13 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.946-1645G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110145308 | ||||||
| chr12:110145443
|
G | GT | 5 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0020others(2): Show | 5 | HG01099.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-1497dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110145443 | |||||
| chr12:110145478
|
G | T | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.946-1475G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110145478 | ||||||
| chr12:110145781
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.946-1172A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110145781 | ||||||
| chr12:110145798
|
ATTTTG | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 108 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.946-1130_946-1126d others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr12 | 110145798 | |||||
| chr12:110145845
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.946-1108C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110145845 | ||||||
| chr12:110146107
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.946-846C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110146107 | ||||||
| chr12:110146446
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.946-507G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110146446 | ||||||
| chr12:110146584
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.946-369A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110146584 | ||||||
| chr12:110146707
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.946-246G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110146707 | ||||||
| chr12:110146721
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.946-232C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 9/18 | chr12 | 110146721 | ||||||
| chr12:110147179
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1041+131T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147179 | ||||||
| chr12:110147275
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1041+227C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147275 | ||||||
| chr12:110147311
|
G | C | 1 | a0001c0001t0001g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1041+263G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147311 | ||||||
| chr12:110147502
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1041+454T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147502 | ||||||
| chr12:110147632
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0004t0001g0019 | 3 | HG02055.hp1 HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1041+584A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147632 | ||||||
| chr12:110147847
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1041+799A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147847 | ||||||
| chr12:110147922
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+874A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110147922 | ||||||
| chr12:110148076
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1041+1028G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148076 | ||||||
| chr12:110148367
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1041+1319T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148367 | ||||||
| chr12:110148473
|
G | A | 34 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0179others(31): Show | 34 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1041+1425G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148473 | ||||||
| chr12:110148724
|
T | A | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1041+1676T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148724 | ||||||
| chr12:110148748
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1041+1700C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148748 | ||||||
| chr12:110148837
|
T | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+1789T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148837 | ||||||
| chr12:110148908
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1041+1860T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110148908 | ||||||
| chr12:110149780
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1041+2732T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149780 | ||||||
| chr12:110149832
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1041+2784G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149832 | ||||||
| chr12:110149846
|
C | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0207 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1041+2798C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149846 | ||||||
| chr12:110149857
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0014 | 2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1041+2809G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149857 | ||||||
| chr12:110149912
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1041+2864C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149912 | ||||||
| chr12:110149927
|
T | A | 1 | a0001c0001t0002g0192 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1041+2879T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149927 | ||||||
| chr12:110149987
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0006g0176 | 2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1041+2939G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110149987 | ||||||
| chr12:110150118
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1041+3070T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150118 | ||||||
| chr12:110150129
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1041+3081C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150129 | ||||||
| chr12:110150263
|
C | A | 1 | a0001c0001t0002g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1041+3215C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150263 | ||||||
| chr12:110150263
|
C | T | 1 | a0001c0001t0002g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1041+3215C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150263 | ||||||
| chr12:110150328
|
A | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+3280A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150328 | ||||||
| chr12:110150656
|
AC | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+3609delC | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150656 | ||||||
| chr12:110150776
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1041+3728C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150776 | ||||||
| chr12:110150823
|
G | C | 1 | a0001c0001t0001g0144 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1041+3775G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150823 | ||||||
| chr12:110150994
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1041+3946T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110150994 | ||||||
| chr12:110151027
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1041+3979A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151027 | ||||||
| chr12:110151187
|
C | T | 1 | a0003c0003t0004g0102 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1041+4139C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151187 | ||||||
| chr12:110151312
|
G | A | 3 | a0001c0001t0001g0061a0003c0003t0004g0077a0004c0006t0004g0076 | 3 | HG03654.hp2 HG03688.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1041+4264G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151312 | ||||||
| chr12:110151352
|
C | G | 2 | a0001c0001t0003g0211a0001c0001t0003g0212 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1041+4304C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151352 | ||||||
| chr12:110151539
|
T | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0020 | 3 | HG01099.hp1 HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1041+4491T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151539 | ||||||
| chr12:110151685
|
C | A | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041+4637C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151685 | ||||||
| chr12:110151764
|
C | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+4716C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110151764 | ||||||
| chr12:110152057
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1041+5009A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110152057 | ||||||
| chr12:110152421
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1041+5373A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110152421 | ||||||
| chr12:110152517
|
G | T | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1041+5469G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110152517 | ||||||
| chr12:110152539
|
G | T | 1 | a0001c0004t0001g0019 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1041+5491G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110152539 | ||||||
| chr12:110152629
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1041+5581G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110152629 | ||||||
| chr12:110152837
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0006g0176 | 2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1041+5789C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110152837 | ||||||
| chr12:110153077
|
C | T | 9 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(6): Show | 9 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1041+6029C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110153077 | ||||||
| chr12:110153443
|
T | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+6395T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110153443 | ||||||
| chr12:110153546
|
G | A | 8 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041+6498G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110153546 | ||||||
| chr12:110153671
|
C | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0207 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1041+6623C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110153671 | ||||||
| chr12:110153824
|
G | A | 24 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0038others(21): Show | 24 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1041+6776G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110153824 | ||||||
| chr12:110154059
|
C | T | 1 | a0001c0001t0002g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1041+7011C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154059 | ||||||
| chr12:110154070
|
G | A | 1 | a0001c0004t0001g0019 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1041+7022G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154070 | ||||||
| chr12:110154163
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1041+7115T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154163 | ||||||
| chr12:110154276
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1041+7228G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154276 | ||||||
| chr12:110154284
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1041+7236G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154284 | ||||||
| chr12:110154353
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1041+7305G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154353 | ||||||
| chr12:110154551
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1041+7503C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154551 | ||||||
| chr12:110154666
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1041+7618A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154666 | ||||||
| chr12:110154758
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1041+7710T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154758 | ||||||
| chr12:110154954
|
C | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+7906C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154954 | ||||||
| chr12:110154975
|
A | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+7927A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154975 | ||||||
| chr12:110154977
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+7929G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154977 | ||||||
| chr12:110154978
|
T | TGAGCCGA others(1): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+7930_1041+793 others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154978 | ||||||
| chr12:110154979
|
C | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+7931C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154979 | ||||||
| chr12:110154983
|
A | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1041+7935A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154983 | ||||||
| chr12:110154986
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-7933T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110154986 | ||||||
| chr12:110154987
|
A | ATTGCACT others(67): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-7930_1042-792 others(78): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110154987 | |||||
| chr12:110155018
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1042-7901A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155018 | ||||||
| chr12:110155319
|
G | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG00642.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1042-7600G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155319 | ||||||
| chr12:110155373
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1042-7546C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155373 | ||||||
| chr12:110155467
|
T | TGCCCAAC others(312): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1042-7436_1042-743 others(323): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110155467 | |||||
| chr12:110155500
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-7419C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155500 | ||||||
| chr12:110155537
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1042-7382C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155537 | ||||||
| chr12:110155604
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1042-7315G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155604 | ||||||
| chr12:110155755
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1042-7164G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110155755 | ||||||
| chr12:110156387
|
A | ACTTATTT others(327): Show |
1 | a0001c0001t0001g0005 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1042-6514_1042-651 others(338): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110156387 | |||||
| chr12:110156387
|
A | ACTTATTT others(328): Show |
1 | a0001c0001t0001g0006 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1042-6514_1042-651 others(339): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110156387 | |||||
| chr12:110156415
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1042-6504G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156415 | ||||||
| chr12:110156418
|
T | A | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1042-6501T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156418 | ||||||
| chr12:110156465
|
T | G | 34 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0179others(31): Show | 34 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1042-6454T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156465 | ||||||
| chr12:110156698
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(56): Show | 59 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.1042-6221C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156698 | ||||||
| chr12:110156779
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-6140G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156779 | ||||||
| chr12:110156806
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1042-6113C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156806 | ||||||
| chr12:110156950
|
T | A | 1 | a0001c0001t0001g0153 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1042-5969T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110156950 | ||||||
| chr12:110157014
|
A | AT | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(2): Show | 5 | HG00423.hp1 HG02258.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-5890dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110157014 | |||||
