Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 283349 |
|---|---|
| ensemblid | ENSG00000153179.14 |
| hgncid | 14271 |
| symbol | RASSF3 |
| name | Ras association domain family member 3 |
| refseq_nuc | NM_178169.4 |
| refseq_prot | NP_835463.1 |
| ensembl_nuc | ENST00000542104.6 |
| ensembl_prot | ENSP00000443021.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 64610495 |
| end | 64697564 |
| strand | + |
| ver | v1.2 |
| region | chr12:64610495-64697564 |
| region5000 | chr12:64605495-64702564 |
| regionname0 | RASSF3_chr12_64610495_64697564 |
| regionname5000 | RASSF3_chr12_64605495_64702564 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 238 | 360 | 78 | 72 | 154 | 16 | 38 | 116 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0002 | 0/0 | 238 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 717 | 327 | 63 | 60 | 154 | 14 | 34 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| c0002 | 0/0 | 717 | 33 | 15 | 12 | 0 | 2 | 4 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| c0003 | 0/0 | 717 | 9 | 9 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| c0004 | 0/0 | 717 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2795 | 60 | 3 | 8 | 46 | 0 | 3 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0002 | 0/0 | 2815 | 34 | 0 | 16 | 12 | 1 | 5 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0003 | 0/0 | 2811 | 31 | 7 | 2 | 19 | 2 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0004 | 0/0 | 2791 | 28 | 1 | 7 | 12 | 2 | 6 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0005 | 0/0 | 2783 | 15 | 0 | 10 | 0 | 1 | 4 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0006 | 0/0 | 2815 | 14 | 2 | 0 | 12 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0007 | 0/0 | 2823 | 14 | 2 | 7 | 1 | 1 | 3 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0008 | 0/0 | 2831 | 13 | 3 | 0 | 8 | 0 | 2 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0009 | 0/0 | 2783 | 10 | 2 | 1 | 6 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0010 | 0/0 | 2823 | 6 | 6 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0011 | 0/0 | 2827 | 6 | 6 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0012 | 0/0 | 2811 | 6 | 4 | 0 | 2 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0013 | 0/0 | 2815 | 6 | 0 | 1 | 0 | 3 | 2 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0014 | 0/0 | 2814 | 5 | 0 | 2 | 1 | 0 | 2 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0015 | 0/0 | 2803 | 5 | 0 | 5 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0016 | 0/0 | 2791 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0017 | 0/0 | 2791 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0018 | 0/0 | 2835 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0019 | 0/0 | 2795 | 4 | 1 | 0 | 0 | 2 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0020 | 0/0 | 2809 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0021 | 0/0 | 2783 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0022 | 0/0 | 2791 | 3 | 0 | 1 | 2 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0023 | 0/0 | 2835 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0024 | 0/0 | 2810 | 3 | 0 | 2 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0025 | 1/0 | 2791 | 3 | 1 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0026 | 0/0 | 2831 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0027 | 0/0 | 2838 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0028 | 0/0 | 2819 | 2 | 1 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0029 | 0/0 | 2827 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0030 | 0/0 | 2827 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0031 | 0/0 | 2791 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0032 | 0/0 | 2831 | 2 | 1 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0033 | 0/0 | 2795 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0034 | 0/0 | 2782 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0035 | 0/0 | 2814 | 2 | 0 | 1 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0036 | 0/0 | 2804 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0037 | 0/0 | 2795 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0038 | 0/0 | 2792 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0039 | 0/0 | 2799 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0040 | 0/0 | 2796 | 2 | 0 | 0 | 1 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0041 | 0/0 | 2790 | 2 | 1 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0042 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0043 | 0/0 | 2823 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0044 | 0/0 | 2815 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0045 | 0/0 | 2826 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0046 | 0/0 | 2803 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0047 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0048 | 0/0 | 2795 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0049 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0050 | 0/0 | 2783 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0051 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0052 | 0/0 | 2819 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0053 | 0/0 | 2816 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0054 | 0/0 | 2819 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0055 | 0/0 | 2824 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0056 | 0/0 | 2815 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0057 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0058 | 0/1 | 2823 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0059 | 0/0 | 2795 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0060 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0061 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0062 | 0/0 | 2795 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0063 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0064 | 0/0 | 2839 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0065 | 0/0 | 2811 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0066 | 0/0 | 2791 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0067 | 0/0 | 2812 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0068 | 0/0 | 2815 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0069 | 0/0 | 2816 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0070 | 0/0 | 2811 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0071 | 0/0 | 2815 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0072 | 0/0 | 2830 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0073 | 0/0 | 2836 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0074 | 0/0 | 2839 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0075 | 0/0 | 2808 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0076 | 0/0 | 2795 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0077 | 0/0 | 2790 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0078 | 0/0 | 2791 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0079 | 0/0 | 2791 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0080 | 0/0 | 2791 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0081 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0082 | 0/0 | 2804 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0083 | 0/0 | 2794 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0084 | 0/0 | 2779 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0085 | 0/0 | 2815 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0086 | 0/0 | 2791 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0087 | 0/0 | 2830 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0088 | 0/0 | 2834 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0089 | 0/0 | 2834 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| t0090 | 0/0 | 2810 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 717 | 327 | 63 | 60 | 154 | 14 | 34 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002 | 0/0 | 717 | 33 | 15 | 12 | 0 | 2 | 4 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0002c0003 | 0/0 | 717 | 9 | 9 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0002c0004 | 0/0 | 717 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3511 | 60 | 3 | 8 | 46 | 0 | 3 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0002 | 0/0 | 3531 | 34 | 0 | 16 | 12 | 1 | 5 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0003 | 0/0 | 3527 | 31 | 7 | 2 | 19 | 2 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0004 | 0/0 | 3507 | 27 | 1 | 7 | 12 | 2 | 5 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0005 | 0/0 | 3499 | 15 | 0 | 10 | 0 | 1 | 4 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0006 | 0/0 | 3531 | 14 | 2 | 0 | 12 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0007 | 0/0 | 3539 | 5 | 1 | 2 | 1 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0008 | 0/0 | 3547 | 13 | 3 | 0 | 8 | 0 | 2 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0009 | 0/0 | 3499 | 10 | 2 | 1 | 6 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0010 | 0/0 | 3539 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0012 | 0/0 | 3527 | 6 | 4 | 0 | 2 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0013 | 0/0 | 3531 | 6 | 0 | 1 | 0 | 3 | 2 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0014 | 0/0 | 3530 | 5 | 0 | 2 | 1 | 0 | 2 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0017 | 0/0 | 3507 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0018 | 0/0 | 3551 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0019 | 0/0 | 3511 | 4 | 1 | 0 | 0 | 2 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0020 | 0/0 | 3525 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0022 | 0/0 | 3507 | 3 | 0 | 1 | 2 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0023 | 0/0 | 3551 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0024 | 0/0 | 3526 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0025 | 1/0 | 3507 | 3 | 1 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0026 | 0/0 | 3547 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0027 | 0/0 | 3554 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0028 | 0/0 | 3535 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0031 | 0/0 | 3507 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0032 | 0/0 | 3547 | 2 | 1 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0033 | 0/0 | 3511 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0034 | 0/0 | 3498 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0035 | 0/0 | 3530 | 2 | 0 | 1 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0036 | 0/0 | 3520 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0037 | 0/0 | 3511 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0038 | 0/0 | 3508 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0039 | 0/0 | 3515 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0040 | 0/0 | 3512 | 2 | 0 | 0 | 1 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0041 | 0/0 | 3506 | 2 | 1 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0043 | 0/0 | 3539 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0044 | 0/0 | 3531 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0046 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0049 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0050 | 0/0 | 3499 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0051 | 0/0 | 3527 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0052 | 0/0 | 3535 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0053 | 0/0 | 3532 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0054 | 0/0 | 3535 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0055 | 0/0 | 3540 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0056 | 0/0 | 3531 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0057 | 0/0 | 3536 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0058 | 0/1 | 3539 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0059 | 0/0 | 3511 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0060 | 0/0 | 3518 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0061 | 0/0 | 3527 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0062 | 0/0 | 3511 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0063 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0064 | 0/0 | 3555 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0065 | 0/0 | 3527 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0066 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0067 | 0/0 | 3528 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0068 | 0/0 | 3531 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0069 | 0/0 | 3532 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0071 | 0/0 | 3531 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0072 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0073 | 0/0 | 3552 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0074 | 0/0 | 3555 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0075 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0076 | 0/0 | 3511 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0077 | 0/0 | 3506 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0078 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0079 | 0/0 | 3507 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0080 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0083 | 0/0 | 3510 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0084 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0085 | 0/0 | 3531 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0086 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0087 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0088 | 0/0 | 3550 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0089 | 0/0 | 3550 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0001t0090 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0004 | 0/0 | 3507 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0007 | 0/0 | 3539 | 9 | 1 | 5 | 0 | 1 | 2 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0015 | 0/0 | 3519 | 5 | 0 | 5 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0016 | 0/0 | 3507 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0021 | 0/0 | 3499 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0024 | 0/0 | 3526 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0028 | 0/0 | 3535 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0029 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0042 | 0/0 | 3515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0045 | 0/0 | 3542 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0047 | 0/0 | 3515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0048 | 0/0 | 3511 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0070 | 0/0 | 3527 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0081 | 0/0 | 3518 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0001c0002t0082 | 0/0 | 3520 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0002c0003t0010 | 0/0 | 3539 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0002c0003t0011 | 0/0 | 3543 | 5 | 5 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0002c0003t0030 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| a0002c0004t0011 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | copy fasta | chr12 | 64605495 | 64702564 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0004g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0006g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0007g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0007g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0007g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0008g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0008g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0008g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0008g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0008g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0008g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0008g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0008g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0008g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0009g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0009g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0009g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0009g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0009g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0009g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0009g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0009g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0010g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0010g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0010g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0010g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0012g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0012g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0012g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0012g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0012g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0013g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0013g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0013g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0013g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0013g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0013g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0014g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0014g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0014g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0014g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0014g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0017g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0017g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0017g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0017g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0018g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0018g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0018g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0018g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0019g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0019g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0019g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0019g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0020g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0020g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0020g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0022g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0022g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0022g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0023g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0023g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0023g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0024g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0024g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0025g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0025g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0025g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0026g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0026g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0026g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0027g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0027g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0027g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0028g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0031g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0031g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0032g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0032g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0033g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0033g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0034g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0034g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0035g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0035g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0036g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0036g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0037g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0037g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0038g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0038g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0039g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0039g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0040g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0040g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0041g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0041g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0043g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0044g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0046g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0049g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0050g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0051g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0052g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0053g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0054g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0055g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0056g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0057g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0058g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0059g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0060g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0061g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0062g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0063g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0064g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0065g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0066g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0067g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0068g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0069g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0071g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0072g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0073g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0074g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0075g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0076g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0077g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0078g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0079g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0080g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0083g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0084g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0085g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0086g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0087g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0088g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0089g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0001t0090g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0007g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0007g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0007g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0007g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0007g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0007g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0007g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0007g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0015g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0015g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0015g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0015g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0015g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0016g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0016g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0016g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0016g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0021g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0021g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0021g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0024g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0028g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0029g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0029g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0042g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0045g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0047g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0048g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0070g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0081g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0001c0002t0082g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0002c0003t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0002c0003t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0002c0003t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0002c0003t0011g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0002c0003t0011g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0002c0003t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0002c0003t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0002c0003t0030g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| a0002c0004t0011g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0007 | g0014 | EUR | GBR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0215 | EUR | GBR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0128 | EUR | FIN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00280 | hp2 | a0001 | c0001 | t0060 | g0134 | EUR | FIN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00323 | hp1 | a0001 | c0001 | t0013 | g0161 | EUR | FIN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00323 | hp2 | a0001 | c0002 | t0024 | g0002 | EUR | FIN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | CHS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0336 | EAS | CHS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00639 | hp2 | a0001 | c0002 | t0007 | g0020 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00642 | hp1 | a0001 | c0002 | t0007 | g0017 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0325 | EAS | CHS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | CHS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0104 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0195 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00741 | hp1 | a0001 | c0002 | t0070 | g0003 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0133 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01069 | hp1 | a0001 | c0002 | t0007 | g0019 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0183 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01071 | hp1 | a0001 | c0002 | t0007 | g0018 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0184 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0301 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01081 | hp1 | a0001 | c0002 | t0015 | g0009 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01099 | hp1 | a0001 | c0001 | t0024 | g0257 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0196 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01106 | hp2 | a0001 | c0002 | t0015 | g0008 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01109 | hp1 | a0001 | c0001 | t0067 | g0210 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01109 | hp2 | a0001 | c0002 | t0082 | g0010 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01167 | hp1 | a0001 | c0002 | t0007 | g0011 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0053 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0100 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01169 | hp2 | a0001 | c0001 | t0014 | g0149 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01175 | hp2 | a0001 | c0002 | t0015 | g0004 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0102 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01243 | hp1 | a0001 | c0001 | t0024 | g0275 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01243 | hp2 | a0001 | c0001 | t0089 | g0355 | AMR | PUR | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01256 | hp1 | a0001 | c0001 | t0055 | g0176 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01256 | hp2 | a0001 | c0001 | t0034 | g0200 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0088 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0201 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01261 | hp1 | a0001 | c0001 | t0022 | g0135 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01261 | hp2 | a0001 | c0001 | t0034 | g0204 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01346 | hp1 | a0001 | c0001 | t0013 | g0166 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01346 | hp2 | a0001 | c0002 | t0015 | g0007 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0348 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0306 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0327 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01361 | hp2 | a0001 | c0001 | t0028 | g0048 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01433 | hp2 | a0001 | c0002 | t0015 | g0006 | AMR | CLM | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0293 | EUR | IBS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01515 | hp2 | a0001 | c0001 | t0019 | g0087 | EUR | IBS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0206 | EUR | IBS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0322 | EUR | IBS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0323 | EUR | IBS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01517 | hp2 | a0001 | c0001 | t0077 | g0292 | EUR | IBS | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0344 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01891 | hp2 | a0002 | c0003 | t0010 | g0116 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0198 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0141 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0321 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0193 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01993 | hp1 | a0001 | c0001 | t0014 | g0320 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG01993 | hp2 | a0001 | c0001 | t0035 | g0096 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02004 | hp1 | a0001 | c0001 | t0052 | g0330 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0197 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02015 | hp1 | a0001 | c0001 | t0007 | g0346 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02015 | hp2 | a0001 | c0001 | t0084 | g0079 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02027 | hp2 | a0001 | c0001 | t0006 | g0278 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02040 | hp1 | a0001 | c0001 | t0025 | g0083 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02040 | hp2 | a0001 | c0001 | t0006 | g0283 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02055 | hp1 | a0001 | c0001 | t0038 | g0359 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02055 | hp2 | a0001 | c0001 | t0020 | g0107 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0332 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02074 | hp2 | a0001 | c0001 | t0080 | g0307 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0324 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02083 | hp2 | a0001 | c0001 | t0009 | g0285 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02129 | hp1 | a0001 | c0001 | t0051 | g0158 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02135 | hp2 | a0001 | c0001 | t0035 | g0341 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0182 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02145 | hp2 | a0001 | c0001 | t0020 | g0108 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CDX | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02155 | hp2 | a0001 | c0001 | t0012 | g0136 | EAS | CDX | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02257 | hp1 | a0001 | c0001 | t0027 | g0356 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02257 | hp2 | a0001 | c0001 | t0017 | g0178 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0364 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0126 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02280 | hp1 | a0002 | c0003 | t0011 | g0115 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02280 | hp2 | a0001 | c0002 | t0048 | g0037 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0091 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02300 | hp2 | a0001 | c0001 | t0009 | g0097 | AMR | PEL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02451 | hp1 | a0001 | c0001 | t0027 | g0351 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02451 | hp2 | a0001 | c0002 | t0016 | g0036 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0277 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0368 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02622 | hp1 | a0001 | c0001 | t0031 | g0113 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02622 | hp2 | a0001 | c0002 | t0021 | g0218 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02630 | hp1 | a0001 | c0002 | t0029 | g0022 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0317 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02647 | hp1 | a0001 | c0001 | t0032 | g0145 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0313 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0205 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02683 | hp2 | a0001 | c0001 | t0013 | g0148 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0203 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02717 | hp1 | a0002 | c0003 | t0011 | g0114 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02717 | hp2 | a0001 | c0002 | t0016 | g0033 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0224 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02723 | hp2 | a0002 | c0003 | t0011 | g0112 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0202 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02738 | hp2 | a0001 | c0001 | t0053 | g0188 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02809 | hp1 | a0001 | c0002 | t0016 | g0035 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02809 | hp2 | a0001 | c0002 | t0021 | g0217 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0366 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02818 | hp2 | a0001 | c0001 | t0065 | g0318 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0244 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02886 | hp2 | a0001 | c0001 | t0027 | g0354 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02895 | hp1 | a0001 | c0001 | t0046 | g0044 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02895 | hp2 | a0001 | c0002 | t0029 | g0021 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02896 | hp1 | a0001 | c0002 | t0042 | g0349 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02896 | hp2 | a0001 | c0001 | t0017 | g0160 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02897 | hp1 | a0001 | c0002 | t0045 | g0024 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02897 | hp2 | a0001 | c0001 | t0017 | g0172 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02922 | hp1 | a0002 | c0004 | t0011 | g0326 | AFR | ESN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02922 | hp2 | a0001 | c0001 | t0044 | g0110 | AFR | ESN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02970 | hp1 | a0001 | c0001 | t0017 | g0179 | AFR | ESN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0308 | AFR | ESN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03041 | hp1 | a0002 | c0003 | t0011 | g0111 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03041 | hp2 | a0001 | c0001 | t0066 | g0220 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03098 | hp1 | a0001 | c0001 | t0020 | g0109 | AFR | MSL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03098 | hp2 | a0001 | c0001 | t0031 | g0118 | AFR | MSL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03130 | hp1 | a0001 | c0001 | t0075 | g0106 | AFR | ESN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03130 | hp2 | a0001 | c0001 | t0012 | g0186 | AFR | ESN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03139 | hp1 | a0001 | c0001 | t0063 | g0170 | AFR | ESN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | ESN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ESN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03195 | hp2 | a0002 | c0003 | t0030 | g0001 | AFR | ESN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03209 | hp1 | a0001 | c0001 | t0043 | g0367 | AFR | MSL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03209 | hp2 | a0001 | c0001 | t0036 | g0314 | AFR | MSL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03239 | hp1 | a0001 | c0001 | t0054 | g0127 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03239 | hp2 | a0001 | c0002 | t0081 | g0005 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0273 | AFR | MSL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0365 | AFR | MSL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0310 | AFR | MSL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03490 | hp1 | a0001 | c0001 | t0019 | g0093 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03490 | hp2 | a0001 | c0001 | t0014 | g0138 