Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 154661 |
|---|---|
| ensemblid | ENSG00000105784.16 |
| hgncid | 30286 |
| symbol | RUNDC3B |
| name | RUN domain containing 3B |
| refseq_nuc | NM_001134405.2 |
| refseq_prot | NP_001127877.1 |
| ensembl_nuc | ENST00000394654.4 |
| ensembl_prot | ENSP00000378149.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 87628398 |
| end | 87832296 |
| strand | + |
| ver | v1.2 |
| region | chr7:87628398-87832296 |
| region5000 | chr7:87623398-87837296 |
| regionname0 | RUNDC3B_chr7_87628398_87832296 |
| regionname5000 | RUNDC3B_chr7_87623398_87837296 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 456 | 199 | 62 | 42 | 65 | 8 | 20 | 47 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0002 | 0/0 | 456 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1371 | 198 | 62 | 42 | 65 | 8 | 19 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| c0002 | 0/0 | 1371 | 3 | 0 | 0 | 3 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| c0003 | 0/0 | 1371 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2683 | 24 | 1 | 6 | 10 | 3 | 4 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0002 | 0/0 | 2689 | 12 | 7 | 2 | 3 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0003 | 0/0 | 2685 | 11 | 1 | 4 | 5 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0004 | 0/0 | 2689 | 10 | 3 | 3 | 3 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0005 | 0/0 | 2691 | 10 | 1 | 2 | 5 | 1 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0006 | 0/0 | 2687 | 8 | 1 | 0 | 5 | 1 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0007 | 0/1 | 2695 | 7 | 4 | 1 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0008 | 0/0 | 2687 | 5 | 0 | 4 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0009 | 1/0 | 2693 | 5 | 1 | 0 | 3 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0010 | 0/0 | 2685 | 4 | 4 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0011 | 0/0 | 2687 | 4 | 0 | 1 | 0 | 1 | 2 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0012 | 0/0 | 2696 | 3 | 0 | 0 | 3 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0013 | 0/0 | 2689 | 3 | 0 | 2 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0014 | 0/0 | 2698 | 3 | 0 | 0 | 3 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0015 | 0/0 | 2684 | 3 | 3 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0016 | 0/0 | 2689 | 3 | 0 | 3 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0017 | 0/0 | 2691 | 3 | 2 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0018 | 0/0 | 2693 | 3 | 3 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0019 | 0/0 | 2695 | 3 | 0 | 2 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0020 | 0/0 | 2689 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0021 | 0/0 | 2691 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0022 | 0/0 | 2691 | 2 | 1 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0023 | 0/0 | 2692 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0024 | 0/0 | 2691 | 2 | 2 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0025 | 0/0 | 2690 | 2 | 1 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0026 | 0/0 | 2693 | 2 | 0 | 1 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0027 | 0/0 | 2696 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0028 | 0/0 | 2681 | 2 | 0 | 0 | 1 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0029 | 0/0 | 2687 | 2 | 1 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0030 | 0/0 | 2686 | 2 | 0 | 2 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0031 | 0/0 | 2688 | 2 | 1 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0032 | 0/0 | 2689 | 2 | 0 | 0 | 0 | 0 | 2 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0033 | 0/0 | 2691 | 2 | 1 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0034 | 0/0 | 2690 | 2 | 2 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0035 | 0/0 | 2689 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0036 | 0/0 | 2688 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0037 | 0/0 | 2691 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0038 | 0/0 | 2693 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0039 | 0/0 | 2694 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0040 | 0/0 | 2694 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0041 | 0/0 | 2687 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0042 | 0/0 | 2689 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0043 | 0/0 | 2689 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0044 | 0/0 | 2688 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0045 | 0/0 | 2688 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0046 | 0/0 | 2691 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0047 | 0/0 | 2694 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0048 | 0/0 | 2695 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0049 | 0/0 | 2695 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0050 | 0/0 | 2696 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0051 | 0/0 | 2697 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0052 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0053 | 0/0 | 2684 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0054 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0055 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0056 | 0/0 | 2683 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0057 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0058 | 0/0 | 2688 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0059 | 0/0 | 2688 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0060 | 0/0 | 2688 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0061 | 0/0 | 2687 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0062 | 0/0 | 2687 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0063 | 0/0 | 2686 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0064 | 0/0 | 2686 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0065 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0066 | 0/0 | 2690 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0067 | 0/0 | 2689 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0068 | 0/0 | 2689 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0069 | 0/0 | 2689 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0070 | 0/0 | 2688 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0071 | 0/0 | 2687 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0072 | 0/0 | 2686 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0073 | 0/0 | 2693 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0074 | 0/0 | 2693 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0075 | 0/0 | 2693 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0076 | 0/0 | 2692 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0077 | 0/0 | 2695 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0078 | 0/0 | 2695 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0079 | 0/0 | 2694 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0080 | 0/0 | 2697 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0081 | 0/0 | 2697 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| t0082 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1371 | 198 | 62 | 42 | 65 | 8 | 19 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0003 | 0/0 | 1371 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0002c0002 | 0/0 | 1371 | 3 | 0 | 0 | 3 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4053 | 23 | 1 | 6 | 10 | 3 | 3 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0002 | 0/0 | 4059 | 10 | 7 | 2 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0003 | 0/0 | 4055 | 11 | 1 | 4 | 5 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0004 | 0/0 | 4059 | 10 | 3 | 3 | 3 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0005 | 0/0 | 4061 | 10 | 1 | 2 | 5 | 1 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0006 | 0/0 | 4057 | 8 | 1 | 0 | 5 | 1 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0007 | 0/1 | 4065 | 7 | 4 | 1 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0008 | 0/0 | 4057 | 5 | 0 | 4 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0009 | 1/0 | 4063 | 5 | 1 | 0 | 3 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0010 | 0/0 | 4055 | 4 | 4 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0011 | 0/0 | 4057 | 4 | 0 | 1 | 0 | 1 | 2 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0012 | 0/0 | 4066 | 3 | 0 | 0 | 3 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0013 | 0/0 | 4059 | 3 | 0 | 2 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0014 | 0/0 | 4068 | 3 | 0 | 0 | 3 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0015 | 0/0 | 4054 | 3 | 3 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0016 | 0/0 | 4059 | 3 | 0 | 3 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0017 | 0/0 | 4061 | 2 | 2 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0018 | 0/0 | 4063 | 3 | 3 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0019 | 0/0 | 4065 | 3 | 0 | 2 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0020 | 0/0 | 4059 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0021 | 0/0 | 4061 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0022 | 0/0 | 4061 | 2 | 1 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0023 | 0/0 | 4062 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0024 | 0/0 | 4061 | 2 | 2 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0025 | 0/0 | 4060 | 2 | 1 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0026 | 0/0 | 4063 | 2 | 0 | 1 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0027 | 0/0 | 4066 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0028 | 0/0 | 4051 | 2 | 0 | 0 | 1 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0029 | 0/0 | 4057 | 2 | 1 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0030 | 0/0 | 4056 | 2 | 0 | 2 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0031 | 0/0 | 4058 | 2 | 1 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0032 | 0/0 | 4059 | 2 | 0 | 0 | 0 | 0 | 2 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0033 | 0/0 | 4061 | 2 | 1 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0034 | 0/0 | 4060 | 2 | 2 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0035 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0036 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0037 | 0/0 | 4061 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0038 | 0/0 | 4063 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0039 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0040 | 0/0 | 4064 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0041 | 0/0 | 4057 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0042 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0043 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0044 | 0/0 | 4058 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0045 | 0/0 | 4058 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0046 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0047 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0048 | 0/0 | 4065 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0049 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0050 | 0/0 | 4066 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0051 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0052 | 0/0 | 4050 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0053 | 0/0 | 4054 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0054 | 0/0 | 4053 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0055 | 0/0 | 4053 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0056 | 0/0 | 4053 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0057 | 0/0 | 4053 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0058 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0059 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0060 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0061 | 0/0 | 4057 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0062 | 0/0 | 4057 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0063 | 0/0 | 4056 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0064 | 0/0 | 4056 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0065 | 0/0 | 4052 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0066 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0067 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0068 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0069 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0070 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0071 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0072 | 0/0 | 4056 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0073 | 0/0 | 4063 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0074 | 0/0 | 4063 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0075 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0076 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0077 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0078 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0079 | 0/0 | 4064 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0080 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0081 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0001t0082 | 0/0 | 4055 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0001c0003t0001 | 0/0 | 4053 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0002c0002t0002 | 0/0 | 4059 | 2 | 0 | 0 | 2 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| a0002c0002t0017 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | copy fasta | chr7 | 87623398 | 87837296 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0008g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0008g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0008g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0008g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0009g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0009g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0009g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0009g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0009g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0010g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0010g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0011g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0011g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0011g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0011g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0012g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0012g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0012g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0013g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0013g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0013g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0014g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0014g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0014g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0015g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0015g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0015g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0016g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0016g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0016g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0017g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0017g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0018g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0018g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0018g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0019g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0019g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0019g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0020g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0020g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0021g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0021g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0022g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0022g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0023g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0023g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0024g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0024g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0025g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0025g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0026g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0026g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0027g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0027g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0028g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0028g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0029g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0029g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0030g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0030g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0031g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0031g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0032g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0032g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0033g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0033g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0034g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0034g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0035g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0036g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0037g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0038g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0039g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0040g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0041g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0042g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0043g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0044g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0045g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0046g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0047g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0048g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0049g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0050g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0051g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0052g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0053g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0054g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0055g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0056g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0057g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0058g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0059g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0060g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0061g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0062g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0063g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0064g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0065g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0066g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0067g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0068g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0069g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0070g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0071g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0072g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0073g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0074g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0075g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0076g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0077g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0078g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0079g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0080g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0081g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0001t0082g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| a0002c0002t0017g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0120 | EUR | FIN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00280 | hp2 | a0001 | c0001 | t0011 | g0194 | EUR | FIN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0104 | EUR | FIN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00323 | hp2 | a0001 | c0001 | t0074 | g0097 | EUR | FIN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00423 | hp1 | a0001 | c0001 | t0012 | g0152 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00423 | hp2 | a0001 | c0001 | t0009 | g0132 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00438 | hp2 | a0001 | c0001 | t0033 | g0073 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00558 | hp1 | a0001 | c0001 | t0031 | g0125 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00621 | hp1 | a0001 | c0001 | t0080 | g0100 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00639 | hp1 | a0001 | c0001 | t0045 | g0078 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00639 | hp2 | a0001 | c0001 | t0037 | g0002 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0116 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00738 | hp1 | a0001 | c0001 | t0016 | g0103 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0111 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG00741 | hp2 | a0001 | c0001 | t0073 | g0098 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01069 | hp1 | a0001 | c0001 | t0065 | g0144 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0197 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0119 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0195 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01074 | hp2 | a0001 | c0001 | t0030 | g0196 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01081 | hp1 | a0001 | c0001 | t0026 | g0146 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01081 | hp2 | a0001 | c0001 | t0013 | g0149 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01099 | hp2 | a0001 | c0001 | t0025 | g0053 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0190 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01169 | hp1 | a0001 | c0001 | t0030 | g0192 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01192 | hp1 | a0001 | c0001 | t0038 | g0182 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01261 | hp2 | a0001 | c0001 | t0016 | g0126 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01346 | hp1 | a0001 | c0001 | t0011 | g0198 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0117 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01358 | hp1 | a0001 | c0001 | t0013 | g0030 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01433 | hp1 | a0001 | c0001 | t0016 | g0129 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0193 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01496 | hp1 | a0001 | c0001 | t0044 | g0033 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0101 | AMR | PEL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01978 | hp1 | a0001 | c0001 | t0019 | g0043 | AMR | PEL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01981 | hp1 | a0001 | c0001 | t0048 | g0028 | AMR | PEL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01981 | hp2 | a0001 | c0001 | t0019 | g0110 | AMR | PEL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02040 | hp1 | a0001 | c0001 | t0046 | g0109 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02040 | hp2 | a0001 | c0001 | t0006 | g0067 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02055 | hp1 | a0001 | c0001 | t0043 | g0011 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0133 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02129 | hp1 | a0001 | c0001 | t0020 | g0036 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0066 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02132 | hp2 | a0001 | c0001 | t0057 | g0138 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02135 | hp1 | a0001 | c0001 | t0007 | g0090 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | KHV | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02165 | hp1 | a0001 | c0001 | t0009 | g0115 | EAS | CDX | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02258 | hp2 | a0001 | c0001 | t0077 | g0169 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02572 | hp1 | a0001 | c0001 | t0068 | g0001 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02572 | hp2 | a0001 | c0001 | t0047 | g0012 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02622 | hp1 | a0001 | c0001 | t0055 | g0199 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02622 | hp2 | a0001 | c0001 | t0017 | g0173 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02630 | hp1 | a0001 | c0001 | t0060 | g0015 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02630 | hp2 | a0001 | c0001 | t0033 | g0065 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02647 | hp1 | a0001 | c0001 | t0024 | g0062 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0007 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02717 | hp1 | a0001 | c0001 | t0022 | g0179 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02717 | hp2 | a0001 | c0001 | t0059 | g0014 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02723 | hp1 | a0001 | c0001 | t0042 | g0148 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02723 | hp2 | a0001 | c0001 | t0078 | g0005 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02818 | hp1 | a0001 | c0001 | t0018 | g0175 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0122 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02895 | hp1 | a0001 | c0001 | t0071 | g0142 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02896 | hp1 | a0001 | c0001 | t0070 | g0017 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02897 | hp1 | a0001 | c0001 | t0069 | g0016 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02897 | hp2 | a0001 | c0001 | t0072 | g0143 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02965 | hp2 | a0001 | c0001 | t0082 | g0023 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02970 | hp1 | a0001 | c0001 | t0081 | g0123 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02970 | hp2 | a0001 | c0001 | t0018 | g0174 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02976 | hp2 | a0001 | c0001 | t0025 | g0004 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03017 | hp1 | a0001 | c0001 | t0064 | g0184 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03017 | hp2 | a0001 | c0001 | t0028 | g0069 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0080 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03041 | hp2 | a0001 | c0001 | t0076 | g0081 | AFR | GWD | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03098 | hp2 | a0001 | c0001 | t0036 | g0160 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0021 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03139 | hp1 | a0001 | c0001 | t0024 | g0003 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0136 | AFR | ESN | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03209 | hp1 | a0001 | c0001 | t0017 | g0170 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03209 | hp2 | a0001 | c0001 | t0066 | g0013 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0186 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0085 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03239 | hp2 | a0001 | c0001 | t0056 | g0086 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03453 | hp1 | a0001 | c0001 | t0052 | g0038 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0108 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03491 | hp1 | a0001 | c0001 | t0032 | g0187 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03492 | hp1 | a0001 | c0001 | t0032 | g0188 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03492 | hp2 | a0001 | c0001 | t0019 | g0024 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0008 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03579 | hp2 | a0001 | c0001 | t0034 | g0079 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03654 | hp1 | a0001 | c0001 | t0079 | g0177 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03654 | hp2 | a0001 | c0001 | t0062 | g0093 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03704 | hp2 | a0001 | c0001 | t0011 | g0200 | SAS | PJL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0089 | SAS | BEB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG04184 | hp1 | a0001 | c0001 | t0061 | g0185 | SAS | BEB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG04199 | hp1 | a0001 | c0001 | t0050 | g0168 | SAS | STU | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0022 | SAS | STU | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG04228 | hp1 | a0001 | c0001 | t0011 | g0189 | SAS | STU | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0145 | SAS | STU | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0009 | AFR | YRI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | YRI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | YRI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18906 | hp2 | a0001 | c0001 | t0015 | g0092 | AFR | YRI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18952 | hp1 | a0001 | c0001 | t0039 | g0158 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18963 | hp1 | a0001 | c0001 | t0023 | g0039 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18968 | hp2 | a0001 | c0001 | t0009 | g0121 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18970 | hp2 | a0001 | c0001 | t0012 | g0150 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18973 | hp1 | a0001 | c0001 | t0006 | g0050 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18974 | hp1 | a0001 | c0001 | t0029 | g0178 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0134 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18975 | hp1 | a0001 | c0001 | t0022 | g0180 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18977 | hp2 | a0001 | c0001 | t0041 | g0183 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0135 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18988 | hp2 | a0001 | c0001 | t0014 | g0155 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18990 | hp1 | a0001 | c0001 | t0028 | g0040 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18990 | hp2 | a0001 | c0001 | t0014 | g0153 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18992 | hp1 | a0001 | c0001 | t0063 | g0060 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18992 | hp2 | a0001 | c0001 | t0051 | g0156 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18994 | hp2 | a0001 | c0001 | t0013 | g0171 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18998 | hp1 | a0001 | c0001 | t0014 | g0157 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA18998 | hp2 | a0001 | c0001 | t0026 | g0083 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19001 | hp2 | a0002 | c0002 | t0017 | g0140 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19005 | hp1 | a0001 | c0001 | t0053 | g0025 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19005 | hp2 | a0001 | c0001 | t0021 | g0032 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19010 | hp1 | a0001 | c0001 | t0006 | g0113 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19030 | hp1 | a0001 | c0001 | t0067 | g0074 | AFR | LWK | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19030 | hp2 | a0001 | c0001 | t0029 | g0181 | AFR | LWK | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19043 | hp1 | a0001 | c0001 | t0015 | g0094 | AFR | LWK | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19043 | hp2 | a0001 | c0001 | t0058 | g0018 | AFR | LWK | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19056 | hp1 | a0001 | c0001 | t0020 | g0034 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19060 | hp2 | a0001 | c0001 | t0023 | g0159 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19062 | hp1 | a0001 | c0001 | t0027 | g0154 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19062 | hp2 | a0001 | c0001 | t0049 | g0201 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19063 | hp2 | a0001 | c0001 | t0021 | g0029 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19082 | hp2 | a0001 | c0001 | t0012 | g0151 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19083 | hp1 | a0001 | c0001 | t0035 | g0035 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19083 | hp2 | a0001 | c0001 | t0054 | g0052 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19087 | hp1 | a0001 | c0001 | t0027 | g0037 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0131 | EAS | JPT | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA20129 | hp1 | a0001 | c0001 | t0018 | g0172 | AFR | ASW | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA20129 | hp2 | a0001 | c0001 | t0015 | g0020 | AFR | ASW | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | TSI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | TSI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0191 | EUR | TSI | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01123 | hp1 | a0001 | c0001 | t0040 | g0161 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02559 | hp1 | a0001 | c0001 | t0034 | g0077 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03471 | hp1 | a0001 | c0001 | t0031 | g0076 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| HG03471 | hp2 | a0001 | c0001 | t0075 | g0006 | AFR | MSL | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0118 | REF | REF | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0009 | g0147 | REF | REF | RUNDC3B_chr7_87623398_87837296 | RUNDC3B | chr7 | 87623398 | 87837296 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87739793
|
G | T | 1 | a0002 | 3 | NA18973.hp2 NA18979.hp1 NA19001.hp2 |
missense_variant&splice_region_variant | MODERATE | c.461G>T | p.Arg154Ile | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/11 | 887/4063 | 461/1371 | 154/456 | chr7 | 87739793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87777887
|
T | C | 1 | a0001c0003 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.888T>C | p.Asp296Asp | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/11 | 1314/4063 | 888/1371 | 296/456 | chr7 | 87777887 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87628549
|
G | C | 3 | a0001c0001t0020a0001c0001t0021a0001c0001t0035 | 5 | HG02129.hp1 NA19005.hp2 NA19056.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-275G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 275 | chr7 | 87628549 | |||||
| chr7:87628552
|
G | A | 1 | a0001c0001t0036 | 1 | HG03098.hp2 | 5_prime_UTR_variant | MODIFIER | c.-272G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 272 | chr7 | 87628552 | |||||
| chr7:87628572
|
G | GGTGC | 3 | a0001c0001t0014a0001c0001t0050a0001c0001t0051 | 5 | HG04199.hp1 NA18988.hp2 NA18990.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-240_-237dupCGTG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 236 | INFO_REALIGN_3_PRIME | chr7 | 87628572 | ||||
| chr7:87628584
|
C | CGT | 5 | a0001c0001t0007a0001c0001t0019a0001c0001t0077others(2): Show | 13 | HG00735.hp2 HG01978.hp1 HG01981.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-200_-199dupTG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 198 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | ||||
| chr7:87628584
|
C | CGTGT | 2 | a0001c0001t0080a0001c0001t0081 | 2 | HG00621.hp1 HG02970.hp1 |
5_prime_UTR_variant | MODIFIER | c.-202_-199dupTGTG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 198 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | ||||
| chr7:87628584
|
CGT | C | 14 | a0001c0001t0005a0001c0001t0017a0001c0001t0021others(11): Show | 31 | HG00280.hp1 HG00438.hp2 HG00639.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-200_-199delTG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 199 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | ||||
| chr7:87628584
|
CGTGT | C | 19 | a0001c0001t0002a0001c0001t0004a0001c0001t0013others(16): Show | 45 | HG00558.hp1 HG00639.hp1 HG00738.hp1 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-202_-199delTGTG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 199 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | ||||
| chr7:87628584
|
CGTGTGT | C | 14 | a0001c0001t0006a0001c0001t0008a0001c0001t0011others(11): Show | 30 | HG00280.hp2 HG00323.hp1 HG01069.hp1 others(27): Show |
5_prime_UTR_variant | MODIFIER | c.-204_-199delTGTGTG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 199 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | ||||
| chr7:87628584
|
CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0003a0001c0001t0010a0001c0001t0015others(1): Show | 19 | HG00438.hp1 HG00741.hp1 HG01074.hp1 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-206_-199delTGTGTG others(2): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 199 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | ||||
| chr7:87628584
|
CGTGTGTG others(3): Show |
C | 7 | a0001c0001t0001a0001c0001t0053a0001c0001t0054others(4): Show | 29 | HG00558.hp2 HG00621.hp2 HG00735.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-208_-199delTGTGTG others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 199 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | ||||
| chr7:87628584
|
CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0028a0001c0001t0052 | 3 | HG03017.hp2 HG03453.hp1 NA18990.hp1 |
5_prime_UTR_variant | MODIFIER | c.-210_-199delTGTGTG others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 199 | INFO_REALIGN_3_PRIME | chr7 | 87628584 | ||||
| chr7:87628586
|
T | TGC | 5 | a0001c0001t0012a0001c0001t0027a0001c0001t0040others(2): Show | 8 | HG00423.hp1 HG01123.hp1 HG01981.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-237_-236insCG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 236 | INFO_REALIGN_3_PRIME | chr7 | 87628586 | ||||
| chr7:87628588
|
T | C | 4 | a0001c0001t0026a0001c0001t0038a0001c0001t0039others(1): Show | 5 | HG01081.hp1 HG01192.hp1 HG02572.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-236T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 236 | chr7 | 87628588 | |||||
| chr7:87628590
|
T | C | 8 | a0001c0001t0012a0001c0001t0022a0001c0001t0023others(5): Show | 14 | HG00423.hp1 HG00639.hp2 HG01099.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-234T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 234 | chr7 | 87628590 | |||||
| chr7:87628592
|
T | C | 7 | a0001c0001t0013a0001c0001t0038a0001c0001t0039others(4): Show | 9 | HG00639.hp1 HG01081.hp2 HG01192.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-232T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 232 | chr7 | 87628592 | |||||
| chr7:87628594
|
T | C | 2 | a0001c0001t0037a0001c0001t0041 | 2 | HG00639.hp2 NA18977.hp2 |
5_prime_UTR_variant | MODIFIER | c.-230T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 230 | chr7 | 87628594 | |||||
| chr7:87628621
|
G | T | 1 | a0001c0001t0082 | 1 | HG02965.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-203G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | chr7 | 87628621 | ||||||
| chr7:87628711
|
C | T | 3 | a0001c0001t0008a0001c0001t0030a0001c0001t0032 | 9 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-113C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/11 | 113 | chr7 | 87628711 | |||||
| chr7:87830440
|
C | CA | 32 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(29): Show | 65 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*429dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 430 | INFO_REALIGN_3_PRIME | chr7 | 87830440 | ||||
| chr7:87830440
|
CA | C | 9 | a0001c0001t0015a0001c0001t0025a0001c0001t0031others(6): Show | 14 | HG00558.hp1 HG00639.hp1 HG01069.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*429delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 429 | INFO_REALIGN_3_PRIME | chr7 | 87830440 | ||||
| chr7:87830518
|
T | C | 1 | a0001c0001t0058 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*488T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 488 | chr7 | 87830518 | |||||
| chr7:87830636
|
C | T | 48 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(45): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*606C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 606 | chr7 | 87830636 | |||||
| chr7:87830715
|
C | A | 1 | a0001c0001t0043 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*685C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 685 | chr7 | 87830715 | |||||
| chr7:87830715
|
C | T | 41 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(38): Show | 75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*685C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 685 | chr7 | 87830715 | |||||
| chr7:87830898
|
ATAGT | A | 3 | a0001c0001t0065a0001c0001t0071a0001c0001t0072 | 3 | HG01069.hp1 HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*871_*874delGTTA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 871 | INFO_REALIGN_3_PRIME | chr7 | 87830898 | ||||
| chr7:87830901
|
G | T | 6 | a0001c0001t0008a0001c0001t0011a0001c0001t0030others(3): Show | 15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*871G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 871 | chr7 | 87830901 | |||||
| chr7:87830991
|
A | G | 1 | a0001c0001t0074 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*961A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 961 | chr7 | 87830991 | |||||
| chr7:87831011
|
C | G | 1 | a0001c0001t0074 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*981C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 981 | chr7 | 87831011 | |||||
| chr7:87831058
|
T | TA | 6 | a0001c0001t0042a0001c0001t0047a0001c0001t0058others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1029dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1030 | INFO_REALIGN_3_PRIME | chr7 | 87831058 | ||||
| chr7:87831060
|