| chr12:110157150
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1042-5769C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157150 | ||||||
| chr12:110157206
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1042-5713G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157206 | ||||||
| chr12:110157329
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1042-5590A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157329 | ||||||
| chr12:110157566
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1042-5353T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157566 | ||||||
| chr12:110157705
|
A | T | 9 | a0002c0002t0001g0012a0002c0002t0001g0046a0002c0002t0001g0048others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1042-5214A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157705 | ||||||
| chr12:110157831
|
T | C | 16 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0116others(13): Show | 16 | HG00423.hp2 HG00558.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1042-5088T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157831 | ||||||
| chr12:110157909
|
T | G | 4 | a0001c0001t0001g0061a0003c0003t0004g0077a0003c0003t0004g0102others(1): Show | 4 | HG03654.hp2 HG03688.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-5010T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110157909 | ||||||
| chr12:110158178
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1042-4741C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158178 | ||||||
| chr12:110158390
|
A | T | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1042-4529A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158390 | ||||||
| chr12:110158598
|
T | A | 3 | a0001c0001t0002g0182a0001c0001t0002g0189a0001c0001t0002g0205 | 3 | HG02717.hp1 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1042-4321T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158598 | ||||||
| chr12:110158763
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1042-4156G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158763 | ||||||
| chr12:110158777
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0033 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1042-4142G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158777 | ||||||
| chr12:110158815
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1042-4104C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158815 | ||||||
| chr12:110158842
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-4077C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158842 | ||||||
| chr12:110158965
|
G | A | 5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1042-3954G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110158965 | ||||||
| chr12:110159266
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-3653C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159266 | ||||||
| chr12:110159371
|
G | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-3548G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159371 | ||||||
| chr12:110159441
|
T | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(57): Show | 60 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1042-3478T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159441 | ||||||
| chr12:110159442
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1042-3477G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159442 | ||||||
| chr12:110159499
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(72): Show | 75 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.1042-3420C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159499 | ||||||
| chr12:110159524
|
T | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0059others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-3395T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159524 | ||||||
| chr12:110159628
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1042-3291C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159628 | ||||||
| chr12:110159741
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1042-3178G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159741 | ||||||
| chr12:110159790
|
TCCAGCAA others(18): Show |
T | 1 | a0001c0001t0001g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1042-3127_1042-310 others(29): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110159790 | |||||
| chr12:110159871
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1042-3048G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110159871 | ||||||
| chr12:110160015
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-2904A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160015 | ||||||
| chr12:110160037
|
C | T | 19 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1042-2882C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160037 | ||||||
| chr12:110160076
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1042-2843G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160076 | ||||||
| chr12:110160252
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1042-2667C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160252 | ||||||
| chr12:110160514
|
G | T | 19 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1042-2405G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160514 | ||||||
| chr12:110160592
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1042-2327A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160592 | ||||||
| chr12:110160906
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02258.hp2 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1042-2013A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110160906 | ||||||
| chr12:110161064
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1042-1855A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110161064 | ||||||
| chr12:110161134
|
C | CT | 37 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0001t0001g0101others(34): Show | 37 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1042-1767dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110161134 | |||||
| chr12:110161654
|
A | G | 1 | a0001c0001t0002g0181 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1042-1265A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110161654 | ||||||
| chr12:110161734
|
G | T | 10 | a0001c0001t0005g0047a0002c0002t0001g0012a0002c0002t0001g0046others(7): Show | 10 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042-1185G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110161734 | ||||||
| chr12:110162148
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(56): Show | 59 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.1042-771C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110162148 | ||||||
| chr12:110162251
|
GGTGTTAC others(43): Show |
G | 1 | a0001c0001t0006g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1042-661_1042-612d others(52): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110162251 | |||||
| chr12:110162331
|
CT | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 122 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1042-567delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr12 | 110162331 | |||||
| chr12:110162336
|
T | C | 1 | a0001c0001t0006g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1042-583T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110162336 | ||||||
| chr12:110162389
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-530C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110162389 | ||||||
| chr12:110162440
|
G | A | 34 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0179others(31): Show | 34 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1042-479G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110162440 | ||||||
| chr12:110162587
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1042-332G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 10/18 | chr12 | 110162587 | ||||||
| chr12:110163312
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0060 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1188+247C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163312 | ||||||
| chr12:110163327
|
G | A | 8 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1188+262G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163327 | ||||||
| chr12:110163614
|
C | CT | 10 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0023others(7): Show | 10 | HG01109.hp2 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1188+568dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110163614 | |||||
| chr12:110163614
|
CT | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0044others(4): Show | 7 | HG00738.hp1 HG01069.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1188+568delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110163614 | |||||
| chr12:110163646
|
C | T | 8 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1188+581C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163646 | ||||||
| chr12:110163650
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1188+585C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163650 | ||||||
| chr12:110163765
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1188+700G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163765 | ||||||
| chr12:110163822
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1188+757G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163822 | ||||||
| chr12:110163866
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1188+801G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110163866 | ||||||
| chr12:110164368
|
C | T | 34 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0179others(31): Show | 34 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1188+1303C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164368 | ||||||
| chr12:110164404
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0035 | 2 | HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1188+1339G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164404 | ||||||
| chr12:110164453
|
G | A | 10 | a0001c0001t0005g0047a0002c0002t0001g0012a0002c0002t0001g0046others(7): Show | 10 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1188+1388G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164453 | ||||||
| chr12:110164470
|
A | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1188+1405A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164470 | ||||||
| chr12:110164571
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1188+1506G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164571 | ||||||
| chr12:110164793
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1188+1728G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164793 | ||||||
| chr12:110164795
|
G | A | 4 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0098others(1): Show | 4 | NA18944.hp2 NA18951.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1188+1730G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110164795 | ||||||
| chr12:110165006
|
G | A | 16 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0116others(13): Show | 16 | HG00423.hp2 HG00558.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1188+1941G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110165006 | ||||||
| chr12:110165038
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1188+1973C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110165038 | ||||||
| chr12:110165125
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1188+2060G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110165125 | ||||||
| chr12:110165401
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1188+2336A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110165401 | ||||||
| chr12:110165504
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1188+2439T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110165504 | ||||||
| chr12:110165956
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1188+2891G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110165956 | ||||||
| chr12:110166385
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1188+3320C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110166385 | ||||||
| chr12:110166413
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1188+3348C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110166413 | ||||||
| chr12:110166638
|
A | G | 1 | a0001c0001t0006g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1188+3573A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110166638 | ||||||
| chr12:110166650
|
T | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1188+3585T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110166650 | ||||||
| chr12:110166954
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1188+3889C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110166954 | ||||||
| chr12:110167010
|
T | C | 1 | a0001c0001t0002g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1188+3945T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110167010 | ||||||
| chr12:110167089
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1188+4024G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110167089 | ||||||
| chr12:110167179
|
T | C | 4 | a0001c0001t0002g0187a0001c0001t0002g0194a0001c0001t0002g0195others(1): Show | 4 | HG00280.hp1 HG01192.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1188+4114T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110167179 | ||||||
| chr12:110167495
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0059others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1188+4430T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110167495 | ||||||
| chr12:110167583
|
A | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0118 | 2 | HG01109.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1188+4518A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110167583 | ||||||
| chr12:110167754
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(57): Show | 60 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1188+4689C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110167754 | ||||||
| chr12:110167847
|
C | CT | 46 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(43): Show | 46 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.1188+4799dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110167847 | |||||
| chr12:110168358
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1188+5293T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110168358 | ||||||
| chr12:110168506
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1188+5441C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110168506 | ||||||
| chr12:110168507
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1188+5442G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110168507 | ||||||
| chr12:110168863
|
T | A | 9 | a0002c0002t0001g0012a0002c0002t0001g0046a0002c0002t0001g0048others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1188+5798T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110168863 | ||||||
| chr12:110168972
|
C | T | 3 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185 | 3 | HG02559.hp1 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1188+5907C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110168972 | ||||||
| chr12:110169023
|
C | CCCTT | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(43): Show | 46 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1188+6014_1188+601 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | |||||
| chr12:110169023
|
C | CCCTTCCT others(1): Show |
12 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0042others(9): Show | 12 | HG00323.hp1 HG01071.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1188+6010_1188+601 others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | |||||
| chr12:110169023
|
C | CCCTTCCT others(5): Show |
10 | a0001c0001t0001g0023a0001c0001t0001g0213a0001c0001t0002g0178others(7): Show | 10 | HG00735.hp2 HG01081.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1188+6006_1188+601 others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | |||||