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03516 | hp1 | a0001 | c0001 | t0078 | g0345 | AFR | ESN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0316 | AFR | ESN | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0352 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03540 | hp2 | a0001 | c0001 | t0049 | g0049 | AFR | GWD | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03579 | hp1 | a0001 | c0002 | t0021 | g0023 | AFR | MSL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03579 | hp2 | a0001 | c0001 | t0087 | g0353 | AFR | MSL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03654 | hp1 | a0001 | c0002 | t0007 | g0012 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0343 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0304 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0305 | SAS | STU | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0246 | SAS | STU | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03704 | hp1 | a0001 | c0001 | t0062 | g0194 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03704 | hp2 | a0001 | c0001 | t0014 | g0137 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03710 | hp1 | a0001 | c0001 | t0009 | g0271 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03831 | hp1 | a0001 | c0001 | t0032 | g0163 | SAS | BEB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0319 | SAS | BEB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | BEB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03834 | hp2 | a0001 | c0001 | t0079 | g0225 | SAS | BEB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03927 | hp1 | a0001 | c0001 | t0056 | g0143 | SAS | BEB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03927 | hp2 | a0001 | c0001 | t0040 | g0084 | SAS | BEB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0207 | SAS | BEB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03942 | hp2 | a0001 | c0001 | t0008 | g0272 | SAS | BEB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG04115 | hp2 | a0001 | c0002 | t0007 | g0013 | SAS | STU | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0303 | SAS | BEB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | BEB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0226 | SAS | STU | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG04204 | hp1 | a0001 | c0001 | t0013 | g0168 | SAS | STU | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG04204 | hp2 | a0001 | c0002 | t0004 | g0015 | SAS | STU | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18522 | hp1 | a0001 | c0001 | t0088 | g0361 | AFR | YRI | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0363 | AFR | YRI | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | CHB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18747 | hp2 | a0001 | c0001 | t0037 | g0297 | EAS | CHB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18906 | hp1 | a0002 | c0003 | t0030 | g0001 | AFR | YRI | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18906 | hp2 | a0001 | c0001 | t0041 | g0312 | AFR | YRI | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18942 | hp1 | a0001 | c0001 | t0037 | g0300 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18942 | hp2 | a0001 | c0001 | t0022 | g0130 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18943 | hp2 | a0001 | c0001 | t0018 | g0236 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0071 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18944 | hp2 | a0001 | c0001 | t0008 | g0222 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18945 | hp1 | a0001 | c0001 | t0026 | g0241 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18946 | hp2 | a0001 | c0001 | t0018 | g0213 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18947 | hp2 | a0001 | c0001 | t0039 | g0038 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18950 | hp1 | a0001 | c0001 | t0076 | g0064 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18952 | hp2 | a0001 | c0001 | t0074 | g0250 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18953 | hp2 | a0001 | c0001 | t0073 | g0238 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18957 | hp1 | a0001 | c0001 | t0008 | g0286 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18962 | hp1 | a0001 | c0001 | t0014 | g0169 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18963 | hp2 | a0001 | c0001 | t0018 | g0237 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18964 | hp1 | a0001 | c0001 | t0072 | g0242 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18964 | hp2 | a0001 | c0001 | t0006 | g0339 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18965 | hp2 | a0001 | c0001 | t0012 | g0190 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18966 | hp1 | a0001 | c0001 | t0023 | g0270 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0287 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18968 | hp2 | a0001 | c0001 | t0033 | g0357 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18978 | hp1 | a0001 | c0001 | t0041 | g0105 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18979 | hp2 | a0001 | c0001 | t0006 | g0334 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18982 | hp1 | a0001 | c0001 | t0033 | g0132 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18982 | hp2 | a0001 | c0001 | t0008 | g0247 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18983 | hp1 | a0001 | c0001 | t0026 | g0240 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0335 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18984 | hp1 | a0001 | c0001 | t0009 | g0281 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18987 | hp2 | a0001 | c0001 | t0083 | g0123 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18988 | hp2 | a0001 | c0001 | t0018 | g0274 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18989 | hp1 | a0001 | c0001 | t0040 | g0098 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18989 | hp2 | a0001 | c0001 | t0026 | g0239 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18995 | hp1 | a0001 | c0001 | t0050 | g0199 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18999 | hp2 | a0001 | c0001 | t0039 | g0031 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0223 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0331 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19004 | hp1 | a0001 | c0001 | t0023 | g0267 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19005 | hp2 | a0001 | c0001 | t0009 | g0284 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19010 | hp1 | a0001 | c0001 | t0009 | g0282 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19011 | hp2 | a0001 | c0001 | t0022 | g0129 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19043 | hp1 | a0001 | c0001 | t0012 | g0125 | AFR | LWK | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19043 | hp2 | a0001 | c0001 | t0036 | g0315 | AFR | LWK | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19057 | hp2 | a0001 | c0001 | t0008 | g0249 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19060 | hp1 | a0001 | c0001 | t0069 | g0046 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19062 | hp2 | a0001 | c0001 | t0009 | g0280 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19064 | hp2 | a0001 | c0001 | t0068 | g0045 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19066 | hp1 | a0001 | c0001 | t0023 | g0269 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19068 | hp1 | a0001 | c0001 | t0008 | g0214 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19068 | hp2 | a0001 | c0001 | t0009 | g0076 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19075 | hp2 | a0001 | c0001 | t0061 | g0139 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19084 | hp1 | a0001 | c0001 | t0008 | g0248 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19085 | hp2 | a0001 | c0001 | t0064 | g0266 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19087 | hp1 | a0001 | c0001 | t0008 | g0276 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0299 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19240 | hp1 | a0001 | c0001 | t0038 | g0243 | AFR | YRI | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA19240 | hp2 | a0001 | c0001 | t0086 | g0362 | AFR | YRI | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA20129 | hp1 | a0001 | c0001 | t0025 | g0075 | AFR | ASW | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0311 | AFR | ASW | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA20752 | hp1 | a0001 | c0001 | t0013 | g0154 | EUR | TSI | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA20752 | hp2 | a0001 | c0001 | t0019 | g0051 | EUR | TSI | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA20805 | hp1 | a0001 | c0001 | t0059 | g0347 | EUR | TSI | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA20805 | hp2 | a0001 | c0001 | t0013 | g0171 | EUR | TSI | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | GIH | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0294 | SAS | GIH | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02109 | hp1 | a0001 | c0002 | t0028 | g0025 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02109 | hp2 | a0002 | c0003 | t0010 | g0119 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0309 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0167 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02559 | hp1 | a0002 | c0003 | t0011 | g0117 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG02559 | hp2 | a0001 | c0002 | t0047 | g0216 | AFR | ACB | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03471 | hp1 | a0001 | c0001 | t0085 | g0029 | AFR | MSL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG03471 | hp2 | a0001 | c0002 | t0016 | g0034 | AFR | MSL | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG06807 | hp1 | a0001 | c0001 | t0090 | g0369 | AFR | USA | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| HG06807 | hp2 | a0001 | c0002 | t0007 | g0016 | AFR | USA | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA20300 | hp1 | a0001 | c0001 | t0019 | g0090 | AFR | USA | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA20300 | hp2 | a0001 | c0001 | t0057 | g0177 | AFR | USA | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA21309 | hp1 | a0001 | c0001 | t0071 | g0360 | AFR | LWK | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0058 | g0151 | REF | REF | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0025 | g0040 | REF | REF | RASSF3_chr12_64605495_64702564 | RASSF3 | chr12 | 64605495 | 64702564 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:64694890
|
G | A | 1 | a0002 | 10 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(7): Show |
missense_variant | MODERATE | c.695G>A | p.Arg232His | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 833/3507 | 695/717 | 232/238 | chr12 | 64694890 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:64610740
|
A | G | 2 | a0001c0002a0002c0004 | 34 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(31): Show |
synonymous_variant | LOW | c.108A>G | p.Gln36Gln | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/5 | 246/3507 | 108/717 | 36/238 | chr12 | 64610740 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:64610536
|
T | C | 44 | a0001c0001t0002a0001c0001t0005a0001c0001t0010others(41): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
5_prime_UTR_variant | MODIFIER | c.-97T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/5 | 97 | chr12 | 64610536 | |||||
| chr12:64610591
|
T | TGCGCCCC others(13): Show |
1 | a0001c0002t0042 | 1 | HG02896.hp1 | 5_prime_UTR_variant | MODIFIER | c.-37_-18dupCCCGGGGA others(12): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/5 | 17 | INFO_REALIGN_3_PRIME | chr12 | 64610591 | ||||
| chr12:64610607
|
C | T | 24 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(21): Show | 93 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-26C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/5 | chr12 | 64610607 | ||||||
| chr12:64694929
|
C | T | 6 | a0001c0001t0027a0001c0001t0086a0001c0001t0087others(3): Show | 8 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*17C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 17 | chr12 | 64694929 | |||||
| chr12:64694949
|
C | T | 1 | a0001c0001t0026 | 3 | NA18945.hp1 NA18983.hp1 NA18989.hp2 |
3_prime_UTR_variant | MODIFIER | c.*37C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 37 | chr12 | 64694949 | |||||
| chr12:64694950
|
G | A | 2 | a0001c0001t0023a0001c0001t0064 | 4 | NA18966.hp1 NA19004.hp1 NA19066.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*38G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 38 | chr12 | 64694950 | |||||
| chr12:64695046
|
C | T | 1 | a0001c0001t0090 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*134C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 134 | chr12 | 64695046 | |||||
| chr12:64695123
|
C | A | 1 | a0001c0001t0065 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*211C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 211 | chr12 | 64695123 | |||||
| chr12:64695277
|
A | G | 1 | a0001c0001t0085 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*365A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 365 | chr12 | 64695277 | |||||
| chr12:64695489
|
G | A | 1 | a0001c0001t0050 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*577G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 577 | chr12 | 64695489 | |||||
| chr12:64695505
|
T | C | 74 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(71): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*593T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 593 | chr12 | 64695505 | |||||
| chr12:64695516
|
A | G | 1 | a0001c0001t0061 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*604A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 604 | chr12 | 64695516 | |||||
| chr12:64695576
|
C | T | 1 | a0001c0001t0020 | 3 | HG02055.hp2 HG02145.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*664C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 664 | chr12 | 64695576 | |||||
| chr12:64695644
|
A | G | 1 | a0001c0001t0013 | 6 | HG00323.hp1 HG01346.hp1 HG02683.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*732A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 732 | chr12 | 64695644 | |||||
| chr12:64695758
|
G | A | 1 | a0001c0001t0086 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*846G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 846 | chr12 | 64695758 | |||||
| chr12:64695765
|
C | T | 1 | a0001c0001t0080 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*853C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 853 | chr12 | 64695765 | |||||
| chr12:64695871
|
G | C | 1 | a0001c0001t0066 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*959G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 959 | chr12 | 64695871 | |||||
| chr12:64696085
|
T | TCCTC | 10 | a0001c0001t0001a0001c0001t0019a0001c0001t0033others(7): Show | 75 | HG00438.hp1 HG00609.hp2 HG00642.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1207_*1210dupCTCC | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696085 | ||||
| chr12:64696085
|
T | TCCTCCCT others(1): Show |
2 | a0001c0001t0039a0001c0002t0047 | 3 | HG02559.hp2 NA18947.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1203_*1210dupCTCC others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696085 | ||||
| chr12:64696085
|
T | TCCTCCCT others(5): Show |
5 | a0001c0001t0036a0001c0001t0046a0001c0002t0015others(2): Show | 10 | HG01081.hp1 HG01106.hp2 HG01109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1199_*1210dupCTCC others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696085 | ||||
| chr12:64696085
|
T | TCCTCCCT others(9): Show |
1 | a0001c0001t0075 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1195_*1210dupCTCC others(12): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696085 | ||||
| chr12:64696085
|
T | TCCTCCCT others(29): Show |
2 | a0001c0002t0029a0001c0002t0045 | 3 | HG02630.hp1 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1205_*1206insACTC others(32): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1206 | INFO_REALIGN_3_PRIME | chr12 | 64696085 | ||||
| chr12:64696085
|
TCCTCCCT others(1): Show |
T | 5 | a0001c0001t0005a0001c0001t0009a0001c0001t0034others(2): Show | 31 | HG00280.hp1 HG00735.hp2 HG01070.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1203_*1210delCTCC others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1203 | INFO_REALIGN_3_PRIME | chr12 | 64696085 | ||||
| chr12:64696085
|
TCCTCCCT others(5): Show |
T | 2 | a0001c0001t0049a0001c0001t0084 | 2 | HG02015.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1199_*1210delCTCC others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1199 | INFO_REALIGN_3_PRIME | chr12 | 64696085 | ||||
| chr12:64696090
|
C | CCTCCCTC others(21): Show |
1 | a0001c0001t0054 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1201_*1202insACTC others(24): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1202 | INFO_REALIGN_3_PRIME | chr12 | 64696090 | ||||
| chr12:64696090
|
C | CCTCCCTC others(21): Show |
3 | a0001c0001t0028a0001c0001t0057a0001c0002t0028 | 3 | HG01361.hp2 HG02109.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1205_*1206insACTC others(24): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1206 | INFO_REALIGN_3_PRIME | chr12 | 64696090 | ||||
| chr12:64696093
|
C | A | 1 | a0001c0001t0043 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1181 | chr12 | 64696093 | |||||
| chr12:64696094
|
C | CCTCCCTC others(13): Show |
7 | a0001c0001t0003a0001c0001t0012a0001c0001t0024others(4): Show | 43 | HG00323.hp2 HG00438.hp2 HG01074.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1197_*1198insACTC others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1198 | INFO_REALIGN_3_PRIME | chr12 | 64696094 | ||||
| chr12:64696094
|
C | CCTCCCTC others(17): Show |
9 | a0001c0001t0002a0001c0001t0006a0001c0001t0013others(6): Show | 65 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1201_*1202insACTC others(20): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1202 | INFO_REALIGN_3_PRIME | chr12 | 64696094 | ||||
| chr12:64696094
|
C | CCTCCCTC others(21): Show |
1 | a0001c0001t0052 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1201_*1202insACTC others(24): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1202 | INFO_REALIGN_3_PRIME | chr12 | 64696094 | ||||
| chr12:64696094
|
C | CCTCCCTC others(17): Show |
3 | a0001c0001t0056a0001c0001t0071a0001c0001t0085 | 3 | HG03471.hp1 HG03927.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1205_*1206insACTC others(20): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1206 | INFO_REALIGN_3_PRIME | chr12 | 64696094 | ||||
| chr12:64696094
|
C | CCTCCCTC others(25): Show |
1 | a0001c0001t0055 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1205_*1206insACTC others(28): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1206 | INFO_REALIGN_3_PRIME | chr12 | 64696094 | ||||
| chr12:64696098
|
C | CCTCCCTC others(13): Show |
1 | a0001c0002t0070 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1201_*1202insACTC others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1202 | INFO_REALIGN_3_PRIME | chr12 | 64696098 | ||||
| chr12:64696107
|
C | CTCACTCA others(13): Show |
1 | a0001c0001t0051 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197_*1198insACTC others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1198 | INFO_REALIGN_3_PRIME | chr12 | 64696107 | ||||
| chr12:64696111
|
C | CTCCCTCC others(5): Show |
1 | a0001c0001t0060 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1210_*1221dupCTTC others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1222 | INFO_REALIGN_3_PRIME | chr12 | 64696111 | ||||
| chr12:64696111
|
CTCCCTCC others(5): Show |
C | 1 | a0001c0002t0042 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1210_*1221delCTTC others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1210 | INFO_REALIGN_3_PRIME | chr12 | 64696111 | ||||
| chr12:64696114
|
C | A | 1 | a0001c0001t0020 | 3 | HG02055.hp2 HG02145.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1202C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1202 | chr12 | 64696114 | |||||
| chr12:64696117
|
C | G | 1 | a0001c0001t0079 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1205C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1205 | chr12 | 64696117 | |||||
| chr12:64696118
|
C | A | 28 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(25): Show | 121 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1206C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1206 | chr12 | 64696118 | |||||
| chr12:64696118
|
C | CCTCACTC others(25): Show |
6 | a0001c0001t0007a0001c0001t0010a0001c0001t0043others(3): Show | 22 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1209_*1210insACTC others(28): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1210 | INFO_REALIGN_3_PRIME | chr12 | 64696118 | ||||
| chr12:64696118
|
C | CCTCCCTC others(29): Show |
3 | a0002c0003t0011a0002c0003t0030a0002c0004t0011 | 8 | HG02280.hp1 HG02559.hp1 HG02717.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1210_*1211insCTCA others(32): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696118 | ||||
| chr12:64696118
|
C | CCTCCCTC others(33): Show |
4 | a0001c0001t0008a0001c0001t0026a0001c0001t0032others(1): Show | 19 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1210_*1211insCTCA others(36): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696118 | ||||
| chr12:64696118
|
C | CCTCCCTC others(37): Show |
1 | a0001c0001t0023 | 3 | NA18966.hp1 NA19004.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1210_*1211insCTCA others(40): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696118 | ||||
| chr12:64696118
|
C | CCTCCCTC others(37): Show |
1 | a0001c0001t0018 | 4 | NA18943.hp2 NA18946.hp2 NA18963.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1210_*1211insCTCC others(40): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696118 | ||||
| chr12:64696118
|
C | CCTCCCTC others(41): Show |
1 | a0001c0001t0064 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1210_*1211insCTCC others(44): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696118 | ||||
| chr12:64696118
|
C | CCTCCCTC others(33): Show |
1 | a0001c0001t0087 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1210_*1211insCTCC others(36): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696118 | ||||
| chr12:64696118
|
C | CCTCCCTC others(41): Show |
1 | a0001c0001t0074 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1210_*1211insCTCC others(44): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696118 | ||||
| chr12:64696118
|
C | CCTCCCTC others(37): Show |
2 | a0001c0001t0088a0001c0001t0089 | 2 | HG01243.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1210_*1211insCTCC others(40): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696118 | ||||
| chr12:64696118
|
C | CCTCCCTC others(13): Show |
1 | a0001c0001t0090 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1210_*1211insCTCC others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696118 | ||||
| chr12:64696118
|
C | CCTCCCTC others(41): Show |
1 | a0001c0001t0027 | 3 | HG02257.hp1 HG02451.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1210_*1211insCTCC others(44): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | INFO_REALIGN_3_PRIME | chr12 | 64696118 | ||||
| chr12:64696122
|
C | CCTCCCTC others(38): Show |
1 | a0001c0001t0073 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1210_*1211insCTCC others(41): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | chr12 | 64696122 | |||||
| chr12:64696123
|
T | C | 2 | a0001c0001t0020a0001c0001t0073 | 4 | HG02055.hp2 HG02145.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1211T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1211 | chr12 | 64696123 | |||||
| chr12:64696132
|
T | TCCCTCAC others(11): Show |
1 | a0001c0001t0020 | 3 | HG02055.hp2 HG02145.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1221_*1222insCCTC others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1222 | INFO_REALIGN_3_PRIME | chr12 | 64696132 | ||||
| chr12:64696140
|
C | T | 1 | a0001c0001t0020 | 3 | HG02055.hp2 HG02145.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1228C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1228 | chr12 | 64696140 | |||||
| chr12:64696276
|
G | A | 2 | a0001c0001t0019a0001c0001t0062 | 5 | HG01515.hp2 HG03490.hp1 HG03704.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1364G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1364 | chr12 | 64696276 | |||||
| chr12:64696353
|
C | T | 2 | a0001c0001t0068a0001c0001t0069 | 2 | NA19060.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1441C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1441 | chr12 | 64696353 | |||||
| chr12:64696743
|
A | G | 1 | a0001c0001t0085 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1831A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1831 | chr12 | 64696743 | |||||
| chr12:64696775
|
A | G | 1 | a0002c0003t0030 | 2 | HG03195.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1863A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1863 | chr12 | 64696775 | |||||
| chr12:64696783
|
C | A | 1 | a0001c0001t0088 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1871C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 1871 | chr12 | 64696783 | |||||
| chr12:64697060
|
A | AT | 10 | a0001c0001t0036a0001c0001t0038a0001c0001t0040others(7): Show | 13 | HG01109.hp1 HG01109.hp2 HG01256.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2170dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 2171 | INFO_REALIGN_3_PRIME | chr12 | 64697060 | ||||
| chr12:64697060
|
AT | A | 18 | a0001c0001t0014a0001c0001t0024a0001c0001t0027others(15): Show | 28 | HG00280.hp2 HG00323.hp2 HG01099.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2170delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 2170 | INFO_REALIGN_3_PRIME | chr12 | 64697060 | ||||
| chr12:64697251
|
G | A | 13 | a0001c0001t0004a0001c0001t0022a0001c0001t0037others(10): Show | 46 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2339G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 2339 | chr12 | 64697251 | |||||
| chr12:64697334
|
C | T | 1 | a0001c0001t0086 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2422C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 2422 | chr12 | 64697334 | |||||
| chr12:64697534
|
T | G | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(19): Show | 114 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2622T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 5/5 | 2622 | chr12 | 64697534 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:64610770
|
G | A | 19 | a0001c0002t0004g0015a0001c0002t0007g0011a0001c0002t0007g0012others(16): Show | 19 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.111+27G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64610770 | ||||||
| chr12:64610816
|
C | A | 5 | a0001c0002t0021g0023a0001c0002t0028g0025a0001c0002t0029g0021others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+73C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64610816 | ||||||
| chr12:64610858
|
G | T | 10 | a0001c0001t0004g0363a0001c0001t0010g0364a0001c0001t0010g0365others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.111+115G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64610858 | ||||||
| chr12:64610859
|
A | T | 10 | a0001c0001t0004g0363a0001c0001t0010g0364a0001c0001t0010g0365others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.111+116A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64610859 | ||||||
| chr12:64610862
|
G | A | 5 | a0001c0002t0021g0023a0001c0002t0028g0025a0001c0002t0029g0021others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+119G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64610862 | ||||||
| chr12:64611046
|
C | T | 1 | a0001c0001t0038g0359 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.111+303C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64611046 | ||||||
| chr12:64611111
|
G | T | 2 | a0001c0001t0002g0358a0001c0001t0033g0357 | 2 | NA18968.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.111+368G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64611111 | ||||||
| chr12:64611235
|
A | C | 259 | a0001c0001t0001g0131a0001c0001t0001g0212a0001c0001t0001g0221others(256): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.111+492A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64611235 | ||||||
| chr12:64611273
|
G | T | 2 | a0001c0001t0001g0124a0001c0001t0083g0123 | 2 | NA18987.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.111+530G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64611273 | ||||||
| chr12:64611285
|
T | G | 240 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0131others(237): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.111+542T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64611285 | ||||||
| chr12:64611299
|
C | G | 147 | a0001c0001t0001g0212a0001c0001t0001g0221a0001c0001t0001g0228others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.111+556C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64611299 | ||||||
| chr12:64611452
|
C | T | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02258.hp1 NA20905.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.111+709C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64611452 | ||||||
| chr12:64611506
|
C | G | 1 | a0001c0001t0002g0208 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.111+763C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64611506 | ||||||
| chr12:64611712
|
C | G | 14 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+969C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64611712 | ||||||
| chr12:64612025
|
A | G | 1 | a0001c0001t0002g0208 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.111+1282A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64612025 | ||||||
| chr12:64612027
|
G | A | 3 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0067g0210 | 3 | HG01109.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.111+1284G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64612027 | ||||||
| chr12:64612037
|
T | G | 1 | a0001c0001t0002g0030 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.111+1294T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64612037 | ||||||
| chr12:64612404
|
T | C | 26 | a0001c0001t0004g0348a0001c0001t0004g0363a0001c0001t0010g0364others(23): Show | 27 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.111+1661T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64612404 | ||||||
| chr12:64612479
|
C | CT | 97 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0050others(94): Show | 97 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.111+1755dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64612479 | |||||
| chr12:64612479
|
CT | C | 8 | a0001c0001t0001g0212a0001c0001t0004g0215a0001c0001t0005g0126others(5): Show | 8 | HG00140.hp2 HG00323.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+1755delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64612479 | |||||
| chr12:64612576
|
A | G | 26 | a0001c0001t0004g0348a0001c0001t0004g0363a0001c0001t0010g0364others(23): Show | 27 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.111+1833A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64612576 | ||||||
| chr12:64612578
|
C | T | 18 | a0001c0001t0007g0346a0001c0001t0007g0352a0001c0001t0027g0351others(15): Show | 18 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.111+1835C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64612578 | ||||||
| chr12:64612590
|
C | T | 9 | a0001c0001t0004g0363a0001c0001t0010g0364a0001c0001t0010g0365others(6): Show | 9 | HG02258.hp2 HG02615.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.111+1847C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64612590 | ||||||
| chr12:64612641
|
C | A | 26 | a0001c0001t0004g0348a0001c0001t0004g0363a0001c0001t0010g0364others(23): Show | 27 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.111+1898C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64612641 | ||||||
| chr12:64612660
|
G | A | 1 | a0001c0001t0005g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.111+1917G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64612660 | ||||||
| chr12:64612771
|
C | T | 17 | a0001c0001t0004g0348a0001c0001t0020g0107a0001c0001t0020g0108others(14): Show | 18 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.111+2028C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64612771 | ||||||
| chr12:64612790
|
A | G | 1 | a0001c0001t0078g0345 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.111+2047A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64612790 | ||||||
| chr12:64612945
|
A | G | 1 | a0002c0003t0010g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.111+2202A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64612945 | ||||||
| chr12:64613054
|
T | C | 2 | a0001c0001t0004g0348a0001c0001t0059g0347 | 2 | HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.111+2311T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64613054 | ||||||
| chr12:64613056
|
C | T | 9 | a0001c0001t0004g0363a0001c0001t0010g0364a0001c0001t0010g0365others(6): Show | 9 | HG02258.hp2 HG02615.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.111+2313C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64613056 | ||||||
| chr12:64613197
|
C | G | 281 | a0001c0001t0001g0042a0001c0001t0001g0131a0001c0001t0001g0212others(278): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.111+2454C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64613197 | ||||||
| chr12:64613212
|
TTTC | T | 125 | a0001c0001t0001g0042a0001c0001t0001g0131a0001c0001t0001g0212others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.111+2473_111+2475d others(5): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64613212 | |||||
| chr12:64613327
|
G | A | 125 | a0001c0001t0001g0042a0001c0001t0001g0131a0001c0001t0001g0212others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.111+2584G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64613327 | ||||||
| chr12:64613347
|
A | AT | 28 | a0001c0001t0002g0206a0001c0001t0003g0319a0001c0001t0005g0207others(25): Show | 28 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.111+2618dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64613347 | |||||
| chr12:64613474
|
G | A | 1 | a0001c0001t0004g0363 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.111+2731G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64613474 | ||||||
| chr12:64613663
|
A | G | 13 | a0001c0001t0001g0333a0001c0001t0001g0337a0001c0001t0001g0338others(10): Show | 13 | HG00597.hp2 HG02074.hp1 NA18957.hp2 others(10): Show |
intron_variant | MODIFIER | c.111+2920A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64613663 | ||||||
| chr12:64613670
|
G | A | 1 | a0001c0001t0012g0136 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.111+2927G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64613670 | ||||||
| chr12:64613708
|
G | A | 1 | a0001c0001t0039g0031 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.111+2965G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64613708 | ||||||
| chr12:64613729
|
T | C | 4 | a0001c0001t0003g0219a0001c0001t0004g0028a0001c0001t0022g0129others(1): Show | 4 | NA18942.hp2 NA18945.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+2986T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64613729 | ||||||
| chr12:64613758
|
C | T | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+3015C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64613758 | ||||||
| chr12:64613841
|
G | A | 2 | a0001c0001t0014g0137a0001c0001t0014g0138 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.111+3098G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64613841 | ||||||
| chr12:64613902
|
C | T | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+3159C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64613902 | ||||||
| chr12:64614039
|
C | G | 29 | a0001c0001t0004g0348a0001c0001t0004g0363a0001c0001t0010g0364others(26): Show | 30 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.111+3296C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64614039 | ||||||
| chr12:64614133
|
C | CT | 18 | a0001c0001t0007g0346a0001c0001t0007g0352a0001c0001t0027g0351others(15): Show | 18 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.111+3407dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64614133 | |||||
| chr12:64614133
|
CT | C | 9 | a0001c0001t0001g0050a0001c0001t0001g0212a0001c0001t0002g0140others(6): Show | 9 | HG00323.hp2 HG01433.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.111+3407delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64614133 | |||||
| chr12:64614259
|
G | A | 110 | a0001c0001t0001g0042a0001c0001t0001g0131a0001c0001t0001g0212others(107): Show | 110 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.111+3516G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64614259 | ||||||
| chr12:64614410
|
G | A | 26 | a0001c0001t0004g0348a0001c0001t0004g0363a0001c0001t0010g0364others(23): Show | 27 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.111+3667G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64614410 | ||||||
| chr12:64614575
|
C | T | 3 | a0001c0002t0021g0217a0001c0002t0021g0218a0001c0002t0047g0216 | 3 | HG02559.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.111+3832C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64614575 | ||||||
| chr12:64614699
|
CT | C | 255 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0131others(252): Show | 256 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.111+3972delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64614699 | |||||
| chr12:64614699
|