T | C | 9 | a0001c0001t0016a0001c0001t0019a0001c0001t0033others(6): Show | 14 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1030T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1030 | chr7 | 87831060 | |||||
| chr7:87831076
|
GT | G | 28 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(25): Show | 56 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1059delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1059 | INFO_REALIGN_3_PRIME | chr7 | 87831076 | ||||
| chr7:87831105
|
AC | A | 2 | a0001c0001t0069a0001c0001t0070 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1076delC | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1076 | chr7 | 87831105 | |||||
| chr7:87831106
|
CT | C | 6 | a0001c0001t0036a0001c0001t0042a0001c0001t0047others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1088delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1088 | INFO_REALIGN_3_PRIME | chr7 | 87831106 | ||||
| chr7:87831107
|
T | A | 2 | a0001c0001t0069a0001c0001t0070 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1077T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1077 | chr7 | 87831107 | |||||
| chr7:87831179
|
G | A | 1 | a0001c0001t0057 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1149G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1149 | chr7 | 87831179 | |||||
| chr7:87831398
|
A | G | 7 | a0001c0001t0008a0001c0001t0011a0001c0001t0030others(4): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1368A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1368 | chr7 | 87831398 | |||||
| chr7:87831560
|
C | T | 1 | a0001c0001t0039 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1530C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1530 | chr7 | 87831560 | |||||
| chr7:87832004
|
C | T | 2 | a0001c0001t0061a0001c0001t0064 | 2 | HG03017.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1974C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 1974 | chr7 | 87832004 | |||||
| chr7:87832092
|
G | A | 6 | a0001c0001t0008a0001c0001t0011a0001c0001t0030others(3): Show | 15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2062G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 2062 | chr7 | 87832092 | |||||
| chr7:87832253
|
G | A | 1 | a0001c0001t0067 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2223G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 11/11 | 2223 | chr7 | 87832253 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87628975
|
C | T | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.122+30C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87628975 | ||||||
| chr7:87629088
|
G | A | 11 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(8): Show | 11 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+143G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629088 | ||||||
| chr7:87629284
|
C | T | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+339C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629284 | ||||||
| chr7:87629410
|
T | C | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.122+465T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629410 | ||||||
| chr7:87629642
|
A | T | 1 | a0001c0001t0049g0201 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.122+697A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629642 | ||||||
| chr7:87629719
|
G | C | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.122+774G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629719 | ||||||
| chr7:87629794
|
C | T | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.122+849C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629794 | ||||||
| chr7:87629845
|
G | A | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.122+900G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629845 | ||||||
| chr7:87629908
|
G | C | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+963G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87629908 | ||||||
| chr7:87629920
|
C | CA | 7 | a0001c0001t0004g0019a0001c0001t0007g0021a0001c0001t0015g0020others(4): Show | 7 | HG00639.hp2 HG02572.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+990dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87629920 | |||||
| chr7:87629920
|
CA | C | 57 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(54): Show | 57 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.122+990delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87629920 | |||||
| chr7:87630069
|
G | A | 200 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(197): Show | 200 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.122+1124G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87630069 | ||||||
| chr7:87630074
|
T | A | 2 | a0001c0001t0061g0185a0001c0001t0064g0184 | 2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.122+1129T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87630074 | ||||||
| chr7:87630154
|
T | A | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.122+1209T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87630154 | ||||||
| chr7:87630533
|
C | T | 3 | a0001c0001t0011g0200a0001c0001t0061g0185a0001c0001t0064g0184 | 3 | HG03017.hp1 HG03704.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.122+1588C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87630533 | ||||||
| chr7:87630688
|
C | CT | 5 | a0001c0001t0003g0141a0001c0001t0006g0145a0001c0001t0065g0144others(2): Show | 5 | HG01069.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+1756dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87630688 | |||||
| chr7:87630688
|
CT | C | 7 | a0001c0001t0006g0186a0001c0001t0013g0149a0001c0001t0047g0012others(4): Show | 7 | HG01081.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+1756delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87630688 | |||||
| chr7:87630830
|
T | C | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.122+1885T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87630830 | ||||||
| chr7:87630926
|
G | A | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.122+1981G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87630926 | ||||||
| chr7:87631296
|
A | G | 1 | a0002c0002t0017g0140 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.122+2351A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631296 | ||||||
| chr7:87631547
|
C | T | 1 | a0001c0001t0010g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.122+2602C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631547 | ||||||
| chr7:87631574
|
T | C | 2 | a0001c0001t0032g0187a0001c0001t0032g0188 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.122+2629T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631574 | ||||||
| chr7:87631628
|
C | T | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.122+2683C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631628 | ||||||
| chr7:87631644
|
C | T | 1 | a0001c0001t0057g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.122+2699C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631644 | ||||||
| chr7:87631861
|
A | T | 1 | a0001c0001t0002g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.122+2916A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631861 | ||||||
| chr7:87631873
|
G | C | 1 | a0001c0001t0019g0024 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.122+2928G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87631873 | ||||||
| chr7:87632112
|
C | CA | 15 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0202others(12): Show | 15 | HG01358.hp1 HG01496.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.122+3180dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87632112 | |||||
| chr7:87632264
|
A | G | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.122+3319A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87632264 | ||||||
| chr7:87632420
|
T | C | 88 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(85): Show | 88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.122+3475T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87632420 | ||||||
| chr7:87632644
|
G | A | 3 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0037g0002 | 3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.122+3699G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87632644 | ||||||
| chr7:87633070
|
T | G | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.122+4125T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633070 | ||||||
| chr7:87633252
|
T | C | 1 | a0001c0001t0028g0040 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.122+4307T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633252 | ||||||
| chr7:87633258
|
C | T | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.122+4313C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633258 | ||||||
| chr7:87633263
|
A | G | 1 | a0001c0001t0023g0039 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.122+4318A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633263 | ||||||
| chr7:87633265
|
G | A | 88 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(85): Show | 88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.122+4320G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633265 | ||||||
| chr7:87633407
|
A | G | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.122+4462A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633407 | ||||||
| chr7:87633627
|
G | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.122+4682G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87633627 | ||||||
| chr7:87633668
|
AT | A | 16 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0012g0150others(13): Show | 16 | HG00423.hp1 HG02165.hp2 HG03098.hp2 others(13): Show |
intron_variant | MODIFIER | c.122+4736delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87633668 | |||||
| chr7:87634244
|
T | G | 2 | a0001c0001t0019g0043a0001c0001t0049g0201 | 2 | HG01978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.122+5299T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634244 | ||||||
| chr7:87634379
|
T | C | 1 | a0001c0001t0040g0161 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.122+5434T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634379 | ||||||
| chr7:87634425
|
C | A | 1 | a0001c0001t0003g0141 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.122+5480C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634425 | ||||||
| chr7:87634487
|
T | G | 1 | a0001c0001t0011g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.122+5542T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634487 | ||||||
| chr7:87634494
|
T | TG | 26 | a0001c0001t0003g0128a0001c0001t0003g0130a0001c0001t0004g0124others(23): Show | 26 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+5560dupG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87634494 | |||||
| chr7:87634494
|
TG | T | 81 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(78): Show | 81 | HG00423.hp1 HG01074.hp1 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.122+5560delG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87634494 | |||||
| chr7:87634559
|
C | T | 2 | a0001c0001t0036g0160a0001c0001t0051g0156 | 2 | HG03098.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.122+5614C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634559 | ||||||
| chr7:87634784
|
T | C | 3 | a0001c0001t0019g0043a0001c0001t0033g0073a0001c0001t0049g0201 | 3 | HG00438.hp2 HG01978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.122+5839T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634784 | ||||||
| chr7:87634831
|
C | G | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+5886C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87634831 | ||||||
| chr7:87635425
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.122+6480G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87635425 | ||||||
| chr7:87635508
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.122+6563A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87635508 | ||||||
| chr7:87635614
|
T | C | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.122+6669T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87635614 | ||||||
| chr7:87635621
|
T | A | 2 | a0001c0001t0012g0150a0001c0001t0012g0151 | 2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.122+6676T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87635621 | ||||||
| chr7:87636734
|
G | A | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122+7789G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87636734 | ||||||
| chr7:87637088
|
T | C | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.122+8143T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637088 | ||||||
| chr7:87637199
|
C | T | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122+8254C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637199 | ||||||
| chr7:87637393
|
C | A | 11 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(8): Show | 11 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+8448C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637393 | ||||||
| chr7:87637495
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.122+8550C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637495 | ||||||
| chr7:87637513
|
C | A | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.122+8568C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637513 | ||||||
| chr7:87637797
|
C | T | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122+8852C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637797 | ||||||
| chr7:87637805
|
T | G | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+8860T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87637805 | ||||||
| chr7:87638077
|
A | C | 3 | a0001c0001t0008g0195a0001c0001t0008g0197a0001c0001t0030g0196 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.122+9132A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87638077 | ||||||
| chr7:87638345
|
T | TTG | 78 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(75): Show | 78 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.122+9434_122+9435d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | |||||
| chr7:87638345
|
T | TTGTG | 15 | a0001c0001t0001g0045a0001c0001t0001g0084a0001c0001t0003g0046others(12): Show | 15 | HG00558.hp1 HG00558.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.122+9432_122+9435d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | |||||
| chr7:87638345
|
T | TTGTGTG | 10 | a0001c0001t0004g0075a0001c0001t0024g0003a0001c0001t0025g0004others(7): Show | 10 | HG00639.hp1 HG00639.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+9430_122+9435d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | |||||
| chr7:87638345
|
T | TTGTGTGT others(1): Show |
3 | a0001c0001t0014g0155a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02896.hp1 HG02897.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.122+9428_122+9435d others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | |||||
| chr7:87638345
|
T | TTGTGTGT others(3): Show |
2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.122+9426_122+9435d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | |||||
| chr7:87638345
|
T | TTGTGTGT others(5): Show |
7 | a0001c0001t0010g0007a0001c0001t0012g0152a0001c0001t0014g0153others(4): Show | 7 | HG00423.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+9424_122+9435d others(14): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | |||||
| chr7:87638345
|
T | TTGTGTGT others(7): Show |
8 | a0001c0001t0010g0010a0001c0001t0014g0157a0001c0001t0027g0037others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+9422_122+9435d others(16): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | |||||
| chr7:87638345
|
T | TTGTGTGT others(9): Show |
3 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0023g0039 | 3 | NA18963.hp1 NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.122+9420_122+9435d others(18): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | |||||
| chr7:87638345
|
TTG | T | 8 | a0001c0001t0001g0070a0001c0001t0002g0163a0001c0001t0002g0164others(5): Show | 8 | HG01192.hp2 HG02559.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+9434_122+9435d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | |||||
| chr7:87638345
|
TTGTG | T | 30 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0176others(27): Show | 30 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.122+9432_122+9435d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638345 | |||||
| chr7:87638371
|
G | GTGTGTA | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.122+9431_122+9432i others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87638371 | |||||
| chr7:87638460
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0028g0069 | 2 | HG01099.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.122+9515C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87638460 | ||||||
| chr7:87638488
|
G | A | 2 | a0001c0001t0061g0185a0001c0001t0064g0184 | 2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.122+9543G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87638488 | ||||||
| chr7:87638503
|
C | T | 1 | a0001c0001t0009g0115 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.122+9558C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87638503 | ||||||
| chr7:87638957
|
C | A | 1 | a0001c0001t0010g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.122+10012C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87638957 | ||||||
| chr7:87638979
|
C | T | 1 | a0001c0001t0055g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.122+10034C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87638979 | ||||||
| chr7:87639077
|
C | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.122+10132C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87639077 | ||||||
| chr7:87639078
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.122+10133G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87639078 | ||||||
| chr7:87639140
|
T | C | 88 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(85): Show | 88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.122+10195T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87639140 | ||||||
| chr7:87639153
|
C | CA | 136 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(133): Show | 136 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.122+10231dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87639153 | |||||
| chr7:87639153
|
C | CAA | 32 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0070others(29): Show | 32 | HG00423.hp2 HG00735.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.122+10230_122+1023 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87639153 | |||||
| chr7:87639153
|
C | CAAA | 7 | a0001c0001t0016g0126a0001c0001t0021g0032a0001c0001t0027g0037others(4): Show | 7 | HG01261.hp2 HG02630.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+10229_122+1023 others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87639153 | |||||
| chr7:87639277
|
T | G | 1 | a0001c0001t0003g0088 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.122+10332T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87639277 | ||||||
| chr7:87639934
|
T | C | 1 | a0001c0001t0012g0152 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.123-10888T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87639934 | ||||||
| chr7:87640072
|
C | T | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.123-10750C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640072 | ||||||
| chr7:87640181
|
T | C | 62 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(59): Show | 62 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.123-10641T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640181 | ||||||
| chr7:87640192
|
G | GTA | 7 | a0001c0001t0052g0038a0001c0001t0057g0138a0001c0001t0058g0018others(4): Show | 7 | HG02132.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-10614_123-1061 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87640192 | |||||
| chr7:87640192
|
GTA | G | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.123-10614_123-1061 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87640192 | |||||
| chr7:87640266
|
A | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.123-10556A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640266 | ||||||
| chr7:87640376
|
G | T | 1 | a0001c0001t0011g0194 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.123-10446G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640376 | ||||||
| chr7:87640503
|
C | A | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-10319C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640503 | ||||||
| chr7:87640708
|
T | C | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.123-10114T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640708 | ||||||
| chr7:87640951
|
G | A | 11 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(8): Show | 11 | HG00639.hp2 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.123-9871G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640951 | ||||||
| chr7:87640955
|
G | A | 1 | a0001c0001t0015g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123-9867G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87640955 | ||||||
| chr7:87641011
|
A | G | 1 | a0001c0001t0010g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123-9811A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87641011 | ||||||
| chr7:87641184
|
T | A | 88 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(85): Show | 88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.123-9638T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87641184 | ||||||
| chr7:87641531
|
C | T | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.123-9291C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87641531 | ||||||
| chr7:87641667
|
T | A | 1 | a0001c0001t0004g0089 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.123-9155T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87641667 | ||||||
| chr7:87641974
|
A | G | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-8848A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87641974 | ||||||
| chr7:87642026
|
G | A | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.123-8796G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87642026 | ||||||
| chr7:87642075
|
C | T | 1 | a0001c0001t0005g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.123-8747C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87642075 | ||||||
| chr7:87642348
|
G | A | 1 | a0001c0001t0019g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.123-8474G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87642348 | ||||||
| chr7:87642522
|
A | G | 41 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(38): Show | 41 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.123-8300A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87642522 | ||||||
| chr7:87642659
|
C | G | 1 | a0001c0001t0003g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.123-8163C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87642659 | ||||||
| chr7:87642736
|
C | T | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.123-8086C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87642736 | ||||||
| chr7:87643195
|
C | T | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.123-7627C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87643195 | ||||||
| chr7:87643687
|
A | AT | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-7123dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87643687 | |||||
| chr7:87643818
|
C | T | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-7004C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87643818 | ||||||
| chr7:87643889
|
C | T | 1 | a0001c0001t0034g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.123-6933C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87643889 | ||||||
| chr7:87643969
|
C | T | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.123-6853C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87643969 | ||||||
| chr7:87643999
|
C | T | 1 | a0001c0001t0013g0171 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.123-6823C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87643999 | ||||||
| chr7:87644123
|
T | C | 37 | a0001c0001t0002g0027a0001c0001t0002g0162a0001c0001t0002g0163others(34): Show | 37 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.123-6699T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87644123 | ||||||
| chr7:87644407
|
A | C | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.123-6415A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87644407 | ||||||
| chr7:87644517
|
G | T | 1 | a0001c0001t0057g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.123-6305G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87644517 | ||||||
| chr7:87644676
|
A | G | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-6146A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87644676 | ||||||
| chr7:87644704
|
T | C | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.123-6118T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87644704 | ||||||
| chr7:87644764
|
G | GAT | 2 | a0001c0001t0003g0095a0001c0001t0004g0089 | 2 | HG00741.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.123-6047_123-6046d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87644764 | |||||
| chr7:87644788
|
A | G | 1 | a0001c0001t0014g0155 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.123-6034A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87644788 | ||||||
| chr7:87645002
|
C | G | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.123-5820C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87645002 | ||||||
| chr7:87645081
|
C | CT | 23 | a0001c0001t0005g0114a0001c0001t0008g0190a0001c0001t0008g0191others(20): Show | 23 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.123-5723dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87645081 | |||||
| chr7:87645206
|
T | C | 7 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-5616T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87645206 | ||||||
| chr7:87645791
|
C | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.123-5031C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87645791 | ||||||
| chr7:87645819
|
A | T | 1 | a0001c0001t0006g0113 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.123-5003A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87645819 | ||||||
| chr7:87645832
|
G | C | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-4990G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87645832 | ||||||
| chr7:87645855
|
ACT | A | 7 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-4964_123-4963d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87645855 | |||||
| chr7:87646073
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.123-4749G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87646073 | ||||||
| chr7:87646225
|
C | T | 3 | a0001c0001t0019g0043a0001c0001t0033g0073a0001c0001t0049g0201 | 3 | HG00438.hp2 HG01978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.123-4597C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87646225 | ||||||
| chr7:87646325
|
A | G | 185 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(182): Show | 185 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.123-4497A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87646325 | ||||||
| chr7:87646341
|
T | C | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.123-4481T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87646341 | ||||||
| chr7:87646732
|
G | A | 1 | a0001c0001t0004g0124 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.123-4090G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87646732 | ||||||
| chr7:87646737
|
CCAGGGAT others(6): Show |
C | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-4082_123-4070d others(15): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87646737 | |||||
| chr7:87646759
|
TTG | T | 2 | a0001c0001t0016g0129a0001c0001t0073g0098 | 2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.123-4059_123-4058d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87646759 | |||||
| chr7:87646796
|
G | T | 1 | a0001c0001t0005g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.123-4026G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87646796 | ||||||
| chr7:87647137
|
G | A | 2 | a0001c0001t0003g0046a0001c0001t0003g0047 | 2 | HG01074.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.123-3685G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647137 | ||||||
| chr7:87647218
|
C | G | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-3604C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647218 | ||||||
| chr7:87647295
|
CT | C | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-3523delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87647295 | |||||
| chr7:87647509
|
A | G | 16 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.123-3313A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647509 | ||||||
| chr7:87647535
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.123-3287T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647535 | ||||||
| chr7:87647575
|
T | C | 1 | a0001c0001t0007g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.123-3247T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647575 | ||||||
| chr7:87647760
|
ACAT | A | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-3058_123-3056d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87647760 | |||||
| chr7:87647925
|
C | G | 2 | a0001c0001t0009g0121a0001c0001t0009g0132 | 2 | HG00423.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.123-2897C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647925 | ||||||
| chr7:87647958
|
G | A | 1 | a0001c0001t0080g0100 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.123-2864G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87647958 | ||||||
| chr7:87648109
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.123-2713G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87648109 | ||||||
| chr7:87648115
|
G | GCATA | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.123-2706_123-2703d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87648115 | |||||
| chr7:87648184
|
C | CA | 46 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(43): Show | 46 | HG00438.hp1 HG01081.hp2 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.123-2621dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87648184 | |||||
| chr7:87648410
|
G | A | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.123-2412G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87648410 | ||||||
| chr7:87648532
|
CA | C | 86 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(83): Show | 86 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.123-2279delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87648532 | |||||
| chr7:87648708
|
G | T | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.123-2114G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87648708 | ||||||
| chr7:87648711
|
A | G | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.123-2111A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87648711 | ||||||
| chr7:87648797
|
A | G | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.123-2025A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87648797 | ||||||
| chr7:87649096
|
C | T | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.123-1726C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87649096 | ||||||
| chr7:87649121
|
TC | T | 13 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(10): Show | 13 | HG00423.hp1 HG03453.hp1 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.123-1699delC | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 87649121 | |||||
| chr7:87649444
|
G | A | 179 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(176): Show | 179 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.123-1378G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87649444 | ||||||
| chr7:87649527
|
G | A | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.123-1295G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87649527 | ||||||
| chr7:87649539
|
T | C | 5 | a0001c0001t0004g0019a0001c0001t0004g0075a0001c0001t0005g0080others(2): Show | 5 | HG02896.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-1283T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87649539 | ||||||
| chr7:87649629
|
A | G | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-1193A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87649629 | ||||||
| chr7:87649645
|
A | G | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-1177A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87649645 | ||||||
| chr7:87650082
|
G | A | 1 | a0001c0001t0073g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.123-740G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87650082 | ||||||
| chr7:87650301
|
A | G | 1 | a0001c0001t0003g0047 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.123-521A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87650301 | ||||||
| chr7:87650436
|
C | T | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.123-386C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87650436 | ||||||
| chr7:87650476
|
A | G | 1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.123-346A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87650476 | ||||||
| chr7:87650492
|
T | C | 1 | a0001c0001t0010g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123-330T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87650492 | ||||||
| chr7:87650540
|
C | T | 88 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(85): Show | 88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.123-282C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 1/10 | chr7 | 87650540 | ||||||
| chr7:87651212
|
G | A | 1 | a0001c0001t0080g0100 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.238+275G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87651212 | ||||||
| chr7:87651517
|
A | G | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+580A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87651517 | ||||||
| chr7:87651699
|
T | C | 1 | a0001c0001t0016g0103 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.238+762T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87651699 | ||||||
| chr7:87651715
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.238+778C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87651715 | ||||||
| chr7:87651768
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+831G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87651768 | ||||||
| chr7:87651843
|
G | A | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.238+906G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87651843 | ||||||
| chr7:87651947
|
G | GT | 4 | a0001c0001t0005g0135a0001c0001t0015g0020a0001c0001t0036g0160others(1): Show | 4 | HG03098.hp2 NA18988.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+1018dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87651947 | |||||
| chr7:87652011
|
T | A | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+1074T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652011 | ||||||
| chr7:87652023
|
A | C | 1 | a0001c0001t0002g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.238+1086A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652023 | ||||||
| chr7:87652136
|
A | G | 1 | a0001c0001t0004g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.238+1199A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652136 | ||||||
| chr7:87652357
|
C | T | 1 | a0001c0001t0028g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.238+1420C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652357 | ||||||
| chr7:87652359
|
C | T | 2 | a0001c0001t0009g0121a0001c0001t0009g0132 | 2 | HG00423.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.238+1422C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652359 | ||||||
| chr7:87652621
|
G | GAGATATA others(11): Show |
1 | a0001c0001t0018g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.238+1685_238+1686i others(20): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GAGATATA others(13): Show |
5 | a0001c0001t0013g0149a0001c0001t0017g0173a0001c0001t0018g0174others(2): Show | 5 | HG01081.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+1685_238+1686i others(22): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GAT | 13 | a0001c0001t0003g0064a0001c0001t0004g0075a0001c0001t0004g0082others(10): Show | 13 | HG00639.hp1 HG02040.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.238+1708_238+1709d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATAT | 11 | a0001c0001t0004g0089a0001c0001t0015g0020a0001c0001t0016g0103others(8): Show | 11 | HG00438.hp2 HG00738.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.238+1706_238+1709d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATAT | 2 | a0001c0001t0019g0043a0001c0001t0062g0093 | 2 | HG01978.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.238+1704_238+1709d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(1): Show |
17 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0195others(14): Show | 17 | HG00423.hp1 HG00621.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.238+1702_238+1709d others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(3): Show |
9 | a0001c0001t0008g0193a0001c0001t0011g0200a0001c0001t0014g0157others(6): Show | 9 | HG01433.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+1700_238+1709d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(5): Show |
2 | a0001c0001t0037g0002a0001c0001t0039g0158 | 2 | HG00639.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.238+1698_238+1709d others(14): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(7): Show |
3 | a0001c0001t0011g0189a0001c0001t0012g0150a0001c0001t0012g0151 | 3 | HG04228.hp1 NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.238+1696_238+1709d others(16): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(9): Show |
4 | a0001c0001t0011g0194a0001c0001t0036g0160a0001c0001t0055g0199others(1): Show | 4 | HG00280.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+1694_238+1709d others(18): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(11): Show |
3 | a0001c0001t0002g0137a0001c0001t0011g0198a0001c0001t0068g0001 | 3 | HG01346.hp1 HG01952.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.238+1692_238+1709d others(20): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(13): Show |
6 | a0001c0001t0002g0163a0001c0001t0002g0176a0001c0001t0017g0170others(3): Show | 6 | HG02572.hp2 HG03209.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.238+1690_238+1709d others(22): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(15): Show |
9 | a0001c0001t0002g0027a0001c0001t0002g0162a0001c0001t0002g0164others(6): Show | 9 | HG01358.hp1 HG01496.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+1688_238+1709d others(24): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(17): Show |
11 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167others(8): Show | 11 | HG01981.hp1 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.238+1686_238+1709d others(26): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(19): Show |
9 | a0001c0001t0006g0186a0001c0001t0010g0007a0001c0001t0010g0008others(6): Show | 9 | HG01123.hp1 HG01192.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+1709_238+1710i others(28): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(21): Show |
4 | a0001c0001t0013g0171a0001c0001t0020g0036a0001c0001t0021g0029others(1): Show | 4 | HG02129.hp1 NA18975.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+1709_238+1710i others(30): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(23): Show |
3 | a0001c0001t0043g0011a0001c0001t0050g0168a0001c0001t0058g0018 | 3 | HG02055.hp1 HG04199.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.238+1709_238+1710i others(32): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(25): Show |
1 | a0001c0001t0041g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.238+1709_238+1710i others(34): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652621
|
G | GATATATA others(39): Show |
1 | a0002c0002t0002g0031 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.238+1709_238+1710i others(48): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87652621 | |||||
| chr7:87652813
|
T | C | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.238+1876T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652813 | ||||||
| chr7:87652888
|
C | T | 1 | a0001c0001t0010g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.238+1951C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87652888 | ||||||
| chr7:87653609
|
T | C | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+2672T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87653609 | ||||||
| chr7:87653734
|
T | C | 1 | a0001c0001t0009g0115 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.238+2797T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87653734 | ||||||
| chr7:87653850
|
T | C | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+2913T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87653850 | ||||||
| chr7:87654163
|
C | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+3226C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87654163 | ||||||
| chr7:87654172
|
C | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+3235C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87654172 | ||||||
| chr7:87654206
|
T | C | 1 | a0001c0001t0006g0050 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.238+3269T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87654206 | ||||||
| chr7:87654346
|
ATT | A | 4 | a0001c0001t0038g0182a0001c0001t0040g0161a0001c0001t0050g0168others(1): Show | 4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+3410_238+3411d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87654346 | ||||||
| chr7:87654640
|
G | T | 3 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0074g0097 | 3 | HG00280.hp1 HG00323.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.238+3703G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87654640 | ||||||
| chr7:87654782
|
G | A | 5 | a0001c0001t0001g0051a0001c0001t0001g0068a0001c0001t0001g0070others(2): Show | 5 | HG01099.hp1 HG01123.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+3845G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87654782 | ||||||