| chr12:110169023
|
C | CCCTTCCT others(9): Show |
2 | a0001c0001t0001g0017a0001c0001t0002g0185 | 2 | HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1188+6002_1188+601 others(20): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | |||||
| chr12:110169023
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0162 | 2 | HG02698.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1188+5958C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110169023 | ||||||
| chr12:110169023
|
CCCTT | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0033others(39): Show | 42 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1188+6014_1188+601 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | |||||
| chr12:110169023
|
CCCTTCCT others(1): Show |
C | 33 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0063others(30): Show | 33 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1188+6010_1188+601 others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | |||||
| chr12:110169023
|
CCCTTCCT others(5): Show |
C | 6 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(3): Show | 6 | HG00642.hp1 HG01074.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+6006_1188+601 others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | |||||
| chr12:110169023
|
CCCTTCCT others(9): Show |
C | 2 | a0001c0001t0001g0135a0001c0001t0005g0047 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1188+6002_1188+601 others(20): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | |||||
| chr12:110169023
|
CCCTTCCT others(13): Show |
C | 2 | a0001c0001t0001g0099a0001c0001t0001g0152 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1188+5998_1188+601 others(24): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169023 | |||||
| chr12:110169072
|
CCTTCCTT others(3): Show |
C | 1 | a0001c0001t0001g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1188+6010_1188+601 others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169072 | |||||
| chr12:110169080
|
C | CCT | 3 | a0002c0002t0001g0048a0002c0002t0001g0049a0002c0002t0001g0054 | 3 | HG03453.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1188+6028_1188+602 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169080 | |||||
| chr12:110169080
|
C | CCTTCCT | 6 | a0002c0002t0001g0012a0002c0002t0001g0046a0002c0002t0001g0050others(3): Show | 6 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1188+6017_1188+601 others(10): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110169080 | |||||
| chr12:110169154
|
C | G | 37 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.1188+6089C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110169154 | ||||||
| chr12:110169334
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1188+6269C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110169334 | ||||||
| chr12:110169398
|
T | A | 1 | a0001c0001t0002g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1188+6333T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110169398 | ||||||
| chr12:110169896
|
C | G | 5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1188+6831C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110169896 | ||||||
| chr12:110170046
|
G | T | 1 | a0001c0001t0002g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1188+6981G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170046 | ||||||
| chr12:110170053
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1188+6988C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170053 | ||||||
| chr12:110170113
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1188+7048C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170113 | ||||||
| chr12:110170554
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1188+7489A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170554 | ||||||
| chr12:110170571
|
C | T | 1 | a0001c0001t0002g0215 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1188+7506C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170571 | ||||||
| chr12:110170688
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1188+7623C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170688 | ||||||
| chr12:110170732
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1188+7667A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110170732 | ||||||
| chr12:110171264
|
A | AT | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(9): Show | 12 | HG00738.hp1 HG01069.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1188+8213dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110171264 | |||||
| chr12:110171587
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1188+8522T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110171587 | ||||||
| chr12:110171707
|
TCTTGCCT others(12): Show |
T | 1 | a0001c0001t0001g0029 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1188+8644_1188+866 others(23): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110171707 | |||||
| chr12:110171909
|
C | T | 36 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.1189-8513C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110171909 | ||||||
| chr12:110172302
|
GCCTCTGC others(2): Show |
G | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0002c0002t0001g0048 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1189-8091_1189-808 others(13): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110172302 | |||||
| chr12:110172358
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1189-8064T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110172358 | ||||||
| chr12:110172358
|
TGGTCTCC others(10): Show |
T | 20 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(17): Show | 20 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1189-8032_1189-801 others(21): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110172358 | |||||
| chr12:110172379
|
C | A | 1 | a0001c0001t0001g0078 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1189-8043C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110172379 | ||||||
| chr12:110172418
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1189-8004G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110172418 | ||||||
| chr12:110172668
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-7754T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110172668 | ||||||
| chr12:110172807
|
A | AC | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0125others(5): Show | 8 | HG01109.hp2 HG01243.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1189-7611dupC | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110172807 | |||||
| chr12:110172858
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1189-7564A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110172858 | ||||||
| chr12:110173040
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0150 | 2 | NA18968.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1189-7382C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173040 | ||||||
| chr12:110173054
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-7368T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173054 | ||||||
| chr12:110173079
|
C | T | 1 | a0001c0004t0001g0019 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1189-7343C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173079 | ||||||
| chr12:110173154
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-7268A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173154 | ||||||
| chr12:110173245
|
CCGTCCGG others(120): Show |
C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-7119_1189-699 others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110173245 | |||||
| chr12:110173329
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1189-7093G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173329 | ||||||
| chr12:110173346
|
G | A | 7 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0142others(4): Show | 7 | HG00423.hp1 NA18944.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-7076G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173346 | ||||||
| chr12:110173357
|
G | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0060 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1189-7065G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173357 | ||||||
| chr12:110173439
|
G | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(8): Show | 11 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1189-6983G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173439 | ||||||
| chr12:110173524
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1189-6898G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173524 | ||||||
| chr12:110173756
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1189-6666C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173756 | ||||||
| chr12:110173774
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1189-6648G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173774 | ||||||
| chr12:110173837
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1189-6585C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173837 | ||||||
| chr12:110173977
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1189-6445G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110173977 | ||||||
| chr12:110174085
|
G | A | 3 | a0001c0001t0002g0182a0001c0001t0002g0189a0001c0001t0002g0205 | 3 | HG02717.hp1 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1189-6337G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174085 | ||||||
| chr12:110174147
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1189-6275G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174147 | ||||||
| chr12:110174258
|
A | G | 1 | a0001c0001t0006g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1189-6164A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174258 | ||||||
| chr12:110174272
|
C | T | 9 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0136others(6): Show | 9 | HG00423.hp1 HG00558.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.1189-6150C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174272 | ||||||
| chr12:110174277
|
C | CA | 12 | a0001c0001t0001g0057a0001c0001t0001g0080a0001c0001t0001g0088others(9): Show | 12 | HG00738.hp2 HG00741.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.1189-6115dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174277 | |||||
| chr12:110174277
|
CA | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 89 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.1189-6115delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174277 | |||||
| chr12:110174277
|
CAA | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(17): Show | 20 | HG00323.hp2 HG01175.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.1189-6116_1189-611 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174277 | |||||
| chr12:110174277
|
CAAA | C | 7 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG01081.hp2 HG01943.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1189-6117_1189-611 others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174277 | |||||
| chr12:110174277
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0044a0001c0001t0001g0075 | 2 | HG02976.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1189-6129_1189-611 others(19): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174277 | |||||
| chr12:110174279
|
AAAAAAAA others(171): Show |
A | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1189-6122_1189-594 others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174279 | |||||
| chr12:110174292
|
A | T | 1 | a0001c0001t0002g0177 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1189-6130A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174292 | ||||||
| chr12:110174293
|
A | T | 1 | a0001c0001t0002g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1189-6129A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174293 | ||||||
| chr12:110174294
|
A | T | 1 | a0001c0001t0002g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1189-6128A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174294 | ||||||
| chr12:110174296
|
A | T | 1 | a0001c0001t0002g0205 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1189-6126A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174296 | ||||||
| chr12:110174300
|
A | T | 1 | a0001c0001t0002g0205 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1189-6122A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174300 | ||||||
| chr12:110174304
|
A | AT | 2 | a0001c0001t0002g0200a0001c0001t0002g0202 | 2 | HG01934.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1189-6118_1189-611 others(5): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174304 | ||||||
| chr12:110174304
|
A | T | 32 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0179others(29): Show | 32 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1189-6118A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174304 | ||||||
| chr12:110174307
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0060 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1189-6115A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174307 | ||||||
| chr12:110174372
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1189-6050T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174372 | ||||||
| chr12:110174412
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1189-6010A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174412 | ||||||
| chr12:110174456
|
A | AG | 6 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1189-5965dupG | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174456 | |||||
| chr12:110174457
|
G | GA | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(14): Show | 17 | HG00738.hp1 HG01069.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1189-5945dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110174457 | |||||
| chr12:110174457
|
G | GGA | 5 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(2): Show | 5 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-5965_1189-596 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174457 | ||||||
| chr12:110174806
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1189-5616A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174806 | ||||||
| chr12:110174810
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1189-5612G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174810 | ||||||
| chr12:110174826
|
A | G | 9 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(6): Show | 9 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1189-5596A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174826 | ||||||
| chr12:110174947
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1189-5475G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110174947 | ||||||
| chr12:110175061
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1189-5361T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175061 | ||||||
| chr12:110175063
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1189-5359G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175063 | ||||||
| chr12:110175349
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1189-5073C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175349 | ||||||
| chr12:110175578
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1189-4844C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175578 | ||||||
| chr12:110175580
|
C | CT | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1189-4842_1189-484 others(5): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175580 | ||||||
| chr12:110175581
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1189-4841G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175581 | ||||||
| chr12:110175692
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1189-4730C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175692 | ||||||
| chr12:110175708
|
A | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0111a0001c0001t0001g0150 | 3 | HG01928.hp1 NA18968.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1189-4714A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110175708 | ||||||
| chr12:110176409
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1189-4013A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176409 | ||||||