CTT | C | 14 | a0001c0001t0001g0221a0001c0001t0002g0142a0001c0001t0007g0352others(11): Show | 14 | HG00323.hp2 HG01070.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.111+3971_111+3972d others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64614699 | |||||
| chr12:64614704
|
T | C | 1 | a0001c0001t0019g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.111+3961T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64614704 | ||||||
| chr12:64614861
|
C | CT | 11 | a0001c0001t0001g0041a0001c0001t0003g0306a0001c0001t0028g0048others(8): Show | 11 | HG01358.hp2 HG01361.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+4128dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64614861 | |||||
| chr12:64614911
|
C | G | 8 | a0001c0002t0004g0015a0001c0002t0007g0013a0001c0002t0007g0014others(5): Show | 8 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+4168C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64614911 | ||||||
| chr12:64614950
|
T | C | 285 | a0001c0001t0001g0042a0001c0001t0001g0131a0001c0001t0001g0212others(282): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.111+4207T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64614950 | ||||||
| chr12:64615295
|
C | A | 1 | a0001c0002t0007g0011 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.111+4552C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64615295 | ||||||
| chr12:64615356
|
G | A | 6 | a0001c0001t0007g0352a0001c0001t0027g0351a0001c0001t0027g0354others(3): Show | 6 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+4613G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64615356 | ||||||
| chr12:64615423
|
C | T | 2 | a0001c0001t0041g0105a0001c0001t0075g0106 | 2 | HG03130.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.111+4680C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64615423 | ||||||
| chr12:64615463
|
C | T | 126 | a0001c0001t0001g0042a0001c0001t0001g0131a0001c0001t0001g0212others(123): Show | 126 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.111+4720C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64615463 | ||||||
| chr12:64615537
|
G | A | 26 | a0001c0001t0001g0032a0001c0001t0001g0055a0001c0001t0001g0056others(23): Show | 26 | HG00438.hp1 HG00609.hp2 HG02132.hp1 others(23): Show |
intron_variant | MODIFIER | c.111+4794G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64615537 | ||||||
| chr12:64615679
|
CT | C | 27 | a0001c0001t0001g0212a0001c0001t0004g0348a0001c0001t0004g0363others(24): Show | 28 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.111+4949delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64615679 | |||||
| chr12:64615760
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.111+5017G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64615760 | ||||||
| chr12:64616543
|
C | T | 1 | a0001c0001t0054g0127 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.111+5800C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64616543 | ||||||
| chr12:64616719
|
C | T | 3 | a0001c0002t0021g0217a0001c0002t0021g0218a0001c0002t0047g0216 | 3 | HG02559.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.111+5976C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64616719 | ||||||
| chr12:64616864
|
C | T | 1 | a0001c0002t0007g0011 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.111+6121C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64616864 | ||||||
| chr12:64616980
|
A | G | 3 | a0001c0002t0021g0217a0001c0002t0021g0218a0001c0002t0047g0216 | 3 | HG02559.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.111+6237A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64616980 | ||||||
| chr12:64617299
|
T | C | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.111+6556T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64617299 | ||||||
| chr12:64617411
|
A | G | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.111+6668A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64617411 | ||||||
| chr12:64617629
|
C | T | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+6886C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64617629 | ||||||
| chr12:64617718
|
G | C | 26 | a0001c0001t0004g0348a0001c0001t0004g0363a0001c0001t0010g0364others(23): Show | 27 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.111+6975G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64617718 | ||||||
| chr12:64617804
|
G | T | 6 | a0001c0001t0028g0048a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+7061G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64617804 | ||||||
| chr12:64617808
|
C | T | 6 | a0001c0001t0028g0048a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+7065C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64617808 | ||||||
| chr12:64617867
|
G | A | 1 | a0001c0001t0008g0224 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.111+7124G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64617867 | ||||||
| chr12:64618200
|
G | A | 103 | a0001c0001t0001g0333a0001c0001t0001g0337a0001c0001t0001g0338others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.111+7457G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64618200 | ||||||
| chr12:64618224
|
C | T | 103 | a0001c0001t0001g0333a0001c0001t0001g0337a0001c0001t0001g0338others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.111+7481C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64618224 | ||||||
| chr12:64618296
|
T | C | 26 | a0001c0001t0004g0348a0001c0001t0004g0363a0001c0001t0010g0364others(23): Show | 27 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.111+7553T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64618296 | ||||||
| chr12:64618445
|
G | C | 5 | a0001c0002t0021g0023a0001c0002t0028g0025a0001c0002t0029g0021others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+7702G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64618445 | ||||||
| chr12:64618569
|
T | A | 3 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0084g0079 | 3 | HG02015.hp2 NA18612.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.111+7826T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64618569 | ||||||
| chr12:64618582
|
C | G | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.111+7839C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64618582 | ||||||
| chr12:64618622
|
C | T | 1 | a0001c0001t0031g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.111+7879C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64618622 | ||||||
| chr12:64618626
|
C | CTTTTGT | 6 | a0001c0001t0028g0048a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+7900_111+7905d others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64618626 | |||||
| chr12:64618639
|
TTTTG | T | 6 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(3): Show | 6 | HG00609.hp2 NA18966.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+7900_111+7903d others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64618639 | |||||
| chr12:64618670
|
AATGCTCT others(7): Show |
A | 3 | a0001c0002t0021g0217a0001c0002t0021g0218a0001c0002t0047g0216 | 3 | HG02559.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.111+7931_111+7944d others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64618670 | |||||
| chr12:64618906
|
C | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | NA20905.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.111+8163C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64618906 | ||||||
| chr12:64618969
|
T | C | 1 | a0001c0001t0085g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.111+8226T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64618969 | ||||||
| chr12:64619044
|
T | C | 85 | a0001c0001t0001g0333a0001c0001t0001g0337a0001c0001t0001g0338others(82): Show | 85 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.111+8301T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64619044 | ||||||
| chr12:64619171
|
A | T | 2 | a0001c0001t0002g0191a0001c0001t0002g0206 | 2 | HG01516.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.111+8428A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64619171 | ||||||
| chr12:64619407
|
G | A | 1 | a0001c0002t0070g0003 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.111+8664G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64619407 | ||||||
| chr12:64619570
|
G | A | 366 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0032others(363): Show | 367 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.111+8827G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64619570 | ||||||
| chr12:64619785
|
A | G | 50 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(47): Show | 51 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.111+9042A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64619785 | ||||||
| chr12:64619813
|
C | T | 6 | a0001c0001t0028g0048a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+9070C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64619813 | ||||||
| chr12:64619863
|
C | T | 2 | a0001c0001t0002g0189a0001c0001t0012g0190 | 2 | NA18965.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.111+9120C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64619863 | ||||||
| chr12:64619872
|
C | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+9129C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64619872 | ||||||
| chr12:64619908
|
A | G | 1 | a0001c0001t0004g0305 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.111+9165A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64619908 | ||||||
| chr12:64619937
|
G | A | 6 | a0001c0001t0002g0321a0001c0001t0002g0327a0001c0001t0002g0328others(3): Show | 6 | HG01255.hp2 HG01361.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+9194G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64619937 | ||||||
| chr12:64619947
|
T | A | 1 | a0001c0001t0008g0286 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.111+9204T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64619947 | ||||||
| chr12:64619979
|
C | CA | 86 | a0001c0001t0001g0333a0001c0001t0002g0140a0001c0001t0002g0142others(83): Show | 86 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.111+9252dupA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64619979 | |||||
| chr12:64620009
|
G | C | 51 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(48): Show | 52 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.111+9266G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64620009 | ||||||
| chr12:64620014
|
C | CTCTGTGT others(7): Show |
1 | a0001c0001t0003g0227 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.111+9272_111+9273i others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64620014 | |||||
| chr12:64620014
|
C | CTGTGTGT others(3): Show |
15 | a0001c0001t0002g0144a0001c0001t0007g0352a0001c0001t0018g0213others(12): Show | 15 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.111+9285_111+9294d others(12): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64620014 | |||||
| chr12:64620014
|
C | CTGTGTGT others(5): Show |
12 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0189others(9): Show | 12 | HG01255.hp1 HG01516.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.111+9283_111+9294d others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64620014 | |||||
| chr12:64620014
|
C | CTGTGTGT others(7): Show |
129 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(126): Show | 129 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.111+9281_111+9294d others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64620014 | |||||
| chr12:64620014
|
C | CTGTGTGT others(9): Show |
36 | a0001c0001t0002g0185a0001c0001t0002g0187a0001c0001t0002g0358others(33): Show | 37 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.111+9279_111+9294d others(18): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64620014 | |||||
| chr12:64620014
|
C | CTGTGTGT others(11): Show |
57 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(54): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.111+9277_111+9294d others(20): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64620014 | |||||
| chr12:64620014
|
C | CTGTGTGT others(13): Show |
11 | a0001c0001t0004g0303a0001c0001t0005g0205a0001c0001t0007g0304others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+9275_111+9294d others(22): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64620014 | |||||
| chr12:64620014
|
C | CTGTGTGT others(17): Show |
4 | a0001c0002t0007g0016a0001c0002t0021g0217a0001c0002t0021g0218others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+9294_111+9295i others(26): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64620014 | |||||
| chr12:64620521
|
A | G | 1 | a0001c0001t0006g0071 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.111+9778A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64620521 | ||||||
| chr12:64620731
|
T | C | 2 | a0001c0001t0006g0331a0001c0001t0006g0339 | 2 | NA18964.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.111+9988T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64620731 | ||||||
| chr12:64620825
|
G | A | 50 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(47): Show | 51 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.111+10082G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64620825 | ||||||
| chr12:64620959
|
T | C | 270 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(267): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.111+10216T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64620959 | ||||||
| chr12:64620999
|
G | A | 2 | a0001c0001t0004g0290a0001c0001t0004g0291 | 2 | NA18612.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.111+10256G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64620999 | ||||||
| chr12:64621092
|
C | T | 62 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(59): Show | 62 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.111+10349C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64621092 | ||||||
| chr12:64621114
|
T | G | 28 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(25): Show | 28 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.111+10371T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64621114 | ||||||
| chr12:64621227
|
C | T | 6 | a0001c0001t0028g0048a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+10484C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64621227 | ||||||
| chr12:64621228
|
G | A | 21 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(18): Show | 21 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.111+10485G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64621228 | ||||||
| chr12:64621464
|
G | A | 152 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.111+10721G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64621464 | ||||||
| chr12:64621508
|
G | C | 1 | a0001c0001t0013g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.111+10765G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64621508 | ||||||
| chr12:64621514
|
G | A | 1 | a0001c0001t0072g0242 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.111+10771G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64621514 | ||||||
| chr12:64621638
|
C | T | 13 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(10): Show | 14 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.111+10895C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64621638 | ||||||
| chr12:64621913
|
G | T | 1 | a0001c0001t0003g0306 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.111+11170G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64621913 | ||||||
| chr12:64621928
|
G | A | 2 | a0001c0001t0008g0222a0001c0001t0008g0223 | 2 | NA18944.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.111+11185G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64621928 | ||||||
| chr12:64621933
|
G | A | 5 | a0001c0001t0009g0244a0001c0001t0009g0273a0001c0001t0038g0243others(2): Show | 5 | HG02886.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.111+11190G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64621933 | ||||||
| chr12:64621955
|
T | TA | 21 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(18): Show | 21 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.111+11220dupA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64621955 | |||||
| chr12:64621956
|
A | T | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.111+11213A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64621956 | ||||||
| chr12:64621971
|
T | C | 1 | a0001c0001t0018g0213 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.111+11228T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64621971 | ||||||
| chr12:64622182
|
T | C | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.111+11439T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64622182 | ||||||
| chr12:64622216
|
A | AT | 67 | a0001c0001t0001g0069a0001c0001t0001g0260a0001c0001t0001g0261others(64): Show | 67 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.111+11490dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64622216 | |||||
| chr12:64622216
|
AT | A | 7 | a0001c0001t0004g0302a0001c0001t0027g0351a0001c0001t0027g0354others(4): Show | 7 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+11490delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64622216 | |||||
| chr12:64622216
|
ATT | A | 48 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(45): Show | 49 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.111+11489_111+1149 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64622216 | |||||
| chr12:64622311
|
T | C | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.111+11568T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64622311 | ||||||
| chr12:64622386
|
T | C | 2 | a0001c0001t0002g0150a0001c0001t0014g0149 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.111+11643T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64622386 | ||||||
| chr12:64622394
|
G | A | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111+11651G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64622394 | ||||||
| chr12:64622474
|
CT | C | 3 | a0001c0001t0008g0247a0001c0001t0008g0248a0001c0001t0008g0249 | 3 | NA18982.hp2 NA19057.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.111+11735delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64622474 | |||||
| chr12:64622491
|
C | T | 1 | a0001c0001t0004g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.111+11748C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64622491 | ||||||
| chr12:64622520
|
A | G | 22 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(19): Show | 22 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.111+11777A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64622520 | ||||||
| chr12:64622764
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.111+12021C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64622764 | ||||||
| chr12:64622948
|
G | A | 2 | a0001c0001t0004g0293a0001c0001t0077g0292 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.111+12205G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64622948 | ||||||
| chr12:64622965
|
C | T | 1 | a0001c0001t0004g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.111+12222C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64622965 | ||||||
| chr12:64622993
|
G | C | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+12250G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64622993 | ||||||
| chr12:64623064
|
G | A | 1 | a0001c0002t0016g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.111+12321G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64623064 | ||||||
| chr12:64623306
|
G | A | 265 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(262): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.111+12563G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64623306 | ||||||
| chr12:64623318
|
G | T | 1 | a0001c0001t0004g0301 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.111+12575G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64623318 | ||||||
| chr12:64623412
|
C | T | 1 | a0001c0001t0008g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.111+12669C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64623412 | ||||||
| chr12:64623682
|
ACCCAGGC others(1010): Show |
A | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+12961_111+1397 others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64623682 | |||||
| chr12:64623918
|
G | A | 83 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(80): Show | 83 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.111+13175G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64623918 | ||||||
| chr12:64623951
|
ATTTCTGT others(11): Show |
A | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.111+13214_111+1323 others(22): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64623951 | |||||
| chr12:64623953
|
T | A | 5 | a0001c0002t0016g0033a0001c0002t0016g0034a0001c0002t0016g0035others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+13210T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64623953 | ||||||
| chr12:64624002
|
C | G | 1 | a0001c0001t0004g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.111+13259C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624002 | ||||||
| chr12:64624064
|
G | T | 83 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(80): Show | 83 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.111+13321G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624064 | ||||||
| chr12:64624074
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.111+13331T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624074 | ||||||
| chr12:64624168
|
C | G | 2 | a0001c0001t0046g0044a0002c0004t0011g0326 | 2 | HG02895.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.111+13425C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624168 | ||||||
| chr12:64624341
|
T | G | 70 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(67): Show | 70 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.111+13598T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624341 | ||||||
| chr12:64624357
|
T | C | 62 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(59): Show | 62 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.111+13614T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624357 | ||||||
| chr12:64624393
|
A | G | 13 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(10): Show | 14 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.111+13650A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624393 | ||||||
| chr12:64624412
|
T | C | 83 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(80): Show | 83 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.111+13669T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624412 | ||||||
| chr12:64624833
|
T | G | 1 | a0001c0001t0058g0151 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.111+14090T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624833 | ||||||
| chr12:64624888
|
C | T | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+14145C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624888 | ||||||
| chr12:64624902
|
C | T | 6 | a0001c0001t0028g0048a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+14159C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624902 | ||||||
| chr12:64624916
|
C | T | 1 | a0001c0001t0010g0364 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.111+14173C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624916 | ||||||
| chr12:64624945
|
G | A | 83 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(80): Show | 83 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.111+14202G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624945 | ||||||
| chr12:64624950
|
A | G | 1 | a0001c0001t0004g0102 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.111+14207A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624950 | ||||||
| chr12:64624956
|
C | T | 1 | a0001c0001t0017g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.111+14213C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64624956 | ||||||
| chr12:64625038
|
A | G | 2 | a0001c0001t0004g0299a0001c0001t0037g0300 | 2 | NA18942.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.111+14295A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64625038 | ||||||
| chr12:64625098
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.111+14355G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64625098 | ||||||
| chr12:64625198
|
C | A | 1 | a0001c0001t0003g0308 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.111+14455C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64625198 | ||||||
| chr12:64625236
|
T | A | 13 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(10): Show | 14 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.111+14493T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64625236 | ||||||
| chr12:64625445
|
C | CT | 62 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(59): Show | 62 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.111+14716dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64625445 | |||||
| chr12:64625669
|
A | G | 1 | a0001c0001t0004g0363 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.111+14926A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64625669 | ||||||
| chr12:64625684
|
G | A | 7 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(4): Show | 7 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+14941G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64625684 | ||||||
| chr12:64625744
|
A | AGCC | 50 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(47): Show | 51 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.111+15002_111+1500 others(7): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64625744 | |||||
| chr12:64625863
|
A | G | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111+15120A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64625863 | ||||||
| chr12:64625943
|
G | T | 83 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(80): Show | 83 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.111+15200G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64625943 | ||||||
| chr12:64625970
|
C | T | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.111+15227C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64625970 | ||||||
| chr12:64626120
|
T | G | 63 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(60): Show | 63 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.111+15377T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64626120 | ||||||
| chr12:64626282
|
C | T | 1 | a0001c0001t0003g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.111+15539C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64626282 | ||||||
| chr12:64626305
|
T | C | 113 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(110): Show | 114 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.111+15562T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64626305 | ||||||
| chr12:64626488
|
C | CA | 57 | a0001c0001t0001g0039a0001c0001t0001g0078a0001c0001t0001g0120others(54): Show | 58 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.111+15762dupA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64626488 | |||||
| chr12:64626529
|
A | G | 1 | a0001c0001t0017g0178 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.111+15786A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64626529 | ||||||
| chr12:64626704
|
G | A | 62 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(59): Show | 62 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.111+15961G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64626704 | ||||||
| chr12:64626814
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.111+16071C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64626814 | ||||||
| chr12:64626954
|
T | C | 2 | a0001c0001t0008g0222a0001c0001t0008g0223 | 2 | NA18944.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.111+16211T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64626954 | ||||||
| chr12:64627048
|
T | C | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+16305T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64627048 | ||||||
| chr12:64627119
|
G | A | 48 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(45): Show | 49 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.111+16376G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64627119 | ||||||
| chr12:64627368
|
A | G | 5 | a0001c0001t0009g0244a0001c0001t0009g0273a0001c0001t0038g0243others(2): Show | 5 | HG02886.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.111+16625A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64627368 | ||||||
| chr12:64627373
|
G | A | 63 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(60): Show | 63 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.111+16630G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64627373 | ||||||
| chr12:64627505
|
A | G | 6 | a0001c0001t0027g0351a0001c0001t0027g0354a0001c0001t0027g0356others(3): Show | 6 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+16762A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64627505 | ||||||
| chr12:64627596
|
C | T | 8 | a0001c0001t0003g0047a0001c0001t0006g0331a0001c0001t0006g0334others(5): Show | 8 | HG00597.hp2 NA18957.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+16853C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64627596 | ||||||
| chr12:64627656
|
G | T | 1 | a0001c0001t0008g0272 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.111+16913G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64627656 | ||||||
| chr12:64627689
|
A | C | 1 | a0001c0001t0009g0271 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.111+16946A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64627689 | ||||||
| chr12:64627947
|
G | C | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+17204G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64627947 | ||||||
| chr12:64628205
|
C | T | 2 | a0001c0001t0086g0362a0001c0001t0088g0361 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+17462C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64628205 | ||||||
| chr12:64628214
|
A | C | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111+17471A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64628214 | ||||||
| chr12:64628281
|
A | G | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0005g0205 | 3 | HG02683.hp1 HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.111+17538A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64628281 | ||||||
| chr12:64628400
|
G | A | 2 | a0001c0001t0006g0054a0001c0001t0006g0071 | 2 | NA18944.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.111+17657G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64628400 | ||||||
| chr12:64628455
|
T | C | 1 | a0001c0001t0006g0332 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.111+17712T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64628455 | ||||||
| chr12:64628614
|
A | G | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+17871A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64628614 | ||||||
| chr12:64629106
|
C | CT | 11 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(8): Show | 11 | HG00438.hp1 HG01361.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+18377dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64629106 | |||||
| chr12:64629141
|
C | T | 31 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(28): Show | 31 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.111+18398C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629141 | ||||||
| chr12:64629193
|
A | G | 1 | a0001c0001t0072g0242 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.111+18450A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629193 | ||||||
| chr12:64629274
|
C | T | 3 | a0001c0001t0055g0176a0001c0001t0057g0177a0001c0001t0058g0151 | 3 | HG01256.hp1 NA20300.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.111+18531C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629274 | ||||||
| chr12:64629347
|
G | A | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.111+18604G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629347 | ||||||
| chr12:64629425
|
C | T | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111+18682C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629425 | ||||||
| chr12:64629451
|
A | G | 1 | a0001c0001t0004g0363 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.111+18708A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629451 | ||||||
| chr12:64629469
|
A | T | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.111+18726A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629469 | ||||||
| chr12:64629538
|
G | T | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.111+18795G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629538 | ||||||
| chr12:64629663
|
G | A | 31 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(28): Show | 31 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.111+18920G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629663 | ||||||
| chr12:64629703
|
G | A | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+18960G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629703 | ||||||
| chr12:64629811
|
A | C | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+19068A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629811 | ||||||
| chr12:64629961
|
C | CA | 9 | a0001c0001t0001g0055a0001c0001t0001g0081a0001c0001t0002g0030others(6): Show | 9 | HG00735.hp2 HG01256.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.111+19234dupA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64629961 | |||||
| chr12:64629961
|
CA | C | 16 | a0001c0001t0006g0054a0001c0001t0007g0100a0001c0001t0020g0107others(13): Show | 17 | HG01169.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.111+19234delA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64629961 | |||||
| chr12:64629961
|
CAA | C | 57 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(54): Show | 57 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.111+19233_111+1923 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64629961 | |||||
| chr12:64629966
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0003g0317 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.111+19229_111+1924 others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64629966 | |||||
| chr12:64629977
|
AG | A | 42 | a0001c0001t0002g0150a0001c0001t0002g0350a0001c0001t0003g0047others(39): Show | 42 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.111+19235delG | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629977 | ||||||
| chr12:64629978
|
G | A | 143 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(140): Show | 143 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.111+19235G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629978 | ||||||
| chr12:64629984
|
G | A | 1 | a0001c0002t0028g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.111+19241G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629984 | ||||||
| chr12:64629988
|
A | G | 1 | a0001c0002t0028g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.111+19245A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64629988 | ||||||
| chr12:64630053
|
CAG | C | 4 | a0001c0001t0002g0147a0001c0001t0002g0152a0001c0001t0002g0175others(1): Show | 4 | HG02135.hp2 NA18941.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+19311_111+1931 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64630053 | ||||||
| chr12:64630350
|
A | G | 1 | a0001c0001t0003g0317 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.111+19607A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64630350 | ||||||
| chr12:64630388
|
T | C | 2 | a0001c0002t0007g0018a0001c0002t0007g0019 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.111+19645T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64630388 | ||||||
| chr12:64630545
|
A | G | 63 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(60): Show | 63 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.111+19802A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64630545 | ||||||
| chr12:64630598
|
A | G | 1 | a0001c0001t0052g0330 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.111+19855A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64630598 | ||||||
| chr12:64630617
|
A | G | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.111+19874A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64630617 | ||||||
| chr12:64630643
|
T | C | 1 | a0001c0001t0002g0327 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.111+19900T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64630643 | ||||||
| chr12:64630764
|
G | A | 27 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(24): Show | 27 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.111+20021G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64630764 | ||||||
| chr12:64630787
|
T | C | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.111+20044T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64630787 | ||||||
| chr12:64630809
|
C | G | 1 | a0001c0001t0004g0215 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.111+20066C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64630809 | ||||||
| chr12:64630846
|
G | T | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+20103G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64630846 | ||||||
| chr12:64630956
|
G | A | 2 | a0001c0001t0014g0137a0001c0001t0014g0138 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.111+20213G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64630956 | ||||||
| chr12:64631026
|
CAG | C | 3 | a0001c0001t0006g0054a0001c0001t0006g0071a0001c0001t0076g0064 | 3 | NA18944.hp1 NA18950.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.111+20290_111+2029 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64631026 | |||||
| chr12:64631171
|