| chr7:87655104
|
A | G | 1 | a0001c0001t0023g0039 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.238+4167A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655104 | ||||||
| chr7:87655339
|
A | G | 1 | a0001c0001t0082g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.238+4402A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655339 | ||||||
| chr7:87655342
|
C | T | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.238+4405C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655342 | ||||||
| chr7:87655344
|
A | AT | 2 | a0001c0001t0004g0124a0001c0001t0005g0127 | 2 | NA18977.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.238+4408dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87655344 | |||||
| chr7:87655439
|
G | A | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+4502G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655439 | ||||||
| chr7:87655790
|
C | A | 1 | a0001c0001t0062g0093 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.238+4853C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655790 | ||||||
| chr7:87655801
|
C | G | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+4864C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655801 | ||||||
| chr7:87655818
|
G | C | 3 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0037g0002 | 3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.238+4881G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87655818 | ||||||
| chr7:87656259
|
T | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+5322T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87656259 | ||||||
| chr7:87656439
|
G | C | 1 | a0001c0001t0006g0104 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.238+5502G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87656439 | ||||||
| chr7:87656614
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+5677G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87656614 | ||||||
| chr7:87656703
|
A | C | 4 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0037g0002others(1): Show | 4 | HG00639.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+5766A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87656703 | ||||||
| chr7:87657062
|
C | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+6125C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657062 | ||||||
| chr7:87657130
|
T | C | 2 | a0001c0001t0003g0130a0001c0001t0006g0104 | 2 | HG00323.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.238+6193T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657130 | ||||||
| chr7:87657131
|
G | A | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+6194G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657131 | ||||||
| chr7:87657165
|
A | G | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.238+6228A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657165 | ||||||
| chr7:87657381
|
C | T | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.238+6444C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657381 | ||||||
| chr7:87657491
|
C | T | 1 | a0001c0001t0003g0141 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.238+6554C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657491 | ||||||
| chr7:87657516
|
C | T | 1 | a0001c0001t0005g0085 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.238+6579C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657516 | ||||||
| chr7:87657608
|
G | A | 2 | a0001c0001t0071g0142a0001c0001t0072g0143 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.238+6671G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657608 | ||||||
| chr7:87657704
|
G | C | 2 | a0001c0001t0003g0128a0001c0001t0007g0090 | 2 | HG00438.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.238+6767G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657704 | ||||||
| chr7:87657975
|
T | C | 1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.238+7038T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87657975 | ||||||
| chr7:87658024
|
C | A | 2 | a0001c0001t0020g0034a0001c0001t0035g0035 | 2 | NA19056.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.238+7087C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87658024 | ||||||
| chr7:87658078
|
C | T | 55 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(52): Show | 55 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.238+7141C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87658078 | ||||||
| chr7:87658564
|
A | G | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+7627A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87658564 | ||||||
| chr7:87658879
|
A | G | 1 | a0001c0001t0009g0121 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.238+7942A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87658879 | ||||||
| chr7:87658898
|
G | C | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+7961G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87658898 | ||||||
| chr7:87658927
|
G | A | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+7990G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87658927 | ||||||
| chr7:87659008
|
T | C | 88 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(85): Show | 88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.238+8071T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659008 | ||||||
| chr7:87659111
|
G | T | 1 | a0001c0001t0050g0168 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.238+8174G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659111 | ||||||
| chr7:87659289
|
T | G | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.238+8352T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659289 | ||||||
| chr7:87659367
|
T | A | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.238+8430T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659367 | ||||||
| chr7:87659410
|
A | G | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.238+8473A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659410 | ||||||
| chr7:87659429
|
G | T | 1 | a0001c0001t0010g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.238+8492G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659429 | ||||||
| chr7:87659781
|
G | T | 1 | a0001c0001t0017g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.238+8844G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659781 | ||||||
| chr7:87659936
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0063a0001c0001t0001g0091 | 3 | HG01496.hp2 HG04184.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.238+8999C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87659936 | ||||||
| chr7:87660323
|
A | T | 1 | a0001c0001t0057g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.238+9386A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660323 | ||||||
| chr7:87660358
|
C | G | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.238+9421C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660358 | ||||||
| chr7:87660526
|
C | T | 1 | a0001c0001t0028g0040 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.238+9589C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660526 | ||||||
| chr7:87660611
|
T | C | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+9674T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660611 | ||||||
| chr7:87660650
|
C | G | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.238+9713C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660650 | ||||||
| chr7:87660903
|
A | G | 1 | a0001c0001t0012g0151 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.238+9966A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660903 | ||||||
| chr7:87660991
|
C | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+10054C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87660991 | ||||||
| chr7:87661117
|
T | A | 1 | a0001c0001t0016g0126 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.238+10180T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87661117 | ||||||
| chr7:87661359
|
TTCTA | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+10427_238+1043 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87661359 | |||||
| chr7:87661424
|
C | T | 3 | a0001c0001t0065g0144a0001c0001t0071g0142a0001c0001t0072g0143 | 3 | HG01069.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.238+10487C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87661424 | ||||||
| chr7:87661496
|
C | G | 1 | a0001c0001t0076g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.238+10559C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87661496 | ||||||
| chr7:87661549
|
T | C | 75 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(72): Show | 75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.238+10612T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87661549 | ||||||
| chr7:87661964
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.238+11027A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87661964 | ||||||
| chr7:87662084
|
A | T | 2 | a0001c0001t0004g0075a0001c0001t0067g0074 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.238+11147A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662084 | ||||||
| chr7:87662169
|
AG | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+11233delG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662169 | ||||||
| chr7:87662243
|
C | G | 3 | a0001c0001t0031g0076a0001c0001t0034g0077a0001c0001t0034g0079 | 3 | HG02559.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.238+11306C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662243 | ||||||
| chr7:87662272
|
C | T | 2 | a0001c0001t0003g0095a0001c0001t0004g0089 | 2 | HG00741.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.238+11335C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662272 | ||||||
| chr7:87662449
|
C | T | 13 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(10): Show | 13 | HG00423.hp1 HG03453.hp1 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.238+11512C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662449 | ||||||
| chr7:87662510
|
G | A | 2 | a0001c0001t0043g0011a0001c0001t0068g0001 | 2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.238+11573G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662510 | ||||||
| chr7:87662715
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.238+11778A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662715 | ||||||
| chr7:87662729
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0063a0001c0001t0001g0091 | 3 | HG01496.hp2 HG04184.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.238+11792T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662729 | ||||||
| chr7:87662846
|
A | G | 1 | a0001c0001t0033g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.238+11909A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87662846 | ||||||
| chr7:87663007
|
T | G | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+12070T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663007 | ||||||
| chr7:87663147
|
C | A | 1 | a0001c0001t0011g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.238+12210C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663147 | ||||||
| chr7:87663195
|
A | G | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+12258A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663195 | ||||||
| chr7:87663199
|
G | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+12262G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663199 | ||||||
| chr7:87663334
|
G | A | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+12397G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663334 | ||||||
| chr7:87663367
|
C | T | 16 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.238+12430C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663367 | ||||||
| chr7:87663369
|
G | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+12432G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663369 | ||||||
| chr7:87663907
|
A | T | 75 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(72): Show | 75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.238+12970A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87663907 | ||||||
| chr7:87664177
|
G | A | 61 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(58): Show | 61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.238+13240G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87664177 | ||||||
| chr7:87664388
|
A | C | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+13451A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87664388 | ||||||
| chr7:87664661
|
G | A | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.238+13724G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87664661 | ||||||
| chr7:87664825
|
G | C | 1 | a0001c0001t0062g0093 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.238+13888G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87664825 | ||||||
| chr7:87664980
|
G | C | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+14043G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87664980 | ||||||
| chr7:87665433
|
TAG | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+14498_238+1449 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87665433 | |||||
| chr7:87665469
|
C | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+14532C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87665469 | ||||||
| chr7:87665470
|
A | T | 1 | a0001c0001t0057g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.238+14533A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87665470 | ||||||
| chr7:87665677
|
C | G | 4 | a0001c0001t0010g0008a0001c0001t0010g0009a0001c0001t0010g0010others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+14740C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87665677 | ||||||
| chr7:87665902
|
A | G | 1 | a0001c0001t0019g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.238+14965A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87665902 | ||||||
| chr7:87665960
|
C | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+15023C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87665960 | ||||||
| chr7:87666082
|
C | G | 1 | a0001c0001t0005g0127 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.238+15145C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87666082 | ||||||
| chr7:87666472
|
G | T | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+15535G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87666472 | ||||||
| chr7:87666581
|
G | A | 1 | a0001c0001t0062g0093 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.238+15644G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87666581 | ||||||
| chr7:87666647
|
T | C | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.238+15710T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87666647 | ||||||
| chr7:87666805
|
T | C | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.238+15868T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87666805 | ||||||
| chr7:87666900
|
A | G | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+15963A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87666900 | ||||||
| chr7:87667015
|
A | G | 1 | a0001c0001t0033g0073 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.238+16078A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87667015 | ||||||
| chr7:87667199
|
C | T | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+16262C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87667199 | ||||||
| chr7:87667279
|
T | C | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+16342T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87667279 | ||||||
| chr7:87667433
|
C | G | 1 | a0001c0001t0009g0121 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.238+16496C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87667433 | ||||||
| chr7:87667842
|
A | G | 1 | a0001c0001t0007g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.238+16905A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87667842 | ||||||
| chr7:87668153
|
T | G | 55 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(52): Show | 55 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.238+17216T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87668153 | ||||||
| chr7:87668252
|
A | C | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.238+17315A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87668252 | ||||||
| chr7:87668317
|
G | A | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+17380G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87668317 | ||||||
| chr7:87668444
|
A | G | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.238+17507A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87668444 | ||||||
| chr7:87668848
|
G | A | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.238+17911G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87668848 | ||||||
| chr7:87668972
|
C | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+18035C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87668972 | ||||||
| chr7:87669423
|
T | C | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+18486T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87669423 | ||||||
| chr7:87669552
|
A | G | 179 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(176): Show | 179 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.238+18615A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87669552 | ||||||
| chr7:87669697
|
T | C | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+18760T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87669697 | ||||||
| chr7:87669931
|
G | A | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.238+18994G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87669931 | ||||||
| chr7:87669938
|
A | G | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.238+19001A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87669938 | ||||||
| chr7:87670024
|
C | T | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.238+19087C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87670024 | ||||||
| chr7:87670604
|
G | A | 7 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0052g0038others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+19667G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87670604 | ||||||
| chr7:87670685
|
G | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+19748G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87670685 | ||||||
| chr7:87670877
|
G | T | 1 | a0001c0001t0011g0194 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.238+19940G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87670877 | ||||||
| chr7:87670940
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.238+20003T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87670940 | ||||||
| chr7:87670970
|
TCA | T | 4 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0037g0002others(1): Show | 4 | HG00639.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+20034_238+2003 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87670970 | ||||||
| chr7:87671038
|
A | C | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+20101A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671038 | ||||||
| chr7:87671063
|
G | A | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+20126G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671063 | ||||||
| chr7:87671165
|
C | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+20228C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671165 | ||||||
| chr7:87671251
|
C | T | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+20314C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671251 | ||||||
| chr7:87671284
|
G | A | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+20347G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671284 | ||||||
| chr7:87671430
|
TGAG | T | 2 | a0001c0001t0069g0016a0001c0001t0070g0017 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.238+20497_238+2049 others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87671430 | |||||
| chr7:87671691
|
G | C | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+20754G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671691 | ||||||
| chr7:87671718
|
C | T | 1 | a0001c0001t0033g0073 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.238+20781C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671718 | ||||||
| chr7:87671938
|
T | C | 1 | a0001c0001t0040g0161 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.238+21001T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87671938 | ||||||
| chr7:87672229
|
A | G | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.238+21292A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672229 | ||||||
| chr7:87672308
|
C | T | 3 | a0001c0001t0019g0043a0001c0001t0033g0073a0001c0001t0049g0201 | 3 | HG00438.hp2 HG01978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.238+21371C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672308 | ||||||
| chr7:87672480
|
G | A | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+21543G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672480 | ||||||
| chr7:87672607
|
A | G | 1 | a0001c0001t0010g0009 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.238+21670A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672607 | ||||||
| chr7:87672683
|
C | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+21746C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672683 | ||||||
| chr7:87672766
|
A | G | 1 | a0001c0001t0057g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.238+21829A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672766 | ||||||
| chr7:87672824
|
A | G | 75 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(72): Show | 75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.238+21887A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672824 | ||||||
| chr7:87672869
|
A | G | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.238+21932A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672869 | ||||||
| chr7:87672893
|
A | C | 1 | a0001c0001t0001g0099 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.238+21956A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87672893 | ||||||
| chr7:87673099
|
G | A | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.238+22162G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673099 | ||||||
| chr7:87673189
|
T | C | 4 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0037g0002others(1): Show | 4 | HG00639.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+22252T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673189 | ||||||
| chr7:87673499
|
G | A | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+22562G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673499 | ||||||
| chr7:87673519
|
T | C | 62 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(59): Show | 62 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.238+22582T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673519 | ||||||
| chr7:87673625
|
C | T | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.238+22688C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673625 | ||||||
| chr7:87673702
|
A | G | 4 | a0001c0001t0003g0088a0001c0001t0006g0066a0001c0001t0006g0067others(1): Show | 4 | HG02040.hp2 HG02129.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+22765A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673702 | ||||||
| chr7:87673767
|
G | T | 1 | a0001c0001t0024g0062 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.238+22830G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87673767 | ||||||
| chr7:87674137
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.238+23200C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87674137 | ||||||
| chr7:87674138
|
G | A | 7 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0052g0038others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+23201G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87674138 | ||||||
| chr7:87674215
|
G | A | 3 | a0001c0001t0005g0096a0001c0001t0005g0134a0001c0001t0005g0135 | 3 | NA18974.hp2 NA18979.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.238+23278G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87674215 | ||||||
| chr7:87674301
|
G | A | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.238+23364G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87674301 | ||||||
| chr7:87674913
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+23976G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87674913 | ||||||
| chr7:87675466
|
T | A | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+24529T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87675466 | ||||||
| chr7:87675653
|
C | CA | 10 | a0001c0001t0001g0070a0001c0001t0004g0111a0001c0001t0004g0112others(7): Show | 10 | HG00738.hp2 HG01192.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+24735dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87675653 | |||||
| chr7:87675653
|
CA | C | 31 | a0001c0001t0001g0061a0001c0001t0006g0186a0001c0001t0008g0190others(28): Show | 31 | HG00280.hp2 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.238+24735delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87675653 | |||||
| chr7:87675653
|
CAA | C | 39 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.238+24734_238+2473 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87675653 | |||||
| chr7:87675653
|
CAAAAAAA others(1): Show |
C | 12 | a0001c0001t0016g0103a0001c0001t0016g0126a0001c0001t0019g0024others(9): Show | 12 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.238+24728_238+2473 others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87675653 | |||||
| chr7:87676283
|
A | C | 2 | a0001c0001t0016g0103a0001c0001t0016g0126 | 2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.239-24138A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87676283 | ||||||
| chr7:87676378
|
AAAC | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.239-24023_239-2402 others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87676378 | |||||
| chr7:87676419
|
G | A | 1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.239-24002G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87676419 | ||||||
| chr7:87676703
|
C | CA | 12 | a0001c0001t0001g0070a0001c0001t0001g0087a0001c0001t0005g0096others(9): Show | 12 | HG00735.hp1 HG00735.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.239-23692dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87676703 | |||||
| chr7:87676703
|
CA | C | 44 | a0001c0001t0002g0167a0001c0001t0004g0019a0001c0001t0004g0075others(41): Show | 44 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.239-23692delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87676703 | |||||
| chr7:87676926
|
A | G | 1 | a0001c0001t0041g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.239-23495A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87676926 | ||||||
| chr7:87676957
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.239-23464A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87676957 | ||||||
| chr7:87677053
|
T | C | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-23368T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87677053 | ||||||
| chr7:87677215
|
A | T | 1 | a0001c0001t0041g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.239-23206A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87677215 | ||||||
| chr7:87677255
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.239-23166A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87677255 | ||||||
| chr7:87677274
|
A | AAC | 28 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0072others(25): Show | 28 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.239-23112_239-2311 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87677274 | |||||
| chr7:87677274
|
A | AACAC | 2 | a0001c0001t0001g0087a0001c0001t0060g0015 | 2 | HG00735.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.239-23114_239-2311 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87677274 | |||||
| chr7:87677274
|
AAC | A | 43 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0163others(40): Show | 43 | HG00323.hp1 HG00735.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.239-23112_239-2311 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87677274 | |||||
| chr7:87677274
|
AACAC | A | 5 | a0001c0001t0001g0107a0001c0001t0015g0020a0001c0001t0015g0092others(2): Show | 5 | HG01167.hp2 HG02818.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-23114_239-2311 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87677274 | |||||
| chr7:87677335
|
T | TA | 45 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(42): Show | 45 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.239-23071dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87677335 | |||||
| chr7:87677335
|
TA | T | 7 | a0001c0001t0001g0044a0001c0001t0005g0135a0001c0001t0015g0020others(4): Show | 7 | HG00639.hp1 HG03098.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-23071delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87677335 | |||||
| chr7:87677504
|
G | T | 3 | a0001c0001t0031g0076a0001c0001t0034g0077a0001c0001t0034g0079 | 3 | HG02559.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239-22917G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87677504 | ||||||
| chr7:87677809
|
T | C | 1 | a0001c0001t0002g0162 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.239-22612T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87677809 | ||||||
| chr7:87678193
|
A | G | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-22228A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87678193 | ||||||
| chr7:87678405
|
T | C | 3 | a0001c0001t0008g0195a0001c0001t0008g0197a0001c0001t0030g0196 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.239-22016T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87678405 | ||||||
| chr7:87678594
|
C | A | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-21827C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87678594 | ||||||
| chr7:87678759
|
GA | G | 7 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-21655delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87678759 | |||||
| chr7:87678817
|
C | T | 7 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-21604C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87678817 | ||||||
| chr7:87679017
|
AGAAAATT others(2762): Show |
A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.239-21401_239-1863 others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87679017 | |||||
| chr7:87679087
|
CT | C | 138 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(135): Show | 138 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.239-21311delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87679087 | |||||
| chr7:87679087
|
CTT | C | 18 | a0001c0001t0003g0049a0001c0001t0006g0186a0001c0001t0008g0190others(15): Show | 18 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.239-21312_239-2131 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87679087 | |||||
| chr7:87679389
|
G | A | 1 | a0001c0001t0045g0078 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.239-21032G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679389 | ||||||
| chr7:87679473
|
C | A | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.239-20948C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679473 | ||||||
| chr7:87679525
|
G | A | 1 | a0001c0001t0080g0100 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.239-20896G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679525 | ||||||
| chr7:87679668
|
G | A | 1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.239-20753G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679668 | ||||||
| chr7:87679794
|
T | C | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-20627T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679794 | ||||||
| chr7:87679832
|
T | C | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-20589T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679832 | ||||||
| chr7:87679852
|
A | G | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.239-20569A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87679852 | ||||||
| chr7:87680097
|
A | G | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-20324A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87680097 | ||||||
| chr7:87680563
|
C | T | 1 | a0001c0001t0010g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.239-19858C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87680563 | ||||||
| chr7:87680750
|
G | A | 2 | a0001c0001t0004g0111a0001c0001t0004g0112 | 2 | HG00738.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.239-19671G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87680750 | ||||||
| chr7:87681004
|
A | G | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.239-19417A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87681004 | ||||||
| chr7:87681058
|
T | C | 50 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(47): Show | 50 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.239-19363T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87681058 | ||||||
| chr7:87681127
|
A | G | 2 | a0001c0001t0016g0103a0001c0001t0016g0126 | 2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.239-19294A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87681127 | ||||||
| chr7:87681634
|
G | A | 1 | a0001c0001t0046g0109 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.239-18787G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87681634 | ||||||
| chr7:87681934
|
C | T | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-18487C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87681934 | ||||||
| chr7:87682204
|
G | A | 1 | a0001c0001t0056g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.239-18217G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87682204 | ||||||
| chr7:87682364
|
C | T | 3 | a0001c0001t0047g0012a0001c0001t0059g0014a0001c0001t0066g0013 | 3 | HG02572.hp2 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.239-18057C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87682364 | ||||||
| chr7:87682561
|
T | C | 1 | a0001c0001t0003g0046 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.239-17860T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87682561 | ||||||
| chr7:87682648
|
A | G | 1 | a0001c0001t0028g0040 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.239-17773A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87682648 | ||||||
| chr7:87682781
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.239-17640T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87682781 | ||||||
| chr7:87682868
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-17553G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87682868 | ||||||
| chr7:87683142
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.239-17279C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87683142 | ||||||
| chr7:87683277
|
G | C | 1 | a0001c0001t0080g0100 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.239-17144G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87683277 | ||||||
| chr7:87683726
|
G | A | 1 | a0001c0001t0078g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.239-16695G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87683726 | ||||||
| chr7:87683799
|
G | A | 4 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0037g0002others(1): Show | 4 | HG00639.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-16622G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87683799 | ||||||
| chr7:87684330
|
T | G | 2 | a0001c0001t0022g0180a0001c0001t0029g0178 | 2 | NA18974.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.239-16091T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87684330 | ||||||
| chr7:87684370
|
A | G | 7 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-16051A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87684370 | ||||||
| chr7:87684746
|
C | CA | 8 | a0001c0001t0004g0124a0001c0001t0009g0132a0001c0001t0010g0010others(5): Show | 8 | HG00423.hp2 HG00621.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.239-15648dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87684746 | |||||
| chr7:87684746
|
C | CAA | 10 | a0001c0001t0012g0150a0001c0001t0012g0152a0001c0001t0014g0153others(7): Show | 10 | HG00423.hp1 HG03098.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-15649_239-1564 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87684746 | |||||
| chr7:87684746
|
C | CAAAA | 44 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(41): Show | 44 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.239-15651_239-1564 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87684746 | |||||
| chr7:87684746
|
C | CAAAAA | 10 | a0001c0001t0002g0165a0001c0001t0002g0202a0001c0001t0017g0173others(7): Show | 10 | HG02622.hp2 HG02970.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-15652_239-1564 others(9): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87684746 | |||||
| chr7:87684746
|
CA | C | 40 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(37): Show | 40 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.239-15648delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87684746 | |||||
| chr7:87684746
|
CAA | C | 5 | a0001c0001t0042g0148a0001c0001t0060g0015a0001c0001t0063g0060others(2): Show | 5 | HG02630.hp1 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-15649_239-1564 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87684746 | |||||
| chr7:87684815
|
A | G | 2 | a0001c0001t0003g0095a0001c0001t0004g0089 | 2 | HG00741.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.239-15606A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87684815 | ||||||
| chr7:87685472
|
G | T | 4 | a0001c0001t0038g0182a0001c0001t0040g0161a0001c0001t0050g0168others(1): Show | 4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-14949G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87685472 | ||||||
| chr7:87685494
|
C | T | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-14927C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87685494 | ||||||
| chr7:87685509
|
G | GA | 13 | a0001c0001t0016g0103a0001c0001t0016g0126a0001c0001t0016g0129others(10): Show | 13 | HG00621.hp1 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.239-14904dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87685509 | |||||
| chr7:87685593
|
G | A | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-14828G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87685593 | ||||||
| chr7:87685942
|
A | G | 1 | a0001c0001t0004g0101 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.239-14479A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87685942 | ||||||
| chr7:87685958
|
A | G | 4 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0037g0002others(1): Show | 4 | HG00639.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-14463A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87685958 | ||||||
| chr7:87685996
|
C | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-14425C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87685996 | ||||||
| chr7:87686323
|
A | G | 4 | a0001c0001t0038g0182a0001c0001t0040g0161a0001c0001t0050g0168others(1): Show | 4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-14098A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686323 | ||||||
| chr7:87686429
|
G | A | 1 | a0001c0001t0046g0109 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.239-13992G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686429 | ||||||
| chr7:87686505
|
C | A | 2 | a0001c0001t0061g0185a0001c0001t0064g0184 | 2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.239-13916C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686505 | ||||||
| chr7:87686565
|
G | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.239-13856G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686565 | ||||||
| chr7:87686570
|
A | C | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-13851A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686570 | ||||||
| chr7:87686606
|
A | C | 1 | a0001c0001t0001g0068 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.239-13815A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686606 | ||||||
| chr7:87686727
|
C | A | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-13694C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686727 | ||||||
| chr7:87686769
|
G | A | 1 | a0001c0001t0010g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.239-13652G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686769 | ||||||
| chr7:87686776
|
G | GA | 5 | a0001c0001t0001g0042a0001c0001t0001g0107a0001c0001t0047g0012others(2): Show | 5 | HG01167.hp2 HG02572.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-13629dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87686776 | |||||
| chr7:87686812
|
G | A | 2 | a0001c0001t0007g0122a0001c0001t0007g0133 | 2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.239-13609G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686812 | ||||||
| chr7:87686848
|
G | A | 1 | a0001c0001t0006g0145 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.239-13573G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686848 | ||||||
| chr7:87686935
|
G | T | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.239-13486G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87686935 | ||||||
| chr7:87687304
|
A | C | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-13117A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687304 | ||||||
| chr7:87687323
|
T | C | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.239-13098T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687323 | ||||||
| chr7:87687324
|
G | C | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.239-13097G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687324 | ||||||
| chr7:87687325
|
G | A | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.239-13096G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687325 | ||||||
| chr7:87687744
|
A | C | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.239-12677A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687744 | ||||||
| chr7:87687778
|
C | T | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.239-12643C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687778 | ||||||