| chr12:110176588
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1189-3834C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176588 | ||||||
| chr12:110176604
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0020 | 3 | HG01099.hp1 HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1189-3818A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176604 | ||||||
| chr12:110176622
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1189-3800A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176622 | ||||||
| chr12:110176683
|
C | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-3739C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176683 | ||||||
| chr12:110176764
|
T | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1189-3658T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176764 | ||||||
| chr12:110176845
|
A | G | 1 | a0001c0001t0002g0205 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1189-3577A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176845 | ||||||
| chr12:110176864
|
C | T | 1 | a0001c0001t0002g0177 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1189-3558C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110176864 | ||||||
| chr12:110177267
|
T | TTTTTG | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(9): Show | 12 | HG00738.hp1 HG01069.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.1189-3126_1189-312 others(9): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110177267 | |||||
| chr12:110177309
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-3113A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177309 | ||||||
| chr12:110177338
|
A | C | 2 | a0001c0001t0001g0171a0001c0001t0006g0176 | 2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1189-3084A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177338 | ||||||
| chr12:110177444
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 109 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1189-2978A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177444 | ||||||
| chr12:110177574
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG01099.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-2848G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177574 | ||||||
| chr12:110177690
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0006g0176 | 2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1189-2732G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177690 | ||||||
| chr12:110177759
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1189-2663C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177759 | ||||||
| chr12:110177869
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1189-2553C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110177869 | ||||||
| chr12:110178076
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1189-2346C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178076 | ||||||
| chr12:110178088
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1189-2334C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178088 | ||||||
| chr12:110178195
|
C | T | 45 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(42): Show | 45 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.1189-2227C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178195 | ||||||
| chr12:110178242
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1189-2180C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178242 | ||||||
| chr12:110178414
|
CA | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0042a0001c0001t0001g0161others(6): Show | 9 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1189-1992delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178414 | |||||
| chr12:110178777
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1189-1645G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178777 | ||||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0005 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0006 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0161 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0120 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
66 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(63): Show | 66 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
2 | a0001c0001t0001g0001a0001c0001t0001g0002 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
6 | a0001c0001t0001g0004a0001c0001t0002g0187a0001c0001t0002g0194others(3): Show | 6 | HG00280.hp1 HG01192.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(40): Show | 43 | HG00323.hp2 HG01167.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
1 | a0001c0004t0001g0019 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
7 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0142others(4): Show | 7 | HG00423.hp1 NA18944.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
80 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178783
|
T | TTTTTTGT others(1868): Show |
1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1189-1601_1189-160 others(1879): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110178783 | |||||
| chr12:110178828
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1189-1594G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178828 | ||||||
| chr12:110178897
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1189-1525G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110178897 | ||||||
| chr12:110179005
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1189-1417G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179005 | ||||||
| chr12:110179187
|
A | G | 1 | a0001c0001t0006g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1189-1235A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179187 | ||||||
| chr12:110179361
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1189-1061G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179361 | ||||||
| chr12:110179441
|
G | T | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1189-981G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179441 | ||||||
| chr12:110179724
|
T | TTA | 3 | a0001c0001t0002g0215a0003c0003t0004g0102a0004c0006t0004g0076 | 3 | HG01074.hp1 HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1189-649_1189-648d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179724
|
T | TTATATA | 2 | a0001c0001t0001g0063a0001c0001t0001g0083 | 2 | HG01169.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1189-653_1189-648d others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179724
|
TTA | T | 14 | a0001c0001t0001g0073a0001c0001t0001g0079a0001c0001t0001g0080others(11): Show | 14 | HG01175.hp1 HG01361.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1189-649_1189-648d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179724
|
TTATA | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0107a0001c0001t0001g0126others(2): Show | 5 | HG01074.hp2 HG01891.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1189-651_1189-648d others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179724
|
TTATATA | T | 3 | a0001c0001t0001g0093a0001c0001t0001g0125a0001c0001t0002g0183 | 3 | HG01243.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1189-653_1189-648d others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179724
|
TTATATAT others(5): Show |
T | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1189-659_1189-648d others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179724
|
TTATATAT others(7): Show |
T | 5 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0119others(2): Show | 5 | HG01099.hp1 HG01099.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-661_1189-648d others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179724
|
TTATATAT others(9): Show |
T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG02630.hp1 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-663_1189-648d others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179724
|
TTATATAT others(11): Show |
T | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1189-665_1189-648d others(20): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179724
|
TTATATAT others(13): Show |
T | 8 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0028others(5): Show | 8 | HG00738.hp1 HG02559.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1189-667_1189-648d others(22): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179724
|
TTATATAT others(15): Show |
T | 16 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0024others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1189-669_1189-648d others(24): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179724
|
TTATATAT others(17): Show |
T | 16 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(13): Show | 16 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.1189-671_1189-648d others(26): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179724
|
TTATATAT others(19): Show |
T | 4 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0122others(1): Show | 4 | HG02257.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-673_1189-648d others(28): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179724
|
TTATATAT others(21): Show |
T | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1189-675_1189-648d others(30): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179724 | |||||
| chr12:110179739
|
TATATATA others(29): Show |
T | 9 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(6): Show | 9 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1189-681_1189-646d others(38): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179739 | |||||
| chr12:110179744
|
A | T | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1189-678A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179744 | ||||||
| chr12:110179745
|
TATATATA others(23): Show |
T | 1 | a0001c0001t0001g0006 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1189-675_1189-646d others(32): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179745 | |||||
| chr12:110179761
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0021others(2): Show | 5 | HG01099.hp1 HG02145.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-661T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179761 | ||||||
| chr12:110179763
|
T | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(6): Show | 9 | HG01099.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1189-659T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179763 | ||||||
| chr12:110179763
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1189-657_1189-644d others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179763 | |||||
| chr12:110179765
|
T | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(18): Show | 21 | HG01099.hp1 HG01099.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1189-657T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179765 | ||||||
| chr12:110179767
|
T | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(24): Show | 27 | HG01099.hp1 HG01099.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1189-655T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179767 | ||||||
| chr12:110179767
|
T | TACAC | 3 | a0001c0001t0003g0208a0001c0001t0003g0211a0001c0001t0003g0212 | 3 | HG01069.hp1 HG01071.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1189-654_1189-653i others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179767 | |||||
| chr12:110179767
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0002g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1189-653_1189-642d others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179767 | |||||
| chr12:110179769
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(64): Show | 67 | HG00323.hp2 HG00735.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.1189-653T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179769 | ||||||
| chr12:110179769
|
T | TAC | 8 | a0001c0001t0001g0124a0001c0001t0001g0156a0001c0001t0001g0163others(5): Show | 8 | HG00280.hp1 HG00642.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1189-652_1189-651i others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179769 | |||||
| chr12:110179769
|
T | TACACAC | 2 | a0001c0001t0001g0154a0001c0001t0001g0162 | 2 | HG00621.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1189-652_1189-651i others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179769 | |||||
| chr12:110179769
|
T | TACACACA others(3): Show |
2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01943.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1189-652_1189-651i others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179769 | |||||
| chr12:110179771
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(94): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1189-651T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179771 | ||||||
| chr12:110179771
|
T | TAC | 5 | a0001c0001t0001g0078a0001c0001t0001g0106a0001c0001t0001g0164others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-650_1189-649i others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179771 | |||||
| chr12:110179771
|
T | TACAC | 3 | a0001c0001t0002g0187a0001c0001t0002g0194a0001c0001t0003g0209 | 3 | HG01433.hp2 HG02293.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1189-650_1189-649i others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179771 | |||||
| chr12:110179771
|
T | TACACACA others(5): Show |
2 | a0001c0001t0001g0136a0001c0001t0001g0167 | 2 | NA18948.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1189-650_1189-649i others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179771 | |||||
| chr12:110179771
|
T | TACACACA others(7): Show |
1 | a0001c0001t0001g0213 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1189-650_1189-649i others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179771 | |||||
| chr12:110179771
|
T | TACACACA others(9): Show |
1 | a0001c0001t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1189-650_1189-649i others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179771 | |||||
| chr12:110179773
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1189-649T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179773 | ||||||
| chr12:110179773
|
T | TAC | 3 | a0001c0001t0001g0065a0001c0001t0001g0088a0001c0001t0001g0113 | 3 | HG02647.hp1 HG03209.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1189-617_1189-616d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TACAC | 7 | a0001c0001t0001g0074a0001c0001t0001g0099a0001c0001t0001g0100others(4): Show | 7 | HG01081.hp1 HG01109.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-619_1189-616d others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TACACAC | 7 | a0001c0001t0001g0103a0001c0001t0001g0116a0001c0001t0001g0118others(4): Show | 7 | HG00323.hp1 HG01168.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-621_1189-616d others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TACACACA others(1): Show |
2 | a0001c0001t0001g0161a0001c0001t0003g0210 | 2 | NA19001.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1189-623_1189-616d others(10): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TACACACA others(3): Show |
1 | a0001c0001t0001g0158 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1189-625_1189-616d others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TACACACA others(5): Show |
3 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0151 | 3 | HG00621.hp2 HG01109.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1189-627_1189-616d others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TACACACA others(7): Show |
3 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0001t0001g0188 | 3 | HG01081.hp2 HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1189-629_1189-616d others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TACACACA others(9): Show |