G | C | 34 | a0001c0001t0005g0126a0001c0001t0005g0128a0001c0001t0005g0141others(31): Show | 34 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.111+20428G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631171 | ||||||
| chr12:64631291
|
A | G | 1 | a0001c0001t0008g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.111+20548A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631291 | ||||||
| chr12:64631307
|
C | T | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.111+20564C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631307 | ||||||
| chr12:64631511
|
T | C | 1 | a0001c0002t0016g0034 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.111+20768T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631511 | ||||||
| chr12:64631520
|
T | C | 4 | a0001c0001t0008g0276a0001c0001t0026g0239a0001c0001t0026g0240others(1): Show | 4 | NA18945.hp1 NA18983.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+20777T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631520 | ||||||
| chr12:64631527
|
A | G | 63 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(60): Show | 63 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.111+20784A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631527 | ||||||
| chr12:64631530
|
G | A | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+20787G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631530 | ||||||
| chr12:64631536
|
A | AATGT | 26 | a0001c0001t0002g0155a0001c0001t0002g0180a0001c0001t0003g0219others(23): Show | 26 | HG00438.hp2 HG00639.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.111+20842_111+2084 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64631536 | |||||
| chr12:64631536
|
A | AATGTATG others(1): Show |
5 | a0001c0001t0003g0252a0001c0001t0035g0341a0001c0001t0071g0360others(2): Show | 5 | HG02135.hp2 HG03130.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+20838_111+2084 others(12): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64631536 | |||||
| chr12:64631536
|
A | AATGTATG others(5): Show |
2 | a0001c0001t0003g0342a0001c0001t0006g0332 | 2 | HG02074.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.111+20834_111+2084 others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64631536 | |||||
| chr12:64631536
|
AATGT | A | 180 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0032others(177): Show | 181 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(178): Show |
intron_variant | MODIFIER | c.111+20842_111+2084 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64631536 | |||||
| chr12:64631536
|
AATGTATG others(1): Show |
A | 37 | a0001c0001t0001g0050a0001c0001t0001g0233a0001c0001t0001g0234others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.111+20838_111+2084 others(12): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64631536 | |||||
| chr12:64631536
|
AATGTATG others(5): Show |
A | 34 | a0001c0001t0001g0077a0001c0001t0001g0099a0001c0001t0004g0103others(31): Show | 34 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.111+20834_111+2084 others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64631536 | |||||
| chr12:64631536
|
AATGTATG others(9): Show |
A | 1 | a0001c0001t0001g0042 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.111+20830_111+2084 others(20): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64631536 | |||||
| chr12:64631610
|
C | T | 2 | a0001c0001t0086g0362a0001c0001t0088g0361 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+20867C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631610 | ||||||
| chr12:64631636
|
A | G | 29 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(26): Show | 29 | HG01109.hp1 HG01361.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.111+20893A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631636 | ||||||
| chr12:64631664
|
C | T | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+20921C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631664 | ||||||
| chr12:64631665
|
G | A | 1 | a0001c0002t0070g0003 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.111+20922G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631665 | ||||||
| chr12:64631772
|
G | T | 63 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(60): Show | 63 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.111+21029G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631772 | ||||||
| chr12:64631907
|
C | G | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.111+21164C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631907 | ||||||
| chr12:64631963
|
C | T | 1 | a0001c0001t0006g0336 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.111+21220C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64631963 | ||||||
| chr12:64632031
|
A | G | 2 | a0001c0002t0007g0011a0001c0002t0007g0012 | 2 | HG01167.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.111+21288A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632031 | ||||||
| chr12:64632082
|
G | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02056.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.111+21339G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632082 | ||||||
| chr12:64632136
|
G | T | 8 | a0001c0002t0004g0015a0001c0002t0007g0013a0001c0002t0007g0014others(5): Show | 8 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+21393G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632136 | ||||||
| chr12:64632149
|
G | T | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+21406G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632149 | ||||||
| chr12:64632226
|
G | C | 49 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(46): Show | 50 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.111+21483G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632226 | ||||||
| chr12:64632260
|
A | G | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.111+21517A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632260 | ||||||
| chr12:64632318
|
C | T | 2 | a0001c0001t0086g0362a0001c0001t0090g0369 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+21575C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632318 | ||||||
| chr12:64632335
|
G | A | 116 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(113): Show | 116 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.111+21592G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632335 | ||||||
| chr12:64632434
|
G | A | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.111+21691G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632434 | ||||||
| chr12:64632552
|
C | T | 2 | a0001c0001t0003g0279a0001c0001t0006g0278 | 2 | HG02027.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.111+21809C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632552 | ||||||
| chr12:64632562
|
A | G | 115 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(112): Show | 115 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.111+21819A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632562 | ||||||
| chr12:64632686
|
T | G | 14 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+21943T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632686 | ||||||
| chr12:64632759
|
A | G | 8 | a0001c0001t0027g0351a0001c0001t0028g0048a0001c0001t0046g0044others(5): Show | 8 | HG01361.hp2 HG02109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+22016A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632759 | ||||||
| chr12:64632897
|
T | C | 7 | a0001c0001t0028g0048a0001c0001t0046g0044a0001c0002t0021g0023others(4): Show | 7 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+22154T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64632897 | ||||||
| chr12:64633005
|
G | A | 1 | a0001c0001t0004g0294 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.111+22262G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64633005 | ||||||
| chr12:64633064
|
T | G | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+22321T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64633064 | ||||||
| chr12:64633083
|
G | A | 2 | a0001c0002t0021g0217a0001c0002t0021g0218 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.111+22340G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64633083 | ||||||
| chr12:64633091
|
CTGTTTCT others(18): Show |
C | 1 | a0001c0001t0026g0239 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.111+22349_111+2237 others(29): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64633091 | ||||||
| chr12:64633395
|
T | A | 1 | a0001c0001t0026g0239 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.111+22652T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64633395 | ||||||
| chr12:64633510
|
ACCTCCTG others(4): Show |
A | 11 | a0001c0001t0028g0048a0001c0001t0046g0044a0001c0001t0086g0362others(8): Show | 11 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+22783_111+2279 others(15): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64633510 | |||||
| chr12:64633634
|
C | T | 8 | a0001c0002t0004g0015a0001c0002t0007g0013a0001c0002t0007g0014others(5): Show | 8 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+22891C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64633634 | ||||||
| chr12:64633641
|
A | G | 42 | a0001c0001t0005g0126a0001c0001t0005g0128a0001c0001t0005g0141others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.111+22898A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64633641 | ||||||
| chr12:64633731
|
C | A | 154 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(151): Show | 154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.111+22988C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64633731 | ||||||
| chr12:64633787
|
G | A | 1 | a0001c0001t0013g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.111+23044G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64633787 | ||||||
| chr12:64633810
|
C | T | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+23067C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64633810 | ||||||
| chr12:64633835
|
A | C | 1 | a0001c0001t0002g0174 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.111+23092A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64633835 | ||||||
| chr12:64633873
|
C | T | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.111+23130C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64633873 | ||||||
| chr12:64634150
|
G | T | 1 | a0001c0001t0001g0124 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.111+23407G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634150 | ||||||
| chr12:64634189
|
G | A | 43 | a0001c0001t0005g0126a0001c0001t0005g0128a0001c0001t0005g0141others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.111+23446G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634189 | ||||||
| chr12:64634278
|
G | C | 6 | a0001c0001t0028g0048a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+23535G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634278 | ||||||
| chr12:64634310
|
C | CT | 57 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(54): Show | 57 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.111+23580dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64634310 | |||||
| chr12:64634310
|
CT | C | 43 | a0001c0001t0005g0126a0001c0001t0005g0128a0001c0001t0005g0141others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.111+23580delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64634310 | |||||
| chr12:64634323
|
T | C | 6 | a0001c0002t0015g0004a0001c0002t0015g0006a0001c0002t0015g0007others(3): Show | 6 | HG01106.hp2 HG01109.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+23580T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634323 | ||||||
| chr12:64634429
|
A | G | 5 | a0001c0001t0003g0313a0001c0001t0003g0316a0001c0001t0036g0314others(2): Show | 5 | HG02647.hp2 HG02818.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+23686A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634429 | ||||||
| chr12:64634520
|
C | T | 154 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(151): Show | 154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.111+23777C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634520 | ||||||
| chr12:64634559
|
C | T | 11 | a0001c0001t0004g0363a0001c0001t0007g0352a0001c0001t0010g0364others(8): Show | 11 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+23816C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634559 | ||||||
| chr12:64634593
|
C | T | 26 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(23): Show | 26 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(23): Show |
intron_variant | MODIFIER | c.111+23850C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634593 | ||||||
| chr12:64634665
|
G | A | 5 | a0001c0002t0021g0023a0001c0002t0028g0025a0001c0002t0029g0021others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+23922G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634665 | ||||||
| chr12:64634693
|
A | G | 1 | a0001c0001t0025g0083 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.111+23950A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634693 | ||||||
| chr12:64634712
|
G | A | 34 | a0001c0001t0005g0126a0001c0001t0005g0128a0001c0001t0005g0141others(31): Show | 34 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.111+23969G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634712 | ||||||
| chr12:64634747
|
C | T | 64 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(61): Show | 64 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.111+24004C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634747 | ||||||
| chr12:64634762
|
T | TA | 26 | a0001c0001t0001g0032a0001c0001t0001g0039a0001c0001t0001g0041others(23): Show | 26 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.111+24047dupA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64634762 | |||||
| chr12:64634762
|
TA | T | 46 | a0001c0001t0001g0221a0001c0001t0003g0252a0001c0001t0004g0215others(43): Show | 47 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.111+24047delA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64634762 | |||||
| chr12:64634762
|
TAA | T | 11 | a0001c0001t0003g0219a0001c0001t0003g0253a0001c0001t0003g0254others(8): Show | 11 | HG00438.hp2 HG02027.hp2 HG03579.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+24046_111+2404 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64634762 | |||||
| chr12:64634762
|
TAAA | T | 48 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(45): Show | 48 | HG00597.hp1 HG01074.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.111+24045_111+2404 others(7): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64634762 | |||||
| chr12:64634762
|
TAAAA | T | 8 | a0001c0001t0002g0156a0001c0001t0002g0159a0001c0001t0002g0189others(5): Show | 8 | HG00323.hp2 HG01175.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+24044_111+2404 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64634762 | |||||
| chr12:64634762
|
TAAAAA | T | 78 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(75): Show | 78 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.111+24043_111+2404 others(9): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64634762 | |||||
| chr12:64634762
|
TAAAAAA | T | 31 | a0001c0001t0002g0173a0001c0001t0003g0209a0001c0001t0003g0211others(28): Show | 31 | HG01109.hp1 HG01169.hp2 HG02258.hp2 others(28): Show |
intron_variant | MODIFIER | c.111+24042_111+2404 others(10): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64634762 | |||||
| chr12:64634764
|
A | T | 14 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+24021A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634764 | ||||||
| chr12:64634778
|
A | T | 1 | a0001c0001t0026g0239 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.111+24035A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634778 | ||||||
| chr12:64634820
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.111+24077G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634820 | ||||||
| chr12:64634864
|
G | T | 1 | a0001c0002t0024g0002 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.111+24121G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634864 | ||||||
| chr12:64634878
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.111+24135A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634878 | ||||||
| chr12:64634914
|
A | G | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+24171A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634914 | ||||||
| chr12:64634967
|
CT | C | 169 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(166): Show | 169 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.111+24240delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64634967 | |||||
| chr12:64634973
|
T | C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+24230T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64634973 | ||||||
| chr12:64635028
|
C | T | 7 | a0001c0001t0028g0048a0001c0001t0046g0044a0001c0002t0021g0023others(4): Show | 7 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+24285C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64635028 | ||||||
| chr12:64635040
|
A | G | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+24297A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64635040 | ||||||
| chr12:64635107
|
C | T | 107 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(104): Show | 107 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.111+24364C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64635107 | ||||||
| chr12:64635302
|
C | T | 4 | a0001c0001t0003g0313a0001c0001t0003g0316a0001c0001t0036g0314others(1): Show | 4 | HG02647.hp2 HG03209.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+24559C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64635302 | ||||||
| chr12:64635515
|
G | A | 2 | a0001c0001t0003g0317a0001c0001t0041g0312 | 2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.111+24772G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64635515 | ||||||
| chr12:64635708
|
G | T | 1 | a0001c0001t0003g0317 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.111+24965G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64635708 | ||||||
| chr12:64635785
|
G | T | 1 | a0001c0001t0003g0268 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.111+25042G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64635785 | ||||||
| chr12:64635811
|
A | G | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+25068A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64635811 | ||||||
| chr12:64635891
|
G | A | 1 | a0001c0001t0031g0113 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.111+25148G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64635891 | ||||||
| chr12:64635968
|
C | T | 1 | a0001c0001t0038g0359 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.111+25225C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64635968 | ||||||
| chr12:64636120
|
GT | G | 79 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0142others(76): Show | 79 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.111+25389delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64636120 | |||||
| chr12:64636202
|
C | T | 14 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+25459C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64636202 | ||||||
| chr12:64636227
|
C | G | 3 | a0001c0001t0006g0310a0001c0001t0006g0311a0001c0001t0044g0110 | 3 | HG02922.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.111+25484C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64636227 | ||||||
| chr12:64636342
|
G | A | 67 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(64): Show | 67 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.111+25599G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64636342 | ||||||
| chr12:64636353
|
A | G | 31 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(28): Show | 31 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.111+25610A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64636353 | ||||||
| chr12:64636511
|
T | C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+25768T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64636511 | ||||||
| chr12:64636603
|
C | A | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+25860C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64636603 | ||||||
| chr12:64636617
|
G | A | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+25874G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64636617 | ||||||
| chr12:64636664
|
G | A | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+25921G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64636664 | ||||||
| chr12:64636723
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.111+25980G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64636723 | ||||||
| chr12:64636764
|
G | A | 60 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.111+26021G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64636764 | ||||||
| chr12:64636831
|
C | T | 1 | a0001c0002t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.111+26088C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64636831 | ||||||
| chr12:64636865
|
C | CA | 8 | a0001c0001t0002g0189a0001c0001t0004g0133a0001c0001t0004g0215others(5): Show | 8 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+26141dupA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64636865 | |||||
| chr12:64636865
|
CA | C | 16 | a0001c0001t0003g0264a0001c0001t0004g0226a0001c0001t0006g0283others(13): Show | 16 | HG01169.hp1 HG02040.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.111+26141delA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64636865 | |||||
| chr12:64637080
|
G | A | 1 | a0001c0001t0003g0317 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.111+26337G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637080 | ||||||
| chr12:64637110
|
G | A | 72 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.111+26367G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637110 | ||||||
| chr12:64637192
|
C | T | 1 | a0001c0001t0003g0263 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.111+26449C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637192 | ||||||
| chr12:64637237
|
A | G | 3 | a0001c0001t0018g0236a0001c0001t0018g0237a0001c0001t0073g0238 | 3 | NA18943.hp2 NA18953.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.111+26494A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637237 | ||||||
| chr12:64637278
|
T | C | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+26535T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637278 | ||||||
| chr12:64637310
|
A | G | 3 | a0001c0001t0004g0298a0001c0001t0004g0302a0001c0001t0037g0297 | 3 | NA18747.hp2 NA19005.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.111+26567A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637310 | ||||||
| chr12:64637341
|
G | C | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | NA19000.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.111+26598G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637341 | ||||||
| chr12:64637423
|
C | CT | 79 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(76): Show | 79 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.111+26698dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64637423 | |||||
| chr12:64637423
|
C | CTT | 6 | a0001c0001t0002g0155a0001c0001t0012g0136a0001c0001t0054g0127others(3): Show | 6 | HG01069.hp2 HG02155.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+26697_111+2669 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64637423 | |||||
| chr12:64637426
|
T | TC | 8 | a0001c0001t0028g0048a0001c0001t0046g0044a0001c0002t0021g0023others(5): Show | 8 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+26683_111+2668 others(5): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637426 | ||||||
| chr12:64637427
|
T | C | 61 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(58): Show | 61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.111+26684T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637427 | ||||||
| chr12:64637468
|
G | A | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.111+26725G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637468 | ||||||
| chr12:64637482
|
T | C | 31 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(28): Show | 31 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.111+26739T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637482 | ||||||
| chr12:64637486
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.111+26743G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637486 | ||||||
| chr12:64637492
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.111+26749T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637492 | ||||||
| chr12:64637519
|
T | A | 14 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+26776T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637519 | ||||||
| chr12:64637519
|
T | G | 1 | a0001c0001t0080g0307 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.111+26776T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637519 | ||||||
| chr12:64637579
|
G | A | 1 | a0001c0001t0027g0354 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.111+26836G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637579 | ||||||
| chr12:64637596
|
G | A | 1 | a0001c0001t0039g0031 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.111+26853G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637596 | ||||||
| chr12:64637695
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.111+26952G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637695 | ||||||
| chr12:64637786
|
T | A | 34 | a0001c0001t0005g0126a0001c0001t0005g0128a0001c0001t0005g0141others(31): Show | 34 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.111+27043T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637786 | ||||||
| chr12:64637799
|
A | G | 2 | a0001c0001t0009g0244a0001c0001t0009g0273 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.111+27056A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637799 | ||||||
| chr12:64637833
|
A | AT | 10 | a0001c0001t0002g0140a0001c0001t0002g0147a0001c0001t0002g0152others(7): Show | 10 | HG01433.hp1 HG03098.hp2 HG03540.hp2 others(7): Show |
intron_variant | MODIFIER | c.111+27106dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64637833 | |||||
| chr12:64637887
|
A | G | 9 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(6): Show | 9 | HG01934.hp1 NA18939.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.111+27144A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637887 | ||||||
| chr12:64637986
|
C | G | 69 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(66): Show | 69 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.111+27243C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64637986 | ||||||
| chr12:64638033
|
T | C | 1 | a0001c0001t0004g0294 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.111+27290T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638033 | ||||||
| chr12:64638066
|
G | A | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.111+27323G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638066 | ||||||
| chr12:64638126
|
G | A | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.111+27383G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638126 | ||||||
| chr12:64638155
|
A | C | 5 | a0001c0002t0016g0033a0001c0002t0016g0034a0001c0002t0016g0035others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+27412A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638155 | ||||||
| chr12:64638209
|
T | G | 1 | a0001c0001t0031g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.111+27466T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638209 | ||||||
| chr12:64638318
|
T | C | 1 | a0001c0001t0065g0318 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.111+27575T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638318 | ||||||
| chr12:64638374
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.111+27631A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638374 | ||||||
| chr12:64638407
|
T | C | 3 | a0001c0001t0017g0160a0001c0001t0017g0172a0001c0001t0049g0049 | 3 | HG02896.hp2 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.111+27664T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638407 | ||||||
| chr12:64638436
|
T | C | 198 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(195): Show | 198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.111+27693T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638436 | ||||||
| chr12:64638520
|
C | T | 1 | a0001c0001t0013g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.111+27777C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638520 | ||||||
| chr12:64638558
|
C | T | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+27815C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638558 | ||||||
| chr12:64638579
|
C | CA | 88 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(85): Show | 88 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.111+27853dupA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64638579 | |||||
| chr12:64638579
|
C | CAA | 38 | a0001c0001t0002g0159a0001c0001t0003g0209a0001c0001t0003g0211others(35): Show | 38 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.111+27852_111+2785 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64638579 | |||||
| chr12:64638640
|
C | G | 3 | a0001c0001t0001g0077a0001c0001t0001g0099a0001c0001t0004g0103 | 3 | HG02071.hp1 NA18747.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.111+27897C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638640 | ||||||
| chr12:64638703
|
G | A | 1 | a0001c0001t0018g0213 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.111+27960G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638703 | ||||||
| chr12:64638717
|
A | G | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.111+27974A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638717 | ||||||
| chr12:64638744
|
T | G | 46 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.111+28001T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638744 | ||||||
| chr12:64638842
|
GTTCC | G | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+28103_111+2810 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64638842 | |||||
| chr12:64638894
|
A | C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+28151A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638894 | ||||||
| chr12:64638960
|
T | C | 1 | a0001c0001t0004g0343 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.111+28217T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638960 | ||||||
| chr12:64638964
|
G | C | 46 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.111+28221G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64638964 | ||||||
| chr12:64639074
|
G | C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+28331G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639074 | ||||||
| chr12:64639355
|
A | G | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+28612A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639355 | ||||||
| chr12:64639362
|
AT | A | 47 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(44): Show | 47 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.111+28631delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64639362 | |||||
| chr12:64639369
|
T | G | 38 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(35): Show | 38 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.111+28626T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639369 | ||||||
| chr12:64639379
|
A | G | 2 | a0001c0001t0057g0177a0001c0001t0058g0151 | 2 | NA20300.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.111+28636A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639379 | ||||||
| chr12:64639394
|
T | C | 1 | a0001c0001t0003g0308 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.111+28651T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639394 | ||||||
| chr12:64639422
|
T | G | 130 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(127): Show | 130 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.111+28679T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639422 | ||||||
| chr12:64639463
|
C | T | 4 | a0001c0001t0009g0097a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG02300.hp2 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+28720C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639463 | ||||||
| chr12:64639464
|
G | A | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.111+28721G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639464 | ||||||
| chr12:64639469
|
C | CT | 49 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(46): Show | 49 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.111+28728dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64639469 | |||||
| chr12:64639481
|
A | G | 1 | a0001c0001t0003g0308 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.111+28738A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639481 | ||||||
| chr12:64639542
|
A | C | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.111+28799A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639542 | ||||||
| chr12:64639698
|
G | C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+28955G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639698 | ||||||
| chr12:64639787
|
C | T | 8 | a0001c0001t0028g0048a0001c0001t0046g0044a0001c0002t0021g0023others(5): Show | 8 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+29044C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639787 | ||||||
| chr12:64639803
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.111+29060C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639803 | ||||||
| chr12:64639853
|
A | G | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+29110A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639853 | ||||||
| chr12:64639906
|
C | T | 1 | a0002c0003t0011g0112 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.111+29163C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639906 | ||||||
| chr12:64639940
|
C | T | 1 | a0001c0002t0047g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.111+29197C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639940 | ||||||
| chr12:64639967
|
A | T | 2 | a0001c0001t0057g0177a0001c0001t0058g0151 | 2 | NA20300.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.111+29224A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64639967 | ||||||
| chr12:64640006
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0068 | 2 | HG00438.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.111+29263A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640006 | ||||||
| chr12:64640051
|
G | C | 7 | a0001c0001t0028g0048a0001c0001t0088g0361a0001c0002t0021g0023others(4): Show | 7 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+29308G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640051 | ||||||
| chr12:64640143
|
A | AT | 5 | a0001c0002t0016g0033a0001c0002t0016g0034a0001c0002t0016g0035others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+29407dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64640143 | |||||
| chr12:64640187
|
T | C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+29444T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640187 | ||||||
| chr12:64640245
|
C | T | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.111+29502C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640245 | ||||||
| chr12:64640392
|
A | G | 26 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(23): Show | 26 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(23): Show |
intron_variant | MODIFIER | c.111+29649A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640392 | ||||||
| chr12:64640498
|
C | G | 2 | a0001c0002t0021g0217a0001c0002t0021g0218 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.111+29755C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640498 | ||||||
| chr12:64640606
|
T | TAAAAAAA others(92): Show |
1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29863_111+2986 others(103): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640606 | ||||||
| chr12:64640608
|
C | A | 1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29865C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640608 | ||||||
| chr12:64640610
|
T | A | 1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29867T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640610 | ||||||
| chr12:64640611
|
C | A | 7 | a0001c0001t0013g0161a0001c0001t0028g0048a0001c0002t0021g0023others(4): Show | 7 | HG00323.hp1 HG01361.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+29868C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640611 | ||||||
| chr12:64640612
|
C | A | 1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29869C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640612 | ||||||
| chr12:64640615
|
G | A | 1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29872G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640615 | ||||||
| chr12:64640616
|
T | A | 1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29873T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640616 | ||||||
| chr12:64640627
|
G | C | 1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29884G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640627 | ||||||
| chr12:64640628
|
G | A | 1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29885G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640628 | ||||||
| chr12:64640634
|
T | G | 1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29891T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640634 | ||||||
| chr12:64640635
|
T | A | 1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29892T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640635 | ||||||
| chr12:64640637
|
C | A | 1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29894C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640637 | ||||||
| chr12:64640638
|