| chr7:87687926
|
C | G | 1 | a0001c0001t0028g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.239-12495C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687926 | ||||||
| chr7:87687949
|
C | T | 1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.239-12472C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87687949 | ||||||
| chr7:87688080
|
A | G | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-12341A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688080 | ||||||
| chr7:87688154
|
G | C | 1 | a0001c0001t0006g0131 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.239-12267G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688154 | ||||||
| chr7:87688220
|
G | A | 1 | a0001c0001t0055g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.239-12201G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688220 | ||||||
| chr7:87688444
|
T | A | 1 | a0001c0001t0058g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.239-11977T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688444 | ||||||
| chr7:87688643
|
G | A | 2 | a0001c0001t0004g0111a0001c0001t0004g0112 | 2 | HG00738.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.239-11778G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688643 | ||||||
| chr7:87688742
|
A | G | 1 | a0001c0001t0006g0113 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.239-11679A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688742 | ||||||
| chr7:87688855
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.239-11566A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688855 | ||||||
| chr7:87688971
|
C | G | 1 | a0001c0001t0004g0082 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.239-11450C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87688971 | ||||||
| chr7:87689133
|
T | C | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.239-11288T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87689133 | ||||||
| chr7:87689492
|
G | A | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-10929G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87689492 | ||||||
| chr7:87689689
|
A | G | 4 | a0001c0001t0038g0182a0001c0001t0040g0161a0001c0001t0050g0168others(1): Show | 4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-10732A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87689689 | ||||||
| chr7:87689991
|
T | A | 58 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(55): Show | 58 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.239-10430T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87689991 | ||||||
| chr7:87689997
|
T | A | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.239-10424T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87689997 | ||||||
| chr7:87690286
|
G | T | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.239-10135G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87690286 | ||||||
| chr7:87690483
|
C | T | 1 | a0001c0001t0058g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.239-9938C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87690483 | ||||||
| chr7:87690928
|
T | C | 2 | a0001c0001t0069g0016a0001c0001t0070g0017 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.239-9493T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87690928 | ||||||
| chr7:87691037
|
A | G | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-9384A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691037 | ||||||
| chr7:87691397
|
A | G | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.239-9024A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691397 | ||||||
| chr7:87691734
|
T | A | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-8687T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691734 | ||||||
| chr7:87691762
|
T | G | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-8659T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691762 | ||||||
| chr7:87691803
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-8618G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691803 | ||||||
| chr7:87691832
|
G | A | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-8589G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691832 | ||||||
| chr7:87691858
|
C | A | 1 | a0001c0001t0025g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.239-8563C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87691858 | ||||||
| chr7:87692155
|
A | G | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.239-8266A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87692155 | ||||||
| chr7:87692255
|
A | G | 1 | a0001c0001t0007g0090 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.239-8166A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87692255 | ||||||
| chr7:87692666
|
A | G | 1 | a0001c0001t0003g0049 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.239-7755A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87692666 | ||||||
| chr7:87692706
|
T | C | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.239-7715T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87692706 | ||||||
| chr7:87692729
|
A | T | 2 | a0001c0001t0020g0034a0001c0001t0035g0035 | 2 | NA19056.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.239-7692A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87692729 | ||||||
| chr7:87693028
|
A | G | 1 | a0001c0001t0021g0032 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.239-7393A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693028 | ||||||
| chr7:87693034
|
G | A | 1 | a0001c0001t0055g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.239-7387G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693034 | ||||||
| chr7:87693070
|
A | G | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-7351A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693070 | ||||||
| chr7:87693123
|
T | C | 1 | a0001c0001t0002g0027 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.239-7298T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693123 | ||||||
| chr7:87693180
|
G | GA | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-7236dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87693180 | |||||
| chr7:87693385
|
T | A | 4 | a0001c0001t0004g0019a0001c0001t0004g0075a0001c0001t0007g0021others(1): Show | 4 | HG02896.hp2 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-7036T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693385 | ||||||
| chr7:87693503
|
A | T | 1 | a0001c0001t0003g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.239-6918A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693503 | ||||||
| chr7:87693507
|
T | C | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.239-6914T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693507 | ||||||
| chr7:87693588
|
C | A | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.239-6833C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693588 | ||||||
| chr7:87693613
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.239-6808G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693613 | ||||||
| chr7:87693695
|
T | A | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-6726T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693695 | ||||||
| chr7:87693829
|
C | T | 16 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-6592C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87693829 | ||||||
| chr7:87694100
|
GT | G | 70 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(67): Show | 70 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(67): Show |
intron_variant | MODIFIER | c.239-6309delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87694100 | |||||
| chr7:87694100
|
GTT | G | 16 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-6310_239-6309d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87694100 | |||||
| chr7:87694271
|
T | A | 1 | a0001c0001t0004g0075 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.239-6150T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87694271 | ||||||
| chr7:87694418
|
A | G | 14 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(11): Show | 14 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.239-6003A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87694418 | ||||||
| chr7:87694702
|
T | A | 2 | a0001c0001t0032g0187a0001c0001t0032g0188 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.239-5719T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87694702 | ||||||
| chr7:87694712
|
C | A | 1 | a0001c0001t0077g0169 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.239-5709C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87694712 | ||||||
| chr7:87695053
|
G | A | 1 | a0001c0001t0017g0173 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.239-5368G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87695053 | ||||||
| chr7:87695070
|
G | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.239-5351G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87695070 | ||||||
| chr7:87695823
|
C | T | 2 | a0001c0001t0004g0075a0001c0001t0067g0074 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.239-4598C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87695823 | ||||||
| chr7:87695862
|
T | C | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.239-4559T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87695862 | ||||||
| chr7:87696418
|
A | T | 1 | a0001c0001t0057g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.239-4003A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87696418 | ||||||
| chr7:87696630
|
T | C | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.239-3791T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87696630 | ||||||
| chr7:87696809
|
T | G | 13 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(10): Show | 13 | HG00423.hp1 HG02723.hp1 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.239-3612T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87696809 | ||||||
| chr7:87696816
|
G | C | 3 | a0001c0001t0004g0082a0001c0001t0004g0124a0001c0001t0005g0127 | 3 | NA18977.hp1 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.239-3605G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87696816 | ||||||
| chr7:87697018
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0072 | 2 | HG01192.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.239-3403C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697018 | ||||||
| chr7:87697146
|
G | A | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.239-3275G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697146 | ||||||
| chr7:87697259
|
G | C | 1 | a0001c0001t0023g0159 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.239-3162G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697259 | ||||||
| chr7:87697273
|
C | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-3148C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697273 | ||||||
| chr7:87697772
|
C | T | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.239-2649C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697772 | ||||||
| chr7:87697886
|
T | C | 1 | a0001c0001t0064g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.239-2535T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697886 | ||||||
| chr7:87697924
|
G | A | 1 | a0001c0001t0040g0161 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.239-2497G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87697924 | ||||||
| chr7:87698383
|
C | T | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.239-2038C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87698383 | ||||||
| chr7:87698687
|
T | C | 88 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(85): Show | 88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.239-1734T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87698687 | ||||||
| chr7:87699099
|
C | T | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.239-1322C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87699099 | ||||||
| chr7:87699415
|
C | CT | 5 | a0001c0001t0001g0048a0001c0001t0001g0063a0001c0001t0047g0012others(2): Show | 5 | HG01496.hp2 HG02572.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-997dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 87699415 | |||||
| chr7:87699870
|
G | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.239-551G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87699870 | ||||||
| chr7:87700342
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.239-79G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 2/10 | chr7 | 87700342 | ||||||
| chr7:87700706
|
A | AAT | 17 | a0001c0001t0006g0186a0001c0001t0008g0190a0001c0001t0008g0191others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.372+153_372+154dup others(2): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87700706 | |||||
| chr7:87700785
|
A | T | 63 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(60): Show | 63 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.372+231A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87700785 | ||||||
| chr7:87701107
|
G | A | 62 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(59): Show | 62 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.372+553G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87701107 | ||||||
| chr7:87701872
|
G | A | 8 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.372+1318G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87701872 | ||||||
| chr7:87701959
|
T | C | 62 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(59): Show | 62 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.372+1405T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87701959 | ||||||
| chr7:87702000
|
A | G | 88 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(85): Show | 88 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.372+1446A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702000 | ||||||
| chr7:87702060
|
G | A | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.372+1506G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702060 | ||||||
| chr7:87702100
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.372+1546G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702100 | ||||||
| chr7:87702142
|
C | CA | 50 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(47): Show | 50 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.372+1618dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | |||||
| chr7:87702142
|
C | CAA | 23 | a0001c0001t0001g0087a0001c0001t0003g0128a0001c0001t0004g0112others(20): Show | 23 | HG00423.hp2 HG00438.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.372+1617_372+1618d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | |||||
| chr7:87702142
|
C | CAAA | 6 | a0001c0001t0004g0111a0001c0001t0006g0186a0001c0001t0007g0133others(3): Show | 6 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.372+1616_372+1618d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | |||||
| chr7:87702142
|
C | CAAAA | 14 | a0001c0001t0008g0191a0001c0001t0008g0193a0001c0001t0010g0007others(11): Show | 14 | HG01123.hp1 HG01346.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.372+1615_372+1618d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | |||||
| chr7:87702142
|
C | CAAAAA | 19 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(16): Show | 19 | HG01081.hp2 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+1614_372+1618d others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | |||||
| chr7:87702142
|
C | CAAAAAA | 16 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0166others(13): Show | 16 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.372+1613_372+1618d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | |||||
| chr7:87702142
|
C | CAAAAAAA | 6 | a0001c0001t0002g0167a0001c0001t0018g0175a0001c0001t0022g0179others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+1612_372+1618d others(9): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | |||||
| chr7:87702142
|
C | CAAAAAAA others(1): Show |
5 | a0001c0001t0012g0150a0001c0001t0023g0039a0001c0001t0051g0156others(2): Show | 5 | HG02572.hp1 HG03209.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1611_372+1618d others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | |||||
| chr7:87702142
|
C | CAAAAAAA others(2): Show |
5 | a0001c0001t0012g0151a0001c0001t0014g0153a0001c0001t0014g0155others(2): Show | 5 | NA18952.hp1 NA18988.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+1610_372+1618d others(11): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | |||||
| chr7:87702142
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0012g0152a0001c0001t0027g0037a0001c0001t0027g0154 | 3 | HG00423.hp1 NA19062.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.372+1609_372+1618d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | |||||
| chr7:87702142
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0023g0159 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.372+1608_372+1618d others(13): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | |||||
| chr7:87702142
|
CAAAAAAA others(9): Show |
C | 3 | a0002c0002t0002g0026a0002c0002t0002g0031a0002c0002t0017g0140 | 3 | NA18973.hp2 NA18979.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.372+1603_372+1618d others(18): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702142 | |||||
| chr7:87702168
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.372+1618_372+1619i others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87702168 | |||||
| chr7:87702175
|
G | C | 1 | a0001c0001t0001g0059 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.372+1621G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702175 | ||||||
| chr7:87702297
|
G | A | 1 | a0001c0001t0010g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.372+1743G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702297 | ||||||
| chr7:87702391
|
A | G | 2 | a0001c0001t0042g0148a0001c0001t0052g0038 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.372+1837A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702391 | ||||||
| chr7:87702540
|
G | T | 1 | a0001c0001t0058g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.372+1986G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702540 | ||||||
| chr7:87702649
|
T | C | 40 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(37): Show | 40 | HG01081.hp2 HG01099.hp2 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.372+2095T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702649 | ||||||
| chr7:87702696
|
T | G | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.372+2142T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87702696 | ||||||
| chr7:87703121
|
G | A | 1 | a0001c0001t0010g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.372+2567G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703121 | ||||||
| chr7:87703122
|
A | G | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.372+2568A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703122 | ||||||
| chr7:87703143
|
C | T | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.372+2589C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703143 | ||||||
| chr7:87703155
|
T | A | 39 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.372+2601T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703155 | ||||||
| chr7:87703381
|
C | G | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.372+2827C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703381 | ||||||
| chr7:87703457
|
G | A | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.372+2903G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703457 | ||||||
| chr7:87703523
|
C | A | 1 | a0001c0001t0009g0136 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.372+2969C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703523 | ||||||
| chr7:87703680
|
AT | A | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+3131delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703680 | |||||
| chr7:87703731
|
C | T | 1 | a0001c0001t0011g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.372+3177C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703731 | ||||||
| chr7:87703755
|
T | C | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.372+3201T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703755 | ||||||
| chr7:87703885
|
CT | C | 15 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0003g0088others(12): Show | 15 | HG00323.hp1 HG00323.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.372+3358delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703885 | |||||
| chr7:87703885
|
CTTTTTTT others(22): Show |
C | 3 | a0001c0001t0001g0107a0001c0001t0065g0144a0001c0001t0071g0142 | 3 | HG01069.hp1 HG01167.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.372+3358_372+3386d others(31): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703885 | |||||
| chr7:87703885
|
CTTTTTTT others(23): Show |
C | 2 | a0001c0001t0035g0035a0001c0001t0045g0078 | 2 | HG00639.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.372+3357_372+3386d others(32): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703885 | |||||
| chr7:87703885
|
CTTTTTTT others(24): Show |
C | 40 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(37): Show | 40 | HG00423.hp1 HG01081.hp2 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.372+3356_372+3386d others(33): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703885 | |||||
| chr7:87703885
|
CTTTTTTT others(25): Show |
C | 27 | a0001c0001t0001g0045a0001c0001t0008g0190a0001c0001t0008g0191others(24): Show | 27 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.372+3355_372+3386d others(34): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703885 | |||||
| chr7:87703885
|
CTTTTTTT others(26): Show |
C | 1 | a0001c0001t0032g0187 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.372+3354_372+3386d others(35): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703885 | |||||
| chr7:87703886
|
TTTTTTTT others(21): Show |
T | 1 | a0001c0001t0072g0143 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.372+3360_372+3387d others(30): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703886 | |||||
| chr7:87703896
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.372+3342T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703896 | ||||||
| chr7:87703897
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.372+3343T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703897 | ||||||
| chr7:87703911
|
TTG | T | 42 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0051others(39): Show | 42 | HG00558.hp2 HG01074.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.372+3358_372+3359d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703911 | ||||||
| chr7:87703912
|
T | G | 5 | a0001c0001t0003g0049a0001c0001t0007g0021a0001c0001t0007g0133others(2): Show | 5 | HG01358.hp2 HG02055.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+3358T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703912 | ||||||
| chr7:87703914
|
G | T | 5 | a0001c0001t0003g0049a0001c0001t0007g0021a0001c0001t0007g0133others(2): Show | 5 | HG01358.hp2 HG02055.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+3360G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703914 | ||||||
| chr7:87703914
|
GT | G | 18 | a0001c0001t0001g0055a0001c0001t0001g0070a0001c0001t0001g0106others(15): Show | 18 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.372+3386delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87703914 | |||||
| chr7:87703915
|
T | G | 51 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0051others(48): Show | 51 | HG00558.hp2 HG01074.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.372+3361T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703915 | ||||||
| chr7:87703919
|
T | G | 2 | a0001c0001t0004g0075a0001c0001t0067g0074 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.372+3365T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703919 | ||||||
| chr7:87703922
|
T | G | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.372+3368T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703922 | ||||||
| chr7:87703991
|
G | T | 1 | a0001c0001t0010g0009 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.372+3437G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87703991 | ||||||
| chr7:87704010
|
T | A | 1 | a0001c0001t0001g0068 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.372+3456T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87704010 | ||||||
| chr7:87704291
|
C | T | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.372+3737C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87704291 | ||||||
| chr7:87704681
|
C | T | 1 | a0001c0001t0010g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.372+4127C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87704681 | ||||||
| chr7:87705068
|
A | G | 63 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(60): Show | 63 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.372+4514A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705068 | ||||||
| chr7:87705295
|
G | A | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.372+4741G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705295 | ||||||
| chr7:87705318
|
T | C | 84 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(81): Show | 84 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.372+4764T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705318 | ||||||
| chr7:87705441
|
C | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.372+4887C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705441 | ||||||
| chr7:87705453
|
A | C | 1 | a0001c0001t0015g0092 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.372+4899A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705453 | ||||||
| chr7:87705525
|
T | C | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.372+4971T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705525 | ||||||
| chr7:87705988
|
G | T | 2 | a0001c0001t0069g0016a0001c0001t0070g0017 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.373-4582G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87705988 | ||||||
| chr7:87706139
|
A | G | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.373-4431A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87706139 | ||||||
| chr7:87706441
|
A | G | 2 | a0001c0001t0016g0103a0001c0001t0016g0126 | 2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.373-4129A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87706441 | ||||||
| chr7:87706707
|
G | A | 1 | a0001c0001t0004g0089 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.373-3863G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87706707 | ||||||
| chr7:87707165
|
C | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0107 | 2 | HG01167.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.373-3405C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87707165 | ||||||
| chr7:87707401
|
C | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.373-3169C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87707401 | ||||||
| chr7:87707402
|
G | A | 1 | a0001c0001t0049g0201 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.373-3168G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87707402 | ||||||
| chr7:87707417
|
T | C | 1 | a0001c0001t0005g0085 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.373-3153T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87707417 | ||||||
| chr7:87707679
|
AAAATAAA others(6): Show |
A | 1 | a0002c0002t0002g0031 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.373-2878_373-2866d others(15): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 87707679 | |||||
| chr7:87707912
|
G | T | 11 | a0001c0001t0003g0128a0001c0001t0004g0082a0001c0001t0004g0101others(8): Show | 11 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.373-2658G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87707912 | ||||||
| chr7:87708196
|
C | A | 2 | a0001c0001t0001g0068a0001c0001t0024g0062 | 2 | HG01099.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.373-2374C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708196 | ||||||
| chr7:87708317
|
A | T | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.373-2253A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708317 | ||||||
| chr7:87708443
|
G | A | 74 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(71): Show | 74 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.373-2127G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708443 | ||||||
| chr7:87708463
|
G | A | 74 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(71): Show | 74 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.373-2107G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708463 | ||||||
| chr7:87708511
|
T | A | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.373-2059T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708511 | ||||||
| chr7:87708727
|
G | A | 1 | a0001c0001t0004g0124 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.373-1843G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708727 | ||||||
| chr7:87708753
|
G | A | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.373-1817G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708753 | ||||||
| chr7:87708792
|
G | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.373-1778G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708792 | ||||||
| chr7:87708793
|
C | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.373-1777C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708793 | ||||||
| chr7:87708937
|
A | C | 1 | a0001c0001t0011g0198 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.373-1633A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708937 | ||||||
| chr7:87708978
|
A | T | 1 | a0001c0001t0003g0141 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.373-1592A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87708978 | ||||||
| chr7:87709298
|
T | C | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.373-1272T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709298 | ||||||
| chr7:87709323
|
G | A | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.373-1247G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709323 | ||||||
| chr7:87709506
|
T | C | 1 | a0001c0001t0058g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.373-1064T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709506 | ||||||
| chr7:87709756
|
A | C | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-814A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709756 | ||||||
| chr7:87709758
|
T | A | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-812T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709758 | ||||||
| chr7:87709760
|
T | A | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-810T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709760 | ||||||
| chr7:87709762
|
T | A | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-808T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709762 | ||||||
| chr7:87709763
|
A | T | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-807A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709763 | ||||||
| chr7:87709764
|
T | A | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-806T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709764 | ||||||
| chr7:87709767
|
A | G | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-803A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709767 | ||||||
| chr7:87709768
|
T | A | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-802T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709768 | ||||||
| chr7:87709770
|
T | G | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-800T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709770 | ||||||
| chr7:87709771
|
A | T | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-799A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709771 | ||||||
| chr7:87709772
|
G | T | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-798G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87709772 | ||||||
| chr7:87710531
|
T | A | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.373-39T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 3/10 | chr7 | 87710531 | ||||||
| chr7:87711067
|
C | T | 2 | a0001c0001t0004g0111a0001c0001t0004g0112 | 2 | HG00738.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.458+412C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87711067 | ||||||
| chr7:87711165
|
C | A | 61 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(58): Show | 61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.458+510C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87711165 | ||||||
| chr7:87711219
|
G | A | 21 | a0001c0001t0015g0020a0001c0001t0015g0092a0001c0001t0015g0094others(18): Show | 21 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.458+564G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87711219 | ||||||
| chr7:87711264
|
T | C | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+609T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87711264 | ||||||
| chr7:87711277
|
GATTGAGC others(1): Show |
G | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.458+627_458+634del others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87711277 | |||||
| chr7:87711293
|
C | T | 2 | a0001c0001t0069g0016a0001c0001t0070g0017 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.458+638C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87711293 | ||||||
| chr7:87711550
|
T | C | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458+895T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87711550 | ||||||
| chr7:87712006
|
G | A | 3 | a0001c0001t0065g0144a0001c0001t0071g0142a0001c0001t0072g0143 | 3 | HG01069.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.458+1351G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87712006 | ||||||
| chr7:87712545
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.458+1890A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87712545 | ||||||
| chr7:87712695
|
C | G | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.458+2040C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87712695 | ||||||
| chr7:87712834
|
G | T | 1 | a0001c0001t0009g0115 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.458+2179G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87712834 | ||||||
| chr7:87713270
|
A | G | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+2615A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713270 | ||||||
| chr7:87713450
|
A | G | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+2795A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713450 | ||||||
| chr7:87713488
|
G | A | 1 | a0001c0001t0041g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.458+2833G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713488 | ||||||
| chr7:87713583
|
T | G | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+2928T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713583 | ||||||
| chr7:87713596
|
G | A | 1 | a0001c0003t0001g0022 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.458+2941G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713596 | ||||||
| chr7:87713663
|
A | G | 2 | a0001c0001t0004g0019a0001c0001t0007g0021 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.458+3008A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713663 | ||||||
| chr7:87713760
|
A | C | 1 | a0001c0001t0007g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.458+3105A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87713760 | ||||||
| chr7:87714216
|
C | T | 1 | a0001c0001t0003g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.458+3561C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714216 | ||||||
| chr7:87714217
|
G | A | 7 | a0001c0001t0015g0020a0001c0001t0015g0092a0001c0001t0015g0094others(4): Show | 7 | HG00639.hp1 HG02559.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.458+3562G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714217 | ||||||
| chr7:87714263
|
C | A | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.458+3608C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714263 | ||||||
| chr7:87714352
|
A | G | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+3697A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714352 | ||||||
| chr7:87714385
|
G | T | 1 | a0001c0001t0001g0105 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.458+3730G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714385 | ||||||
| chr7:87714393
|
G | A | 1 | a0001c0001t0003g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.458+3738G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714393 | ||||||
| chr7:87714592
|
G | T | 1 | a0001c0001t0003g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.458+3937G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714592 | ||||||
| chr7:87714706
|
T | C | 47 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(44): Show | 47 | HG00558.hp2 HG00621.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.458+4051T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714706 | ||||||
| chr7:87714707
|
G | C | 47 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(44): Show | 47 | HG00558.hp2 HG00621.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.458+4052G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714707 | ||||||
| chr7:87714733
|
C | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4078C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87714733 | ||||||
| chr7:87715034
|
G | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4379G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715034 | ||||||
| chr7:87715102
|
A | C | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4447A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715102 | ||||||
| chr7:87715139
|
G | A | 1 | a0001c0001t0011g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.458+4484G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715139 | ||||||
| chr7:87715202
|
A | G | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.458+4547A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715202 | ||||||
| chr7:87715251
|
T | TATTATAT others(17): Show |
21 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0055others(18): Show | 21 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.458+4701_458+4724d others(26): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715251 | |||||
| chr7:87715251
|
T | TATTATAT others(41): Show |
3 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0075g0006 | 3 | HG02976.hp2 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.458+4677_458+4724d others(50): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715251 | |||||
| chr7:87715251
|
T | TATTATAT others(89): Show |
1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.458+4629_458+4724d others(98): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715251 | |||||
| chr7:87715251
|
TATTATAT others(17): Show |
T | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.458+4701_458+4724d others(26): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715251 | |||||
| chr7:87715251
|
TATTATAT others(41): Show |
T | 3 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018 | 3 | HG02572.hp2 HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.458+4677_458+4724d others(50): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715251 | |||||
| chr7:87715274
|
T | A | 1 | a0001c0001t0005g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.458+4619T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715274 | ||||||
| chr7:87715292
|
T | G | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4637T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715292 | ||||||
| chr7:87715321
|
A | ATAATTAT others(17): Show |
1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.458+4689_458+4690i others(26): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715321 | |||||
| chr7:87715321
|
A | T | 39 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.458+4666A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715321 | ||||||
| chr7:87715331
|
ATAAT | A | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.458+4682_458+4685d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715331 | |||||
| chr7:87715331
|
ATAATTAA others(47): Show |
A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4677_458+4730d others(56): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715331 | ||||||
| chr7:87715341
|
TATAATAA others(20): Show |
T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+4692_458+4718d others(29): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715341 | |||||
| chr7:87715345
|
A | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.458+4690A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715345 | ||||||
| chr7:87715369
|
A | ATAATTAT others(17): Show |
3 | a0001c0001t0008g0193a0001c0001t0011g0198a0001c0001t0064g0184 | 3 | HG01346.hp1 HG01433.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.458+4724_458+4725i others(26): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715369 | |||||
| chr7:87715369
|
A | T | 20 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0195others(17): Show | 20 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.458+4714A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715369 | ||||||
| chr7:87715382
|
CAATAT | C | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.458+4739_458+4743d others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715382 | |||||
| chr7:87715387
|
T | TC | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4732_458+4733i others(3): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715387 | ||||||
| chr7:87715421
|
TTAATATA others(14): Show |
T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+4785_458+4805d others(23): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715421 | |||||
| chr7:87715473
|
TTAA | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4821_458+4823d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715473 | |||||
| chr7:87715516
|
TTA | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+4870_458+4871d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87715516 | |||||
| chr7:87715648
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.458+4993T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715648 | ||||||