1 | a0001c0001t0001g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1189-631_1189-616d others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATAC | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0002g0217 | 3 | HG00741.hp2 HG01928.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1189-648_1189-647i others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATACAC | 5 | a0001c0001t0001g0071a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 5 | HG00280.hp2 HG01123.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1189-648_1189-647i others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATACACA others(1): Show |
2 | a0001c0001t0001g0114a0001c0001t0002g0197 | 2 | HG00741.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1189-648_1189-647i others(10): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATACACA others(3): Show |
3 | a0001c0001t0001g0153a0001c0001t0001g0157a0001c0001t0002g0199 | 3 | HG00423.hp2 HG04204.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1189-648_1189-647i others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATACACA others(7): Show |
5 | a0001c0001t0001g0069a0001c0001t0001g0137a0001c0001t0001g0141others(2): Show | 5 | HG00558.hp1 HG00558.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.1189-648_1189-647i others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATACACA others(9): Show |
1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1189-648_1189-647i others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATACACA others(15): Show |
1 | a0001c0001t0001g0170 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1189-648_1189-647i others(24): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATATACA others(7): Show |
3 | a0001c0001t0001g0068a0001c0001t0001g0148a0001c0001t0001g0159 | 3 | HG04204.hp1 NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1189-648_1189-647i others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATATACA others(9): Show |
1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1189-648_1189-647i others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATATATA others(5): Show |
1 | a0001c0001t0002g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1189-648_1189-647i others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATATATA others(7): Show |
2 | a0001c0001t0001g0067a0001c0001t0001g0070 | 2 | NA19078.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1189-648_1189-647i others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATATATA others(3): Show |
1 | a0001c0001t0001g0072 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1189-648_1189-647i others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATATATA others(9): Show |
2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG00423.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1189-648_1189-647i others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATATATA others(7): Show |
1 | a0001c0001t0002g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1189-648_1189-647i others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0139 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1189-648_1189-647i others(24): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0142 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1189-648_1189-647i others(24): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATATATA others(17): Show |
1 | a0001c0001t0001g0145 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1189-648_1189-647i others(26): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179773
|
T | TATATATA others(23): Show |
1 | a0001c0001t0001g0143 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1189-648_1189-647i others(32): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179773 | |||||
| chr12:110179805
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1189-617C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179805 | ||||||
| chr12:110179806
|
A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0174 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1189-616_1189-615i others(17): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179806 | ||||||
| chr12:110179842
|
A | AAT | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1189-568_1189-567d others(4): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr12 | 110179842 | |||||
| chr12:110179910
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0006 | 2 | HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1189-512G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110179910 | ||||||
| chr12:110180364
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1189-58A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 11/18 | chr12 | 110180364 | ||||||
| chr12:110180707
|
A | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(56): Show | 59 | HG00323.hp2 HG01069.hp2 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.1338+136A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110180707 | ||||||
| chr12:110180805
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1338+234A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110180805 | ||||||
| chr12:110180863
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1338+292G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110180863 | ||||||
| chr12:110181001
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1338+430G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110181001 | ||||||
| chr12:110181085
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(56): Show | 59 | HG00323.hp2 HG01069.hp2 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.1338+514C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110181085 | ||||||
| chr12:110181453
|
G | C | 1 | a0001c0004t0001g0019 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1338+882G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110181453 | ||||||
| chr12:110181544
|
G | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0124a0001c0001t0001g0129others(5): Show | 8 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1338+973G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110181544 | ||||||
| chr12:110181754
|
C | T | 8 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1338+1183C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110181754 | ||||||
| chr12:110181992
|
T | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(58): Show | 61 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1338+1421T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110181992 | ||||||
| chr12:110182602
|
A | T | 1 | a0001c0001t0002g0197 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1338+2031A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182602 | ||||||
| chr12:110182631
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1338+2060G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182631 | ||||||
| chr12:110182856
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1338+2285C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182856 | ||||||
| chr12:110182871
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1338+2300C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182871 | ||||||
| chr12:110182952
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1338+2381G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182952 | ||||||
| chr12:110182960
|
G | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(10): Show | 13 | HG01099.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1338+2389G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182960 | ||||||
| chr12:110182976
|
A | C | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1338+2405A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110182976 | ||||||
| chr12:110183010
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1338+2439C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110183010 | ||||||
| chr12:110183616
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1338+3045A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110183616 | ||||||
| chr12:110183638
|
C | T | 12 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0005g0047others(9): Show | 12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1338+3067C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110183638 | ||||||
| chr12:110183803
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1338+3232G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110183803 | ||||||
| chr12:110184089
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1338+3518G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184089 | ||||||
| chr12:110184139
|
A | G | 1 | a0001c0001t0002g0177 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1338+3568A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184139 | ||||||
| chr12:110184153
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1338+3582A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184153 | ||||||
| chr12:110184243
|
G | C | 1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1338+3672G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184243 | ||||||
| chr12:110184246
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1338+3675A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184246 | ||||||
| chr12:110184247
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1338+3676G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184247 | ||||||
| chr12:110184267
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1338+3696G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184267 | ||||||
| chr12:110184356
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1338+3785A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184356 | ||||||
| chr12:110184358
|
T | A | 1 | a0001c0001t0001g0139 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1338+3787T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184358 | ||||||
| chr12:110184419
|
T | G | 20 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(17): Show | 20 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1338+3848T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184419 | ||||||
| chr12:110184505
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1338+3934C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184505 | ||||||
| chr12:110184738
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(57): Show | 60 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1338+4167C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184738 | ||||||
| chr12:110184908
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1338+4337A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110184908 | ||||||
| chr12:110185185
|
A | T | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1338+4614A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110185185 | ||||||
| chr12:110185380
|
C | T | 2 | a0001c0001t0002g0179a0001c0001t0002g0206 | 2 | HG00642.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1338+4809C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110185380 | ||||||
| chr12:110185442
|
G | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0081others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+4871G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110185442 | ||||||
| chr12:110185852
|
A | T | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1339-5068A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110185852 | ||||||
| chr12:110185907
|
G | GA | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1339-5012dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110185907 | |||||
| chr12:110186132
|
T | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0059others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1339-4788T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186132 | ||||||
| chr12:110186169
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1339-4751G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186169 | ||||||
| chr12:110186238
|
C | CTTGT | 14 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(11): Show | 14 | HG00621.hp1 HG01099.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1339-4647_1339-464 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110186238 | |||||
| chr12:110186238
|
CTTGT | C | 71 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0017others(68): Show | 71 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1339-4647_1339-464 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110186238 | |||||
| chr12:110186238
|
CTTGTTTG others(1): Show |
C | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(14): Show | 17 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1339-4651_1339-464 others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110186238 | |||||
| chr12:110186288
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-4632G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186288 | ||||||
| chr12:110186415
|
G | A | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1339-4505G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186415 | ||||||
| chr12:110186484
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-4436C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186484 | ||||||
| chr12:110186496
|
TC | T | 11 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(8): Show | 11 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1339-4423delC | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186496 | ||||||
| chr12:110186717
|
C | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-4203C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186717 | ||||||
| chr12:110186746
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1339-4174G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186746 | ||||||
| chr12:110186863
|
G | A | 26 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0179others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1339-4057G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186863 | ||||||
| chr12:110186941
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1339-3979G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110186941 | ||||||
| chr12:110187254
|
GTTGTTT | G | 26 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0179others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1339-3645_1339-364 others(10): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110187254 | |||||
| chr12:110187344
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 129 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1339-3576G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187344 | ||||||
| chr12:110187504
|
A | G | 1 | a0001c0001t0002g0218 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1339-3416A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187504 | ||||||
| chr12:110187517
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1339-3403G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187517 | ||||||
| chr12:110187545
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-3375A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187545 | ||||||
| chr12:110187704
|
A | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-3216A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187704 | ||||||
| chr12:110187772
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0145 | 2 | NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1339-3148T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187772 | ||||||
| chr12:110187847
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1339-3073G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110187847 | ||||||
| chr12:110188058
|
C | T | 3 | a0001c0001t0003g0208a0001c0001t0003g0211a0001c0001t0003g0212 | 3 | HG01069.hp1 HG01071.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1339-2862C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188058 | ||||||
| chr12:110188070
|
C | T | 5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1339-2850C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188070 | ||||||
| chr12:110188186
|
G | A | 1 | a0001c0001t0006g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1339-2734G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188186 | ||||||
| chr12:110188208
|
G | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1339-2712G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188208 | ||||||
| chr12:110188346
|
A | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-2574A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188346 | ||||||
| chr12:110188752