C | G | 1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29895C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640638 | ||||||
| chr12:64640640
|
T | A | 1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29897T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640640 | ||||||
| chr12:64640643
|
CATTTTAT others(87): Show |
C | 1 | a0001c0001t0013g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.111+29901_111+2999 others(98): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640643 | ||||||
| chr12:64640659
|
T | G | 80 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(77): Show | 80 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.111+29916T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640659 | ||||||
| chr12:64640679
|
G | A | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+29936G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640679 | ||||||
| chr12:64640679
|
G | T | 5 | a0001c0001t0027g0351a0001c0001t0027g0354a0001c0001t0027g0356others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.111+29936G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640679 | ||||||
| chr12:64640688
|
G | C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+29945G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640688 | ||||||
| chr12:64640737
|
G | C | 143 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(140): Show | 143 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.111+29994G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640737 | ||||||
| chr12:64640739
|
C | T | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.111+29996C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640739 | ||||||
| chr12:64640780
|
C | T | 46 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.111+30037C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640780 | ||||||
| chr12:64640861
|
C | T | 46 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.111+30118C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640861 | ||||||
| chr12:64640889
|
T | G | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.111+30146T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64640889 | ||||||
| chr12:64641016
|
T | G | 61 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(58): Show | 61 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.111+30273T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641016 | ||||||
| chr12:64641046
|
ATATACT | A | 8 | a0001c0001t0028g0048a0001c0001t0046g0044a0001c0002t0021g0023others(5): Show | 8 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+30307_111+3031 others(10): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641046 | |||||
| chr12:64641065
|
A | G | 13 | a0001c0001t0003g0306a0001c0001t0007g0346a0001c0002t0004g0015others(10): Show | 13 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.111+30322A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641065 | ||||||
| chr12:64641070
|
C | T | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+30327C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641070 | ||||||
| chr12:64641079
|
C | T | 193 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(190): Show | 193 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.111+30336C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641079 | ||||||
| chr12:64641339
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0080others(2): Show | 5 | HG02015.hp2 HG02080.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+30596T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641339 | ||||||
| chr12:64641398
|
A | G | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+30655A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641398 | ||||||
| chr12:64641399
|
G | GGC | 6 | a0001c0001t0004g0288a0001c0001t0005g0196a0001c0001t0005g0197others(3): Show | 6 | HG01099.hp2 HG01934.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+30659_111+3066 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641399 | |||||
| chr12:64641400
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+30658_111+3065 others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641400 | |||||
| chr12:64641400
|
G | GCACACAC others(11): Show |
1 | a0001c0001t0004g0363 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.111+30658_111+3065 others(22): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641400 | |||||
| chr12:64641400
|
G | GCACACAC others(13): Show |
6 | a0001c0002t0007g0013a0001c0002t0007g0016a0001c0002t0007g0017others(3): Show | 6 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+30658_111+3065 others(24): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641400 | |||||
| chr12:64641400
|
G | GCACACAC others(15): Show |
3 | a0001c0001t0090g0369a0001c0002t0004g0015a0001c0002t0007g0014 | 3 | HG00140.hp1 HG04204.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.111+30658_111+3065 others(26): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641400 | |||||
| chr12:64641400
|
G | GCACACAC others(17): Show |
5 | a0001c0001t0007g0346a0001c0001t0086g0362a0001c0001t0088g0361others(2): Show | 5 | HG01167.hp1 HG02015.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.111+30658_111+3065 others(28): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641400 | |||||
| chr12:64641402
|
G | A | 43 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(40): Show | 43 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.111+30659G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641402 | ||||||
| chr12:64641404
|
A | G | 48 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0289others(45): Show | 48 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.111+30661A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641404 | ||||||
| chr12:64641414
|
A | ACACACAC others(31): Show |
1 | a0001c0002t0045g0024 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.111+30672_111+3067 others(42): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(27): Show |
1 | a0001c0002t0021g0023 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.111+30672_111+3067 others(38): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(29): Show |
2 | a0001c0002t0029g0021a0001c0002t0029g0022 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.111+30672_111+3067 others(40): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(31): Show |
1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.111+30672_111+3067 others(42): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(23): Show |
1 | a0001c0002t0028g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.111+30672_111+3067 others(34): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(23): Show |
1 | a0001c0001t0065g0318 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.111+30672_111+3067 others(34): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(19): Show |
1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.111+30672_111+3067 others(30): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(21): Show |
1 | a0001c0001t0038g0243 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.111+30672_111+3067 others(32): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(23): Show |
1 | a0001c0001t0036g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.111+30672_111+3067 others(34): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(25): Show |
2 | a0001c0001t0003g0313a0001c0001t0036g0314 | 2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.111+30672_111+3067 others(36): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(19): Show |
2 | a0001c0001t0085g0029a0001c0002t0047g0216 | 2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.111+30672_111+3067 others(30): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(21): Show |
2 | a0001c0001t0003g0317a0001c0001t0041g0312 | 2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.111+30672_111+3067 others(32): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(23): Show |
1 | a0001c0001t0003g0316 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.111+30672_111+3067 others(34): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(25): Show |
1 | a0001c0001t0066g0220 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.111+30672_111+3067 others(36): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(13): Show |
1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+30672_111+3067 others(24): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(19): Show |
2 | a0001c0001t0003g0209a0001c0001t0067g0210 | 2 | HG01109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.111+30672_111+3067 others(30): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(23): Show |
2 | a0001c0001t0006g0310a0001c0001t0044g0110 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.111+30672_111+3067 others(34): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(11): Show |
1 | a0001c0001t0006g0311 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.111+30672_111+3067 others(22): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(15): Show |
1 | a0001c0001t0003g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.111+30672_111+3067 others(26): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(15): Show |
1 | a0001c0001t0003g0308 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.111+30672_111+3067 others(26): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACACACAC others(7): Show |
1 | a0001c0001t0003g0309 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.111+30672_111+3067 others(18): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ACG | 14 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0085others(11): Show | 14 | HG00609.hp2 HG01099.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.111+30684_111+3068 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641414 | |||||
| chr12:64641414
|
A | ATGCGCGC others(3): Show |
1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.111+30671_111+3067 others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641414 | ||||||
| chr12:64641414
|
A | G | 6 | a0001c0001t0004g0288a0001c0001t0005g0196a0001c0001t0005g0197others(3): Show | 6 | HG01099.hp2 HG01934.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+30671A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641414 | ||||||
| chr12:64641415
|
C | T | 1 | a0001c0001t0006g0287 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.111+30672C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641415 | ||||||
| chr12:64641416
|
G | A | 90 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(87): Show | 90 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.111+30673G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641416 | ||||||
| chr12:64641417
|
C | T | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.111+30674C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641417 | ||||||
| chr12:64641418
|
G | A | 89 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(86): Show | 89 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.111+30675G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641418 | ||||||
| chr12:64641419
|
C | CACACACA others(17): Show |
1 | a0001c0001t0002g0153 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.111+30676_111+3067 others(28): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641419 | ||||||
| chr12:64641419
|
C | CACACACA others(13): Show |
5 | a0001c0001t0004g0226a0001c0001t0004g0325a0001c0001t0006g0324others(2): Show | 5 | HG00673.hp1 HG01256.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+30676_111+3067 others(24): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641419 | ||||||
| chr12:64641419
|
C | CACACACA others(11): Show |
66 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(63): Show | 66 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.111+30676_111+3067 others(22): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641419 | ||||||
| chr12:64641419
|
C | CACACACA others(9): Show |
13 | a0001c0001t0007g0352a0001c0001t0009g0244a0001c0001t0009g0273others(10): Show | 13 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.111+30676_111+3067 others(20): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641419 | ||||||
| chr12:64641419
|
C | CACACACA others(7): Show |
2 | a0001c0001t0017g0160a0001c0001t0017g0172 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.111+30676_111+3067 others(18): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641419 | ||||||
| chr12:64641419
|
C | T | 1 | a0001c0001t0079g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.111+30676C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641419 | ||||||
| chr12:64641421
|
C | T | 7 | a0001c0001t0028g0048a0001c0001t0046g0044a0001c0002t0021g0023others(4): Show | 7 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+30678C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641421 | ||||||
| chr12:64641429
|
T | C | 1 | a0001c0001t0038g0359 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.111+30686T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641429 | ||||||
| chr12:64641442
|
A | G | 43 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(40): Show | 43 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.111+30699A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641442 | ||||||
| chr12:64641474
|
T | C | 6 | a0001c0001t0007g0352a0001c0001t0010g0364a0001c0001t0010g0365others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+30731T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641474 | ||||||
| chr12:64641521
|
G | T | 130 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(127): Show | 130 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.111+30778G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641521 | ||||||
| chr12:64641625
|
ATC | A | 38 | a0001c0001t0002g0144a0001c0001t0002g0155a0001c0001t0002g0321others(35): Show | 38 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+30894_111+3089 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641625 | |||||
| chr12:64641636
|
TC | T | 189 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(186): Show | 189 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.111+30894delC | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641636 | ||||||
| chr12:64641637
|
C | T | 4 | a0001c0001t0003g0262a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG06807.hp1 NA18522.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+30894C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641637 | ||||||
| chr12:64641637
|
CT | C | 35 | a0001c0001t0001g0026a0001c0001t0001g0042a0001c0001t0001g0059others(32): Show | 36 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.111+30911delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641637 | |||||
| chr12:64641748
|
A | AT | 63 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0189others(60): Show | 63 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.111+31017dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641748 | |||||
| chr12:64641748
|
AT | A | 15 | a0001c0001t0007g0346a0001c0001t0049g0049a0001c0001t0086g0362others(12): Show | 15 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.111+31017delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64641748 | |||||
| chr12:64641801
|
A | G | 130 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(127): Show | 130 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.111+31058A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641801 | ||||||
| chr12:64641835
|
C | T | 1 | a0001c0001t0051g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.111+31092C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641835 | ||||||
| chr12:64641870
|
G | C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+31127G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641870 | ||||||
| chr12:64641881
|
A | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+31138A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641881 | ||||||
| chr12:64641891
|
T | C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+31148T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641891 | ||||||
| chr12:64641923
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.111+31180G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641923 | ||||||
| chr12:64641928
|
G | A | 1 | a0002c0003t0011g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.111+31185G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641928 | ||||||
| chr12:64641930
|
C | T | 8 | a0001c0001t0028g0048a0001c0001t0046g0044a0001c0002t0021g0023others(5): Show | 8 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+31187C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64641930 | ||||||
| chr12:64642037
|
C | T | 1 | a0001c0001t0013g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.111+31294C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642037 | ||||||
| chr12:64642058
|
A | G | 1 | a0001c0001t0003g0316 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.111+31315A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642058 | ||||||
| chr12:64642239
|
G | A | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+31496G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642239 | ||||||
| chr12:64642325
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.111+31582C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642325 | ||||||
| chr12:64642361
|
A | C | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+31618A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642361 | ||||||
| chr12:64642394
|
T | C | 2 | a0001c0002t0021g0217a0001c0002t0021g0218 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.111+31651T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642394 | ||||||
| chr12:64642397
|
T | A | 62 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(59): Show | 62 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.111+31654T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642397 | ||||||
| chr12:64642415
|
C | T | 3 | a0001c0001t0018g0236a0001c0001t0018g0237a0001c0001t0073g0238 | 3 | NA18943.hp2 NA18953.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.111+31672C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642415 | ||||||
| chr12:64642538
|
C | T | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.111+31795C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642538 | ||||||
| chr12:64642559
|
C | CA | 24 | a0001c0001t0001g0073a0001c0001t0001g0086a0001c0001t0001g0340others(21): Show | 24 | HG00597.hp2 HG00609.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.111+31845dupA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64642559 | |||||
| chr12:64642559
|
CA | C | 58 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0032others(55): Show | 58 | HG00642.hp2 HG01106.hp2 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.111+31845delA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64642559 | |||||
| chr12:64642559
|
CAA | C | 18 | a0001c0001t0001g0042a0001c0001t0001g0067a0001c0001t0001g0080others(15): Show | 18 | HG01243.hp1 HG01243.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.111+31844_111+3184 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64642559 | |||||
| chr12:64642559
|
CAAA | C | 62 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(59): Show | 62 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.111+31843_111+3184 others(7): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64642559 | |||||
| chr12:64642559
|
CAAAA | C | 43 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0289others(40): Show | 43 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.111+31842_111+3184 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64642559 | |||||
| chr12:64642559
|
CAAAAAAA others(2): Show |
C | 12 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(9): Show | 13 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.111+31837_111+3184 others(13): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64642559 | |||||
| chr12:64642559
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+31835_111+3184 others(15): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64642559 | |||||
| chr12:64642574
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+31832_111+3184 others(21): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642574 | ||||||
| chr12:64642586
|
AAAG | A | 19 | a0001c0001t0003g0211a0001c0001t0003g0308a0001c0001t0003g0317others(16): Show | 19 | HG01109.hp1 HG02258.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.111+31845_111+3184 others(7): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64642586 | |||||
| chr12:64642587
|
AAG | A | 17 | a0001c0001t0003g0209a0001c0001t0003g0309a0001c0001t0003g0313others(14): Show | 17 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.111+31846_111+3184 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64642587 | |||||
| chr12:64642588
|
AG | A | 8 | a0001c0001t0028g0048a0001c0001t0046g0044a0001c0002t0007g0012others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+31846delG | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642588 | ||||||
| chr12:64642589
|
G | A | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+31846G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642589 | ||||||
| chr12:64642605
|
GTAATTAA others(16): Show |
G | 1 | a0001c0001t0002g0208 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.111+31879_111+3190 others(27): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64642605 | |||||
| chr12:64642624
|
GTAAT | G | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+31890_111+3189 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64642624 | |||||
| chr12:64642654
|
AAATTAAT others(12): Show |
A | 73 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(70): Show | 74 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.111+31934_111+3195 others(23): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64642654 | |||||
| chr12:64642715
|
A | G | 1 | a0001c0002t0007g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.111+31972A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642715 | ||||||
| chr12:64642846
|
T | C | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111+32103T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642846 | ||||||
| chr12:64642869
|
T | C | 11 | a0001c0001t0006g0283a0001c0001t0009g0280a0001c0001t0009g0281others(8): Show | 11 | HG02040.hp2 HG02083.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+32126T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642869 | ||||||
| chr12:64642951
|
C | T | 82 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(79): Show | 82 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.111+32208C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642951 | ||||||
| chr12:64642961
|
G | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+32218G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64642961 | ||||||
| chr12:64643143
|
G | A | 1 | a0002c0003t0011g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.111+32400G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64643143 | ||||||
| chr12:64643322
|
T | A | 1 | a0001c0001t0003g0245 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.111+32579T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64643322 | ||||||
| chr12:64643543
|
G | A | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+32800G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64643543 | ||||||
| chr12:64643560
|
T | A | 2 | a0001c0001t0086g0362a0001c0001t0088g0361 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+32817T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64643560 | ||||||
| chr12:64643560
|
T | C | 1 | a0001c0001t0090g0369 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.111+32817T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64643560 | ||||||
| chr12:64643583
|
C | A | 2 | a0001c0001t0003g0256a0001c0001t0003g0259 | 2 | NA18971.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.111+32840C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64643583 | ||||||
| chr12:64643632
|
A | G | 1 | a0001c0001t0003g0256 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.111+32889A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64643632 | ||||||
| chr12:64643645
|
A | C | 8 | a0001c0001t0028g0048a0001c0001t0046g0044a0001c0002t0021g0023others(5): Show | 8 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+32902A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64643645 | ||||||
| chr12:64643703
|
G | C | 262 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(259): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.111+32960G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64643703 | ||||||
| chr12:64643703
|
G | T | 4 | a0001c0001t0049g0049a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+32960G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64643703 | ||||||
| chr12:64643712
|
C | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+32969C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64643712 | ||||||
| chr12:64644235
|
G | C | 37 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(34): Show | 37 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.111+33492G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64644235 | ||||||
| chr12:64644375
|
C | T | 14 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+33632C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64644375 | ||||||
| chr12:64644431
|
C | G | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.111+33688C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64644431 | ||||||
| chr12:64644432
|
A | G | 7 | a0001c0001t0028g0048a0001c0001t0046g0044a0001c0002t0021g0023others(4): Show | 7 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+33689A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64644432 | ||||||
| chr12:64644466
|
T | C | 50 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(47): Show | 50 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.111+33723T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64644466 | ||||||
| chr12:64644625
|
A | G | 1 | a0001c0001t0008g0276 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.111+33882A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64644625 | ||||||
| chr12:64644699
|
A | AAAACAAA others(1): Show |
52 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(49): Show | 52 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.111+33968_111+3397 others(12): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64644699 | |||||
| chr12:64644699
|
A | AAAACAAA others(5): Show |
190 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(187): Show | 191 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.111+33964_111+3397 others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64644699 | |||||
| chr12:64644699
|
A | AAAACAAA others(9): Show |
10 | a0001c0001t0028g0048a0001c0001t0046g0044a0001c0001t0086g0362others(7): Show | 10 | HG01361.hp2 HG02630.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.111+33960_111+3397 others(20): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64644699 | |||||
| chr12:64644699
|
A | AAAACAAA others(13): Show |
8 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0013others(5): Show | 8 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+33975_111+3397 others(24): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64644699 | |||||
| chr12:64644699
|
A | AAAACAAA others(17): Show |
3 | a0001c0002t0007g0011a0001c0002t0007g0012a0001c0002t0007g0016 | 3 | HG01167.hp1 HG03654.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.111+33975_111+3397 others(28): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64644699 | |||||
| chr12:64644733
|
A | G | 49 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(46): Show | 49 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.111+33990A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64644733 | ||||||
| chr12:64644739
|
A | AT | 58 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(55): Show | 58 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.111+33997dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64644739 | |||||
| chr12:64644751
|
T | C | 2 | a0001c0001t0086g0362a0001c0001t0088g0361 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+34008T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64644751 | ||||||
| chr12:64644814
|
A | G | 3 | a0001c0002t0029g0021a0001c0002t0029g0022a0001c0002t0045g0024 | 3 | HG02630.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.111+34071A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64644814 | ||||||
| chr12:64644852
|
A | C | 3 | a0001c0002t0029g0021a0001c0002t0029g0022a0001c0002t0045g0024 | 3 | HG02630.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.111+34109A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64644852 | ||||||
| chr12:64644943
|
G | A | 4 | a0001c0001t0049g0049a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG03540.hp2 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+34200G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64644943 | ||||||
| chr12:64645133
|
A | G | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+34390A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64645133 | ||||||
| chr12:64645369
|
A | G | 1 | a0001c0001t0018g0213 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.111+34626A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64645369 | ||||||
| chr12:64645476
|
C | G | 1 | a0001c0001t0039g0031 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.111+34733C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64645476 | ||||||
| chr12:64645536
|
TAAAG | T | 3 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0067g0210 | 3 | HG01109.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.111+34797_111+3480 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64645536 | |||||
| chr12:64645628
|
C | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111+34885C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64645628 | ||||||
| chr12:64645866
|
G | C | 45 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(42): Show | 45 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.111+35123G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64645866 | ||||||
| chr12:64645873
|
T | C | 7 | a0001c0001t0028g0048a0001c0001t0046g0044a0001c0002t0021g0023others(4): Show | 7 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+35130T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64645873 | ||||||
| chr12:64646036
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.111+35293A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64646036 | ||||||
| chr12:64646112
|
ATTAT | A | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+35374_111+3537 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64646112 | |||||
| chr12:64646378
|
A | C | 15 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(12): Show | 15 | HG01109.hp1 HG02486.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+35635A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64646378 | ||||||
| chr12:64646460
|
T | C | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+35717T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64646460 | ||||||
| chr12:64646610
|
G | A | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.111+35867G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64646610 | ||||||
| chr12:64646697
|
A | G | 95 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0032others(92): Show | 95 | HG00438.hp1 HG00609.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.111+35954A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64646697 | ||||||
| chr12:64646746
|
AT | A | 132 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0140others(129): Show | 132 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.111+36017delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64646746 | |||||
| chr12:64646781
|
A | G | 7 | a0001c0001t0028g0048a0001c0002t0021g0023a0001c0002t0028g0025others(4): Show | 7 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+36038A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64646781 | ||||||
| chr12:64646843
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.111+36100G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64646843 | ||||||
| chr12:64646896
|
T | C | 2 | a0001c0001t0003g0251a0001c0001t0003g0264 | 2 | NA19001.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.111+36153T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64646896 | ||||||
| chr12:64646922
|
C | G | 5 | a0001c0002t0021g0023a0001c0002t0028g0025a0001c0002t0029g0021others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+36179C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64646922 | ||||||
| chr12:64646929
|
G | A | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111+36186G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64646929 | ||||||
| chr12:64647154
|
C | T | 6 | a0001c0002t0021g0023a0001c0002t0028g0025a0001c0002t0029g0021others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+36411C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647154 | ||||||
| chr12:64647159
|
A | C | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+36416A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647159 | ||||||
| chr12:64647233
|
T | TTTTA | 26 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(23): Show | 26 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(23): Show |
intron_variant | MODIFIER | c.111+36510_111+3651 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64647233 | |||||
| chr12:64647305
|
G | A | 64 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(61): Show | 64 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.111+36562G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647305 | ||||||
| chr12:64647331
|
C | T | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+36588C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647331 | ||||||
| chr12:64647412
|
C | CTT | 79 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(76): Show | 79 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.111+36681_111+3668 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64647412 | |||||
| chr12:64647498
|
C | T | 1 | a0001c0001t0004g0288 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.111+36755C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647498 | ||||||
| chr12:64647537
|
A | T | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.111+36794A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647537 | ||||||
| chr12:64647571
|
C | T | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.111+36828C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647571 | ||||||
| chr12:64647610
|
A | G | 1 | a0001c0001t0001g0340 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.111+36867A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647610 | ||||||
| chr12:64647662
|
C | T | 27 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(24): Show | 27 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.111+36919C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647662 | ||||||
| chr12:64647690
|
C | T | 1 | a0001c0001t0051g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.111+36947C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647690 | ||||||
| chr12:64647691
|
A | G | 1 | a0001c0001t0051g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.111+36948A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647691 | ||||||
| chr12:64647695
|
A | G | 1 | a0001c0001t0051g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.111+36952A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647695 | ||||||
| chr12:64647703
|
G | A | 1 | a0001c0001t0051g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.111+36960G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647703 | ||||||
| chr12:64647706
|
C | T | 43 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(40): Show | 43 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.111+36963C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647706 | ||||||
| chr12:64647707
|
G | C | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.111+36964G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647707 | ||||||
| chr12:64647714
|
G | A | 37 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(34): Show | 37 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.111+36971G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647714 | ||||||
| chr12:64647724
|
T | G | 1 | a0001c0001t0007g0346 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.111+36981T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647724 | ||||||
| chr12:64647762
|
A | AT | 5 | a0001c0002t0021g0023a0001c0002t0028g0025a0001c0002t0029g0021others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+37020dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64647762 | |||||
| chr12:64647961
|
C | T | 1 | a0001c0001t0038g0243 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.112-36826C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64647961 | ||||||
| chr12:64648050
|
G | A | 17 | a0001c0001t0007g0346a0001c0001t0028g0048a0001c0001t0075g0106others(14): Show | 17 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.112-36737G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64648050 | ||||||
| chr12:64648095
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.112-36692C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64648095 | ||||||
| chr12:64648269
|
C | T | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-36518C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64648269 | ||||||
| chr12:64648354
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.112-36433T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64648354 | ||||||
| chr12:64648403
|
A | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-36384A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64648403 | ||||||
| chr12:64648489
|