| chr7:87715665
|
A | G | 1 | a0001c0001t0026g0083 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.458+5010A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715665 | ||||||
| chr7:87715808
|
G | T | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458+5153G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715808 | ||||||
| chr7:87715892
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.458+5237C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715892 | ||||||
| chr7:87715937
|
C | T | 1 | a0001c0001t0046g0109 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.458+5282C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87715937 | ||||||
| chr7:87716090
|
T | A | 1 | a0001c0001t0010g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.458+5435T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87716090 | ||||||
| chr7:87716091
|
A | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+5436A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87716091 | ||||||
| chr7:87716133
|
T | C | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.458+5478T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87716133 | ||||||
| chr7:87716202
|
A | C | 7 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0052g0038others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.458+5547A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87716202 | ||||||
| chr7:87716875
|
C | T | 1 | a0001c0001t0004g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.458+6220C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87716875 | ||||||
| chr7:87717024
|
C | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+6369C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87717024 | ||||||
| chr7:87717344
|
TAAAG | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+6690_458+6693d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87717344 | ||||||
| chr7:87717464
|
A | G | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.458+6809A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87717464 | ||||||
| chr7:87717485
|
G | A | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.458+6830G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87717485 | ||||||
| chr7:87717503
|
G | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0105 | 2 | NA18952.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.458+6848G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87717503 | ||||||
| chr7:87718072
|
A | C | 39 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.458+7417A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87718072 | ||||||
| chr7:87718213
|
T | C | 2 | a0001c0001t0022g0180a0001c0001t0029g0178 | 2 | NA18974.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.458+7558T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87718213 | ||||||
| chr7:87718269
|
A | G | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.458+7614A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87718269 | ||||||
| chr7:87718269
|
A | T | 1 | a0001c0001t0001g0044 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.458+7614A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87718269 | ||||||
| chr7:87718695
|
A | C | 2 | a0001c0001t0069g0016a0001c0001t0070g0017 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.458+8040A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87718695 | ||||||
| chr7:87718916
|
A | G | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.458+8261A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87718916 | ||||||
| chr7:87719329
|
T | G | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+8674T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719329 | ||||||
| chr7:87719458
|
A | G | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.458+8803A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719458 | ||||||
| chr7:87719465
|
C | T | 2 | a0001c0001t0004g0102a0001c0001t0031g0125 | 2 | HG00558.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.458+8810C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719465 | ||||||
| chr7:87719665
|
G | T | 1 | a0001c0001t0004g0124 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.458+9010G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719665 | ||||||
| chr7:87719680
|
A | G | 15 | a0001c0001t0001g0059a0001c0001t0016g0103a0001c0001t0016g0126others(12): Show | 15 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.458+9025A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719680 | ||||||
| chr7:87719703
|
A | G | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.458+9048A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719703 | ||||||
| chr7:87719911
|
C | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.458+9256C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87719911 | ||||||
| chr7:87719990
|
C | CA | 11 | a0001c0001t0001g0068a0001c0001t0004g0019a0001c0001t0004g0075others(8): Show | 11 | HG00639.hp2 HG01099.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.458+9351dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87719990 | |||||
| chr7:87719990
|
CA | C | 47 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(44): Show | 47 | HG00558.hp2 HG00621.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.458+9351delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87719990 | |||||
| chr7:87720002
|
A | AAAGAAAG | 6 | a0001c0001t0020g0034a0001c0001t0020g0036a0001c0001t0021g0029others(3): Show | 6 | HG02129.hp1 HG02258.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.458+9349_458+9350i others(9): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720002 | |||||
| chr7:87720002
|
A | AAGAAAG | 55 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(52): Show | 55 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.458+9348_458+9349i others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720002 | |||||
| chr7:87720055
|
A | G | 1 | a0001c0001t0007g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.458+9400A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720055 | ||||||
| chr7:87720131
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.458+9476G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720131 | ||||||
| chr7:87720362
|
C | T | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.458+9707C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720362 | ||||||
| chr7:87720394
|
A | G | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.458+9739A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720394 | ||||||
| chr7:87720540
|
A | ATG | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.458+9886_458+9887i others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720540 | |||||
| chr7:87720542
|
A | ATG | 2 | a0001c0001t0015g0094a0001c0001t0016g0126 | 2 | HG01261.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.458+9919_458+9920d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | |||||
| chr7:87720542
|
A | ATGTG | 10 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0013g0030others(7): Show | 10 | HG01358.hp1 HG01496.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.458+9917_458+9920d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | |||||
| chr7:87720542
|
A | ATGTGTG | 33 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(30): Show | 33 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.458+9915_458+9920d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | |||||
| chr7:87720542
|
A | ATGTGTGT others(1): Show |
23 | a0001c0001t0002g0202a0001c0001t0011g0200a0001c0001t0013g0149others(20): Show | 23 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.458+9913_458+9920d others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | |||||
| chr7:87720542
|
A | ATGTGTGT others(3): Show |
2 | a0001c0001t0014g0157a0001c0001t0027g0037 | 2 | NA18998.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.458+9911_458+9920d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | |||||
| chr7:87720542
|
A | ATGTGTGT others(5): Show |
1 | a0002c0002t0017g0140 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.458+9909_458+9920d others(14): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | |||||
| chr7:87720542
|
A | G | 4 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0069g0016others(1): Show | 4 | HG02572.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+9887A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720542 | ||||||
| chr7:87720542
|
ATG | A | 88 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(85): Show | 88 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.458+9919_458+9920d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | |||||
| chr7:87720542
|
ATGTGTG | A | 2 | a0001c0001t0017g0170a0001c0001t0036g0160 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.458+9915_458+9920d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720542 | |||||
| chr7:87720624
|
CAG | C | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+9972_458+9973d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720624 | |||||
| chr7:87720683
|
C | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+10028C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720683 | ||||||
| chr7:87720747
|
C | T | 1 | a0001c0001t0024g0062 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.458+10092C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720747 | ||||||
| chr7:87720758
|
G | A | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458+10103G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720758 | ||||||
| chr7:87720776
|
A | G | 5 | a0001c0001t0001g0068a0001c0001t0024g0003a0001c0001t0024g0062others(2): Show | 5 | HG00639.hp2 HG01099.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+10121A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720776 | ||||||
| chr7:87720857
|
C | G | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.458+10202C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720857 | ||||||
| chr7:87720919
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0068g0001 | 2 | HG01099.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.458+10264A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87720919 | ||||||
| chr7:87720932
|
T | TAGTTAAA others(30): Show |
201 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(198): Show | 201 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.458+10286_458+1028 others(41): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87720932 | |||||
| chr7:87721744
|
A | G | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.458+11089A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87721744 | ||||||
| chr7:87721862
|
C | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+11207C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87721862 | ||||||
| chr7:87721951
|
G | A | 2 | a0001c0001t0042g0148a0001c0001t0052g0038 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.458+11296G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87721951 | ||||||
| chr7:87722007
|
G | A | 3 | a0001c0001t0008g0195a0001c0001t0008g0197a0001c0001t0030g0196 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.458+11352G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87722007 | ||||||
| chr7:87722270
|
T | C | 2 | a0001c0001t0016g0129a0001c0001t0073g0098 | 2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.458+11615T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87722270 | ||||||
| chr7:87722881
|
C | T | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.458+12226C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87722881 | ||||||
| chr7:87722958
|
G | A | 1 | a0001c0001t0057g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.458+12303G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87722958 | ||||||
| chr7:87722975
|
G | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+12320G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87722975 | ||||||
| chr7:87723033
|
T | C | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.458+12378T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723033 | ||||||
| chr7:87723328
|
C | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.458+12673C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723328 | ||||||
| chr7:87723412
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0107 | 2 | HG01167.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.458+12757G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723412 | ||||||
| chr7:87723527
|
C | T | 8 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.458+12872C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723527 | ||||||
| chr7:87723632
|
T | C | 61 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(58): Show | 61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.458+12977T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723632 | ||||||
| chr7:87723760
|
C | T | 4 | a0001c0001t0038g0182a0001c0001t0040g0161a0001c0001t0050g0168others(1): Show | 4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+13105C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723760 | ||||||
| chr7:87723904
|
G | A | 1 | a0001c0001t0006g0145 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.458+13249G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723904 | ||||||
| chr7:87723907
|
C | T | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.458+13252C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87723907 | ||||||
| chr7:87724234
|
T | C | 2 | a0001c0001t0025g0053a0001c0001t0028g0069 | 2 | HG01099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.458+13579T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87724234 | ||||||
| chr7:87724607
|
A | G | 4 | a0001c0001t0038g0182a0001c0001t0040g0161a0001c0001t0050g0168others(1): Show | 4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+13952A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87724607 | ||||||
| chr7:87724887
|
T | C | 1 | a0001c0001t0003g0064 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.458+14232T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87724887 | ||||||
| chr7:87724888
|
A | G | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.458+14233A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87724888 | ||||||
| chr7:87724976
|
A | G | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+14321A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87724976 | ||||||
| chr7:87725264
|
C | T | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-14527C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725264 | ||||||
| chr7:87725294
|
A | G | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-14497A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725294 | ||||||
| chr7:87725337
|
G | A | 2 | a0001c0001t0003g0130a0001c0001t0006g0131 | 2 | HG03098.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.459-14454G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725337 | ||||||
| chr7:87725501
|
T | G | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.459-14290T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725501 | ||||||
| chr7:87725660
|
T | C | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459-14131T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725660 | ||||||
| chr7:87725778
|
C | A | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-14013C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725778 | ||||||
| chr7:87725922
|
A | C | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.459-13869A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87725922 | ||||||
| chr7:87726059
|
A | G | 2 | a0001c0001t0069g0016a0001c0001t0070g0017 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.459-13732A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726059 | ||||||
| chr7:87726085
|
CT | C | 201 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(198): Show | 201 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.459-13703delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87726085 | |||||
| chr7:87726147
|
T | C | 1 | a0001c0001t0078g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.459-13644T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726147 | ||||||
| chr7:87726357
|
C | T | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.459-13434C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726357 | ||||||
| chr7:87726382
|
G | A | 1 | a0001c0001t0010g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.459-13409G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726382 | ||||||
| chr7:87726528
|
T | G | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.459-13263T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726528 | ||||||
| chr7:87726589
|
C | G | 8 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.459-13202C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726589 | ||||||
| chr7:87726614
|
T | C | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.459-13177T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726614 | ||||||
| chr7:87726620
|
T | G | 1 | a0001c0001t0009g0115 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.459-13171T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726620 | ||||||
| chr7:87726690
|
C | T | 8 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.459-13101C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726690 | ||||||
| chr7:87726816
|
T | C | 3 | a0001c0001t0004g0101a0001c0001t0005g0114a0001c0001t0026g0083 | 3 | HG01952.hp1 NA18975.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.459-12975T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726816 | ||||||
| chr7:87726826
|
A | G | 2 | a0001c0001t0016g0103a0001c0001t0016g0126 | 2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.459-12965A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726826 | ||||||
| chr7:87726914
|
T | C | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.459-12877T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726914 | ||||||
| chr7:87726926
|
C | G | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459-12865C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726926 | ||||||
| chr7:87726942
|
C | A | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459-12849C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87726942 | ||||||
| chr7:87727110
|
A | G | 7 | a0001c0001t0001g0068a0001c0001t0004g0019a0001c0001t0004g0075others(4): Show | 7 | HG01099.hp1 HG01261.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-12681A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87727110 | ||||||
| chr7:87727286
|
G | C | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.459-12505G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87727286 | ||||||
| chr7:87727587
|
AT | A | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.459-12197delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87727587 | |||||
| chr7:87727675
|
C | T | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-12116C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87727675 | ||||||
| chr7:87727723
|
T | C | 1 | a0001c0001t0022g0179 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.459-12068T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87727723 | ||||||
| chr7:87728096
|
A | G | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.459-11695A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87728096 | ||||||
| chr7:87728411
|
G | C | 6 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0165others(3): Show | 6 | HG02559.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-11380G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87728411 | ||||||
| chr7:87728474
|
C | T | 2 | a0001c0001t0019g0043a0001c0001t0049g0201 | 2 | HG01978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.459-11317C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87728474 | ||||||
| chr7:87728487
|
T | G | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-11304T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87728487 | ||||||
| chr7:87728550
|
T | A | 54 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(51): Show | 54 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.459-11241T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87728550 | ||||||
| chr7:87728830
|
G | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-10961G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87728830 | ||||||
| chr7:87729048
|
ATCTG | A | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-10739_459-1073 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87729048 | |||||
| chr7:87729170
|
G | A | 2 | a0001c0001t0004g0102a0001c0001t0031g0125 | 2 | HG00558.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.459-10621G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729170 | ||||||
| chr7:87729176
|
A | G | 2 | a0001c0001t0003g0046a0001c0001t0003g0047 | 2 | HG01074.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.459-10615A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729176 | ||||||
| chr7:87729202
|
T | C | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-10589T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729202 | ||||||
| chr7:87729460
|
G | A | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.459-10331G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729460 | ||||||
| chr7:87729674
|
G | A | 1 | a0001c0001t0078g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.459-10117G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729674 | ||||||
| chr7:87729712
|
C | T | 11 | a0001c0001t0003g0128a0001c0001t0004g0082a0001c0001t0004g0101others(8): Show | 11 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.459-10079C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729712 | ||||||
| chr7:87729770
|
C | T | 1 | a0001c0001t0056g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.459-10021C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87729770 | ||||||
| chr7:87730015
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.459-9776G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87730015 | ||||||
| chr7:87730189
|
G | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-9602G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87730189 | ||||||
| chr7:87730525
|
G | C | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.459-9266G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87730525 | ||||||
| chr7:87730582
|
C | T | 5 | a0001c0001t0003g0141a0001c0001t0006g0050a0001c0001t0006g0113others(2): Show | 5 | HG02132.hp2 NA18970.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-9209C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87730582 | ||||||
| chr7:87730851
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0072 | 2 | HG01192.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.459-8940G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87730851 | ||||||
| chr7:87731008
|
G | A | 1 | a0001c0001t0063g0060 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.459-8783G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731008 | ||||||
| chr7:87731310
|
T | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-8481T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731310 | ||||||
| chr7:87731512
|
C | A | 1 | a0001c0001t0001g0051 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.459-8279C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731512 | ||||||
| chr7:87731612
|
G | T | 8 | a0001c0001t0003g0128a0001c0001t0004g0082a0001c0001t0004g0101others(5): Show | 8 | HG00438.hp1 HG01952.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.459-8179G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731612 | ||||||
| chr7:87731729
|
T | C | 7 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-8062T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731729 | ||||||
| chr7:87731823
|
G | A | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.459-7968G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731823 | ||||||
| chr7:87731887
|
C | T | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-7904C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731887 | ||||||
| chr7:87731940
|
A | G | 2 | a0001c0001t0042g0148a0001c0001t0052g0038 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.459-7851A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87731940 | ||||||
| chr7:87732053
|
A | G | 1 | a0001c0001t0004g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459-7738A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87732053 | ||||||
| chr7:87732202
|
C | A | 3 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0037g0002 | 3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.459-7589C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87732202 | ||||||
| chr7:87732227
|
C | T | 54 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(51): Show | 54 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.459-7564C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87732227 | ||||||
| chr7:87732249
|
C | A | 7 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0052g0038others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-7542C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87732249 | ||||||
| chr7:87732322
|
A | G | 1 | a0001c0001t0031g0125 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.459-7469A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87732322 | ||||||
| chr7:87732385
|
G | GAAAGAAA others(272): Show |
2 | a0001c0001t0004g0075a0001c0001t0067g0074 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.459-7397_459-7396i others(281): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87732385 | |||||
| chr7:87732932
|
A | G | 3 | a0001c0001t0031g0076a0001c0001t0034g0077a0001c0001t0034g0079 | 3 | HG02559.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.459-6859A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87732932 | ||||||
| chr7:87733132
|
GC | G | 14 | a0001c0001t0016g0103a0001c0001t0016g0126a0001c0001t0016g0129others(11): Show | 14 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.459-6652delC | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87733132 | |||||
| chr7:87733376
|
T | G | 9 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-6415T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733376 | ||||||
| chr7:87733392
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.459-6399T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733392 | ||||||
| chr7:87733568
|
G | A | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-6223G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733568 | ||||||
| chr7:87733627
|
C | T | 1 | a0001c0001t0062g0093 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.459-6164C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733627 | ||||||
| chr7:87733711
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.459-6080A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733711 | ||||||
| chr7:87733791
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.459-6000C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733791 | ||||||
| chr7:87733901
|
C | T | 1 | a0001c0001t0005g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.459-5890C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733901 | ||||||
| chr7:87733902
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0107 | 2 | HG01167.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.459-5889G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733902 | ||||||
| chr7:87733940
|
T | C | 2 | a0001c0001t0013g0030a0001c0001t0044g0033 | 2 | HG01358.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.459-5851T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87733940 | ||||||
| chr7:87734011
|
G | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0107 | 2 | HG01167.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.459-5780G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734011 | ||||||
| chr7:87734526
|
A | G | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.459-5265A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734526 | ||||||
| chr7:87734662
|
T | C | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.459-5129T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734662 | ||||||
| chr7:87734738
|
A | G | 3 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0037g0002 | 3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.459-5053A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734738 | ||||||
| chr7:87734781
|
T | C | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.459-5010T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734781 | ||||||
| chr7:87734787
|
ACTCCAT | A | 2 | a0001c0001t0019g0110a0001c0001t0056g0086 | 2 | HG01981.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.459-4999_459-4994d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87734787 | |||||
| chr7:87734874
|
A | C | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.459-4917A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734874 | ||||||
| chr7:87734891
|
G | A | 7 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-4900G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87734891 | ||||||
| chr7:87735106
|
T | G | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.459-4685T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735106 | ||||||
| chr7:87735325
|
C | A | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.459-4466C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735325 | ||||||
| chr7:87735846
|
G | C | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.459-3945G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735846 | ||||||
| chr7:87735932
|
C | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-3859C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735932 | ||||||
| chr7:87735933
|
G | A | 1 | a0001c0001t0011g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.459-3858G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735933 | ||||||
| chr7:87735949
|
A | G | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.459-3842A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735949 | ||||||
| chr7:87735966
|
A | T | 61 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(58): Show | 61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.459-3825A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87735966 | ||||||
| chr7:87736102
|
T | C | 1 | a0001c0001t0004g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459-3689T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736102 | ||||||
| chr7:87736226
|
T | C | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.459-3565T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736226 | ||||||
| chr7:87736296
|
A | G | 2 | a0001c0001t0069g0016a0001c0001t0070g0017 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.459-3495A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736296 | ||||||
| chr7:87736441
|
A | G | 1 | a0001c0001t0025g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.459-3350A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736441 | ||||||
| chr7:87736450
|
A | G | 1 | a0001c0001t0006g0131 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.459-3341A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736450 | ||||||
| chr7:87736548
|
C | T | 2 | a0001c0001t0016g0103a0001c0001t0016g0126 | 2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.459-3243C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736548 | ||||||
| chr7:87736750
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.459-3041G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736750 | ||||||
| chr7:87736804
|
ATATATT | A | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.459-2975_459-2970d others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736804 | |||||
| chr7:87736808
|
A | T | 1 | a0001c0001t0004g0102 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.459-2983A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736808 | ||||||
| chr7:87736855
|
C | CTA | 3 | a0001c0001t0004g0111a0001c0001t0016g0103a0001c0001t0033g0073 | 3 | HG00438.hp2 HG00738.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.459-2902_459-2901d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736855 | |||||
| chr7:87736855
|
CTA | C | 7 | a0001c0001t0003g0049a0001c0001t0006g0104a0001c0001t0006g0145others(4): Show | 7 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-2902_459-2901d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736855 | |||||
| chr7:87736855
|
CTATA | C | 5 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0003g0057others(2): Show | 5 | HG01123.hp2 HG03098.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-2904_459-2901d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736855 | |||||
| chr7:87736855
|
CTATATAT others(7): Show |
C | 6 | a0001c0001t0010g0007a0001c0001t0010g0010a0001c0001t0039g0158others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.459-2914_459-2901d others(16): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736855 | |||||
| chr7:87736855
|
CTATATAT others(9): Show |
C | 9 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0014g0153others(6): Show | 9 | NA18963.hp1 NA18970.hp2 NA18988.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-2916_459-2901d others(18): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736855 | |||||
| chr7:87736869
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-2920_459-2898d others(25): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736869 | |||||
| chr7:87736869
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.459-2920_459-2894d others(29): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736869 | |||||
| chr7:87736870
|
TATATATA others(10): Show |
T | 1 | a0001c0001t0051g0156 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.459-2920_459-2904d others(19): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736870 | ||||||
| chr7:87736871
|
ATATATAT others(15): Show |
A | 22 | a0001c0001t0002g0027a0001c0001t0002g0162a0001c0001t0002g0163others(19): Show | 22 | HG01123.hp1 HG01358.hp1 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.459-2918_459-2897d others(24): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736871 | |||||
| chr7:87736871
|
ATATATAT others(16): Show |
A | 5 | a0001c0001t0002g0137a0001c0001t0002g0167a0001c0001t0018g0172others(2): Show | 5 | HG01496.hp1 HG01952.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-2918_459-2896d others(25): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736871 | |||||
| chr7:87736871
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0058g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.459-2918_459-2894d others(27): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736871 | |||||
| chr7:87736872
|
TATATATA others(8): Show |
T | 2 | a0001c0001t0010g0008a0001c0001t0012g0152 | 2 | HG00423.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.459-2918_459-2904d others(17): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736872 | ||||||
| chr7:87736873
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0055g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.459-2916_459-2897d others(22): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736873 | |||||
| chr7:87736873
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0013g0149 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.459-2916_459-2896d others(23): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736873 | |||||
| chr7:87736873
|
ATATATAT others(15): Show |
A | 11 | a0001c0001t0020g0034a0001c0001t0020g0036a0001c0001t0021g0029others(8): Show | 11 | HG01192.hp1 HG02129.hp1 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.459-2916_459-2895d others(24): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736873 | |||||
| chr7:87736873
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.459-2916_459-2892d others(27): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736873 | |||||
| chr7:87736874
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0010g0009 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.459-2916_459-2904d others(15): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736874 | ||||||
| chr7:87736875
|
ATATATAT others(13): Show |
A | 12 | a0001c0001t0008g0191a0001c0001t0008g0193a0001c0001t0008g0195others(9): Show | 12 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.459-2914_459-2895d others(22): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736875 | |||||
| chr7:87736875
|
ATATATAT others(14): Show |
A | 2 | a0001c0001t0008g0190a0001c0001t0030g0192 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.459-2914_459-2894d others(23): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736875 | |||||
| chr7:87736876
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459-2914_459-2902d others(15): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736876 | ||||||
| chr7:87736877
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0069g0016 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.459-2912_459-2891d others(24): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736877 | |||||
| chr7:87736877
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0070g0017 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.459-2912_459-2890d others(25): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736877 | |||||
| chr7:87736879
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.459-2910_459-2899d others(14): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736879 | |||||
| chr7:87736879
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0011g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.459-2910_459-2891d others(22): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736879 | |||||
| chr7:87736881
|
ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0068a0001c0001t0076g0081 | 2 | HG01099.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.459-2908_459-2899d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736881 | |||||
| chr7:87736881
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.459-2908_459-2897d others(14): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736881 | |||||
| chr7:87736882
|
TATA | T | 3 | a0001c0001t0004g0082a0001c0001t0004g0124a0001c0001t0005g0127 | 3 | NA18977.hp1 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.459-2908_459-2906d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736882 | ||||||
| chr7:87736883
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0037g0002 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459-2906_459-2897d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736883 | |||||
| chr7:87736883
|
ATATATAT others(4): Show |
A | 4 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0059g0014others(1): Show | 4 | HG02717.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-2906_459-2896d others(13): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736883 | |||||
| chr7:87736884
|
TATA | T | 4 | a0001c0001t0007g0122a0001c0001t0007g0133a0001c0001t0009g0136others(1): Show | 4 | HG02055.hp2 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-2906_459-2904d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736884 | ||||||
| chr7:87736885
|
A | T | 2 | a0001c0001t0005g0080a0001c0001t0068g0001 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.459-2906A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736885 | ||||||
| chr7:87736886
|
TA | T | 2 | a0001c0001t0005g0134a0001c0001t0005g0135 | 2 | NA18974.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.459-2904delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736886 | ||||||
| chr7:87736886
|
TATA | T | 7 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0061others(4): Show | 7 | HG00558.hp2 HG02132.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-2904_459-2902d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736886 | ||||||
| chr7:87736887
|
A | T | 17 | a0001c0001t0004g0082a0001c0001t0004g0124a0001c0001t0005g0080others(14): Show | 17 | HG00280.hp1 HG02055.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.459-2904A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736887 | ||||||
| chr7:87736887
|
ATAT | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0055a0001c0001t0001g0058others(6): Show | 9 | HG02165.hp2 HG02965.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-2902_459-2900d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736887 | |||||
| chr7:87736888
|
TA | T | 3 | a0001c0001t0001g0087a0001c0001t0006g0067a0001c0001t0053g0025 | 3 | HG00735.hp1 HG02040.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.459-2902delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736888 | ||||||
| chr7:87736889
|
A | T | 38 | a0001c0001t0001g0044a0001c0001t0003g0057a0001c0001t0003g0130others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.459-2902A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736889 | ||||||
| chr7:87736889
|
AT | A | 13 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0003g0088others(10): Show | 13 | HG01081.hp1 HG01496.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.459-2876delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736889 | |||||
| chr7:87736889
|
ATT | A | 6 | a0001c0001t0003g0128a0001c0001t0004g0101a0001c0001t0004g0102others(3): Show | 6 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.459-2877_459-2876d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87736889 | |||||
| chr7:87736890
|
T | TA | 9 | a0001c0001t0001g0042a0001c0001t0001g0070a0001c0001t0001g0072others(6): Show | 9 | HG00423.hp2 HG00741.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-2901_459-2900i others(3): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736890 | ||||||
| chr7:87736890
|
T | TATATA | 3 | a0001c0001t0016g0129a0001c0001t0033g0065a0001c0001t0046g0109 | 3 | HG01433.hp1 HG02040.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.459-2901_459-2900i others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736890 | ||||||
| chr7:87736891
|
T | A | 9 | a0001c0001t0001g0063a0001c0001t0001g0106a0001c0001t0003g0046others(6): Show | 9 | HG00438.hp2 HG00621.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.459-2900T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736891 | ||||||
| chr7:87736892
|
T | A | 15 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0005g0114others(12): Show | 15 | HG00741.hp2 HG01099.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.459-2899T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736892 | ||||||