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1339-2168A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188752 | ||||||
| chr12:110188768
|
C | CA | 15 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(12): Show | 15 | HG01109.hp2 HG02145.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.1339-2137dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110188768 | |||||
| chr12:110188768
|
CA | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG00738.hp1 HG01069.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1339-2137delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110188768 | |||||
| chr12:110188853
|
C | T | 9 | a0002c0002t0001g0012a0002c0002t0001g0046a0002c0002t0001g0048others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1339-2067C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188853 | ||||||
| chr12:110188933
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1339-1987A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110188933 | ||||||
| chr12:110189272
|
G | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1339-1648G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110189272 | ||||||
| chr12:110189282
|
A | G | 5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1339-1638A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110189282 | ||||||
| chr12:110189336
|
TTTTA | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1339-1560_1339-155 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110189336 | |||||
| chr12:110189506
|
A | G | 1 | a0001c0001t0002g0205 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1339-1414A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110189506 | ||||||
| chr12:110189624
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1339-1296C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110189624 | ||||||
| chr12:110189629
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1339-1291G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110189629 | ||||||
| chr12:110189876
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1339-1044A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110189876 | ||||||
| chr12:110190107
|
C | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0034 | 3 | HG00323.hp2 HG01175.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1339-813C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110190107 | ||||||
| chr12:110190192
|
A | AGAGTGCA others(4): Show |
1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1339-727_1339-717d others(13): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110190192 | |||||
| chr12:110190475
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1339-445C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | chr12 | 110190475 | ||||||
| chr12:110190504
|
A | AT | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0036others(9): Show | 12 | HG00738.hp1 HG01069.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1339-406dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr12 | 110190504 | |||||
| chr12:110191168
|
CT | C | 9 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0153others(6): Show | 9 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1467+134delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr12 | 110191168 | |||||
| chr12:110191441
|
G | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1467+393G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110191441 | ||||||
| chr12:110191461
|
A | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 129 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1467+413A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110191461 | ||||||
| chr12:110191619
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1467+571G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110191619 | ||||||
| chr12:110191687
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 108 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1467+639T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110191687 | ||||||
| chr12:110191766
|
C | A | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1467+718C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110191766 | ||||||
| chr12:110191792
|
C | T | 9 | a0002c0002t0001g0012a0002c0002t0001g0046a0002c0002t0001g0048others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1467+744C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110191792 | ||||||
| chr12:110191899
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1468-718G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110191899 | ||||||
| chr12:110192011
|
A | C | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1468-606A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192011 | ||||||
| chr12:110192114
|
T | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-503T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192114 | ||||||
| chr12:110192149
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1468-468C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192149 | ||||||
| chr12:110192415
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1468-202C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192415 | ||||||
| chr12:110192421
|
G | A | 1 | a0001c0001t0003g0208 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1468-196G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192421 | ||||||
| chr12:110192453
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1468-164T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192453 | ||||||
| chr12:110192555
|
A | C | 1 | a0001c0001t0001g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1468-62A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 13/18 | chr12 | 110192555 | ||||||
| chr12:110192933
|
A | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1557+227A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110192933 | ||||||
| chr12:110193263
|
G | C | 2 | a0001c0001t0002g0186a0001c0001t0002g0207 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1557+557G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110193263 | ||||||
| chr12:110193316
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1557+610A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110193316 | ||||||
| chr12:110193323
|
T | C | 1 | a0001c0001t0006g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1557+617T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110193323 | ||||||
| chr12:110193486
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1557+780A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110193486 | ||||||
| chr12:110193581
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1557+875A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110193581 | ||||||
| chr12:110193647
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1557+941A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110193647 | ||||||
| chr12:110194076
|
C | T | 5 | a0001c0001t0001g0142a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 5 | HG00423.hp1 NA18944.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557+1370C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110194076 | ||||||
| chr12:110194137
|
C | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0087a0001c0001t0001g0090others(4): Show | 7 | HG01516.hp2 HG01928.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1557+1431C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110194137 | ||||||
| chr12:110194901
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1557+2195C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110194901 | ||||||
| chr12:110195986
|
A | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1557+3280A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110195986 | ||||||
| chr12:110195991
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1557+3285T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110195991 | ||||||
| chr12:110196005
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1557+3299C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196005 | ||||||
| chr12:110196185
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1557+3479T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196185 | ||||||
| chr12:110196300
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0059 | 2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1557+3594C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196300 | ||||||
| chr12:110196510
|
A | C | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1557+3804A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196510 | ||||||
| chr12:110196576
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1557+3870G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196576 | ||||||
| chr12:110196713
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1557+4007C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196713 | ||||||
| chr12:110196836
|
A | C | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1557+4130A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110196836 | ||||||
| chr12:110197076
|
A | G | 16 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0116others(13): Show | 16 | HG00423.hp2 HG00558.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1557+4370A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197076 | ||||||
| chr12:110197172
|
G | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1557+4466G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197172 | ||||||
| chr12:110197199
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1557+4493G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197199 | ||||||
| chr12:110197248
|
G | GTAGA | 27 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0068others(24): Show | 27 | HG00099.hp1 HG00423.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.1557+4584_1557+458 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197248 | |||||
| chr12:110197248
|
G | GTAGATAG others(1): Show |
5 | a0001c0001t0001g0062a0001c0001t0001g0103a0001c0001t0001g0158others(2): Show | 5 | HG01243.hp2 HG02071.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557+4580_1557+458 others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197248 | |||||
| chr12:110197248
|
GTAGA | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(58): Show | 61 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1557+4584_1557+458 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197248 | |||||
| chr12:110197248
|
GTAGATAG others(1): Show |
G | 19 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 19 | HG00323.hp2 HG01074.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1557+4580_1557+458 others(12): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197248 | |||||
| chr12:110197248
|
GTAGATAG others(5): Show |
G | 3 | a0001c0001t0001g0004a0001c0001t0003g0209a0001c0001t0003g0210 | 3 | HG02293.hp1 HG03579.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1557+4576_1557+458 others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197248 | |||||
| chr12:110197248
|
GTAGATAG others(9): Show |
G | 3 | a0001c0001t0003g0208a0001c0001t0003g0211a0001c0001t0003g0212 | 3 | HG01069.hp1 HG01071.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1557+4572_1557+458 others(20): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197248 | |||||
| chr12:110197252
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0002g0193 | 2 | HG02683.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1557+4546A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197252 | ||||||
| chr12:110197256
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1557+4550A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197256 | ||||||
| chr12:110197414
|
A | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1557+4708A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197414 | ||||||
| chr12:110197438
|
C | G | 1 | a0001c0001t0002g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1557+4732C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197438 | ||||||
| chr12:110197445
|
CT | C | 19 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0090others(16): Show | 19 | HG00423.hp2 HG00558.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.1557+4750delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197445 | |||||
| chr12:110197555
|
C | CAT | 24 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0063others(21): Show | 24 | HG00423.hp2 HG00558.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1557+4877_1557+487 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | |||||
| chr12:110197555
|
C | CATAT | 14 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0121others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1557+4875_1557+487 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | |||||
| chr12:110197555
|
C | CATATAT | 3 | a0001c0001t0001g0004a0001c0001t0001g0093a0001c0001t0002g0195 | 3 | HG00280.hp1 HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1557+4873_1557+487 others(10): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | |||||
| chr12:110197555
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1557+4867_1557+487 others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | |||||
| chr12:110197555
|
C | CATATATA others(7): Show |
1 | a0001c0001t0001g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1557+4865_1557+487 others(18): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | |||||
| chr12:110197555
|
C | CATATATA others(9): Show |
1 | a0001c0001t0001g0005 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1557+4863_1557+487 others(20): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | |||||
| chr12:110197555
|
C | CATATATA others(11): Show |
1 | a0001c0001t0001g0006 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1557+4861_1557+487 others(22): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | |||||
| chr12:110197555
|
CAT | C | 13 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0042others(10): Show | 13 | HG01081.hp2 HG01943.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1557+4877_1557+487 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | |||||
| chr12:110197555
|
CATAT | C | 33 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(30): Show | 33 | HG00323.hp2 HG01167.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1557+4875_1557+487 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | |||||
| chr12:110197555
|
CATATATA others(5): Show |
C | 1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1557+4867_1557+487 others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110197555 | |||||
| chr12:110197567
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1557+4861T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197567 | ||||||
| chr12:110197583
|
T | C | 11 | a0001c0001t0001g0058a0001c0001t0005g0047a0002c0002t0001g0012others(8): Show | 11 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1557+4877T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197583 | ||||||
| chr12:110197714
|
T | A | 1 | a0001c0001t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1557+5008T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197714 | ||||||
| chr12:110197799
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1557+5093G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197799 | ||||||
| chr12:110197932
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1557+5226G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197932 | ||||||
| chr12:110197958
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(6): Show | 9 | HG01099.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1557+5252C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110197958 | ||||||
| chr12:110198209
|
T | C | 5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557+5503T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198209 | ||||||
| chr12:110198286
|
T | G | 6 | a0001c0001t0002g0178a0001c0001t0002g0191a0001c0001t0002g0192others(3): Show | 6 | HG01071.hp1 HG01081.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-5578T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198286 | ||||||
| chr12:110198287
|
T | A | 1 | a0001c0001t0001g0167 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1558-5577T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198287 | ||||||