G | A | 2 | a0001c0001t0005g0201a0001c0001t0034g0200 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.112-36298G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64648489 | ||||||
| chr12:64648702
|
C | T | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.112-36085C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64648702 | ||||||
| chr12:64648724
|
G | A | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-36063G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64648724 | ||||||
| chr12:64648776
|
C | T | 5 | a0001c0001t0027g0351a0001c0001t0027g0354a0001c0001t0027g0356others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-36011C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64648776 | ||||||
| chr12:64648802
|
A | ATTTT | 58 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(55): Show | 59 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.112-35968_112-3596 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64648802 | |||||
| chr12:64648802
|
A | ATTTTT | 96 | a0001c0001t0002g0206a0001c0001t0003g0209a0001c0001t0003g0211others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.112-35969_112-3596 others(9): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64648802 | |||||
| chr12:64648802
|
A | ATTTTTT | 95 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(92): Show | 95 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.112-35970_112-3596 others(10): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64648802 | |||||
| chr12:64648802
|
A | ATTTTTTT | 7 | a0001c0001t0002g0329a0001c0001t0006g0339a0001c0001t0012g0182others(4): Show | 7 | HG01943.hp2 HG02145.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-35971_112-3596 others(11): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64648802 | |||||
| chr12:64648802
|
A | ATTTTTTT others(4): Show |
2 | a0001c0002t0021g0023a0001c0002t0028g0025 | 2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.112-35975_112-3596 others(15): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64648802 | |||||
| chr12:64648802
|
A | ATTTTTTT others(7): Show |
3 | a0001c0002t0029g0021a0001c0002t0029g0022a0001c0002t0045g0024 | 3 | HG02630.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.112-35978_112-3596 others(18): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64648802 | |||||
| chr12:64648850
|
G | C | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.112-35937G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64648850 | ||||||
| chr12:64649003
|
T | C | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.112-35784T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649003 | ||||||
| chr12:64649015
|
G | A | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-35772G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649015 | ||||||
| chr12:64649107
|
C | T | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-35680C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649107 | ||||||
| chr12:64649121
|
GA | G | 45 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(42): Show | 45 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.112-35662delA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64649121 | |||||
| chr12:64649191
|
G | GT | 82 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(79): Show | 82 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.112-35585dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64649191 | |||||
| chr12:64649229
|
G | A | 1 | a0001c0001t0009g0282 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.112-35558G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649229 | ||||||
| chr12:64649273
|
A | G | 2 | a0001c0001t0009g0244a0001c0001t0009g0273 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.112-35514A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649273 | ||||||
| chr12:64649285
|
C | T | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-35502C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649285 | ||||||
| chr12:64649451
|
G | A | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112-35336G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649451 | ||||||
| chr12:64649551
|
A | G | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.112-35236A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649551 | ||||||
| chr12:64649623
|
G | A | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-35164G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649623 | ||||||
| chr12:64649679
|
G | T | 1 | a0001c0001t0004g0290 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.112-35108G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649679 | ||||||
| chr12:64649807
|
C | T | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.112-34980C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649807 | ||||||
| chr12:64649808
|
G | A | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.112-34979G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649808 | ||||||
| chr12:64649959
|
G | A | 1 | a0001c0001t0005g0193 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.112-34828G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649959 | ||||||
| chr12:64649994
|
G | T | 1 | a0001c0002t0015g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.112-34793G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64649994 | ||||||
| chr12:64650293
|
G | A | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-34494G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64650293 | ||||||
| chr12:64650408
|
C | CT | 27 | a0001c0001t0001g0027a0001c0001t0001g0041a0001c0001t0001g0055others(24): Show | 27 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.112-34355dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64650408 | |||||
| chr12:64650408
|
C | CTT | 69 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0142others(66): Show | 69 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.112-34356_112-3435 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64650408 | |||||
| chr12:64650408
|
C | CTTT | 25 | a0001c0001t0002g0140a0001c0001t0002g0156a0001c0001t0002g0189others(22): Show | 25 | HG01175.hp1 HG01433.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.112-34357_112-3435 others(7): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64650408 | |||||
| chr12:64650408
|
CT | C | 51 | a0001c0001t0001g0260a0001c0001t0003g0262a0001c0001t0004g0133others(48): Show | 51 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.112-34355delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64650408 | |||||
| chr12:64650408
|
CTTTTT | C | 6 | a0001c0001t0007g0352a0001c0001t0010g0364a0001c0001t0010g0365others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-34359_112-3435 others(9): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64650408 | |||||
| chr12:64650408
|
CTTTTTTT | C | 7 | a0001c0001t0049g0049a0001c0001t0075g0106a0001c0002t0021g0023others(4): Show | 7 | HG02630.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-34361_112-3435 others(11): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64650408 | |||||
| chr12:64650662
|
G | A | 6 | a0001c0001t0049g0049a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-34125G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64650662 | ||||||
| chr12:64650680
|
G | T | 1 | a0001c0002t0007g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.112-34107G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64650680 | ||||||
| chr12:64650691
|
A | G | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.112-34096A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64650691 | ||||||
| chr12:64650878
|
G | A | 1 | a0001c0002t0029g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112-33909G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64650878 | ||||||
| chr12:64650929
|
C | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-33858C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64650929 | ||||||
| chr12:64651006
|
T | A | 1 | a0001c0001t0007g0304 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.112-33781T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651006 | ||||||
| chr12:64651020
|
T | G | 1 | a0001c0001t0038g0359 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.112-33767T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651020 | ||||||
| chr12:64651034
|
G | T | 92 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(89): Show | 92 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.112-33753G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651034 | ||||||
| chr12:64651143
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.112-33644A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651143 | ||||||
| chr12:64651156
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.112-33631G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651156 | ||||||
| chr12:64651254
|
T | G | 92 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(89): Show | 92 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.112-33533T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651254 | ||||||
| chr12:64651311
|
G | A | 1 | a0001c0001t0004g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.112-33476G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651311 | ||||||
| chr12:64651353
|
C | T | 1 | a0001c0001t0006g0287 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.112-33434C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651353 | ||||||
| chr12:64651395
|
G | C | 8 | a0001c0001t0049g0049a0001c0001t0075g0106a0001c0002t0021g0023others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.112-33392G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651395 | ||||||
| chr12:64651417
|
G | A | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.112-33370G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651417 | ||||||
| chr12:64651418
|
G | A | 5 | a0001c0001t0027g0351a0001c0001t0027g0354a0001c0001t0027g0356others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-33369G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651418 | ||||||
| chr12:64651463
|
G | A | 12 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(9): Show | 13 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.112-33324G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651463 | ||||||
| chr12:64651620
|
A | T | 1 | a0001c0001t0002g0156 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.112-33167A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651620 | ||||||
| chr12:64651714
|
G | A | 53 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(50): Show | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.112-33073G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651714 | ||||||
| chr12:64651918
|
C | T | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.112-32869C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651918 | ||||||
| chr12:64651946
|
C | T | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112-32841C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64651946 | ||||||
| chr12:64652209
|
G | GTAGT | 14 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.112-32576_112-3257 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64652209 | |||||
| chr12:64652242
|
T | C | 5 | a0001c0002t0021g0023a0001c0002t0028g0025a0001c0002t0029g0021others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-32545T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64652242 | ||||||
| chr12:64652311
|
G | A | 26 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(23): Show | 26 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(23): Show |
intron_variant | MODIFIER | c.112-32476G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64652311 | ||||||
| chr12:64652368
|
T | A | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-32419T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64652368 | ||||||
| chr12:64652415
|
T | TC | 195 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0041others(192): Show | 195 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.112-32365dupC | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64652415 | |||||
| chr12:64652519
|
T | A | 8 | a0001c0001t0049g0049a0001c0001t0075g0106a0001c0002t0021g0023others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.112-32268T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64652519 | ||||||
| chr12:64652572
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0099 | 2 | HG02071.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.112-32215G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64652572 | ||||||
| chr12:64652911
|
C | A | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-31876C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64652911 | ||||||
| chr12:64653256
|
T | G | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-31531T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64653256 | ||||||
| chr12:64653399
|
T | A | 92 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(89): Show | 92 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.112-31388T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64653399 | ||||||
| chr12:64653409
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.112-31378C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64653409 | ||||||
| chr12:64653569
|
C | CT | 6 | a0001c0001t0004g0363a0001c0001t0028g0048a0001c0001t0038g0243others(3): Show | 6 | HG01361.hp2 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-31205dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64653569 | |||||
| chr12:64653753
|
G | A | 53 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(50): Show | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.112-31034G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64653753 | ||||||
| chr12:64653950
|
C | T | 13 | a0001c0001t0027g0351a0001c0001t0027g0354a0001c0001t0027g0356others(10): Show | 13 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.112-30837C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64653950 | ||||||
| chr12:64653951
|
G | C | 31 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(28): Show | 31 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.112-30836G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64653951 | ||||||
| chr12:64653987
|
A | G | 14 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.112-30800A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64653987 | ||||||
| chr12:64654005
|
T | C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-30782T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654005 | ||||||
| chr12:64654057
|
T | C | 1 | a0001c0001t0031g0113 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.112-30730T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654057 | ||||||
| chr12:64654224
|
G | A | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112-30563G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654224 | ||||||
| chr12:64654258
|
G | A | 1 | a0001c0002t0016g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.112-30529G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654258 | ||||||
| chr12:64654548
|
C | T | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.112-30239C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654548 | ||||||
| chr12:64654554
|
C | T | 7 | a0001c0001t0049g0049a0001c0001t0075g0106a0001c0002t0021g0023others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-30233C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654554 | ||||||
| chr12:64654602
|
T | C | 9 | a0001c0001t0049g0049a0001c0001t0086g0362a0001c0001t0088g0361others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.112-30185T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654602 | ||||||
| chr12:64654643
|
C | CG | 38 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0042others(35): Show | 38 | HG00735.hp2 HG00741.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.112-30131dupG | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64654643 | |||||
| chr12:64654643
|
C | CGG | 34 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0056others(31): Show | 34 | HG00642.hp2 HG00735.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.112-30132_112-3013 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64654643 | |||||
| chr12:64654643
|
CG | C | 30 | a0001c0001t0004g0215a0001c0001t0004g0288a0001c0001t0004g0289others(27): Show | 30 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.112-30131delG | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64654643 | |||||
| chr12:64654648
|
G | T | 120 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(117): Show | 121 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.112-30139G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654648 | ||||||
| chr12:64654650
|
G | C | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-30137G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654650 | ||||||
| chr12:64654650
|
G | T | 8 | a0001c0001t0003g0227a0001c0001t0049g0049a0001c0001t0075g0106others(5): Show | 8 | HG02027.hp1 HG02109.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-30137G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654650 | ||||||
| chr12:64654651
|
G | T | 5 | a0001c0002t0016g0033a0001c0002t0016g0034a0001c0002t0016g0035others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-30136G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654651 | ||||||
| chr12:64654652
|
G | C | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.112-30135G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654652 | ||||||
| chr12:64654653
|
G | T | 61 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(58): Show | 61 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.112-30134G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654653 | ||||||
| chr12:64654655
|
G | T | 1 | a0001c0001t0003g0227 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.112-30132G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654655 | ||||||
| chr12:64654655
|
GGT | G | 82 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0003g0043others(79): Show | 82 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.112-30130_112-3012 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64654655 | |||||
| chr12:64654656
|
GT | G | 108 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(105): Show | 108 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.112-30130delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654656 | ||||||
| chr12:64654657
|
T | C | 1 | a0001c0001t0003g0227 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.112-30130T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654657 | ||||||
| chr12:64654657
|
T | G | 6 | a0001c0001t0001g0235a0001c0001t0002g0189a0001c0001t0006g0336others(3): Show | 6 | HG00597.hp2 HG01361.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-30130T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654657 | ||||||
| chr12:64654658
|
G | C | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-30129G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654658 | ||||||
| chr12:64654658
|
G | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-30129G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654658 | ||||||
| chr12:64654709
|
AC | A | 53 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(50): Show | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.112-30077delC | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654709 | ||||||
| chr12:64654789
|
T | C | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.112-29998T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654789 | ||||||
| chr12:64654853
|
G | A | 1 | a0001c0001t0009g0273 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.112-29934G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64654853 | ||||||
| chr12:64654873
|
TAAATA | T | 5 | a0001c0001t0027g0351a0001c0001t0027g0354a0001c0001t0027g0356others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-29903_112-2989 others(9): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64654873 | |||||
| chr12:64655128
|
C | G | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.112-29659C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655128 | ||||||
| chr12:64655210
|
A | C | 2 | a0002c0003t0011g0114a0002c0003t0011g0115 | 2 | HG02280.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.112-29577A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655210 | ||||||
| chr12:64655411
|
A | G | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-29376A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655411 | ||||||
| chr12:64655438
|
G | A | 53 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(50): Show | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.112-29349G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655438 | ||||||
| chr12:64655440
|
C | G | 1 | a0001c0001t0008g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.112-29347C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655440 | ||||||
| chr12:64655472
|
T | A | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.112-29315T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655472 | ||||||
| chr12:64655488
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.112-29299T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655488 | ||||||
| chr12:64655489
|
C | A | 1 | a0001c0001t0001g0235 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.112-29298C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655489 | ||||||
| chr12:64655577
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.112-29210T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655577 | ||||||
| chr12:64655664
|
A | G | 1 | a0001c0001t0054g0127 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.112-29123A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655664 | ||||||
| chr12:64655718
|
T | C | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.112-29069T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655718 | ||||||
| chr12:64655753
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.112-29034G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655753 | ||||||
| chr12:64655760
|
C | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-29027C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655760 | ||||||
| chr12:64655809
|
G | A | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-28978G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655809 | ||||||
| chr12:64655864
|
T | C | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.112-28923T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64655864 | ||||||
| chr12:64656028
|
G | GA | 7 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0019g0087others(4): Show | 7 | HG00438.hp1 HG01515.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-28741dupA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64656028 | |||||
| chr12:64656028
|
GA | G | 103 | a0001c0001t0001g0070a0001c0001t0001g0099a0001c0001t0001g0234others(100): Show | 103 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.112-28741delA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64656028 | |||||
| chr12:64656030
|
A | G | 1 | a0001c0001t0013g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.112-28757A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64656030 | ||||||
| chr12:64656102
|
A | G | 1 | a0002c0003t0011g0112 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.112-28685A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64656102 | ||||||
| chr12:64656168
|
G | A | 7 | a0001c0001t0049g0049a0001c0001t0075g0106a0001c0002t0021g0023others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-28619G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64656168 | ||||||
| chr12:64656284
|
A | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-28503A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64656284 | ||||||
| chr12:64656323
|
A | G | 1 | a0001c0001t0036g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.112-28464A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64656323 | ||||||
| chr12:64656374
|
G | A | 79 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(76): Show | 79 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.112-28413G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64656374 | ||||||
| chr12:64656654
|
T | G | 1 | a0001c0001t0008g0286 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.112-28133T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64656654 | ||||||
| chr12:64656828
|
A | C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-27959A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64656828 | ||||||
| chr12:64656847
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.112-27940T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64656847 | ||||||
| chr12:64656935
|
A | G | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.112-27852A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64656935 | ||||||
| chr12:64657011
|
C | CT | 88 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0082others(85): Show | 88 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.112-27760dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64657011 | |||||
| chr12:64657100
|
A | G | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-27687A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64657100 | ||||||
| chr12:64657168
|
C | A | 54 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(51): Show | 54 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.112-27619C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64657168 | ||||||
| chr12:64657168
|
C | T | 3 | a0001c0001t0006g0310a0001c0001t0006g0311a0001c0001t0044g0110 | 3 | HG02922.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.112-27619C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64657168 | ||||||
| chr12:64657224
|
A | G | 1 | a0001c0002t0024g0002 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.112-27563A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64657224 | ||||||
| chr12:64657226
|
G | C | 3 | a0001c0001t0002g0174a0001c0001t0014g0137a0001c0001t0014g0138 | 3 | HG03490.hp2 HG03704.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.112-27561G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64657226 | ||||||
| chr12:64657283
|
G | T | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.112-27504G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64657283 | ||||||
| chr12:64657297
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | NA18951.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.112-27490G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64657297 | ||||||
| chr12:64657475
|
G | T | 54 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(51): Show | 54 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.112-27312G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64657475 | ||||||
| chr12:64657518
|
G | T | 26 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(23): Show | 26 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(23): Show |
intron_variant | MODIFIER | c.112-27269G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64657518 | ||||||
| chr12:64658079
|
G | A | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-26708G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64658079 | ||||||
| chr12:64658140
|
C | T | 82 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(79): Show | 82 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.112-26647C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64658140 | ||||||
| chr12:64658343
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0083g0123 | 2 | NA18987.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.112-26444G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64658343 | ||||||
| chr12:64658434
|
T | A | 1 | a0001c0001t0001g0078 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.112-26353T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64658434 | ||||||
| chr12:64658453
|
C | T | 1 | a0001c0001t0085g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.112-26334C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64658453 | ||||||
| chr12:64658479
|
C | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-26308C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64658479 | ||||||
| chr12:64658764
|
A | T | 5 | a0001c0002t0021g0023a0001c0002t0028g0025a0001c0002t0029g0021others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-26023A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64658764 | ||||||
| chr12:64658877
|
T | C | 1 | a0001c0002t0015g0004 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.112-25910T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64658877 | ||||||
| chr12:64658890
|
C | T | 1 | a0001c0001t0079g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.112-25897C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64658890 | ||||||
| chr12:64658906
|
A | G | 2 | a0001c0001t0002g0208a0001c0001t0032g0163 | 2 | HG01978.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.112-25881A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64658906 | ||||||
| chr12:64658930
|
T | C | 92 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(89): Show | 92 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.112-25857T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64658930 | ||||||
| chr12:64658932
|
T | A | 1 | a0001c0001t0002g0206 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.112-25855T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64658932 | ||||||
| chr12:64658967
|
A | G | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112-25820A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64658967 | ||||||
| chr12:64659113
|
A | AG | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-25673dupG | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64659113 | |||||
| chr12:64659324
|
T | G | 1 | a0001c0002t0007g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.112-25463T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64659324 | ||||||
| chr12:64659328
|
C | A | 1 | a0001c0002t0007g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.112-25459C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64659328 | ||||||
| chr12:64659441
|
G | A | 7 | a0001c0001t0049g0049a0001c0001t0075g0106a0001c0002t0021g0023others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-25346G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64659441 | ||||||
| chr12:64659502
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.112-25285C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64659502 | ||||||
| chr12:64659688
|
C | T | 2 | a0001c0001t0086g0362a0001c0001t0088g0361 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-25099C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64659688 | ||||||
| chr12:64659715
|
A | G | 1 | a0001c0001t0036g0315 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.112-25072A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64659715 | ||||||
| chr12:64659806
|
G | A | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112-24981G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64659806 | ||||||
| chr12:64659879
|
C | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-24908C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64659879 | ||||||
| chr12:64659893
|
A | G | 1 | a0001c0001t0002g0152 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.112-24894A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64659893 | ||||||
| chr12:64659916
|
C | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-24871C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64659916 | ||||||
| chr12:64659951
|
C | CGT | 68 | a0001c0001t0002g0192a0001c0001t0003g0219a0001c0001t0003g0227others(65): Show | 68 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.112-24805_112-2480 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64659951 | |||||
| chr12:64659951
|
C | CGTGT | 7 | a0001c0001t0004g0293a0001c0001t0005g0207a0001c0001t0006g0287others(4): Show | 7 | HG01515.hp1 HG01517.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-24807_112-2480 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64659951 | |||||
| chr12:64659951
|
C | CGTGTGT | 3 | a0001c0002t0016g0035a0001c0002t0029g0021a0001c0002t0045g0024 | 3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.112-24809_112-2480 others(10): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64659951 | |||||
| chr12:64659951
|
CGT | C | 99 | a0001c0001t0001g0056a0001c0001t0001g0333a0001c0001t0001g0340others(96): Show | 100 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.112-24805_112-2480 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64659951 | |||||
| chr12:64659951
|
CGTGT | C | 9 | a0001c0001t0001g0070a0001c0001t0003g0306a0001c0001t0004g0133others(6): Show | 9 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.112-24807_112-2480 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64659951 | |||||
| chr12:64659951
|
CGTGTGT | C | 16 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(13): Show | 16 | HG01109.hp1 HG02486.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.112-24809_112-2480 others(10): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64659951 | |||||
| chr12:64659951
|
CGTGTGTG others(3): Show |
C | 15 | a0001c0001t0007g0346a0001c0001t0075g0106a0001c0001t0086g0362others(12): Show | 15 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.112-24813_112-2480 others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64659951 | |||||
| chr12:64660006
|
G | GTA | 82 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(79): Show | 82 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.112-24773_112-2477 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64660006 | |||||
| chr12:64660006
|
G | GTATATAT others(41): Show |
1 | a0001c0001t0013g0166 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.112-24772_112-2477 others(52): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64660006 | |||||
| chr12:64660006
|
G | GTATATAT others(43): Show |
8 | a0001c0001t0013g0148a0001c0001t0013g0154a0001c0001t0013g0161others(5): Show | 8 | HG00323.hp1 HG01256.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.112-24772_112-2477 others(54): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64660006 | |||||
| chr12:64660014
|
A | ATG | 87 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(84): Show | 88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.112-24761_112-2476 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64660014 | |||||
| chr12:64660014
|
A | ATGTG | 26 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(23): Show | 26 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(23): Show |
intron_variant | MODIFIER | c.112-24763_112-2476 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64660014 | |||||
| chr12:64660016
|
G | A | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112-24771G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660016 | ||||||
| chr12:64660018
|
G | A | 1 | a0001c0001t0009g0273 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.112-24769G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660018 | ||||||
| chr12:64660020
|
GTGTGTGT others(13): Show |
G | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112-24759_112-2474 others(24): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64660020 | |||||
| chr12:64660040
|
A | G | 1 | a0001c0001t0039g0031 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.112-24747A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660040 | ||||||
| chr12:64660046
|
G | GTA | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-24740_112-2473 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64660046 | |||||
| chr12:64660052
|
G | A | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-24735G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660052 | ||||||
| chr12:64660052
|
G | GTA | 157 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(154): Show | 158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.112-24725_112-2472 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64660052 | |||||
| chr12:64660052
|
G | GTATA | 6 | a0001c0001t0049g0049a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-24727_112-2472 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64660052 | |||||
| chr12:64660054
|
A | G | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112-24733A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660054 | ||||||
| chr12:64660062
|
A | ATATG | 13 | a0001c0001t0007g0346a0001c0001t0028g0048a0001c0002t0004g0015others(10): Show | 13 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.112-24724_112-2472 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64660062 | |||||
| chr12:64660062
|
A | G | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-24725A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660062 | ||||||
| chr12:64660069
|
T | C | 1 | a0001c0001t0004g0305 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.112-24718T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660069 | ||||||
| chr12:64660087
|
T | C | 1 | a0001c0001t0019g0090 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.112-24700T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660087 | ||||||
| chr12:64660453
|
C | A | 6 | a0001c0001t0049g0049a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-24334C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660453 | ||||||
| chr12:64660454
|
A | C | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.112-24333A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660454 | ||||||
| chr12:64660555
|
A | C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-24232A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660555 | ||||||
| chr12:64660564
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.112-24223G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660564 | ||||||
| chr12:64660672
|