| chr7:87736893
|
T | A | 3 | a0001c0001t0003g0046a0001c0001t0003g0047a0001c0001t0016g0103 | 3 | HG00738.hp1 HG01074.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.459-2898T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736893 | ||||||
| chr7:87736894
|
T | A | 5 | a0001c0001t0016g0129a0001c0001t0019g0110a0001c0001t0056g0086others(2): Show | 5 | HG00741.hp2 HG01433.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.459-2897T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736894 | ||||||
| chr7:87736916
|
G | T | 1 | a0001c0001t0003g0046 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.459-2875G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87736916 | ||||||
| chr7:87737055
|
G | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-2736G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737055 | ||||||
| chr7:87737146
|
G | A | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459-2645G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737146 | ||||||
| chr7:87737342
|
T | C | 5 | a0001c0001t0001g0099a0001c0001t0005g0096a0001c0001t0005g0134others(2): Show | 5 | HG00423.hp2 NA18968.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.459-2449T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737342 | ||||||
| chr7:87737484
|
C | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-2307C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737484 | ||||||
| chr7:87737564
|
C | A | 1 | a0001c0001t0001g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.459-2227C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737564 | ||||||
| chr7:87737832
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.459-1959G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737832 | ||||||
| chr7:87737906
|
C | T | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.459-1885C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737906 | ||||||
| chr7:87737961
|
G | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-1830G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87737961 | ||||||
| chr7:87738005
|
G | C | 24 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(21): Show | 24 | HG00423.hp1 HG02055.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.459-1786G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87738005 | ||||||
| chr7:87738026
|
C | T | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.459-1765C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87738026 | ||||||
| chr7:87738165
|
A | G | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459-1626A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87738165 | ||||||
| chr7:87738208
|
A | T | 3 | a0001c0001t0065g0144a0001c0001t0071g0142a0001c0001t0072g0143 | 3 | HG01069.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.459-1583A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87738208 | ||||||
| chr7:87738217
|
AG | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-1570delG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 87738217 | |||||
| chr7:87738411
|
G | A | 1 | a0001c0001t0010g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.459-1380G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87738411 | ||||||
| chr7:87738529
|
C | T | 3 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0037g0002 | 3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.459-1262C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87738529 | ||||||
| chr7:87739026
|
T | G | 1 | a0001c0001t0008g0191 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.459-765T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87739026 | ||||||
| chr7:87739381
|
A | G | 1 | a0001c0001t0003g0128 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.459-410A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87739381 | ||||||
| chr7:87739415
|
G | A | 75 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(72): Show | 75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.459-376G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87739415 | ||||||
| chr7:87739556
|
C | A | 1 | a0001c0001t0003g0064 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.459-235C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87739556 | ||||||
| chr7:87739669
|
T | A | 1 | a0001c0001t0006g0145 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.459-122T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87739669 | ||||||
| chr7:87739746
|
C | T | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-45C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 4/10 | chr7 | 87739746 | ||||||
| chr7:87740145
|
C | T | 6 | a0001c0001t0010g0008a0001c0001t0010g0009a0001c0001t0010g0010others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.548+265C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740145 | ||||||
| chr7:87740347
|
A | T | 1 | a0001c0001t0058g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.548+467A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740347 | ||||||
| chr7:87740369
|
G | A | 75 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(72): Show | 75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.548+489G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740369 | ||||||
| chr7:87740393
|
A | G | 1 | a0001c0001t0080g0100 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.548+513A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740393 | ||||||
| chr7:87740867
|
A | G | 14 | a0001c0001t0016g0103a0001c0001t0016g0126a0001c0001t0016g0129others(11): Show | 14 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.549-632A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740867 | ||||||
| chr7:87740953
|
C | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.549-546C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740953 | ||||||
| chr7:87740955
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0061 | 2 | NA19063.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.549-544A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87740955 | ||||||
| chr7:87741226
|
C | G | 1 | a0001c0001t0028g0040 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.549-273C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87741226 | ||||||
| chr7:87741300
|
A | G | 1 | a0001c0001t0031g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.549-199A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87741300 | ||||||
| chr7:87741344
|
G | A | 1 | a0001c0001t0038g0182 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.549-155G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 5/10 | chr7 | 87741344 | ||||||
| chr7:87741848
|
TATA | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+274_629+276del others(3): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87741848 | |||||
| chr7:87741915
|
G | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+336G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87741915 | ||||||
| chr7:87742044
|
T | C | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.629+465T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87742044 | ||||||
| chr7:87742503
|
A | G | 2 | a0001c0001t0012g0150a0001c0001t0012g0151 | 2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.629+924A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87742503 | ||||||
| chr7:87742575
|
A | AATAG | 38 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0048others(35): Show | 38 | HG00558.hp2 HG01099.hp2 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+1040_629+1043d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87742575 | |||||
| chr7:87742575
|
A | AATAGATA others(1): Show |
4 | a0001c0001t0001g0042a0001c0001t0019g0110a0001c0001t0027g0037others(1): Show | 4 | HG01981.hp2 HG03239.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.629+1036_629+1043d others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87742575 | |||||
| chr7:87742575
|
A | G | 1 | a0001c0001t0057g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.629+996A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87742575 | ||||||
| chr7:87742575
|
AATAG | A | 33 | a0001c0001t0001g0106a0001c0001t0002g0137a0001c0001t0002g0166others(30): Show | 33 | HG00621.hp2 HG00639.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.629+1040_629+1043d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87742575 | |||||
| chr7:87742575
|
AATAGATA others(1): Show |
A | 17 | a0001c0001t0002g0027a0001c0001t0002g0202a0001c0001t0005g0096others(14): Show | 17 | HG01192.hp1 HG01358.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.629+1036_629+1043d others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87742575 | |||||
| chr7:87742575
|
AATAGATA others(21): Show |
A | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.629+1016_629+1043d others(30): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87742575 | |||||
| chr7:87742824
|
C | T | 1 | a0001c0001t0025g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.629+1245C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87742824 | ||||||
| chr7:87742930
|
G | A | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.629+1351G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87742930 | ||||||
| chr7:87742962
|
A | C | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+1383A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87742962 | ||||||
| chr7:87743113
|
C | CA | 17 | a0001c0001t0006g0131a0001c0001t0008g0191a0001c0001t0008g0193others(14): Show | 17 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.629+1548dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87743113 | |||||
| chr7:87743113
|
CA | C | 10 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(7): Show | 10 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.629+1548delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87743113 | |||||
| chr7:87743278
|
C | T | 6 | a0001c0001t0013g0149a0001c0001t0017g0173a0001c0001t0018g0172others(3): Show | 6 | HG01081.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.629+1699C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87743278 | ||||||
| chr7:87743576
|
C | T | 1 | a0001c0001t0026g0083 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.629+1997C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87743576 | ||||||
| chr7:87743666
|
GT | G | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629+2094delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87743666 | |||||
| chr7:87743671
|
T | C | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.629+2092T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87743671 | ||||||
| chr7:87743811
|
G | A | 1 | a0001c0001t0003g0064 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.629+2232G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87743811 | ||||||
| chr7:87743857
|
T | C | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629+2278T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87743857 | ||||||
| chr7:87744125
|
T | C | 7 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.629+2546T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744125 | ||||||
| chr7:87744169
|
A | G | 2 | a0001c0001t0003g0095a0001c0001t0004g0089 | 2 | HG00741.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.629+2590A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744169 | ||||||
| chr7:87744219
|
A | G | 1 | a0001c0001t0006g0145 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.629+2640A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744219 | ||||||
| chr7:87744257
|
A | G | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.629+2678A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744257 | ||||||
| chr7:87744271
|
C | T | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.629+2692C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744271 | ||||||
| chr7:87744292
|
T | C | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.629+2713T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744292 | ||||||
| chr7:87744726
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.629+3147C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744726 | ||||||
| chr7:87744791
|
C | T | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629+3212C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744791 | ||||||
| chr7:87744899
|
CAGAG | C | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.629+3321_629+3324d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87744899 | ||||||
| chr7:87745025
|
G | T | 1 | a0001c0001t0015g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.629+3446G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745025 | ||||||
| chr7:87745129
|
G | A | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.629+3550G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745129 | ||||||
| chr7:87745170
|
C | G | 1 | a0001c0001t0074g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.629+3591C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745170 | ||||||
| chr7:87745468
|
T | A | 14 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(11): Show | 14 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.629+3889T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745468 | ||||||
| chr7:87745512
|
G | A | 11 | a0001c0001t0003g0128a0001c0001t0004g0082a0001c0001t0004g0101others(8): Show | 11 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.629+3933G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745512 | ||||||
| chr7:87745512
|
GTA | G | 7 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.629+3935_629+3936d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87745512 | |||||
| chr7:87745553
|
T | G | 6 | a0001c0001t0004g0019a0001c0001t0004g0075a0001c0001t0004g0139others(3): Show | 6 | HG01261.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.629+3974T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745553 | ||||||
| chr7:87745779
|
A | AT | 84 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(81): Show | 84 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.629+4207dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87745779 | |||||
| chr7:87745893
|
G | A | 2 | a0001c0001t0003g0064a0001c0001t0028g0040 | 2 | HG03704.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.629+4314G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745893 | ||||||
| chr7:87745896
|
C | T | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.629+4317C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745896 | ||||||
| chr7:87745946
|
A | G | 1 | a0001c0001t0080g0100 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.629+4367A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87745946 | ||||||
| chr7:87746005
|
ATTG | A | 4 | a0001c0001t0038g0182a0001c0001t0040g0161a0001c0001t0050g0168others(1): Show | 4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.629+4432_629+4434d others(5): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87746005 | |||||
| chr7:87746205
|
C | T | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629+4626C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87746205 | ||||||
| chr7:87746317
|
A | G | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+4738A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87746317 | ||||||
| chr7:87746335
|
T | C | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.629+4756T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87746335 | ||||||
| chr7:87746506
|
C | T | 1 | a0001c0001t0003g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.629+4927C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87746506 | ||||||
| chr7:87746775
|
A | G | 7 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0052g0038others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.629+5196A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87746775 | ||||||
| chr7:87747292
|
G | C | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.629+5713G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87747292 | ||||||
| chr7:87747564
|
G | C | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.629+5985G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87747564 | ||||||
| chr7:87747600
|
A | G | 1 | a0001c0001t0004g0124 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.629+6021A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87747600 | ||||||
| chr7:87748314
|
G | T | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+6735G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87748314 | ||||||
| chr7:87748376
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.629+6797A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87748376 | ||||||
| chr7:87748549
|
G | T | 3 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0037g0002 | 3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.629+6970G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87748549 | ||||||
| chr7:87748604
|
A | G | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.629+7025A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87748604 | ||||||
| chr7:87748663
|
C | T | 1 | a0001c0001t0078g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.629+7084C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87748663 | ||||||
| chr7:87748832
|
G | T | 1 | a0001c0001t0016g0129 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.629+7253G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87748832 | ||||||
| chr7:87749120
|
T | C | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+7541T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749120 | ||||||
| chr7:87749334
|
C | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+7755C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749334 | ||||||
| chr7:87749518
|
T | C | 2 | a0001c0001t0069g0016a0001c0001t0070g0017 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629+7939T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749518 | ||||||
| chr7:87749520
|
A | T | 2 | a0001c0001t0069g0016a0001c0001t0070g0017 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629+7941A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749520 | ||||||
| chr7:87749745
|
G | A | 3 | a0001c0001t0008g0190a0001c0001t0030g0192a0001c0001t0076g0081 | 3 | HG01167.hp1 HG01169.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.629+8166G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749745 | ||||||
| chr7:87749859
|
C | CT | 14 | a0001c0001t0005g0096a0001c0001t0005g0117a0001c0001t0005g0119others(11): Show | 14 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(11): Show |
intron_variant | MODIFIER | c.629+8289dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87749859 | |||||
| chr7:87749868
|
T | A | 1 | a0001c0001t0007g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.629+8289T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749868 | ||||||
| chr7:87749907
|
T | C | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+8328T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749907 | ||||||
| chr7:87749944
|
T | A | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629+8365T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749944 | ||||||
| chr7:87749972
|
C | T | 39 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.629+8393C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87749972 | ||||||
| chr7:87750117
|
G | C | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.629+8538G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750117 | ||||||
| chr7:87750169
|
A | G | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+8590A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750169 | ||||||
| chr7:87750176
|
A | G | 1 | a0001c0001t0055g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.629+8597A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750176 | ||||||
| chr7:87750198
|
G | C | 1 | a0001c0001t0005g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.629+8619G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750198 | ||||||
| chr7:87750226
|
T | C | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.629+8647T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750226 | ||||||
| chr7:87750341
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.629+8762G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750341 | ||||||
| chr7:87750362
|
A | G | 1 | a0001c0001t0076g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.629+8783A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750362 | ||||||
| chr7:87750390
|
A | G | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629+8811A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750390 | ||||||
| chr7:87750582
|
C | G | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.629+9003C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750582 | ||||||
| chr7:87750674
|
C | G | 1 | a0001c0001t0002g0176 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.629+9095C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750674 | ||||||
| chr7:87750718
|
A | T | 1 | a0001c0001t0016g0103 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.629+9139A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750718 | ||||||
| chr7:87750752
|
G | T | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.629+9173G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750752 | ||||||
| chr7:87750795
|
G | A | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629+9216G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750795 | ||||||
| chr7:87750862
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.629+9283G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750862 | ||||||
| chr7:87750891
|
T | C | 15 | a0001c0001t0008g0191a0001c0001t0016g0103a0001c0001t0016g0126others(12): Show | 15 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.629+9312T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750891 | ||||||
| chr7:87750992
|
C | G | 1 | a0001c0001t0050g0168 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.629+9413C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87750992 | ||||||
| chr7:87751021
|
T | A | 2 | a0001c0001t0001g0068a0001c0001t0024g0062 | 2 | HG01099.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.629+9442T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87751021 | ||||||
| chr7:87751369
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.629+9790T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87751369 | ||||||
| chr7:87751406
|
A | G | 1 | a0001c0001t0011g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.629+9827A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87751406 | ||||||
| chr7:87751653
|
G | C | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.629+10074G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87751653 | ||||||
| chr7:87751683
|
TC | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+10105delC | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87751683 | ||||||
| chr7:87751686
|
G | GTTA | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+10109_629+1011 others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87751686 | |||||
| chr7:87751725
|
T | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+10146T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87751725 | ||||||
| chr7:87752015
|
C | T | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+10436C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752015 | ||||||
| chr7:87752086
|
C | G | 23 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(20): Show | 23 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.629+10507C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752086 | ||||||
| chr7:87752087
|
G | A | 13 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(10): Show | 13 | HG00423.hp1 HG03139.hp1 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.629+10508G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752087 | ||||||
| chr7:87752199
|
C | A | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.629+10620C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752199 | ||||||
| chr7:87752244
|
A | C | 1 | a0001c0001t0033g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.629+10665A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752244 | ||||||
| chr7:87752270
|
T | A | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.629+10691T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752270 | ||||||
| chr7:87752292
|
G | C | 1 | a0001c0001t0025g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.629+10713G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752292 | ||||||
| chr7:87752359
|
A | G | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.629+10780A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752359 | ||||||
| chr7:87752464
|
A | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+10885A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752464 | ||||||
| chr7:87752551
|
G | C | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.629+10972G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752551 | ||||||
| chr7:87752555
|
C | G | 2 | a0001c0001t0003g0130a0001c0001t0074g0097 | 2 | HG00323.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.629+10976C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752555 | ||||||
| chr7:87752791
|
GGTTTATC others(21): Show |
G | 1 | a0001c0001t0007g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.629+11213_629+1124 others(32): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752791 | ||||||
| chr7:87752794
|
T | C | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+11215T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752794 | ||||||
| chr7:87752800
|
G | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+11221G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752800 | ||||||
| chr7:87752822
|
A | T | 1 | a0001c0001t0007g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.629+11243A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752822 | ||||||
| chr7:87752883
|
T | C | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.629+11304T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752883 | ||||||
| chr7:87752982
|
G | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+11403G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87752982 | ||||||
| chr7:87753193
|
A | T | 1 | a0001c0001t0024g0062 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.629+11614A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87753193 | ||||||
| chr7:87753286
|
A | C | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629+11707A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87753286 | ||||||
| chr7:87753294
|
G | C | 2 | a0001c0001t0022g0180a0001c0001t0029g0178 | 2 | NA18974.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.629+11715G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87753294 | ||||||
| chr7:87753620
|
G | A | 61 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(58): Show | 61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.629+12041G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87753620 | ||||||
| chr7:87753715
|
T | C | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.629+12136T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87753715 | ||||||
| chr7:87753861
|
T | A | 39 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.629+12282T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87753861 | ||||||
| chr7:87754066
|
G | C | 1 | a0001c0001t0005g0134 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.629+12487G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754066 | ||||||
| chr7:87754086
|
C | A | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+12507C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754086 | ||||||
| chr7:87754312
|
G | A | 1 | a0001c0001t0034g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.629+12733G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754312 | ||||||
| chr7:87754352
|
A | C | 7 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0052g0038others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.629+12773A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754352 | ||||||
| chr7:87754416
|
G | T | 1 | a0001c0001t0009g0115 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.629+12837G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754416 | ||||||
| chr7:87754487
|
A | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+12908A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754487 | ||||||
| chr7:87754599
|
A | C | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.629+13020A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754599 | ||||||
| chr7:87754854
|
T | G | 1 | a0001c0001t0003g0046 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.629+13275T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754854 | ||||||
| chr7:87754857
|
C | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+13278C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754857 | ||||||
| chr7:87754905
|
A | C | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.629+13326A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754905 | ||||||
| chr7:87754943
|
C | CA | 26 | a0001c0001t0001g0087a0001c0001t0001g0099a0001c0001t0001g0106others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.629+13382dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87754943 | |||||
| chr7:87754943
|
CA | C | 14 | a0001c0001t0003g0046a0001c0001t0004g0019a0001c0001t0007g0021others(11): Show | 14 | HG00639.hp1 HG01169.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.629+13382delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87754943 | |||||
| chr7:87754996
|
C | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+13417C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87754996 | ||||||
| chr7:87755027
|
C | CT | 39 | a0001c0001t0001g0054a0001c0001t0002g0027a0001c0001t0002g0137others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.629+13461dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87755027 | |||||
| chr7:87755116
|
G | A | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629+13537G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87755116 | ||||||
| chr7:87755148
|
G | A | 1 | a0001c0001t0031g0125 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.629+13569G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87755148 | ||||||
| chr7:87755295
|
A | G | 4 | a0001c0001t0003g0088a0001c0001t0006g0066a0001c0001t0006g0067others(1): Show | 4 | HG02040.hp2 HG02129.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.629+13716A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87755295 | ||||||
| chr7:87755851
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0009g0132 | 2 | HG00423.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.629+14272G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87755851 | ||||||
| chr7:87756051
|
C | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.629+14472C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87756051 | ||||||
| chr7:87756279
|
C | T | 1 | a0001c0001t0010g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.630-14302C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87756279 | ||||||
| chr7:87756627
|
C | T | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-13954C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87756627 | ||||||
| chr7:87756770
|
G | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.630-13811G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87756770 | ||||||
| chr7:87756796
|
T | C | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.630-13785T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87756796 | ||||||
| chr7:87757153
|
C | T | 2 | a0001c0001t0022g0180a0001c0001t0029g0178 | 2 | NA18974.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.630-13428C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87757153 | ||||||
| chr7:87757288
|
A | T | 63 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(60): Show | 63 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.630-13293A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87757288 | ||||||
| chr7:87757353
|
T | G | 55 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(52): Show | 55 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.630-13228T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87757353 | ||||||
| chr7:87757678
|
G | A | 1 | a0001c0001t0007g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.630-12903G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87757678 | ||||||
| chr7:87757802
|
A | C | 1 | a0001c0001t0020g0036 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.630-12779A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87757802 | ||||||
| chr7:87758024
|
A | C | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.630-12557A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87758024 | ||||||
| chr7:87758082
|
G | T | 14 | a0001c0001t0016g0103a0001c0001t0016g0126a0001c0001t0016g0129others(11): Show | 14 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.630-12499G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87758082 | ||||||
| chr7:87758358
|
C | T | 14 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(11): Show | 14 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.630-12223C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87758358 | ||||||
| chr7:87758803
|
T | C | 1 | a0001c0001t0082g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.630-11778T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87758803 | ||||||
| chr7:87759233
|
A | C | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.630-11348A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759233 | ||||||
| chr7:87759236
|
A | G | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.630-11345A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759236 | ||||||
| chr7:87759325
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.630-11256C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759325 | ||||||
| chr7:87759443
|
A | G | 7 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.630-11138A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759443 | ||||||
| chr7:87759466
|
C | A | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.630-11115C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759466 | ||||||
| chr7:87759605
|
T | G | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.630-10976T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759605 | ||||||
| chr7:87759658
|
T | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.630-10923T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759658 | ||||||
| chr7:87759735
|
C | CTACA | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-10846_630-1084 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759735 | ||||||
| chr7:87759736
|
A | G | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-10845A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87759736 | ||||||
| chr7:87759793
|
C | CA | 13 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(10): Show | 13 | HG00423.hp1 HG02559.hp1 HG03471.hp1 others(10): Show |
intron_variant | MODIFIER | c.630-10774dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87759793 | |||||
| chr7:87760069
|
G | T | 1 | a0001c0001t0005g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.630-10512G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87760069 | ||||||
| chr7:87760069
|
GT | G | 61 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(58): Show | 61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.630-10500delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87760069 | |||||
| chr7:87760135
|
C | T | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.630-10446C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87760135 | ||||||
| chr7:87760866
|
A | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0072 | 2 | HG01192.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.630-9715A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87760866 | ||||||
| chr7:87761014
|
A | G | 63 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(60): Show | 63 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.630-9567A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87761014 | ||||||
| chr7:87761148
|
G | A | 61 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(58): Show | 61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.630-9433G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87761148 | ||||||
| chr7:87761506
|
G | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.630-9075G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87761506 | ||||||
| chr7:87761593
|
A | G | 39 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.630-8988A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87761593 | ||||||
| chr7:87761845
|
G | C | 16 | a0001c0001t0001g0087a0001c0001t0001g0099a0001c0001t0005g0096others(13): Show | 16 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(13): Show |
intron_variant | MODIFIER | c.630-8736G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87761845 | ||||||
| chr7:87761990
|
G | T | 1 | a0001c0001t0003g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.630-8591G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87761990 | ||||||
| chr7:87762300
|
T | C | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-8281T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762300 | ||||||
| chr7:87762330
|
G | A | 1 | a0001c0001t0033g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.630-8251G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762330 | ||||||
| chr7:87762418
|
A | G | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.630-8163A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762418 | ||||||
| chr7:87762445
|
A | G | 154 | a0001c0001t0001g0055a0001c0001t0001g0068a0001c0001t0001g0087others(151): Show | 154 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.630-8136A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762445 | ||||||
| chr7:87762583
|
T | C | 4 | a0001c0001t0003g0088a0001c0001t0006g0066a0001c0001t0006g0067others(1): Show | 4 | HG02040.hp2 HG02129.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.630-7998T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762583 | ||||||
| chr7:87762693
|
G | A | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.630-7888G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762693 | ||||||
| chr7:87762728
|
A | T | 1 | a0001c0001t0026g0083 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.630-7853A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762728 | ||||||
| chr7:87762878
|
TA | T | 61 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(58): Show | 61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.630-7694delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87762878 | |||||
| chr7:87762894
|
C | T | 14 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0202others(11): Show | 14 | HG01358.hp1 HG01496.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.630-7687C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762894 | ||||||
| chr7:87762896
|
G | A | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.630-7685G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87762896 | ||||||
| chr7:87762979
|
TACTTATC others(5): Show |
T | 39 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.630-7597_630-7586d others(14): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87762979 | |||||
| chr7:87763203
|
T | C | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.630-7378T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87763203 | ||||||
| chr7:87763627
|
A | G | 11 | a0001c0001t0003g0128a0001c0001t0004g0082a0001c0001t0004g0101others(8): Show | 11 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.630-6954A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87763627 | ||||||
| chr7:87763821
|
C | A | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-6760C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87763821 | ||||||
| chr7:87764203
|
A | G | 3 | a0001c0001t0024g0003a0001c0001t0025g0004a0001c0001t0037g0002 | 3 | HG00639.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.630-6378A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87764203 | ||||||
| chr7:87764355
|
T | G | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.630-6226T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87764355 | ||||||
| chr7:87764434
|
G | C | 2 | a0001c0001t0022g0180a0001c0001t0029g0178 | 2 | NA18974.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.630-6147G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87764434 | ||||||
| chr7:87764447
|
A | G | 5 | a0001c0001t0003g0128a0001c0001t0004g0101a0001c0001t0005g0114others(2): Show | 5 | HG00438.hp1 HG01952.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.630-6134A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87764447 | ||||||
| chr7:87764459
|
G | C | 200 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(197): Show | 200 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.630-6122G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87764459 | ||||||
| chr7:87765019
|
C | T | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.630-5562C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765019 | ||||||
| chr7:87765037
|
G | C | 54 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(51): Show | 54 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.630-5544G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765037 | ||||||
| chr7:87765230
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.630-5351C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765230 | ||||||
| chr7:87765274
|
AT | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.630-5298delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 87765274 | |||||
| chr7:87765337
|
C | G | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.630-5244C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765337 | ||||||
| chr7:87765435
|
T | G | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.630-5146T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765435 | ||||||
| chr7:87765451
|
C | A | 2 | a0001c0001t0016g0129a0001c0001t0073g0098 | 2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.630-5130C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765451 | ||||||
| chr7:87765890
|