| chr12:110198505
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG01099.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-5359A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198505 | ||||||
| chr12:110198562
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1558-5302C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198562 | ||||||
| chr12:110198563
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1558-5301G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198563 | ||||||
| chr12:110198671
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1558-5193T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198671 | ||||||
| chr12:110198755
|
A | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1558-5109A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198755 | ||||||
| chr12:110198816
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0002g0207 | 2 | HG01109.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1558-5048T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198816 | ||||||
| chr12:110198849
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1558-5015G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198849 | ||||||
| chr12:110198885
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0014 | 2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1558-4979C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110198885 | ||||||
| chr12:110199361
|
C | T | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0081 | 3 | HG01167.hp1 HG01169.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1558-4503C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110199361 | ||||||
| chr12:110199450
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0014 | 2 | HG01099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1558-4414T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110199450 | ||||||
| chr12:110199738
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1558-4126T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110199738 | ||||||
| chr12:110199883
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1558-3981C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110199883 | ||||||
| chr12:110200399
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1558-3465C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200399 | ||||||
| chr12:110200508
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1558-3356C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200508 | ||||||
| chr12:110200674
|
GCACGGTG others(3): Show |
G | 9 | a0002c0002t0001g0012a0002c0002t0001g0046a0002c0002t0001g0048others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1558-3185_1558-317 others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110200674 | |||||
| chr12:110200720
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1558-3144C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200720 | ||||||
| chr12:110200729
|
G | T | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1558-3135G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200729 | ||||||
| chr12:110200824
|
G | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1558-3040G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200824 | ||||||
| chr12:110200906
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1558-2958C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200906 | ||||||
| chr12:110200907
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1558-2957G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200907 | ||||||
| chr12:110200960
|
A | T | 1 | a0001c0001t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1558-2904A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110200960 | ||||||
| chr12:110201187
|
G | C | 3 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185 | 3 | HG02559.hp1 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1558-2677G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110201187 | ||||||
| chr12:110201402
|
CA | C | 7 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0107others(4): Show | 7 | HG00735.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558-2447delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110201402 | |||||
| chr12:110201470
|
C | T | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0081 | 3 | HG01167.hp1 HG01169.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1558-2394C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110201470 | ||||||
| chr12:110201520
|
T | G | 5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558-2344T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110201520 | ||||||
| chr12:110201524
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1558-2340G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110201524 | ||||||
| chr12:110201599
|
T | TTTTA | 8 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1558-2241_1558-223 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110201599 | |||||
| chr12:110201807
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1558-2057G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110201807 | ||||||
| chr12:110201910
|
T | C | 1 | a0001c0001t0002g0198 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1558-1954T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110201910 | ||||||
| chr12:110202248
|
T | G | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-1616T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202248 | ||||||
| chr12:110202254
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1558-1610G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202254 | ||||||
| chr12:110202269
|
T | G | 1 | a0001c0001t0001g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1558-1595T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202269 | ||||||
| chr12:110202349
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1558-1515A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202349 | ||||||
| chr12:110202393
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1558-1471A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202393 | ||||||
| chr12:110202453
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(54): Show | 57 | HG00323.hp2 HG01099.hp1 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.1558-1411C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202453 | ||||||
| chr12:110202457
|
C | CT | 10 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(7): Show | 10 | HG01167.hp2 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1558-1393dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110202457 | |||||
| chr12:110202512
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1558-1352G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202512 | ||||||
| chr12:110202522
|
G | A | 8 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1558-1342G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202522 | ||||||
| chr12:110202703
|
T | TG | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1558-1159dupG | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr12 | 110202703 | |||||
| chr12:110202854
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1558-1010C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202854 | ||||||
| chr12:110202923
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1558-941A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202923 | ||||||
| chr12:110202923
|
A | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1558-941A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202923 | ||||||
| chr12:110202994
|
G | A | 5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558-870G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110202994 | ||||||
| chr12:110203064
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1558-800A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110203064 | ||||||
| chr12:110203127
|
A | T | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1558-737A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110203127 | ||||||
| chr12:110203470
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1558-394A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110203470 | ||||||
| chr12:110203498
|
T | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1558-366T>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 14/18 | chr12 | 110203498 | ||||||
| chr12:110204091
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1644+141C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110204091 | ||||||
| chr12:110204380
|
T | C | 9 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(6): Show | 9 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+430T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110204380 | ||||||
| chr12:110204385
|
A | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(71): Show | 74 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.1644+435A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110204385 | ||||||
| chr12:110204821
|
C | G | 2 | a0001c0001t0002g0201a0001c0001t0002g0202 | 2 | HG01071.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1645-622C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110204821 | ||||||
| chr12:110204965
|
C | T | 8 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1645-478C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110204965 | ||||||
| chr12:110205052
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1645-391G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110205052 | ||||||
| chr12:110205247
|
G | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1645-196G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110205247 | ||||||
| chr12:110205409
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1645-34G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 15/18 | chr12 | 110205409 | ||||||
| chr12:110205955
|
T | C | 4 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0143others(1): Show | 4 | HG01934.hp1 HG02004.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1802+275T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110205955 | ||||||
| chr12:110205974
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0060 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1802+294C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110205974 | ||||||
| chr12:110206003
|
G | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1802+323G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206003 | ||||||
| chr12:110206240
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(57): Show | 60 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1802+560G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206240 | ||||||
| chr12:110206490
|
A | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1802+810A>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206490 | ||||||
| chr12:110206491
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1802+811G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206491 | ||||||
| chr12:110206547
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1802+867C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206547 | ||||||
| chr12:110206548
|
G | A | 5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1802+868G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206548 | ||||||
| chr12:110206675
|
T | TA | 12 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(9): Show | 12 | HG00741.hp1 HG00741.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1802+1015dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr12 | 110206675 | |||||
| chr12:110206890
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1802+1210G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110206890 | ||||||
| chr12:110207034
|
A | AT | 5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1802+1367dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr12 | 110207034 | |||||
| chr12:110207121
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1802+1441C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110207121 | ||||||
| chr12:110207499
|
C | T | 1 | a0002c0002t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1803-1672C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110207499 | ||||||
| chr12:110207545
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1803-1626C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110207545 | ||||||
| chr12:110207556
|
C | CT | 16 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0034others(13): Show | 16 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1803-1591dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr12 | 110207556 | |||||
| chr12:110207785
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1803-1386G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110207785 | ||||||
| chr12:110207808
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0035 | 2 | HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1803-1363C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110207808 | ||||||
| chr12:110207949
|
A | T | 1 | a0002c0002t0001g0054 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1803-1222A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110207949 | ||||||
| chr12:110208024
|
G | A | 19 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1803-1147G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208024 | ||||||
| chr12:110208106
|
C | T | 1 | a0001c0001t0002g0177 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1803-1065C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208106 | ||||||
| chr12:110208403
|
G | A | 2 | a0001c0001t0002g0186a0001c0001t0002g0207 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1803-768G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208403 | ||||||
| chr12:110208475
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1803-696C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208475 | ||||||
| chr12:110208656
|
C | G | 1 | a0001c0001t0001g0073 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1803-515C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208656 | ||||||
| chr12:110208665
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0002 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1803-506A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208665 | ||||||
| chr12:110208898
|
G | A | 9 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(6): Show | 9 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1803-273G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110208898 | ||||||
| chr12:110209030
|
T | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1803-141T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110209030 | ||||||
| chr12:110209035
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1803-136T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110209035 | ||||||
| chr12:110209069
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1803-102A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 17/18 | chr12 | 110209069 | ||||||
| chr12:110209394
|
T | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1848+178T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110209394 | ||||||
| chr12:110209768
|
C | CA | 9 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0170others(6): Show | 9 | HG01081.hp2 HG01243.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1848+572dupA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110209768 | |||||
| chr12:110209768
|
CA | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0030others(4): Show | 7 | HG00738.hp2 HG02486.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1848+572delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110209768 | |||||
| chr12:110209924
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1848+708G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110209924 | ||||||
| chr12:110210086
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1848+870A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210086 | ||||||
| chr12:110210257
|
G | C | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1848+1041G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210257 | ||||||
| chr12:110210564
|
C | A | 1 | a0001c0001t0001g0067 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1848+1348C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210564 | ||||||