G | A | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.112-24115G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660672 | ||||||
| chr12:64660686
|
G | A | 1 | a0001c0001t0031g0113 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.112-24101G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660686 | ||||||
| chr12:64660695
|
A | G | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.112-24092A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660695 | ||||||
| chr12:64660811
|
C | T | 1 | a0001c0001t0008g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.112-23976C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660811 | ||||||
| chr12:64660978
|
A | C | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-23809A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64660978 | ||||||
| chr12:64661111
|
C | G | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-23676C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64661111 | ||||||
| chr12:64661157
|
G | A | 1 | a0001c0002t0007g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.112-23630G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64661157 | ||||||
| chr12:64661239
|
G | A | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-23548G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64661239 | ||||||
| chr12:64661277
|
C | T | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-23510C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64661277 | ||||||
| chr12:64661353
|
G | A | 2 | a0001c0001t0023g0269a0001c0001t0023g0270 | 2 | NA18966.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.112-23434G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64661353 | ||||||
| chr12:64661528
|
A | T | 64 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(61): Show | 64 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.112-23259A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64661528 | ||||||
| chr12:64661535
|
C | T | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-23252C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64661535 | ||||||
| chr12:64661677
|
C | CT | 6 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0001g0057others(3): Show | 6 | HG01175.hp2 HG02135.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-23087dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64661677 | |||||
| chr12:64661677
|
CT | C | 180 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0058others(177): Show | 181 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.112-23087delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64661677 | |||||
| chr12:64661677
|
CTT | C | 14 | a0001c0001t0002g0181a0001c0001t0004g0343a0001c0001t0007g0346others(11): Show | 14 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-23088_112-2308 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64661677 | |||||
| chr12:64661677
|
CTTT | C | 6 | a0001c0001t0049g0049a0001c0001t0075g0106a0001c0002t0021g0023others(3): Show | 6 | HG02630.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-23089_112-2308 others(7): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64661677 | |||||
| chr12:64661680
|
T | TC | 5 | a0001c0001t0003g0262a0001c0001t0003g0268a0001c0001t0008g0247others(2): Show | 5 | HG02071.hp2 NA18979.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-23107_112-2310 others(5): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64661680 | ||||||
| chr12:64661681
|
T | C | 56 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(53): Show | 56 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.112-23106T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64661681 | ||||||
| chr12:64661683
|
T | C | 3 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0067g0210 | 3 | HG01109.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.112-23104T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64661683 | ||||||
| chr12:64661684
|
T | C | 26 | a0001c0001t0003g0308a0001c0001t0003g0309a0001c0001t0003g0313others(23): Show | 26 | HG02258.hp2 HG02486.hp1 HG02559.hp2 others(23): Show |
intron_variant | MODIFIER | c.112-23103T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64661684 | ||||||
| chr12:64661755
|
T | C | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.112-23032T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64661755 | ||||||
| chr12:64661990
|
TA | T | 196 | a0001c0001t0001g0069a0001c0001t0001g0233a0001c0001t0001g0338others(193): Show | 197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.112-22782delA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64661990 | |||||
| chr12:64661990
|
TAA | T | 66 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(63): Show | 66 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.112-22783_112-2278 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64661990 | |||||
| chr12:64662089
|
C | G | 26 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(23): Show | 26 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(23): Show |
intron_variant | MODIFIER | c.112-22698C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64662089 | ||||||
| chr12:64662129
|
A | C | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-22658A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64662129 | ||||||
| chr12:64662255
|
C | CA | 6 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0232others(3): Show | 6 | HG00438.hp1 HG01934.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-22516dupA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64662255 | |||||
| chr12:64662255
|
CA | C | 236 | a0001c0001t0001g0058a0001c0001t0001g0333a0001c0001t0001g0340others(233): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.112-22516delA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64662255 | |||||
| chr12:64662274
|
A | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-22513A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64662274 | ||||||
| chr12:64662451
|
T | A | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-22336T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64662451 | ||||||
| chr12:64662458
|
C | A | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-22329C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64662458 | ||||||
| chr12:64662555
|
T | C | 5 | a0001c0001t0027g0351a0001c0001t0027g0354a0001c0001t0027g0356others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-22232T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64662555 | ||||||
| chr12:64662602
|
A | T | 19 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(16): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.112-22185A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64662602 | ||||||
| chr12:64662652
|
G | A | 1 | a0001c0001t0005g0202 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.112-22135G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64662652 | ||||||
| chr12:64662843
|
G | A | 2 | a0001c0001t0014g0137a0001c0001t0014g0138 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.112-21944G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64662843 | ||||||
| chr12:64662856
|
T | C | 26 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(23): Show | 26 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(23): Show |
intron_variant | MODIFIER | c.112-21931T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64662856 | ||||||
| chr12:64662997
|
T | C | 2 | a0001c0002t0021g0217a0001c0002t0021g0218 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.112-21790T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64662997 | ||||||
| chr12:64663023
|
T | C | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.112-21764T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64663023 | ||||||
| chr12:64663155
|
T | C | 31 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(28): Show | 31 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.112-21632T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64663155 | ||||||
| chr12:64663252
|
G | T | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.112-21535G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64663252 | ||||||
| chr12:64663377
|
T | A | 14 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.112-21410T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64663377 | ||||||
| chr12:64663406
|
T | G | 2 | a0001c0002t0021g0217a0001c0002t0021g0218 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.112-21381T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64663406 | ||||||
| chr12:64663526
|
AT | A | 93 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(90): Show | 93 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.112-21248delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64663526 | |||||
| chr12:64663552
|
T | C | 86 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(83): Show | 86 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.112-21235T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64663552 | ||||||
| chr12:64663553
|
G | A | 2 | a0001c0002t0029g0021a0001c0002t0045g0024 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.112-21234G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64663553 | ||||||
| chr12:64663666
|
C | T | 4 | a0001c0001t0075g0106a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG03130.hp1 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-21121C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64663666 | ||||||
| chr12:64663681
|
T | A | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112-21106T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64663681 | ||||||
| chr12:64663840
|
C | CT | 40 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0001g0059others(37): Show | 40 | HG01109.hp2 HG01243.hp2 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-20925dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64663840 | |||||
| chr12:64663840
|
C | CTT | 10 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0003g0209others(7): Show | 10 | HG01109.hp1 HG01952.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.112-20926_112-2092 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64663840 | |||||
| chr12:64663840
|
CT | C | 110 | a0001c0001t0001g0052a0001c0001t0001g0131a0001c0001t0001g0260others(107): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.112-20925delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64663840 | |||||
| chr12:64663840
|
CTTTTTTT others(3): Show |
C | 14 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.112-20934_112-2092 others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64663840 | |||||
| chr12:64663955
|
C | T | 7 | a0001c0001t0049g0049a0001c0002t0021g0023a0001c0002t0028g0025others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-20832C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64663955 | ||||||
| chr12:64663991
|
A | G | 266 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.112-20796A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64663991 | ||||||
| chr12:64664191
|
T | C | 4 | a0001c0001t0018g0213a0001c0001t0018g0236a0001c0001t0018g0237others(1): Show | 4 | NA18943.hp2 NA18946.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-20596T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664191 | ||||||
| chr12:64664289
|
A | G | 3 | a0001c0001t0008g0247a0001c0001t0008g0248a0001c0001t0008g0249 | 3 | NA18982.hp2 NA19057.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.112-20498A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664289 | ||||||
| chr12:64664309
|
G | T | 5 | a0001c0001t0027g0351a0001c0001t0027g0354a0001c0001t0027g0356others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-20478G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664309 | ||||||
| chr12:64664460
|
G | A | 4 | a0001c0001t0075g0106a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG03130.hp1 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-20327G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664460 | ||||||
| chr12:64664501
|
C | A | 1 | a0001c0001t0003g0264 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.112-20286C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664501 | ||||||
| chr12:64664515
|
A | G | 28 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(25): Show | 28 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.112-20272A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664515 | ||||||
| chr12:64664660
|
T | C | 1 | a0001c0001t0003g0264 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.112-20127T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664660 | ||||||
| chr12:64664661
|
C | T | 1 | a0001c0001t0003g0264 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.112-20126C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664661 | ||||||
| chr12:64664761
|
A | G | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-20026A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664761 | ||||||
| chr12:64664790
|
G | A | 1 | a0001c0001t0013g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.112-19997G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664790 | ||||||
| chr12:64664832
|
A | G | 92 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(89): Show | 92 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.112-19955A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664832 | ||||||
| chr12:64664839
|
G | A | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112-19948G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664839 | ||||||
| chr12:64664846
|
G | C | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-19941G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664846 | ||||||
| chr12:64664913
|
T | A | 7 | a0001c0001t0049g0049a0001c0002t0021g0023a0001c0002t0028g0025others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-19874T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664913 | ||||||
| chr12:64664941
|
C | T | 1 | a0001c0001t0003g0263 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.112-19846C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64664941 | ||||||
| chr12:64665066
|
G | A | 3 | a0001c0001t0004g0298a0001c0001t0004g0302a0001c0001t0037g0297 | 3 | NA18747.hp2 NA19005.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.112-19721G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64665066 | ||||||
| chr12:64665156
|
C | G | 2 | a0001c0001t0086g0362a0001c0001t0088g0361 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-19631C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64665156 | ||||||
| chr12:64665195
|
A | G | 1 | a0001c0001t0022g0135 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.112-19592A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64665195 | ||||||
| chr12:64665264
|
G | T | 1 | a0001c0001t0001g0058 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.112-19523G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64665264 | ||||||
| chr12:64665270
|
C | T | 212 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(209): Show | 213 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.112-19517C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64665270 | ||||||
| chr12:64665412
|
A | G | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-19375A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64665412 | ||||||
| chr12:64665681
|
G | A | 1 | a0001c0001t0008g0286 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.112-19106G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64665681 | ||||||
| chr12:64665776
|
T | C | 1 | a0001c0001t0017g0178 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.112-19011T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64665776 | ||||||
| chr12:64665891
|
A | T | 1 | a0001c0001t0038g0359 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.112-18896A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64665891 | ||||||
| chr12:64666115
|
C | T | 60 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(57): Show | 60 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.112-18672C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64666115 | ||||||
| chr12:64666176
|
C | T | 1 | a0002c0003t0011g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.112-18611C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64666176 | ||||||
| chr12:64666365
|
C | CT | 85 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(82): Show | 85 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.112-18413dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64666365 | |||||
| chr12:64666365
|
C | CTT | 8 | a0001c0001t0006g0334a0001c0001t0049g0049a0001c0002t0021g0023others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.112-18414_112-1841 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64666365 | |||||
| chr12:64666440
|
G | A | 4 | a0001c0001t0075g0106a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG03130.hp1 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-18347G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64666440 | ||||||
| chr12:64666474
|
TAGCAGAT others(3): Show |
T | 1 | a0001c0001t0062g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.112-18297_112-1828 others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64666474 | |||||
| chr12:64666508
|
G | C | 92 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(89): Show | 92 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.112-18279G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64666508 | ||||||
| chr12:64666509
|
G | T | 4 | a0001c0001t0075g0106a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG03130.hp1 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-18278G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64666509 | ||||||
| chr12:64666533
|
G | A | 6 | a0001c0002t0015g0004a0001c0002t0015g0006a0001c0002t0015g0007others(3): Show | 6 | HG01106.hp2 HG01109.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-18254G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64666533 | ||||||
| chr12:64666584
|
G | A | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-18203G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64666584 | ||||||
| chr12:64666691
|
T | G | 6 | a0001c0001t0027g0351a0001c0001t0027g0354a0001c0001t0027g0356others(3): Show | 6 | HG01243.hp2 HG01361.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-18096T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64666691 | ||||||
| chr12:64667011
|
C | T | 4 | a0001c0001t0075g0106a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG03130.hp1 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-17776C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64667011 | ||||||
| chr12:64667046
|
G | C | 12 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(9): Show | 13 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.112-17741G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64667046 | ||||||
| chr12:64667060
|
G | A | 1 | a0001c0001t0059g0347 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.112-17727G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64667060 | ||||||
| chr12:64667196
|
T | G | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-17591T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64667196 | ||||||
| chr12:64667252
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.112-17535G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64667252 | ||||||
| chr12:64667357
|
C | T | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-17430C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64667357 | ||||||
| chr12:64667484
|
G | T | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.112-17303G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64667484 | ||||||
| chr12:64667485
|
C | T | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-17302C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64667485 | ||||||
| chr12:64667487
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.112-17300C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64667487 | ||||||
| chr12:64667837
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.112-16950A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64667837 | ||||||
| chr12:64667930
|
C | T | 29 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.112-16857C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64667930 | ||||||
| chr12:64668256
|
T | TTTC | 8 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(5): Show | 8 | HG01934.hp1 NA18939.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.112-16516_112-1651 others(7): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64668256 | |||||
| chr12:64668256
|
T | TTTCTTCT others(2): Show |
7 | a0001c0001t0049g0049a0001c0002t0021g0023a0001c0002t0028g0025others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-16522_112-1651 others(13): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64668256 | |||||
| chr12:64668256
|
T | TTTCTTCT others(5): Show |
63 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0142others(60): Show | 63 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.112-16525_112-1651 others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64668256 | |||||
| chr12:64668256
|
T | TTTCTTCT others(8): Show |
17 | a0001c0001t0002g0140a0001c0001t0002g0144a0001c0001t0002g0156others(14): Show | 17 | HG01106.hp1 HG01175.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.112-16528_112-1651 others(19): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64668256 | |||||
| chr12:64668271
|
CT | C | 18 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(15): Show | 19 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.112-16503delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64668271 | |||||
| chr12:64668272
|
T | TTCTTCTT others(4): Show |
1 | a0001c0001t0002g0321 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.112-16514_112-1651 others(15): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64668272 | |||||
| chr12:64668274
|
T | C | 6 | a0001c0001t0049g0049a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-16513T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64668274 | ||||||
| chr12:64668608
|
C | T | 62 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(59): Show | 62 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.112-16179C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64668608 | ||||||
| chr12:64668642
|
A | AGCAG | 4 | a0001c0001t0075g0106a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG03130.hp1 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-16143_112-1614 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64668642 | |||||
| chr12:64668680
|
A | AT | 129 | a0001c0001t0001g0061a0001c0001t0001g0124a0001c0001t0001g0260others(126): Show | 129 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.112-16088dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64668680 | |||||
| chr12:64668680
|
A | ATT | 22 | a0001c0001t0002g0140a0001c0001t0002g0156a0001c0001t0002g0164others(19): Show | 22 | HG00597.hp1 HG01175.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.112-16089_112-1608 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64668680 | |||||
| chr12:64668680
|
AT | A | 9 | a0001c0001t0001g0041a0001c0001t0003g0309a0001c0001t0004g0302others(6): Show | 9 | HG01993.hp2 HG02486.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.112-16088delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64668680 | |||||
| chr12:64668701
|
A | G | 62 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(59): Show | 62 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.112-16086A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64668701 | ||||||
| chr12:64668705
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.112-16082G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64668705 | ||||||
| chr12:64668714
|
C | T | 1 | a0001c0001t0004g0305 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.112-16073C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64668714 | ||||||
| chr12:64668828
|
C | T | 6 | a0001c0002t0015g0004a0001c0002t0015g0006a0001c0002t0015g0007others(3): Show | 6 | HG01106.hp2 HG01109.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-15959C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64668828 | ||||||
| chr12:64668854
|
TG | T | 7 | a0001c0001t0049g0049a0001c0002t0021g0023a0001c0002t0028g0025others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-15932delG | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64668854 | ||||||
| chr12:64668883
|
G | A | 1 | a0001c0001t0085g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.112-15904G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64668883 | ||||||
| chr12:64668938
|
G | A | 4 | a0001c0001t0001g0055a0001c0001t0001g0059a0001c0001t0001g0061others(1): Show | 4 | HG02155.hp1 NA19057.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-15849G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64668938 | ||||||
| chr12:64669009
|
G | T | 1 | a0001c0001t0001g0094 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.112-15778G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64669009 | ||||||
| chr12:64669010
|
A | T | 1 | a0001c0001t0001g0094 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.112-15777A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64669010 | ||||||
| chr12:64669236
|
A | G | 1 | a0001c0001t0084g0079 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.112-15551A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64669236 | ||||||
| chr12:64669394
|
C | G | 4 | a0001c0001t0075g0106a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG03130.hp1 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-15393C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64669394 | ||||||
| chr12:64669405
|
G | A | 2 | a0001c0001t0002g0150a0001c0001t0014g0149 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.112-15382G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64669405 | ||||||
| chr12:64669464
|
CTTCTT | C | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0003g0258 | 3 | HG02132.hp2 NA18951.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.112-15320_112-1531 others(9): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64669464 | |||||
| chr12:64669494
|
T | TGCCTAGG others(16): Show |
1 | a0001c0001t0061g0139 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.112-15292_112-1527 others(27): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64669494 | |||||
| chr12:64669556
|
C | T | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.112-15231C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64669556 | ||||||
| chr12:64669564
|
A | G | 4 | a0001c0001t0075g0106a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG03130.hp1 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-15223A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64669564 | ||||||
| chr12:64669636
|
A | G | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.112-15151A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64669636 | ||||||
| chr12:64669664
|
T | C | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-15123T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64669664 | ||||||
| chr12:64669691
|
C | A | 5 | a0001c0002t0016g0033a0001c0002t0016g0034a0001c0002t0016g0035others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-15096C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64669691 | ||||||
| chr12:64669890
|
C | CA | 20 | a0001c0001t0001g0032a0001c0001t0001g0039a0001c0001t0001g0041others(17): Show | 20 | HG00438.hp1 HG01109.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.112-14875dupA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64669890 | |||||
| chr12:64669890
|
CA | C | 25 | a0001c0001t0001g0260a0001c0001t0002g0159a0001c0001t0003g0219others(22): Show | 25 | HG00438.hp2 HG01361.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.112-14875delA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64669890 | |||||
| chr12:64669890
|
CAA | C | 97 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(94): Show | 98 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.112-14876_112-1487 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64669890 | |||||
| chr12:64669890
|
CAAA | C | 14 | a0001c0001t0002g0208a0001c0001t0013g0161a0001c0001t0017g0179others(11): Show | 14 | HG00323.hp1 HG01891.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.112-14877_112-1487 others(7): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64669890 | |||||
| chr12:64669912
|
A | AG | 3 | a0001c0001t0006g0054a0001c0001t0006g0071a0001c0001t0076g0064 | 3 | NA18944.hp1 NA18950.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.112-14875_112-1487 others(5): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64669912 | ||||||
| chr12:64669923
|
T | A | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.112-14864T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64669923 | ||||||
| chr12:64670029
|
G | GT | 23 | a0001c0001t0002g0140a0001c0001t0002g0144a0001c0001t0002g0156others(20): Show | 23 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.112-14746dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64670029 | |||||
| chr12:64670029
|
GT | G | 26 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(23): Show | 26 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(23): Show |
intron_variant | MODIFIER | c.112-14746delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64670029 | |||||
| chr12:64670044
|
T | C | 1 | a0001c0001t0090g0369 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.112-14743T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64670044 | ||||||
| chr12:64670111
|
G | A | 4 | a0001c0001t0075g0106a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG03130.hp1 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-14676G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64670111 | ||||||
| chr12:64670189
|
G | A | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112-14598G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64670189 | ||||||
| chr12:64670191
|
G | A | 26 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(23): Show | 26 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(23): Show |
intron_variant | MODIFIER | c.112-14596G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64670191 | ||||||
| chr12:64670370
|
G | GT | 132 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0032others(129): Show | 133 | HG00438.hp1 HG00609.hp2 HG00642.hp2 others(130): Show |
intron_variant | MODIFIER | c.112-14404dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64670370 | |||||
| chr12:64670370
|
G | GTT | 6 | a0001c0001t0001g0058a0001c0001t0001g0077a0001c0001t0001g0099others(3): Show | 6 | HG01168.hp2 HG01993.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-14405_112-1440 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64670370 | |||||
| chr12:64670370
|
G | GTTTT | 18 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0001t0004g0295others(15): Show | 18 | HG01358.hp1 HG01952.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.112-14407_112-1440 others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64670370 | |||||
| chr12:64670370
|
G | GTTTTT | 33 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0289others(30): Show | 33 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.112-14408_112-1440 others(9): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64670370 | |||||
| chr12:64670370
|
GT | G | 83 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(80): Show | 83 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.112-14404delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64670370 | |||||
| chr12:64670370
|
GTT | G | 7 | a0001c0001t0009g0244a0001c0001t0009g0273a0001c0002t0021g0023others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-14405_112-1440 others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64670370 | |||||
| chr12:64670544
|
C | CT | 66 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(63): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.112-14226dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64670544 | |||||
| chr12:64670544
|
CT | C | 154 | a0001c0001t0001g0070a0001c0001t0001g0260a0001c0001t0001g0261others(151): Show | 154 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.112-14226delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64670544 | |||||
| chr12:64670545
|
T | TC | 4 | a0002c0003t0010g0119a0002c0003t0011g0114a0002c0003t0011g0115others(1): Show | 5 | HG02109.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-14242_112-1424 others(5): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64670545 | ||||||
| chr12:64670546
|
T | C | 2 | a0001c0001t0049g0049a0002c0003t0010g0116 | 2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.112-14241T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64670546 | ||||||
| chr12:64670547
|
T | C | 1 | a0001c0001t0074g0250 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.112-14240T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64670547 | ||||||
| chr12:64670878
|
G | A | 4 | a0001c0001t0075g0106a0001c0001t0086g0362a0001c0001t0088g0361others(1): Show | 4 | HG03130.hp1 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-13909G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64670878 | ||||||
| chr12:64670929
|
T | TC | 5 | a0001c0001t0004g0363a0001c0001t0038g0243a0001c0001t0066g0220others(2): Show | 5 | HG02559.hp2 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-13856dupC | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64670929 | |||||
| chr12:64670932
|
G | A | 7 | a0001c0001t0049g0049a0001c0002t0021g0023a0001c0002t0028g0025others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-13855G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64670932 | ||||||
| chr12:64670952
|
G | A | 1 | a0001c0001t0075g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112-13835G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64670952 | ||||||
| chr12:64670994
|
C | G | 1 | a0001c0001t0012g0136 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.112-13793C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64670994 | ||||||
| chr12:64671008
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.112-13779T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64671008 | ||||||
| chr12:64671389
|
C | T | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-13398C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64671389 | ||||||
| chr12:64671411
|
T | C | 81 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-13376T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64671411 | ||||||
| chr12:64671518
|
C | T | 61 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(58): Show | 61 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.112-13269C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64671518 | ||||||
| chr12:64671557
|
G | A | 3 | a0001c0001t0002g0142a0001c0001t0002g0150a0001c0001t0014g0149 | 3 | HG01070.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.112-13230G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64671557 | ||||||
| chr12:64671632
|
C | T | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.112-13155C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64671632 | ||||||
| chr12:64671807
|
G | T | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-12980G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64671807 | ||||||
| chr12:64671828
|
T | C | 11 | a0001c0001t0049g0049a0001c0001t0075g0106a0001c0001t0086g0362others(8): Show | 11 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.112-12959T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64671828 | ||||||
| chr12:64671878
|
A | G | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.112-12909A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64671878 | ||||||
| chr12:64671907
|
T | C | 5 | a0001c0001t0004g0363a0001c0001t0038g0243a0001c0001t0066g0220others(2): Show | 5 | HG02559.hp2 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-12880T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64671907 | ||||||
| chr12:64671972
|
A | G | 1 | a0001c0001t0090g0369 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.112-12815A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64671972 | ||||||
| chr12:64672051
|
T | G | 14 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.112-12736T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64672051 | ||||||
| chr12:64672119
|
G | T | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.112-12668G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64672119 | ||||||
| chr12:64672127
|
C | CATATA | 5 | a0001c0001t0028g0048a0001c0001t0075g0106a0001c0001t0086g0362others(2): Show | 5 | HG01361.hp2 HG03130.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-12656_112-1265 others(9): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64672127 | |||||
| chr12:64672150
|
A | G | 2 | a0001c0002t0021g0217a0001c0002t0021g0218 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.112-12637A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64672150 | ||||||
| chr12:64672162
|
G | A | 7 | a0001c0001t0049g0049a0001c0002t0021g0023a0001c0002t0028g0025others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-12625G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64672162 | ||||||
| chr12:64672232
|
T | A | 1 | a0001c0001t0018g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.112-12555T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64672232 | ||||||
| chr12:64672311
|
C | T | 23 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0041others(20): Show | 23 | HG00642.hp2 HG00735.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.112-12476C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64672311 | ||||||
| chr12:64672465
|
T | A | 93 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(90): Show | 93 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.112-12322T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64672465 | ||||||