A | G | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-4691A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765890 | ||||||
| chr7:87765926
|
T | A | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.630-4655T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87765926 | ||||||
| chr7:87766086
|
G | C | 15 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(12): Show | 15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.630-4495G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766086 | ||||||
| chr7:87766206
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.630-4375G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766206 | ||||||
| chr7:87766439
|
C | T | 1 | a0001c0001t0005g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.630-4142C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766439 | ||||||
| chr7:87766710
|
T | C | 2 | a0001c0001t0013g0171a0001c0001t0041g0183 | 2 | NA18977.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.630-3871T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766710 | ||||||
| chr7:87766871
|
A | C | 39 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.630-3710A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766871 | ||||||
| chr7:87766877
|
G | A | 1 | a0001c0001t0008g0191 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.630-3704G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766877 | ||||||
| chr7:87766936
|
A | T | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.630-3645A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87766936 | ||||||
| chr7:87767025
|
A | T | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.630-3556A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767025 | ||||||
| chr7:87767086
|
G | A | 2 | a0001c0001t0003g0095a0001c0001t0004g0089 | 2 | HG00741.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.630-3495G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767086 | ||||||
| chr7:87767130
|
G | A | 75 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(72): Show | 75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.630-3451G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767130 | ||||||
| chr7:87767296
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.630-3285A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767296 | ||||||
| chr7:87767302
|
C | T | 1 | a0001c0001t0004g0101 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.630-3279C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767302 | ||||||
| chr7:87767730
|
C | T | 1 | a0001c0001t0082g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.630-2851C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767730 | ||||||
| chr7:87767816
|
G | A | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.630-2765G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87767816 | ||||||
| chr7:87768029
|
T | C | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.630-2552T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87768029 | ||||||
| chr7:87768284
|
G | C | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.630-2297G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87768284 | ||||||
| chr7:87768472
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.630-2109G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87768472 | ||||||
| chr7:87768540
|
C | T | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.630-2041C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87768540 | ||||||
| chr7:87768704
|
C | T | 4 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0006g0104others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.630-1877C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87768704 | ||||||
| chr7:87768862
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.630-1719G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87768862 | ||||||
| chr7:87769026
|
G | A | 1 | a0001c0001t0010g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.630-1555G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769026 | ||||||
| chr7:87769157
|
C | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.630-1424C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769157 | ||||||
| chr7:87769210
|
C | T | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.630-1371C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769210 | ||||||
| chr7:87769211
|
A | G | 2 | a0001c0001t0002g0162a0001c0001t0002g0176 | 2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.630-1370A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769211 | ||||||
| chr7:87769330
|
C | A | 1 | a0001c0001t0019g0024 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.630-1251C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769330 | ||||||
| chr7:87769386
|
G | A | 1 | a0001c0001t0007g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.630-1195G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769386 | ||||||
| chr7:87769601
|
T | C | 1 | a0001c0001t0050g0168 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.630-980T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769601 | ||||||
| chr7:87769640
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.630-941T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769640 | ||||||
| chr7:87769826
|
C | T | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.630-755C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769826 | ||||||
| chr7:87769942
|
T | C | 1 | a0001c0001t0003g0128 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.630-639T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87769942 | ||||||
| chr7:87770038
|
C | G | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.630-543C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87770038 | ||||||
| chr7:87770081
|
C | T | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.630-500C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87770081 | ||||||
| chr7:87770121
|
A | T | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.630-460A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87770121 | ||||||
| chr7:87770318
|
G | C | 1 | a0001c0001t0074g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.630-263G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87770318 | ||||||
| chr7:87770455
|
A | G | 3 | a0002c0002t0002g0026a0002c0002t0002g0031a0002c0002t0017g0140 | 3 | NA18973.hp2 NA18979.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.630-126A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87770455 | ||||||
| chr7:87770572
|
T | C | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.630-9T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 6/10 | chr7 | 87770572 | ||||||
| chr7:87771286
|
C | G | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.798+537C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87771286 | ||||||
| chr7:87771295
|
T | C | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.798+546T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87771295 | ||||||
| chr7:87771339
|
T | A | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.798+590T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87771339 | ||||||
| chr7:87771782
|
A | G | 1 | a0001c0001t0058g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.798+1033A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87771782 | ||||||
| chr7:87772460
|
G | A | 1 | a0001c0001t0049g0201 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.798+1711G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87772460 | ||||||
| chr7:87772762
|
A | G | 3 | a0001c0001t0015g0020a0001c0001t0015g0092a0001c0001t0015g0094 | 3 | NA18906.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.798+2013A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87772762 | ||||||
| chr7:87772870
|
G | A | 2 | a0001c0001t0061g0185a0001c0001t0064g0184 | 2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.798+2121G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87772870 | ||||||
| chr7:87772995
|
T | TAAGACTA others(321): Show |
2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.798+2260_798+2261i others(330): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87772995 | |||||
| chr7:87773031
|
A | T | 1 | a0001c0001t0001g0061 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.798+2282A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773031 | ||||||
| chr7:87773051
|
T | C | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.798+2302T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773051 | ||||||
| chr7:87773180
|
G | A | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.798+2431G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773180 | ||||||
| chr7:87773220
|
A | G | 153 | a0001c0001t0001g0068a0001c0001t0001g0087a0001c0001t0001g0099others(150): Show | 153 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.798+2471A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773220 | ||||||
| chr7:87773317
|
C | T | 1 | a0001c0001t0026g0083 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.798+2568C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773317 | ||||||
| chr7:87773322
|
C | CA | 8 | a0001c0001t0002g0202a0001c0001t0006g0104a0001c0001t0007g0116others(5): Show | 8 | HG00323.hp1 HG00735.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.798+2594dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773322 | |||||
| chr7:87773322
|
CA | C | 23 | a0001c0001t0005g0117a0001c0001t0008g0190a0001c0001t0008g0191others(20): Show | 23 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.798+2594delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773322 | |||||
| chr7:87773526
|
G | A | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.798+2777G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773526 | ||||||
| chr7:87773630
|
TGTTTG | T | 6 | a0001c0001t0010g0007a0001c0001t0010g0010a0001c0001t0043g0011others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+2887_798+2891d others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773630 | |||||
| chr7:87773636
|
G | T | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.798+2887G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773636 | ||||||
| chr7:87773645
|
G | T | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.798+2896G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773645 | ||||||
| chr7:87773646
|
T | G | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.798+2897T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773646 | ||||||
| chr7:87773648
|
T | C | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.798+2899T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773648 | ||||||
| chr7:87773658
|
C | CTTGTT | 89 | a0001c0001t0001g0068a0001c0001t0001g0087a0001c0001t0002g0027others(86): Show | 89 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.798+2943_798+2947d others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773658 | |||||
| chr7:87773658
|
C | CTTGTTTT others(3): Show |
31 | a0001c0001t0002g0165a0001c0001t0003g0130a0001c0001t0004g0082others(28): Show | 31 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.798+2938_798+2947d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773658 | |||||
| chr7:87773658
|
C | T | 5 | a0001c0001t0010g0008a0001c0001t0010g0009a0001c0001t0060g0015others(2): Show | 5 | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.798+2909C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773658 | ||||||
| chr7:87773658
|
CTTGTT | C | 15 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(12): Show | 15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.798+2943_798+2947d others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773658 | |||||
| chr7:87773658
|
CTTGTTTT others(3): Show |
C | 4 | a0001c0001t0031g0076a0001c0001t0034g0077a0001c0001t0034g0079others(1): Show | 4 | HG00639.hp1 HG02559.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+2938_798+2947d others(12): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87773658 | |||||
| chr7:87773768
|
C | T | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.798+3019C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773768 | ||||||
| chr7:87773849
|
T | C | 3 | a0001c0001t0004g0082a0001c0001t0004g0124a0001c0001t0005g0127 | 3 | NA18977.hp1 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.798+3100T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773849 | ||||||
| chr7:87773876
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.798+3127C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773876 | ||||||
| chr7:87773877
|
G | A | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.798+3128G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87773877 | ||||||
| chr7:87774029
|
A | G | 1 | a0001c0001t0010g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.798+3280A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87774029 | ||||||
| chr7:87774104
|
T | A | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.798+3355T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87774104 | ||||||
| chr7:87774329
|
T | A | 1 | a0001c0001t0003g0057 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.799-3469T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87774329 | ||||||
| chr7:87774418
|
A | G | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.799-3380A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87774418 | ||||||
| chr7:87774426
|
C | G | 1 | a0001c0001t0079g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.799-3372C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87774426 | ||||||
| chr7:87775309
|
A | G | 1 | a0001c0001t0028g0040 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.799-2489A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775309 | ||||||
| chr7:87775360
|
A | G | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.799-2438A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775360 | ||||||
| chr7:87775516
|
A | G | 2 | a0001c0001t0004g0111a0001c0001t0004g0112 | 2 | HG00738.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.799-2282A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775516 | ||||||
| chr7:87775635
|
T | C | 1 | a0001c0001t0077g0169 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.799-2163T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775635 | ||||||
| chr7:87775761
|
C | T | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.799-2037C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775761 | ||||||
| chr7:87775810
|
T | C | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.799-1988T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775810 | ||||||
| chr7:87775905
|
G | T | 1 | a0001c0001t0053g0025 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.799-1893G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87775905 | ||||||
| chr7:87776035
|
A | C | 75 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(72): Show | 75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.799-1763A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776035 | ||||||
| chr7:87776075
|
A | G | 1 | a0001c0001t0017g0173 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.799-1723A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776075 | ||||||
| chr7:87776147
|
A | T | 1 | a0001c0003t0001g0022 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.799-1651A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776147 | ||||||
| chr7:87776325
|
A | G | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.799-1473A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776325 | ||||||
| chr7:87776574
|
G | T | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.799-1224G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776574 | ||||||
| chr7:87776717
|
A | G | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.799-1081A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776717 | ||||||
| chr7:87776772
|
A | G | 1 | a0001c0001t0007g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.799-1026A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776772 | ||||||
| chr7:87776859
|
T | C | 1 | a0001c0001t0055g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.799-939T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87776859 | ||||||
| chr7:87777061
|
A | G | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.799-737A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87777061 | ||||||
| chr7:87777336
|
G | A | 1 | a0001c0001t0009g0136 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.799-462G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87777336 | ||||||
| chr7:87777399
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.799-399C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87777399 | ||||||
| chr7:87777400
|
TCTCA | T | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.799-395_799-392del others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 87777400 | |||||
| chr7:87777582
|
T | C | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.799-216T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 7/10 | chr7 | 87777582 | ||||||
| chr7:87778056
|
T | C | 4 | a0001c0001t0031g0076a0001c0001t0034g0077a0001c0001t0034g0079others(1): Show | 4 | HG00639.hp1 HG02559.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.956+101T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778056 | ||||||
| chr7:87778115
|
G | A | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.956+160G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778115 | ||||||
| chr7:87778205
|
G | C | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.956+250G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778205 | ||||||
| chr7:87778284
|
A | G | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.956+329A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778284 | ||||||
| chr7:87778390
|
C | T | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.956+435C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778390 | ||||||
| chr7:87778440
|
C | CA | 81 | a0001c0001t0001g0051a0001c0001t0002g0027a0001c0001t0002g0137others(78): Show | 81 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(78): Show |
intron_variant | MODIFIER | c.956+501dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87778440 | |||||
| chr7:87778465
|
A | G | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.956+510A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778465 | ||||||
| chr7:87778694
|
A | G | 6 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.956+739A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778694 | ||||||
| chr7:87778875
|
AT | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.956+921delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778875 | ||||||
| chr7:87778928
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0105 | 2 | NA18952.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.956+973C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778928 | ||||||
| chr7:87778949
|
A | G | 8 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.956+994A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87778949 | ||||||
| chr7:87779023
|
C | T | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.956+1068C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87779023 | ||||||
| chr7:87779030
|
A | G | 41 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(38): Show | 41 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.956+1075A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87779030 | ||||||
| chr7:87779145
|
T | G | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.956+1190T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87779145 | ||||||
| chr7:87779167
|
G | A | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.956+1212G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87779167 | ||||||
| chr7:87779875
|
C | T | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.956+1920C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87779875 | ||||||
| chr7:87780142
|
T | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0105 | 2 | NA18952.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.956+2187T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87780142 | ||||||
| chr7:87780209
|
T | A | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.956+2254T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87780209 | ||||||
| chr7:87780428
|
C | T | 42 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(39): Show | 42 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.956+2473C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87780428 | ||||||
| chr7:87780449
|
GTTAT | G | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.956+2497_956+2500d others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87780449 | |||||
| chr7:87780775
|
AAGATAAG others(17): Show |
A | 1 | a0001c0001t0080g0100 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.956+2823_956+2846d others(26): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87780775 | |||||
| chr7:87781019
|
T | C | 1 | a0001c0001t0004g0102 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.956+3064T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87781019 | ||||||
| chr7:87781292
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0072 | 2 | HG01192.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.956+3337G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87781292 | ||||||
| chr7:87781304
|
T | TAGAAGTA others(313): Show |
16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.956+3368_956+3369i others(322): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87781304 | |||||
| chr7:87781421
|
C | A | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.956+3466C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87781421 | ||||||
| chr7:87781579
|
T | A | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.956+3624T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87781579 | ||||||
| chr7:87781676
|
G | A | 2 | a0001c0001t0011g0194a0001c0001t0011g0198 | 2 | HG00280.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.956+3721G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87781676 | ||||||
| chr7:87782214
|
C | T | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.956+4259C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87782214 | ||||||
| chr7:87782267
|
C | G | 2 | a0001c0001t0003g0095a0001c0001t0004g0089 | 2 | HG00741.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.956+4312C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87782267 | ||||||
| chr7:87782534
|
T | C | 1 | a0001c0001t0046g0109 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.956+4579T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87782534 | ||||||
| chr7:87783007
|
T | A | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.956+5052T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783007 | ||||||
| chr7:87783053
|
G | A | 1 | a0001c0001t0020g0036 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.956+5098G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783053 | ||||||
| chr7:87783100
|
C | G | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.956+5145C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783100 | ||||||
| chr7:87783173
|
T | G | 88 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(85): Show | 88 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(85): Show |
intron_variant | MODIFIER | c.956+5218T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783173 | ||||||
| chr7:87783197
|
A | G | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.956+5242A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783197 | ||||||
| chr7:87783238
|
A | G | 1 | a0001c0001t0015g0092 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.956+5283A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783238 | ||||||
| chr7:87783242
|
T | C | 1 | a0001c0001t0076g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.956+5287T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783242 | ||||||
| chr7:87783337
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.956+5382T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783337 | ||||||
| chr7:87783395
|
C | T | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.956+5440C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783395 | ||||||
| chr7:87783500
|
C | T | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.956+5545C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783500 | ||||||
| chr7:87783595
|
C | T | 1 | a0001c0001t0005g0127 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.956+5640C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783595 | ||||||
| chr7:87783647
|
A | G | 1 | a0001c0001t0058g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.956+5692A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783647 | ||||||
| chr7:87783764
|
G | A | 78 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(75): Show | 78 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.956+5809G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783764 | ||||||
| chr7:87783956
|
C | A | 78 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(75): Show | 78 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.956+6001C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87783956 | ||||||
| chr7:87784593
|
T | C | 14 | a0001c0001t0016g0103a0001c0001t0016g0126a0001c0001t0016g0129others(11): Show | 14 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.956+6638T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87784593 | ||||||
| chr7:87784795
|
G | A | 1 | a0001c0001t0040g0161 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.956+6840G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87784795 | ||||||
| chr7:87784811
|
T | C | 1 | a0001c0001t0004g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.956+6856T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87784811 | ||||||
| chr7:87785071
|
G | A | 1 | a0001c0001t0074g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.956+7116G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785071 | ||||||
| chr7:87785130
|
G | A | 41 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(38): Show | 41 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.956+7175G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785130 | ||||||
| chr7:87785309
|
G | C | 1 | a0001c0001t0078g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.956+7354G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785309 | ||||||
| chr7:87785709
|
G | T | 1 | a0001c0001t0010g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.956+7754G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785709 | ||||||
| chr7:87785777
|
C | T | 6 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0165others(3): Show | 6 | HG02559.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.956+7822C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785777 | ||||||
| chr7:87785887
|
T | C | 1 | a0001c0001t0037g0002 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.956+7932T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785887 | ||||||
| chr7:87785922
|
G | A | 2 | a0001c0001t0004g0075a0001c0001t0067g0074 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.956+7967G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87785922 | ||||||
| chr7:87786407
|
A | T | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.956+8452A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87786407 | ||||||
| chr7:87786454
|
A | G | 7 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0052g0038others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.956+8499A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87786454 | ||||||
| chr7:87786668
|
A | T | 4 | a0001c0001t0038g0182a0001c0001t0040g0161a0001c0001t0050g0168others(1): Show | 4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.956+8713A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87786668 | ||||||
| chr7:87786835
|
G | A | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.956+8880G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87786835 | ||||||
| chr7:87786985
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.956+9030T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87786985 | ||||||
| chr7:87787010
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.956+9055G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87787010 | ||||||
| chr7:87787022
|
T | C | 1 | a0001c0001t0055g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.956+9067T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87787022 | ||||||
| chr7:87787066
|
G | C | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.956+9111G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87787066 | ||||||
| chr7:87787524
|
C | T | 154 | a0001c0001t0001g0068a0001c0001t0001g0087a0001c0001t0001g0099others(151): Show | 154 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.956+9569C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87787524 | ||||||
| chr7:87787560
|
T | C | 1 | a0001c0001t0009g0115 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.956+9605T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87787560 | ||||||
| chr7:87787891
|
T | C | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.956+9936T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87787891 | ||||||
| chr7:87788058
|
A | G | 1 | a0001c0001t0055g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.956+10103A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788058 | ||||||
| chr7:87788060
|
T | C | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.956+10105T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788060 | ||||||
| chr7:87788076
|
A | G | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.956+10121A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788076 | ||||||
| chr7:87788152
|
G | A | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.956+10197G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788152 | ||||||
| chr7:87788378
|
A | C | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.956+10423A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788378 | ||||||
| chr7:87788627
|
C | T | 2 | a0001c0001t0069g0016a0001c0001t0070g0017 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.956+10672C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788627 | ||||||
| chr7:87788647
|
A | T | 21 | a0001c0001t0015g0020a0001c0001t0015g0092a0001c0001t0015g0094others(18): Show | 21 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.956+10692A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788647 | ||||||
| chr7:87788663
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0009g0132 | 2 | HG00423.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.956+10708A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788663 | ||||||
| chr7:87788703
|
C | CT | 15 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(12): Show | 15 | HG00280.hp2 HG01071.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.956+10765dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87788703 | |||||
| chr7:87788703
|
CT | C | 35 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0068others(32): Show | 35 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.956+10765delT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87788703 | |||||
| chr7:87788703
|
CTT | C | 24 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(21): Show | 24 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.956+10764_956+1076 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87788703 | |||||
| chr7:87788703
|
CTTT | C | 24 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0202others(21): Show | 24 | HG01123.hp1 HG01192.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.956+10763_956+1076 others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87788703 | |||||
| chr7:87788832
|
A | C | 5 | a0001c0001t0047g0012a0001c0001t0058g0018a0001c0001t0060g0015others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.956+10877A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87788832 | ||||||
| chr7:87789527
|
C | T | 4 | a0001c0001t0010g0008a0001c0001t0010g0009a0001c0001t0010g0010others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.956+11572C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87789527 | ||||||
| chr7:87789546
|
T | C | 154 | a0001c0001t0001g0068a0001c0001t0001g0087a0001c0001t0001g0099others(151): Show | 154 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.956+11591T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87789546 | ||||||
| chr7:87789572
|
T | A | 8 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.956+11617T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87789572 | ||||||
| chr7:87790032
|
A | G | 40 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(37): Show | 40 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.956+12077A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87790032 | ||||||
| chr7:87790541
|
G | T | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.956+12586G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87790541 | ||||||
| chr7:87790652
|
AAG | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.956+12700_956+1270 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87790652 | |||||
| chr7:87790775
|
T | C | 2 | a0001c0001t0016g0129a0001c0001t0073g0098 | 2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.956+12820T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87790775 | ||||||
| chr7:87791387
|
A | G | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.956+13432A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87791387 | ||||||
| chr7:87791664
|
A | G | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.956+13709A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87791664 | ||||||
| chr7:87791668
|
C | A | 2 | a0001c0001t0069g0016a0001c0001t0070g0017 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.956+13713C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87791668 | ||||||
| chr7:87791681
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.956+13726C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87791681 | ||||||
| chr7:87792350
|
A | G | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.956+14395A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87792350 | ||||||
| chr7:87792635
|
G | T | 1 | a0001c0001t0056g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.956+14680G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87792635 | ||||||
| chr7:87793003
|
A | G | 2 | a0001c0001t0012g0150a0001c0001t0012g0151 | 2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.957-14370A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87793003 | ||||||
| chr7:87793429
|
G | A | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.957-13944G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87793429 | ||||||
| chr7:87793509
|
G | A | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.957-13864G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87793509 | ||||||
| chr7:87793820
|
G | A | 2 | a0001c0001t0016g0103a0001c0001t0016g0126 | 2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.957-13553G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87793820 | ||||||
| chr7:87794309
|
C | T | 1 | a0001c0001t0006g0050 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.957-13064C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87794309 | ||||||
| chr7:87794625
|
CA | C | 82 | a0001c0001t0001g0058a0001c0001t0002g0027a0001c0001t0002g0137others(79): Show | 82 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(79): Show |
intron_variant | MODIFIER | c.957-12734delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87794625 | |||||
| chr7:87794633
|
A | T | 1 | a0001c0001t0001g0045 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.957-12740A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87794633 | ||||||
| chr7:87794652
|
A | G | 1 | a0001c0001t0082g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.957-12721A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87794652 | ||||||
| chr7:87795014
|
G | T | 1 | a0001c0001t0003g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.957-12359G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87795014 | ||||||
| chr7:87795231
|
T | A | 1 | a0001c0001t0001g0084 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.957-12142T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87795231 | ||||||
| chr7:87795413
|
C | A | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.957-11960C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87795413 | ||||||
| chr7:87795706
|
C | T | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.957-11667C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87795706 | ||||||
| chr7:87795723
|
C | CA | 45 | a0001c0001t0001g0061a0001c0001t0004g0075a0001c0001t0007g0090others(42): Show | 45 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.957-11633dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87795723 | |||||
| chr7:87795723
|
C | CAAA | 35 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0163others(32): Show | 35 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.957-11635_957-1163 others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87795723 | |||||
| chr7:87795723
|
CA | C | 5 | a0001c0001t0006g0067a0001c0001t0007g0133a0001c0001t0043g0011others(2): Show | 5 | HG02040.hp2 HG02055.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.957-11633delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87795723 | |||||
| chr7:87795757
|
C | T | 1 | a0001c0001t0011g0194 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.957-11616C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87795757 | ||||||
| chr7:87795847
|
G | T | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.957-11526G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87795847 | ||||||
| chr7:87796051
|
A | G | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.957-11322A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87796051 | ||||||
| chr7:87796183
|
G | A | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.957-11190G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87796183 | ||||||
| chr7:87796234
|
T | C | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.957-11139T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87796234 | ||||||
| chr7:87796347
|
G | A | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.957-11026G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87796347 | ||||||
| chr7:87796650
|
T | C | 7 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.957-10723T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87796650 | ||||||
| chr7:87797538
|
C | T | 61 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(58): Show | 61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.957-9835C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87797538 | ||||||
| chr7:87797730
|
T | C | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.957-9643T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87797730 | ||||||
| chr7:87798070
|
T | C | 1 | a0001c0001t0012g0152 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.957-9303T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87798070 | ||||||
| chr7:87798376
|
A | G | 75 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(72): Show | 75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.957-8997A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87798376 | ||||||
| chr7:87798844
|
T | C | 2 | a0001c0001t0004g0019a0001c0001t0024g0003 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.957-8529T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87798844 | ||||||
| chr7:87798963
|
T | C | 6 | a0001c0001t0010g0008a0001c0001t0010g0009a0001c0001t0010g0010others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-8410T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87798963 | ||||||
| chr7:87799111
|
T | A | 1 | a0001c0001t0055g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.957-8262T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799111 | ||||||
| chr7:87799145
|
T | C | 1 | a0001c0001t0003g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.957-8228T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799145 | ||||||
| chr7:87799348
|
C | T | 1 | a0001c0001t0074g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.957-8025C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799348 | ||||||
| chr7:87799398
|
C | G | 2 | a0001c0001t0004g0111a0001c0001t0004g0112 | 2 | HG00738.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.957-7975C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799398 | ||||||
| chr7:87799616
|
C | T | 1 | a0001c0001t0010g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.957-7757C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799616 | ||||||
| chr7:87799817
|
C | T | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.957-7556C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799817 | ||||||
| chr7:87799845
|
C | T | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.957-7528C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799845 | ||||||
| chr7:87799872
|
C | T | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.957-7501C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87799872 | ||||||
| chr7:87799885
|
CA | C | 65 | a0001c0001t0001g0056a0001c0001t0001g0068a0001c0001t0002g0027others(62): Show | 65 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.957-7467delA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87799885 | |||||
| chr7:87800121
|
G | C | 1 | a0001c0001t0023g0039 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.957-7252G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87800121 | ||||||
| chr7:87800653
|
C | CT | 15 | a0001c0001t0002g0202a0001c0001t0004g0019a0001c0001t0012g0150others(12): Show | 15 | HG00423.hp1 HG02976.hp1 HG03139.hp1 others(12): Show |
intron_variant | MODIFIER | c.957-6704dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87800653 | |||||
| chr7:87800653
|
C | CTT | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.957-6705_957-6704d others(4): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87800653 | |||||
| chr7:87800735
|
C | T | 1 | a0001c0001t0017g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.957-6638C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87800735 | ||||||
| chr7:87801254
|