| chr12:110210687
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1848+1471C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210687 | ||||||
| chr12:110210793
|
A | G | 10 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG01099.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1848+1577A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210793 | ||||||
| chr12:110210849
|
A | T | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1848+1633A>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210849 | ||||||
| chr12:110210946
|
C | G | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1848+1730C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210946 | ||||||
| chr12:110210951
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1848+1735G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210951 | ||||||
| chr12:110210954
|
C | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1848+1738C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210954 | ||||||
| chr12:110210958
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1848+1742C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210958 | ||||||
| chr12:110210998
|
G | A | 1 | a0001c0004t0001g0019 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1848+1782G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110210998 | ||||||
| chr12:110211030
|
A | AT | 6 | a0001c0001t0001g0004a0001c0001t0001g0069a0001c0001t0001g0113others(3): Show | 6 | HG00741.hp1 HG01243.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1848+1828dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110211030 | |||||
| chr12:110211133
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1848+1917T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211133 | ||||||
| chr12:110211139
|
C | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1848+1923C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211139 | ||||||
| chr12:110211175
|
C | CT | 23 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(20): Show | 23 | HG01071.hp2 HG01099.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1848+1980dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110211175 | |||||
| chr12:110211175
|
CT | C | 10 | a0001c0001t0001g0162a0001c0001t0001g0170a0001c0001t0001g0172others(7): Show | 10 | HG01943.hp1 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1848+1980delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110211175 | |||||
| chr12:110211175
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0025a0001c0001t0001g0029 | 2 | NA18952.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1848+1971_1848+198 others(14): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110211175 | |||||
| chr12:110211175
|
CTTTTTTT others(5): Show |
C | 9 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(6): Show | 9 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1848+1969_1848+198 others(16): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110211175 | |||||
| chr12:110211179
|
T | C | 14 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(11): Show | 14 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1848+1963T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211179 | ||||||
| chr12:110211188
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1848+1972T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211188 | ||||||
| chr12:110211190
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1848+1974T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211190 | ||||||
| chr12:110211191
|
T | C | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1848+1975T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211191 | ||||||
| chr12:110211216
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1848+2000G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211216 | ||||||
| chr12:110211302
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1848+2086G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211302 | ||||||
| chr12:110211719
|
C | T | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1848+2503C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211719 | ||||||
| chr12:110211806
|
C | A | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1848+2590C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211806 | ||||||
| chr12:110211873
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1848+2657A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211873 | ||||||
| chr12:110211931
|
A | G | 1 | a0001c0001t0002g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1848+2715A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211931 | ||||||
| chr12:110211985
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1848+2769G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110211985 | ||||||
| chr12:110212226
|
G | A | 24 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0038others(21): Show | 24 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1848+3010G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110212226 | ||||||
| chr12:110212242
|
TA | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 126 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1848+3044delA | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110212242 | |||||
| chr12:110212537
|
T | TAA | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1848+3334_1848+333 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110212537 | |||||
| chr12:110212635
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1848+3419A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110212635 | ||||||
| chr12:110212693
|
C | T | 8 | a0001c0001t0001g0114a0001c0001t0001g0124a0001c0001t0001g0129others(5): Show | 8 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1848+3477C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110212693 | ||||||
| chr12:110212697
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1848+3481C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110212697 | ||||||
| chr12:110213062
|
ACT | A | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1848+3849_1848+385 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110213062 | |||||
| chr12:110213105
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1848+3889G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110213105 | ||||||
| chr12:110213122
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1848+3906G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110213122 | ||||||
| chr12:110213654
|
C | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | NA18948.hp1 NA18952.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.1849-4390C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110213654 | ||||||
| chr12:110213729
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1849-4315G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110213729 | ||||||
| chr12:110213733
|
C | A | 5 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1849-4311C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110213733 | ||||||
| chr12:110213783
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1849-4261G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110213783 | ||||||
| chr12:110214004
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0174 | 2 | HG01943.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1849-4040G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110214004 | ||||||
| chr12:110214055
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1849-3989C>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110214055 | ||||||
| chr12:110214154
|
G | T | 1 | a0001c0004t0001g0019 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1849-3890G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110214154 | ||||||
| chr12:110214284
|
G | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0037others(22): Show | 25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1849-3760G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110214284 | ||||||
| chr12:110214758
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1849-3286A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110214758 | ||||||
| chr12:110215080
|
C | G | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1849-2964C>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215080 | ||||||
| chr12:110215175
|
C | T | 1 | a0002c0002t0001g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1849-2869C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215175 | ||||||
| chr12:110215232
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2812G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215232 | ||||||
| chr12:110215325
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2719A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215325 | ||||||
| chr12:110215431
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1849-2613T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215431 | ||||||
| chr12:110215433
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1849-2611C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215433 | ||||||
| chr12:110215453
|
C | CT | 42 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(39): Show | 42 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.1849-2562dupT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | |||||
| chr12:110215453
|
C | CTT | 19 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(16): Show | 19 | HG01099.hp1 HG01167.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1849-2563_1849-256 others(6): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | |||||
| chr12:110215453
|
C | CTTT | 6 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(3): Show | 6 | HG02486.hp1 HG02717.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1849-2564_1849-256 others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | |||||
| chr12:110215453
|
C | CTTTT | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0060others(3): Show | 6 | HG01168.hp1 HG01169.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1849-2565_1849-256 others(8): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | |||||
| chr12:110215453
|
C | CTTTTT | 5 | a0001c0001t0001g0013a0002c0002t0001g0049a0002c0002t0001g0050others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1849-2566_1849-256 others(9): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | |||||
| chr12:110215453
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1849-2591C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215453 | ||||||
| chr12:110215453
|
CT | C | 15 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0092others(12): Show | 15 | HG01074.hp1 HG01074.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1849-2562delT | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | |||||
| chr12:110215453
|
CTTT | C | 20 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0002g0177others(17): Show | 20 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1849-2564_1849-256 others(7): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215453 | |||||
| chr12:110215524
|
T | G | 10 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0081others(7): Show | 10 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1849-2520T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215524 | ||||||
| chr12:110215537
|
C | T | 8 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG01081.hp2 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1849-2507C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215537 | ||||||
| chr12:110215584
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2460C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215584 | ||||||
| chr12:110215628
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2416A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215628 | ||||||
| chr12:110215677
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1849-2367G>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215677 | ||||||
| chr12:110215701
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2343T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215701 | ||||||
| chr12:110215736
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2308G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215736 | ||||||
| chr12:110215789
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-2255A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215789 | ||||||
| chr12:110215839
|
T | G | 1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1849-2205T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215839 | ||||||
| chr12:110215892
|
T | TAACAAAA others(335): Show |
1 | a0001c0001t0001g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1849-2136_1849-213 others(346): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215892 | |||||
| chr12:110215894
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1849-2150A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110215894 | ||||||
| chr12:110215895
|
C | CAAAAACA others(337): Show |
1 | a0001c0001t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1849-2136_1849-213 others(348): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215895 | |||||
| chr12:110215895
|
C | CAAAAACA others(338): Show |
1 | a0001c0001t0001g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1849-2136_1849-213 others(349): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110215895 | |||||
| chr12:110216052
|
T | C | 19 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 19 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1849-1992T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110216052 | ||||||
| chr12:110216173
|
G | GTTGTT | 2 | a0001c0001t0001g0135a0001c0004t0001g0019 | 2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1849-1843_1849-183 others(9): Show |
IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr12 | 110216173 | |||||
| chr12:110216442
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1849-1602G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110216442 | ||||||
| chr12:110216516
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1849-1528T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110216516 | ||||||
| chr12:110216746
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1849-1298G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110216746 | ||||||
| chr12:110216899
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1849-1145G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110216899 | ||||||
| chr12:110217325
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1849-719G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217325 | ||||||
| chr12:110217622
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1849-422C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217622 | ||||||
| chr12:110217665
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0004t0001g0019 | 3 | HG02055.hp1 HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1849-379G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217665 | ||||||
| chr12:110217786
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1849-258A>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217786 | ||||||
| chr12:110217814
|
T | G | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1849-230T>G | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217814 | ||||||
| chr12:110217818
|
G | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1849-226G>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217818 | ||||||
| chr12:110217877
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0059 | 2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1849-167G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217877 | ||||||
| chr12:110217900
|
T | C | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1849-144T>C | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217900 | ||||||
| chr12:110217907
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1849-137G>A | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217907 | ||||||
| chr12:110217985
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1849-59C>T | IFT81 | ENSG00000122970.16 | transcript | ENST00000242591.10 | protein_coding | 18/18 | chr12 | 110217985 |