C | T | 1 | a0001c0001t0005g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.957-6119C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87801254 | ||||||
| chr7:87801354
|
G | A | 153 | a0001c0001t0001g0068a0001c0001t0001g0087a0001c0001t0001g0099others(150): Show | 153 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.957-6019G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87801354 | ||||||
| chr7:87801401
|
A | G | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.957-5972A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87801401 | ||||||
| chr7:87801656
|
C | A | 2 | a0001c0001t0004g0075a0001c0001t0067g0074 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.957-5717C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87801656 | ||||||
| chr7:87801670
|
G | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.957-5703G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87801670 | ||||||
| chr7:87801838
|
A | C | 1 | a0001c0001t0058g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.957-5535A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87801838 | ||||||
| chr7:87802247
|
G | T | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-5126G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802247 | ||||||
| chr7:87802321
|
A | G | 2 | a0001c0001t0025g0053a0001c0001t0028g0069 | 2 | HG01099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.957-5052A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802321 | ||||||
| chr7:87802373
|
C | T | 15 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(12): Show | 15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.957-5000C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802373 | ||||||
| chr7:87802493
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0107 | 2 | HG01167.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.957-4880T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802493 | ||||||
| chr7:87802543
|
A | G | 2 | a0001c0001t0013g0171a0001c0001t0041g0183 | 2 | NA18977.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.957-4830A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802543 | ||||||
| chr7:87802762
|
T | C | 1 | a0001c0001t0007g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.957-4611T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802762 | ||||||
| chr7:87802965
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.957-4408A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87802965 | ||||||
| chr7:87803324
|
G | A | 1 | a0001c0001t0005g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.957-4049G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803324 | ||||||
| chr7:87803383
|
C | A | 4 | a0001c0001t0010g0008a0001c0001t0010g0009a0001c0001t0010g0010others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-3990C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803383 | ||||||
| chr7:87803444
|
C | T | 3 | a0001c0001t0047g0012a0001c0001t0059g0014a0001c0001t0066g0013 | 3 | HG02572.hp2 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.957-3929C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803444 | ||||||
| chr7:87803459
|
A | C | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.957-3914A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803459 | ||||||
| chr7:87803512
|
A | G | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.957-3861A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803512 | ||||||
| chr7:87803623
|
C | G | 2 | a0001c0001t0010g0008a0001c0001t0010g0009 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.957-3750C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803623 | ||||||
| chr7:87803692
|
A | G | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.957-3681A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803692 | ||||||
| chr7:87803833
|
C | A | 1 | a0001c0001t0076g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.957-3540C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803833 | ||||||
| chr7:87803849
|
G | A | 1 | a0001c0001t0015g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.957-3524G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803849 | ||||||
| chr7:87803870
|
A | G | 3 | a0001c0001t0004g0082a0001c0001t0004g0124a0001c0001t0005g0127 | 3 | NA18977.hp1 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.957-3503A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87803870 | ||||||
| chr7:87804143
|
G | C | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.957-3230G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87804143 | ||||||
| chr7:87804569
|
A | G | 6 | a0001c0001t0010g0008a0001c0001t0010g0009a0001c0001t0010g0010others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-2804A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87804569 | ||||||
| chr7:87805255
|
CAACTT | C | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-2110_957-2106d others(7): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 87805255 | |||||
| chr7:87805284
|
A | G | 2 | a0001c0001t0008g0190a0001c0001t0030g0192 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.957-2089A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87805284 | ||||||
| chr7:87805298
|
T | C | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-2075T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87805298 | ||||||
| chr7:87805468
|
G | A | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.957-1905G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87805468 | ||||||
| chr7:87805944
|
T | C | 2 | a0001c0001t0042g0148a0001c0001t0052g0038 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.957-1429T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87805944 | ||||||
| chr7:87806293
|
G | T | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.957-1080G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87806293 | ||||||
| chr7:87806615
|
T | C | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.957-758T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 8/10 | chr7 | 87806615 | ||||||
| chr7:87807837
|
A | G | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1103+318A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87807837 | ||||||
| chr7:87807867
|
A | G | 3 | a0001c0001t0019g0043a0001c0001t0033g0073a0001c0001t0049g0201 | 3 | HG00438.hp2 HG01978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1103+348A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87807867 | ||||||
| chr7:87807895
|
A | T | 1 | a0001c0001t0016g0126 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1103+376A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87807895 | ||||||
| chr7:87807896
|
T | C | 14 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(11): Show | 14 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1103+377T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87807896 | ||||||
| chr7:87807940
|
A | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1103+421A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87807940 | ||||||
| chr7:87807943
|
T | G | 2 | a0001c0001t0069g0016a0001c0001t0070g0017 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1103+424T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87807943 | ||||||
| chr7:87808454
|
G | C | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1103+935G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87808454 | ||||||
| chr7:87808460
|
C | T | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1103+941C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87808460 | ||||||
| chr7:87808766
|
C | T | 61 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(58): Show | 61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.1103+1247C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87808766 | ||||||
| chr7:87809032
|
C | T | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1103+1513C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87809032 | ||||||
| chr7:87809430
|
T | TA | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1103+1912dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 87809430 | |||||
| chr7:87809832
|
C | T | 1 | a0001c0001t0002g0202 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1103+2313C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87809832 | ||||||
| chr7:87809943
|
G | A | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1103+2424G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87809943 | ||||||
| chr7:87810029
|
CCCTATAA others(34): Show |
C | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1103+2514_1103+255 others(45): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 87810029 | |||||
| chr7:87810060
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1103+2541A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87810060 | ||||||
| chr7:87810368
|
G | A | 2 | a0001c0001t0004g0075a0001c0001t0067g0074 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1103+2849G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87810368 | ||||||
| chr7:87810523
|
C | A | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1103+3004C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87810523 | ||||||
| chr7:87810711
|
G | A | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1103+3192G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87810711 | ||||||
| chr7:87810755
|
G | A | 1 | a0001c0001t0055g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1103+3236G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87810755 | ||||||
| chr7:87810757
|
C | A | 1 | a0001c0001t0036g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1103+3238C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87810757 | ||||||
| chr7:87811068
|
T | C | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1103+3549T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811068 | ||||||
| chr7:87811261
|
T | A | 4 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0063others(1): Show | 4 | HG01496.hp2 HG02280.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1103+3742T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811261 | ||||||
| chr7:87811339
|
A | AT | 89 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(86): Show | 89 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1103+3835dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 87811339 | |||||
| chr7:87811539
|
T | C | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1103+4020T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811539 | ||||||
| chr7:87811548
|
G | A | 3 | a0001c0001t0014g0153a0001c0001t0014g0155a0001c0001t0051g0156 | 3 | NA18988.hp2 NA18990.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1103+4029G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811548 | ||||||
| chr7:87811640
|
G | A | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1103+4121G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811640 | ||||||
| chr7:87811706
|
T | A | 3 | a0001c0001t0004g0019a0001c0001t0024g0003a0001c0001t0037g0002 | 3 | HG00639.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1103+4187T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811706 | ||||||
| chr7:87811775
|
T | G | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1103+4256T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87811775 | ||||||
| chr7:87812446
|
T | C | 1 | a0001c0001t0037g0002 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1104-3695T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87812446 | ||||||
| chr7:87812619
|
G | C | 1 | a0001c0001t0006g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1104-3522G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87812619 | ||||||
| chr7:87812721
|
T | G | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1104-3420T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87812721 | ||||||
| chr7:87812923
|
G | A | 4 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0006g0104others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1104-3218G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87812923 | ||||||
| chr7:87813062
|
G | A | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1104-3079G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813062 | ||||||
| chr7:87813660
|
T | C | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1104-2481T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813660 | ||||||
| chr7:87813849
|
C | T | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1104-2292C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813849 | ||||||
| chr7:87813850
|
A | G | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1104-2291A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813850 | ||||||
| chr7:87813949
|
C | A | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1104-2192C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813949 | ||||||
| chr7:87813961
|
A | G | 3 | a0001c0001t0065g0144a0001c0001t0071g0142a0001c0001t0072g0143 | 3 | HG01069.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1104-2180A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813961 | ||||||
| chr7:87813975
|
C | T | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1104-2166C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813975 | ||||||
| chr7:87813980
|
C | CA | 14 | a0001c0001t0003g0128a0001c0001t0004g0101a0001c0001t0004g0102others(11): Show | 14 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1104-2147dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 87813980 | |||||
| chr7:87813995
|
G | A | 1 | a0001c0001t0005g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1104-2146G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813995 | ||||||
| chr7:87813996
|
A | G | 1 | a0001c0001t0005g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1104-2145A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813996 | ||||||
| chr7:87813997
|
T | A | 1 | a0001c0001t0005g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1104-2144T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87813997 | ||||||
| chr7:87814101
|
C | CT | 20 | a0001c0001t0001g0091a0001c0001t0012g0150a0001c0001t0012g0151others(17): Show | 20 | HG00423.hp1 HG01978.hp1 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.1104-2024dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 87814101 | |||||
| chr7:87814257
|
C | T | 1 | a0001c0001t0010g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1104-1884C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814257 | ||||||
| chr7:87814432
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1104-1709A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814432 | ||||||
| chr7:87814611
|
A | G | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1104-1530A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814611 | ||||||
| chr7:87814626
|
G | T | 1 | a0001c0001t0006g0104 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1104-1515G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814626 | ||||||
| chr7:87814657
|
G | A | 61 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(58): Show | 61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.1104-1484G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814657 | ||||||
| chr7:87814661
|
G | T | 2 | a0001c0001t0018g0172a0001c0001t0018g0174 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1104-1480G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814661 | ||||||
| chr7:87814736
|
G | A | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1104-1405G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814736 | ||||||
| chr7:87814825
|
C | T | 1 | a0001c0001t0033g0073 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1104-1316C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814825 | ||||||
| chr7:87814850
|
T | G | 1 | a0001c0001t0076g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1104-1291T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87814850 | ||||||
| chr7:87815090
|
C | G | 39 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.1104-1051C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87815090 | ||||||
| chr7:87815323
|
A | G | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1104-818A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87815323 | ||||||
| chr7:87815556
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1104-585G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87815556 | ||||||
| chr7:87815570
|
C | G | 2 | a0001c0001t0042g0148a0001c0001t0052g0038 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1104-571C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87815570 | ||||||
| chr7:87815633
|
C | A | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1104-508C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | chr7 | 87815633 | ||||||
| chr7:87815915
|
C | CT | 8 | a0001c0001t0005g0114a0001c0001t0042g0148a0001c0001t0047g0012others(5): Show | 8 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1104-217dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 87815915 | |||||
| chr7:87816312
|
A | G | 7 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0052g0038others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1225+50A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816312 | ||||||
| chr7:87816376
|
T | G | 1 | a0001c0001t0010g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1225+114T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816376 | ||||||
| chr7:87816433
|
G | T | 131 | a0001c0001t0001g0042a0001c0001t0001g0048a0001c0001t0001g0051others(128): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1225+171G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816433 | ||||||
| chr7:87816434
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1225+172G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816434 | ||||||
| chr7:87816438
|
G | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1225+176G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816438 | ||||||
| chr7:87816683
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1225+421G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816683 | ||||||
| chr7:87816735
|
A | T | 1 | a0001c0001t0055g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1225+473A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816735 | ||||||
| chr7:87816757
|
T | C | 1 | a0001c0001t0055g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1225+495T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816757 | ||||||
| chr7:87816959
|
T | C | 1 | a0001c0001t0052g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1225+697T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87816959 | ||||||
| chr7:87817076
|
C | A | 1 | a0001c0001t0001g0084 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1225+814C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87817076 | ||||||
| chr7:87817514
|
T | C | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1225+1252T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87817514 | ||||||
| chr7:87817614
|
C | T | 3 | a0001c0001t0019g0024a0001c0001t0019g0110a0001c0001t0056g0086 | 3 | HG01981.hp2 HG03239.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1225+1352C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87817614 | ||||||
| chr7:87817724
|
C | A | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1225+1462C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87817724 | ||||||
| chr7:87817825
|
G | C | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1225+1563G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87817825 | ||||||
| chr7:87818202
|
T | A | 1 | a0001c0001t0001g0099 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1225+1940T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87818202 | ||||||
| chr7:87818756
|
T | C | 1 | a0001c0001t0005g0085 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1225+2494T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87818756 | ||||||
| chr7:87818809
|
T | G | 3 | a0001c0001t0004g0019a0001c0001t0024g0003a0001c0001t0037g0002 | 3 | HG00639.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1225+2547T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87818809 | ||||||
| chr7:87818998
|
G | A | 1 | a0001c0001t0008g0193 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1225+2736G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87818998 | ||||||
| chr7:87819038
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1225+2776C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87819038 | ||||||
| chr7:87819145
|
C | T | 1 | a0001c0001t0080g0100 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1225+2883C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87819145 | ||||||
| chr7:87819529
|
A | G | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1225+3267A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87819529 | ||||||
| chr7:87819724
|
C | T | 1 | a0001c0001t0026g0083 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1225+3462C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87819724 | ||||||
| chr7:87819961
|
C | T | 3 | a0001c0001t0014g0153a0001c0001t0014g0155a0001c0001t0051g0156 | 3 | NA18988.hp2 NA18990.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1225+3699C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87819961 | ||||||
| chr7:87820134
|
C | T | 7 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1225+3872C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820134 | ||||||
| chr7:87820197
|
A | C | 39 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.1225+3935A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820197 | ||||||
| chr7:87820215
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1225+3953G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820215 | ||||||
| chr7:87820219
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1225+3957T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820219 | ||||||
| chr7:87820266
|
A | G | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.1225+4004A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820266 | ||||||
| chr7:87820491
|
C | A | 1 | a0001c0001t0004g0082 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1225+4229C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820491 | ||||||
| chr7:87820515
|
A | G | 4 | a0001c0001t0019g0024a0001c0001t0060g0015a0001c0001t0069g0016others(1): Show | 4 | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1225+4253A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820515 | ||||||
| chr7:87820521
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1225+4259C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820521 | ||||||
| chr7:87820536
|
T | C | 21 | a0001c0001t0015g0020a0001c0001t0015g0092a0001c0001t0015g0094others(18): Show | 21 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1225+4274T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820536 | ||||||
| chr7:87820774
|
C | A | 1 | a0001c0001t0060g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1225+4512C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820774 | ||||||
| chr7:87820838
|
G | A | 61 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(58): Show | 61 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.1225+4576G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820838 | ||||||
| chr7:87820962
|
C | T | 1 | a0001c0001t0022g0179 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1225+4700C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87820962 | ||||||
| chr7:87821115
|
T | A | 3 | a0001c0001t0004g0019a0001c0001t0024g0003a0001c0001t0037g0002 | 3 | HG00639.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1225+4853T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821115 | ||||||
| chr7:87821170
|
C | T | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1225+4908C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821170 | ||||||
| chr7:87821173
|
A | T | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1225+4911A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821173 | ||||||
| chr7:87821198
|
G | T | 1 | a0001c0001t0007g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1225+4936G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821198 | ||||||
| chr7:87821263
|
G | C | 41 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(38): Show | 41 | HG01074.hp1 HG01081.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.1225+5001G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821263 | ||||||
| chr7:87821423
|
C | T | 39 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.1225+5161C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821423 | ||||||
| chr7:87821492
|
C | T | 1 | a0001c0001t0023g0039 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1225+5230C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821492 | ||||||
| chr7:87821573
|
G | A | 1 | a0001c0001t0082g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1225+5311G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821573 | ||||||
| chr7:87821578
|
G | A | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1225+5316G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821578 | ||||||
| chr7:87821622
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1225+5360G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821622 | ||||||
| chr7:87821735
|
C | T | 1 | a0001c0001t0047g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1225+5473C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821735 | ||||||
| chr7:87821813
|
G | C | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1225+5551G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821813 | ||||||
| chr7:87821870
|
C | G | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1225+5608C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821870 | ||||||
| chr7:87821881
|
A | C | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1225+5619A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821881 | ||||||
| chr7:87821886
|
T | C | 1 | a0001c0001t0026g0146 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1225+5624T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87821886 | ||||||
| chr7:87822041
|
G | C | 1 | a0001c0001t0082g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1225+5779G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822041 | ||||||
| chr7:87822224
|
G | A | 1 | a0001c0001t0075g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225+5962G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822224 | ||||||
| chr7:87822236
|
C | A | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1225+5974C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822236 | ||||||
| chr7:87822321
|
G | A | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1225+6059G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822321 | ||||||
| chr7:87822343
|
G | A | 1 | a0001c0001t0005g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1225+6081G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822343 | ||||||
| chr7:87822441
|
A | G | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1225+6179A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822441 | ||||||
| chr7:87822678
|
C | G | 3 | a0001c0001t0005g0096a0001c0001t0005g0134a0001c0001t0005g0135 | 3 | NA18974.hp2 NA18979.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1225+6416C>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822678 | ||||||
| chr7:87822814
|
C | T | 1 | a0001c0001t0010g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1225+6552C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822814 | ||||||
| chr7:87822859
|
A | C | 2 | a0001c0001t0008g0190a0001c0001t0030g0192 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1225+6597A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822859 | ||||||
| chr7:87822878
|
G | C | 39 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(36): Show | 39 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.1225+6616G>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87822878 | ||||||
| chr7:87823007
|
T | G | 63 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(60): Show | 63 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.1225+6745T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823007 | ||||||
| chr7:87823056
|
A | T | 64 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(61): Show | 64 | HG00280.hp2 HG00438.hp1 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1225+6794A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823056 | ||||||
| chr7:87823070
|
C | T | 1 | a0001c0001t0005g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1225+6808C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823070 | ||||||
| chr7:87823110
|
C | A | 1 | a0001c0001t0078g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1226-6775C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823110 | ||||||
| chr7:87823141
|
G | A | 1 | a0001c0001t0078g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1226-6744G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823141 | ||||||
| chr7:87823264
|
G | A | 3 | a0001c0001t0060g0015a0001c0001t0069g0016a0001c0001t0070g0017 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1226-6621G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823264 | ||||||
| chr7:87823318
|
C | T | 2 | a0001c0001t0059g0014a0001c0001t0066g0013 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1226-6567C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823318 | ||||||
| chr7:87823380
|
TTTAAAA | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1226-6502_1226-649 others(10): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823380 | |||||
| chr7:87823393
|
A | T | 2 | a0001c0001t0001g0044a0001c0001t0007g0116 | 2 | HG00735.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1226-6492A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823393 | ||||||
| chr7:87823412
|
A | AT | 74 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(71): Show | 74 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.1226-6465dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823412 | |||||
| chr7:87823783
|
C | CAT | 8 | a0001c0001t0010g0007a0001c0001t0010g0008a0001c0001t0010g0009others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1226-6094_1226-609 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823783 | |||||
| chr7:87823791
|
T | C | 6 | a0001c0001t0001g0068a0001c0001t0004g0139a0001c0001t0024g0062others(3): Show | 6 | HG01099.hp1 HG01261.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1226-6094T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823791 | ||||||
| chr7:87823791
|
T | TAC | 10 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0084others(7): Show | 10 | HG00558.hp2 HG00621.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1226-6062_1226-606 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823791 | |||||
| chr7:87823791
|
T | TACAC | 2 | a0001c0001t0001g0070a0001c0001t0045g0078 | 2 | HG00639.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1226-6064_1226-606 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823791 | |||||
| chr7:87823791
|
TAC | T | 5 | a0001c0001t0003g0141a0001c0001t0006g0066a0001c0001t0009g0121others(2): Show | 5 | HG02129.hp2 HG03041.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1226-6062_1226-606 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823791 | |||||
| chr7:87823791
|
TACAC | T | 17 | a0001c0001t0001g0091a0001c0001t0002g0166a0001c0001t0005g0117others(14): Show | 17 | HG00423.hp1 HG01346.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1226-6064_1226-606 others(8): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823791 | |||||
| chr7:87823793
|
C | T | 60 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(57): Show | 60 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1226-6092C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823793 | ||||||
| chr7:87823795
|
C | T | 22 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0202others(19): Show | 22 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1226-6090C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823795 | ||||||
| chr7:87823797
|
C | T | 15 | a0001c0001t0002g0166a0001c0001t0012g0150a0001c0001t0012g0151others(12): Show | 15 | HG00423.hp1 HG02559.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1226-6088C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823797 | ||||||
| chr7:87823823
|
C | CAT | 3 | a0001c0001t0003g0088a0001c0001t0005g0080a0001c0001t0006g0131 | 3 | HG02135.hp2 HG03041.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1226-6052_1226-605 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823823 | |||||
| chr7:87823823
|
C | T | 4 | a0001c0001t0006g0066a0001c0001t0006g0067a0001c0001t0069g0016others(1): Show | 4 | HG02040.hp2 HG02129.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1226-6062C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823823 | ||||||
| chr7:87823823
|
CAT | C | 9 | a0001c0001t0004g0082a0001c0001t0004g0101a0001c0001t0004g0102others(6): Show | 9 | HG00558.hp1 HG01952.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1226-6052_1226-605 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87823823 | |||||
| chr7:87823825
|
T | C | 3 | a0001c0001t0003g0128a0001c0001t0007g0090a0001c0001t0047g0012 | 3 | HG00438.hp1 HG02135.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1226-6060T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823825 | ||||||
| chr7:87823827
|
T | C | 11 | a0001c0001t0003g0128a0001c0001t0004g0082a0001c0001t0004g0101others(8): Show | 11 | HG00438.hp1 HG00558.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.1226-6058T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87823827 | ||||||
| chr7:87824084
|
T | C | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1226-5801T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87824084 | ||||||
| chr7:87824159
|
GCAATTAG others(19): Show |
G | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1226-5722_1226-569 others(30): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87824159 | |||||
| chr7:87824287
|
A | G | 75 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(72): Show | 75 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.1226-5598A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87824287 | ||||||
| chr7:87824466
|
C | CT | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1226-5412dupT | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87824466 | |||||
| chr7:87824504
|
T | C | 1 | a0001c0001t0005g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1226-5381T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87824504 | ||||||
| chr7:87825042
|
A | T | 6 | a0001c0001t0042g0148a0001c0001t0047g0012a0001c0001t0058g0018others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1226-4843A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825042 | ||||||
| chr7:87825063
|
C | CA | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1226-4813dupA | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87825063 | |||||
| chr7:87825139
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1226-4746G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825139 | ||||||
| chr7:87825419
|
C | T | 11 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(8): Show | 11 | HG00423.hp1 NA18952.hp1 NA18970.hp2 others(8): Show |
intron_variant | MODIFIER | c.1226-4466C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825419 | ||||||
| chr7:87825432
|
G | A | 2 | a0001c0001t0047g0012a0001c0001t0058g0018 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1226-4453G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825432 | ||||||
| chr7:87825669
|
G | A | 2 | a0001c0001t0004g0111a0001c0001t0004g0112 | 2 | HG00738.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1226-4216G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825669 | ||||||
| chr7:87825749
|
T | C | 63 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(60): Show | 63 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.1226-4136T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825749 | ||||||
| chr7:87825840
|
C | T | 155 | a0001c0001t0001g0068a0001c0001t0001g0087a0001c0001t0001g0099others(152): Show | 155 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1226-4045C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825840 | ||||||
| chr7:87825856
|
T | C | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1226-4029T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825856 | ||||||
| chr7:87825971
|
A | C | 1 | a0001c0001t0003g0128 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1226-3914A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825971 | ||||||
| chr7:87825973
|
A | G | 1 | a0001c0001t0003g0128 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1226-3912A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87825973 | ||||||
| chr7:87826043
|
T | G | 1 | a0001c0001t0007g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1226-3842T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826043 | ||||||
| chr7:87826046
|
G | A | 12 | a0001c0001t0012g0150a0001c0001t0012g0151a0001c0001t0012g0152others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.1226-3839G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826046 | ||||||
| chr7:87826112
|
G | T | 1 | a0001c0001t0016g0126 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1226-3773G>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826112 | ||||||
| chr7:87826390
|
T | TG | 85 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.1226-3494dupG | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87826390 | |||||
| chr7:87826404
|
A | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1226-3481A>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826404 | ||||||
| chr7:87826415
|
T | C | 2 | a0001c0001t0007g0021a0001c0001t0025g0004 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1226-3470T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826415 | ||||||
| chr7:87826451
|
T | G | 2 | a0001c0001t0001g0099a0001c0001t0009g0132 | 2 | HG00423.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1226-3434T>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826451 | ||||||
| chr7:87826507
|
A | G | 1 | a0001c0001t0033g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1226-3378A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826507 | ||||||
| chr7:87826523
|
C | A | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1226-3362C>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826523 | ||||||
| chr7:87826524
|
A | C | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1226-3361A>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826524 | ||||||
| chr7:87826905
|
T | C | 1 | a0001c0001t0006g0050 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1226-2980T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87826905 | ||||||
| chr7:87827377
|
C | T | 15 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(12): Show | 15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1226-2508C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87827377 | ||||||
| chr7:87827443
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0003g0064a0001c0001t0004g0089others(1): Show | 4 | HG03704.hp1 HG03831.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1226-2442C>T | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87827443 | ||||||
| chr7:87827663
|
G | A | 5 | a0001c0001t0001g0051a0001c0001t0001g0070a0001c0001t0001g0072others(2): Show | 5 | HG01099.hp2 HG01123.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1226-2222G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87827663 | ||||||
| chr7:87827952
|
T | A | 1 | a0001c0001t0003g0057 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1226-1933T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87827952 | ||||||
| chr7:87828030
|
A | G | 15 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(12): Show | 15 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1226-1855A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87828030 | ||||||
| chr7:87828170
|
TTC | T | 38 | a0001c0001t0002g0027a0001c0001t0002g0137a0001c0001t0002g0162others(35): Show | 38 | HG01081.hp2 HG01123.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1226-1713_1226-171 others(6): Show |
RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 87828170 | |||||
| chr7:87828209
|
G | A | 1 | a0001c0001t0003g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1226-1676G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87828209 | ||||||
| chr7:87828217
|
T | A | 1 | a0001c0001t0042g0148 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1226-1668T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87828217 | ||||||
| chr7:87828455
|
T | C | 2 | a0001c0001t0001g0056a0001c0001t0035g0035 | 2 | NA19001.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1226-1430T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87828455 | ||||||
| chr7:87829080
|
G | A | 1 | a0001c0001t0043g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1226-805G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829080 | ||||||
| chr7:87829117
|
T | C | 1 | a0001c0001t0068g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1226-768T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829117 | ||||||
| chr7:87829207
|
A | G | 16 | a0001c0001t0008g0190a0001c0001t0008g0191a0001c0001t0008g0193others(13): Show | 16 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1226-678A>G | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829207 | ||||||
| chr7:87829262
|
T | C | 1 | a0001c0001t0005g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1226-623T>C | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829262 | ||||||
| chr7:87829318
|
T | A | 1 | a0001c0001t0004g0102 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1226-567T>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829318 | ||||||
| chr7:87829510
|
G | A | 4 | a0001c0001t0031g0076a0001c0001t0034g0077a0001c0001t0034g0079others(1): Show | 4 | HG00639.hp1 HG02559.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1226-375G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829510 | ||||||
| chr7:87829593
|
G | A | 2 | a0001c0001t0036g0160a0001c0001t0076g0081 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1226-292G>A | RUNDC3B | ENSG00000105784.16 | transcript | ENST00000394654.4 | protein_coding | 10/10 | chr7 | 87829593 |