| chr12:64672764
|
C | T | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.112-12023C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64672764 | ||||||
| chr12:64672846
|
G | A | 5 | a0001c0001t0027g0351a0001c0001t0027g0354a0001c0001t0027g0356others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-11941G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64672846 | ||||||
| chr12:64672895
|
C | G | 62 | a0001c0001t0001g0072a0001c0001t0001g0260a0001c0001t0001g0261others(59): Show | 62 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.112-11892C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64672895 | ||||||
| chr12:64672989
|
G | A | 6 | a0001c0001t0007g0352a0001c0001t0010g0364a0001c0001t0010g0365others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-11798G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64672989 | ||||||
| chr12:64673042
|
A | T | 6 | a0001c0002t0015g0004a0001c0002t0015g0006a0001c0002t0015g0007others(3): Show | 6 | HG01106.hp2 HG01109.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-11745A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673042 | ||||||
| chr12:64673052
|
T | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02056.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.112-11735T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673052 | ||||||
| chr12:64673063
|
C | T | 1 | a0001c0001t0004g0303 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.112-11724C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673063 | ||||||
| chr12:64673163
|
T | G | 1 | a0001c0001t0004g0303 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.112-11624T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673163 | ||||||
| chr12:64673258
|
T | A | 1 | a0001c0001t0004g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.112-11529T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673258 | ||||||
| chr12:64673295
|
T | G | 1 | a0001c0001t0003g0265 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.112-11492T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673295 | ||||||
| chr12:64673404
|
A | G | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.112-11383A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673404 | ||||||
| chr12:64673409
|
T | G | 70 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(67): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.112-11378T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673409 | ||||||
| chr12:64673589
|
A | G | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-11198A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673589 | ||||||
| chr12:64673591
|
G | A | 1 | a0001c0001t0065g0318 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.112-11196G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673591 | ||||||
| chr12:64673598
|
G | A | 31 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(28): Show | 31 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.112-11189G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673598 | ||||||
| chr12:64673680
|
A | G | 1 | a0001c0001t0086g0362 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.112-11107A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673680 | ||||||
| chr12:64673768
|
A | G | 5 | a0001c0001t0007g0352a0001c0001t0010g0365a0001c0001t0010g0366others(2): Show | 5 | HG02615.hp2 HG02818.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-11019A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673768 | ||||||
| chr12:64673932
|
C | A | 5 | a0001c0001t0004g0088a0001c0001t0004g0091a0001c0001t0004g0102others(2): Show | 5 | HG00735.hp1 HG01192.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-10855C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673932 | ||||||
| chr12:64673955
|
A | G | 8 | a0001c0002t0004g0015a0001c0002t0007g0013a0001c0002t0007g0014others(5): Show | 8 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-10832A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673955 | ||||||
| chr12:64673998
|
G | T | 1 | a0001c0001t0018g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.112-10789G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64673998 | ||||||
| chr12:64674001
|
T | A | 1 | a0001c0001t0018g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.112-10786T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64674001 | ||||||
| chr12:64674110
|
G | A | 1 | a0001c0001t0086g0362 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.112-10677G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64674110 | ||||||
| chr12:64674293
|
G | A | 5 | a0002c0003t0010g0116a0002c0003t0010g0119a0002c0003t0011g0114others(2): Show | 6 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-10494G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64674293 | ||||||
| chr12:64674301
|
T | C | 1 | a0001c0002t0047g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.112-10486T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64674301 | ||||||
| chr12:64674375
|
A | C | 3 | a0001c0001t0006g0310a0001c0001t0006g0311a0001c0001t0044g0110 | 3 | HG02922.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.112-10412A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64674375 | ||||||
| chr12:64674389
|
G | A | 2 | a0001c0001t0005g0195a0001c0001t0034g0204 | 2 | HG00735.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.112-10398G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64674389 | ||||||
| chr12:64674453
|
T | C | 59 | a0001c0001t0004g0133a0001c0001t0004g0215a0001c0001t0004g0288others(56): Show | 59 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.112-10334T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64674453 | ||||||
| chr12:64674522
|
A | G | 3 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369 | 3 | HG06807.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.112-10265A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64674522 | ||||||
| chr12:64674559
|
C | T | 8 | a0001c0001t0086g0362a0001c0001t0088g0361a0001c0001t0090g0369others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.112-10228C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64674559 | ||||||
| chr12:64674889
|
C | T | 1 | a0001c0002t0081g0005 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.112-9898C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64674889 | ||||||
| chr12:64674906
|
T | C | 65 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(62): Show | 65 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.112-9881T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64674906 | ||||||
| chr12:64674990
|
C | T | 65 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(62): Show | 65 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.112-9797C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64674990 | ||||||
| chr12:64675031
|
A | G | 81 | a0001c0001t0001g0082a0001c0001t0001g0333a0001c0001t0001g0340others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-9756A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675031 | ||||||
| chr12:64675045
|
G | GC | 43 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0042others(40): Show | 44 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.112-9728dupC | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675045 | |||||
| chr12:64675045
|
G | GCC | 41 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0059others(38): Show | 41 | HG00438.hp1 HG01081.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.112-9729_112-9728d others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675045 | |||||
| chr12:64675045
|
G | GCCC | 30 | a0001c0001t0001g0032a0001c0001t0001g0062a0001c0001t0001g0063others(27): Show | 30 | HG00140.hp1 HG00639.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.112-9730_112-9728d others(5): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675045 | |||||
| chr12:64675045
|
G | GCCCCCCC others(3): Show |
1 | a0001c0001t0009g0282 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.112-9737_112-9728d others(12): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675045 | |||||
| chr12:64675045
|
G | GCCCCCCC others(4): Show |
2 | a0001c0001t0005g0193a0001c0001t0006g0283 | 2 | HG01975.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.112-9738_112-9728d others(13): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675045 | |||||
| chr12:64675045
|
G | GCCCCCCC others(5): Show |
7 | a0001c0001t0004g0289a0001c0001t0004g0348a0001c0001t0005g0195others(4): Show | 7 | HG00735.hp2 HG01258.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-9739_112-9728d others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675045 | |||||
| chr12:64675045
|
G | GCCCCCCC others(6): Show |
7 | a0001c0001t0005g0126a0001c0001t0005g0141a0001c0001t0005g0203others(4): Show | 7 | HG01256.hp2 HG01261.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-9740_112-9728d others(15): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675045 | |||||
| chr12:64675045
|
G | GCCCCCCC others(7): Show |
1 | a0001c0001t0062g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.112-9741_112-9728d others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675045 | |||||
| chr12:64675045
|
G | GCCCCCCC others(8): Show |
3 | a0001c0001t0005g0196a0001c0001t0005g0202a0001c0001t0088g0361 | 3 | HG01099.hp2 HG02738.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.112-9728_112-9727i others(17): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675045 | |||||
| chr12:64675051
|
C | CCCCCCCC others(10): Show |
1 | a0001c0001t0007g0304 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.112-9728_112-9727i others(19): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675051 | |||||
| chr12:64675051
|
C | CCCCCCCC others(7): Show |
1 | a0001c0001t0004g0343 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.112-9728_112-9727i others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675051 | |||||
| chr12:64675051
|
C | CCCCCCCC others(5): Show |
1 | a0001c0001t0004g0295 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.112-9728_112-9727i others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675051 | |||||
| chr12:64675052
|
C | CCCCCCCC others(10): Show |
1 | a0001c0001t0004g0305 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.112-9728_112-9727i others(19): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675052 | |||||
| chr12:64675052
|
C | CCCCCCCC others(9): Show |
2 | a0001c0001t0004g0296a0001c0001t0060g0134 | 2 | HG00280.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.112-9728_112-9727i others(18): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675052 | |||||
| chr12:64675052
|
C | CCCCCCCC others(8): Show |
4 | a0001c0001t0004g0133a0001c0001t0004g0301a0001c0001t0008g0286others(1): Show | 4 | HG00741.hp2 HG01074.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-9728_112-9727i others(17): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675052 | |||||
| chr12:64675052
|
C | CCCCCCCC others(7): Show |
6 | a0001c0001t0004g0215a0001c0001t0004g0293a0001c0001t0004g0299others(3): Show | 6 | HG00140.hp2 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-9728_112-9727i others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675052 | |||||
| chr12:64675052
|
C | CCCCCCCC others(6): Show |
7 | a0001c0001t0004g0288a0001c0001t0004g0290a0001c0001t0004g0294others(4): Show | 7 | HG02896.hp1 NA18612.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-9728_112-9727i others(15): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675052 | |||||
| chr12:64675052
|
C | CCCCCCCC others(5): Show |
4 | a0001c0001t0004g0291a0001c0001t0004g0298a0001c0001t0006g0287others(1): Show | 4 | HG02074.hp2 NA18968.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-9728_112-9727i others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675052 | |||||
| chr12:64675053
|
C | CT | 6 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(3): Show | 6 | HG00609.hp2 NA18966.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-9734_112-9733i others(3): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675053 | ||||||
| chr12:64675054
|
C | CG | 6 | a0001c0001t0006g0334a0001c0001t0006g0336a0001c0001t0014g0169others(3): Show | 6 | HG00597.hp2 HG02135.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-9733_112-9732i others(3): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675054 | ||||||
| chr12:64675054
|
C | G | 75 | a0001c0001t0001g0082a0001c0001t0001g0333a0001c0001t0001g0340others(72): Show | 75 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.112-9733C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675054 | ||||||
| chr12:64675055
|
C | T | 59 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(56): Show | 59 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.112-9732C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675055 | ||||||
| chr12:64675060
|
G | A | 40 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(37): Show | 40 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.112-9727G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675060 | ||||||
| chr12:64675063
|
A | AC | 5 | a0001c0001t0001g0055a0001c0001t0001g0234a0001c0001t0002g0208others(2): Show | 5 | HG01175.hp2 HG01952.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-9720dupC | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64675063 | |||||
| chr12:64675103
|
A | G | 1 | a0001c0001t0018g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.112-9684A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675103 | ||||||
| chr12:64675113
|
A | C | 23 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(20): Show | 23 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.112-9674A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675113 | ||||||
| chr12:64675346
|
C | T | 7 | a0001c0001t0006g0283a0001c0001t0009g0280a0001c0001t0009g0281others(4): Show | 7 | HG02040.hp2 HG02083.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-9441C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675346 | ||||||
| chr12:64675347
|
G | A | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.112-9440G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675347 | ||||||
| chr12:64675372
|
A | T | 1 | a0001c0001t0006g0324 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.112-9415A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675372 | ||||||
| chr12:64675413
|
G | C | 1 | a0001c0001t0005g0196 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.112-9374G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675413 | ||||||
| chr12:64675444
|
C | A | 1 | a0001c0001t0018g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.112-9343C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675444 | ||||||
| chr12:64675446
|
G | C | 1 | a0001c0001t0018g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.112-9341G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675446 | ||||||
| chr12:64675448
|
C | G | 1 | a0001c0001t0018g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.112-9339C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675448 | ||||||
| chr12:64675488
|
T | G | 63 | a0001c0001t0004g0088a0001c0001t0004g0091a0001c0001t0004g0102others(60): Show | 63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.112-9299T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675488 | ||||||
| chr12:64675616
|
G | A | 1 | a0001c0001t0032g0145 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.112-9171G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675616 | ||||||
| chr12:64675741
|
G | A | 1 | a0001c0002t0048g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.112-9046G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675741 | ||||||
| chr12:64675773
|
C | T | 5 | a0001c0001t0027g0351a0001c0001t0027g0354a0001c0001t0027g0356others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-9014C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675773 | ||||||
| chr12:64675832
|
C | G | 1 | a0001c0001t0018g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.112-8955C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675832 | ||||||
| chr12:64675833
|
G | C | 1 | a0001c0001t0018g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.112-8954G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675833 | ||||||
| chr12:64675995
|
G | A | 1 | a0001c0001t0005g0202 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.112-8792G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64675995 | ||||||
| chr12:64676060
|
G | A | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.112-8727G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64676060 | ||||||
| chr12:64676166
|
A | AT | 58 | a0001c0001t0001g0228a0001c0001t0002g0162a0001c0001t0002g0165others(55): Show | 58 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.112-8598dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64676166 | |||||
| chr12:64676166
|
A | ATT | 16 | a0001c0001t0004g0091a0001c0001t0004g0296a0001c0001t0004g0298others(13): Show | 16 | HG00140.hp1 HG00639.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.112-8599_112-8598d others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64676166 | |||||
| chr12:64676166
|
AT | A | 164 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0032others(161): Show | 164 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.112-8598delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64676166 | |||||
| chr12:64676166
|
ATT | A | 22 | a0001c0001t0001g0231a0001c0001t0003g0252a0001c0001t0008g0247others(19): Show | 23 | HG01081.hp1 HG01891.hp2 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.112-8599_112-8598d others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64676166 | |||||
| chr12:64676327
|
T | C | 269 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(266): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.112-8460T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64676327 | ||||||
| chr12:64676397
|
G | A | 13 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0308others(10): Show | 13 | HG01109.hp1 HG02486.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.112-8390G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64676397 | ||||||
| chr12:64676467
|
C | CT | 9 | a0001c0001t0001g0039a0001c0001t0001g0050a0001c0001t0001g0055others(6): Show | 9 | HG01109.hp2 HG02071.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.112-8296dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64676467 | |||||
| chr12:64676467
|
CT | C | 36 | a0001c0001t0001g0042a0001c0001t0001g0069a0001c0001t0001g0080others(33): Show | 37 | HG01169.hp2 HG01943.hp1 HG01993.hp2 others(34): Show |
intron_variant | MODIFIER | c.112-8296delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64676467 | |||||
| chr12:64676467
|
CTT | C | 94 | a0001c0001t0001g0333a0001c0001t0002g0140a0001c0001t0002g0142others(91): Show | 94 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.112-8297_112-8296d others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64676467 | |||||
| chr12:64676467
|
CTTT | C | 119 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0003g0043others(116): Show | 119 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.112-8298_112-8296d others(5): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64676467 | |||||
| chr12:64676467
|
CTTTT | C | 22 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0309others(19): Show | 22 | HG01074.hp2 HG01109.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.112-8299_112-8296d others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64676467 | |||||
| chr12:64676467
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0340 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.112-8306_112-8296d others(13): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64676467 | |||||
| chr12:64676514
|
C | T | 14 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.112-8273C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64676514 | ||||||
| chr12:64676620
|
C | T | 1 | a0001c0001t0074g0250 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.112-8167C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64676620 | ||||||
| chr12:64676621
|
G | A | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.112-8166G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64676621 | ||||||
| chr12:64676652
|
A | G | 4 | a0001c0001t0012g0125a0001c0001t0012g0167a0001c0001t0012g0182others(1): Show | 4 | HG02145.hp1 HG02486.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-8135A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64676652 | ||||||
| chr12:64676663
|
G | T | 1 | a0001c0001t0018g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.112-8124G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64676663 | ||||||
| chr12:64676719
|
C | T | 1 | a0001c0001t0008g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.112-8068C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64676719 | ||||||
| chr12:64676750
|
C | T | 2 | a0001c0001t0003g0313a0001c0001t0003g0316 | 2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.112-8037C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64676750 | ||||||
| chr12:64676832
|
G | A | 5 | a0001c0002t0021g0023a0001c0002t0028g0025a0001c0002t0029g0021others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-7955G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64676832 | ||||||
| chr12:64676913
|
C | T | 1 | a0001c0002t0021g0023 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.112-7874C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64676913 | ||||||
| chr12:64676956
|
C | T | 1 | a0001c0001t0003g0263 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.112-7831C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64676956 | ||||||
| chr12:64677101
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.112-7686C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64677101 | ||||||
| chr12:64677116
|
T | C | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.112-7671T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64677116 | ||||||
| chr12:64677326
|
A | G | 2 | a0001c0001t0017g0160a0001c0001t0017g0172 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.112-7461A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64677326 | ||||||
| chr12:64677353
|
G | A | 57 | a0001c0001t0004g0088a0001c0001t0004g0091a0001c0001t0004g0102others(54): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.112-7434G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64677353 | ||||||
| chr12:64677378
|
C | T | 1 | a0001c0001t0003g0279 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.112-7409C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64677378 | ||||||
| chr12:64677554
|
C | T | 1 | a0001c0001t0002g0350 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.112-7233C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64677554 | ||||||
| chr12:64677580
|
G | T | 2 | a0001c0001t0049g0049a0001c0001t0085g0029 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.112-7207G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64677580 | ||||||
| chr12:64677600
|
A | C | 1 | a0001c0001t0090g0369 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.112-7187A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64677600 | ||||||
| chr12:64677748
|
T | G | 3 | a0001c0001t0004g0133a0001c0001t0004g0301a0001c0001t0060g0134 | 3 | HG00280.hp2 HG00741.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.112-7039T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64677748 | ||||||
| chr12:64677840
|
C | T | 57 | a0001c0001t0004g0088a0001c0001t0004g0091a0001c0001t0004g0102others(54): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.112-6947C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64677840 | ||||||
| chr12:64677894
|
T | C | 1 | a0001c0001t0006g0324 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.112-6893T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64677894 | ||||||
| chr12:64678104
|
G | C | 2 | a0001c0001t0009g0244a0001c0001t0009g0273 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.112-6683G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64678104 | ||||||
| chr12:64678461
|
A | G | 1 | a0001c0001t0052g0330 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.112-6326A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64678461 | ||||||
| chr12:64678640
|
C | T | 1 | a0001c0001t0004g0343 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.112-6147C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64678640 | ||||||
| chr12:64678641
|
G | A | 1 | a0001c0001t0018g0213 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.112-6146G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64678641 | ||||||
| chr12:64678648
|
C | A | 1 | a0001c0001t0035g0096 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.112-6139C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64678648 | ||||||
| chr12:64678648
|
C | CA | 12 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0085others(9): Show | 12 | HG00438.hp1 HG00642.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.112-6122dupA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64678648 | |||||
| chr12:64678648
|
C | CAA | 13 | a0001c0001t0020g0107a0001c0001t0020g0109a0001c0001t0031g0113others(10): Show | 14 | HG01256.hp2 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.112-6123_112-6122d others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64678648 | |||||
| chr12:64678648
|
C | CAAAAA | 17 | a0001c0001t0002g0146a0001c0001t0002g0321a0001c0001t0002g0327others(14): Show | 17 | HG01255.hp1 HG01255.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.112-6126_112-6122d others(7): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64678648 | |||||
| chr12:64678648
|
C | CAAAAAA | 119 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(116): Show | 119 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.112-6127_112-6122d others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64678648 | |||||
| chr12:64678648
|
C | CAAAAAAA | 59 | a0001c0001t0002g0140a0001c0001t0002g0144a0001c0001t0002g0155others(56): Show | 59 | HG00597.hp2 HG00673.hp2 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.112-6128_112-6122d others(9): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64678648 | |||||
| chr12:64678648
|
C | CAAAAAAA others(1): Show |
19 | a0001c0001t0002g0192a0001c0001t0003g0227a0001c0001t0003g0252others(16): Show | 19 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.112-6129_112-6122d others(10): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64678648 | |||||
| chr12:64678648
|
C | CAAAAAAA others(2): Show |
19 | a0001c0001t0004g0289a0001c0001t0005g0126a0001c0001t0005g0193others(16): Show | 19 | HG00642.hp1 HG01071.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.112-6130_112-6122d others(11): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64678648 | |||||
| chr12:64678648
|
C | CAAAAAAA others(3): Show |
12 | a0001c0001t0005g0128a0001c0001t0005g0141a0001c0001t0005g0195others(9): Show | 12 | HG00280.hp1 HG00735.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.112-6131_112-6122d others(12): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64678648 | |||||
| chr12:64678648
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0006g0283a0001c0001t0009g0282 | 2 | HG02040.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.112-6133_112-6122d others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64678648 | |||||
| chr12:64678666
|
C | A | 30 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0041others(27): Show | 30 | HG00642.hp2 HG00673.hp1 HG01952.hp1 others(27): Show |
intron_variant | MODIFIER | c.112-6121C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64678666 | ||||||
| chr12:64678667
|
C | A | 1 | a0001c0001t0039g0038 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.112-6120C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64678667 | ||||||
| chr12:64678794
|
A | G | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.112-5993A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64678794 | ||||||
| chr12:64678848
|
A | G | 79 | a0001c0001t0001g0333a0001c0001t0001g0340a0001c0001t0002g0140others(76): Show | 79 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.112-5939A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64678848 | ||||||
| chr12:64678968
|
T | G | 2 | a0001c0002t0021g0217a0001c0002t0021g0218 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.112-5819T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64678968 | ||||||
| chr12:64679310
|
T | C | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.112-5477T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64679310 | ||||||
| chr12:64679383
|
A | G | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.112-5404A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64679383 | ||||||
| chr12:64679428
|
A | G | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.112-5359A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64679428 | ||||||
| chr12:64679530
|
T | C | 253 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.112-5257T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64679530 | ||||||
| chr12:64679640
|
T | G | 1 | a0001c0001t0018g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.112-5147T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64679640 | ||||||
| chr12:64679641
|
G | A | 1 | a0001c0001t0018g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.112-5146G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64679641 | ||||||
| chr12:64679967
|
A | G | 5 | a0001c0002t0021g0023a0001c0002t0028g0025a0001c0002t0029g0021others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-4820A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64679967 | ||||||
| chr12:64679999
|
G | A | 2 | a0001c0001t0049g0049a0001c0001t0085g0029 | 2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.112-4788G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64679999 | ||||||
| chr12:64680565
|
G | T | 262 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(259): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.112-4222G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64680565 | ||||||
| chr12:64680682
|
C | T | 3 | a0001c0001t0026g0239a0001c0001t0026g0240a0001c0001t0026g0241 | 3 | NA18945.hp1 NA18983.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.112-4105C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64680682 | ||||||
| chr12:64680693
|
G | A | 262 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(259): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.112-4094G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64680693 | ||||||
| chr12:64680695
|
T | C | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.112-4092T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64680695 | ||||||
| chr12:64680706
|
C | G | 1 | a0001c0001t0019g0093 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.112-4081C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64680706 | ||||||
| chr12:64680707
|
G | C | 1 | a0001c0001t0019g0093 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.112-4080G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64680707 | ||||||
| chr12:64680716
|
C | T | 1 | a0001c0001t0007g0346 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.112-4071C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64680716 | ||||||
| chr12:64680755
|
A | T | 1 | a0001c0001t0052g0330 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.112-4032A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64680755 | ||||||
| chr12:64680842
|
T | C | 263 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(260): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.112-3945T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64680842 | ||||||
| chr12:64680858
|
C | T | 1 | a0001c0001t0074g0250 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.112-3929C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64680858 | ||||||
| chr12:64681011
|
C | T | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0005g0205 | 3 | HG02683.hp1 HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.112-3776C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64681011 | ||||||
| chr12:64681552
|
T | G | 85 | a0001c0001t0001g0234a0001c0001t0001g0333a0001c0001t0001g0340others(82): Show | 85 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.112-3235T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64681552 | ||||||
| chr12:64681816
|
C | A | 1 | a0001c0001t0003g0268 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.112-2971C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64681816 | ||||||
| chr12:64681930
|
A | C | 1 | a0001c0002t0007g0017 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.112-2857A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64681930 | ||||||
| chr12:64682037
|
T | A | 260 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.112-2750T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682037 | ||||||
| chr12:64682163
|
C | T | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.112-2624C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682163 | ||||||
| chr12:64682201
|
G | T | 1 | a0001c0001t0004g0302 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.112-2586G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682201 | ||||||
| chr12:64682273
|
C | T | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.112-2514C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682273 | ||||||
| chr12:64682284
|
C | T | 1 | a0001c0001t0004g0305 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.112-2503C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682284 | ||||||
| chr12:64682437
|
G | T | 63 | a0001c0001t0004g0088a0001c0001t0004g0091a0001c0001t0004g0102others(60): Show | 63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.112-2350G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682437 | ||||||
| chr12:64682447
|
G | A | 2 | a0001c0001t0008g0222a0001c0001t0008g0223 | 2 | NA18944.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.112-2340G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682447 | ||||||
| chr12:64682460
|
G | A | 10 | a0001c0002t0004g0015a0001c0002t0007g0011a0001c0002t0007g0012others(7): Show | 10 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.112-2327G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682460 | ||||||
| chr12:64682475
|
G | A | 6 | a0001c0001t0001g0234a0001c0001t0002g0173a0001c0001t0002g0181others(3): Show | 6 | NA18951.hp2 NA18962.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-2312G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682475 | ||||||
| chr12:64682566
|
C | CA | 21 | a0001c0001t0001g0055a0001c0001t0002g0189a0001c0001t0002g0350others(18): Show | 22 | HG01261.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.112-2205dupA | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64682566 | |||||
| chr12:64682580
|
A | C | 1 | a0002c0004t0011g0326 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.112-2207A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682580 | ||||||
| chr12:64682655
|
A | G | 1 | a0001c0001t0008g0276 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.112-2132A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682655 | ||||||
| chr12:64682682
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | NA18963.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.112-2105C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682682 | ||||||
| chr12:64682693
|
C | T | 11 | a0001c0001t0007g0346a0001c0002t0004g0015a0001c0002t0007g0011others(8): Show | 11 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.112-2094C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682693 | ||||||
| chr12:64682718
|
G | T | 82 | a0001c0001t0001g0234a0001c0001t0001g0333a0001c0001t0001g0340others(79): Show | 82 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.112-2069G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682718 | ||||||
| chr12:64682768
|
C | T | 5 | a0001c0001t0009g0244a0001c0001t0009g0273a0001c0001t0032g0145others(2): Show | 5 | HG02647.hp1 HG02886.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-2019C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682768 | ||||||
| chr12:64682801
|
T | C | 5 | a0001c0001t0027g0351a0001c0001t0027g0354a0001c0001t0027g0356others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-1986T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682801 | ||||||
| chr12:64682850
|
T | C | 5 | a0001c0001t0007g0352a0001c0001t0010g0365a0001c0001t0010g0366others(2): Show | 5 | HG02615.hp2 HG02818.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-1937T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682850 | ||||||
| chr12:64682902
|
G | A | 1 | a0001c0001t0004g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.112-1885G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64682902 | ||||||
| chr12:64683154
|
G | A | 1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.112-1633G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64683154 | ||||||
| chr12:64683445
|
C | T | 5 | a0001c0001t0009g0244a0001c0001t0009g0273a0001c0001t0032g0145others(2): Show | 5 | HG02647.hp1 HG02886.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-1342C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64683445 | ||||||
| chr12:64683480
|
A | G | 1 | a0001c0001t0052g0330 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.112-1307A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64683480 | ||||||
| chr12:64683951
|
T | C | 3 | a0001c0001t0036g0314a0001c0001t0036g0315a0001c0001t0075g0106 | 3 | HG03130.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.112-836T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64683951 | ||||||
| chr12:64683989
|
G | GGA | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0025g0075 | 3 | NA18963.hp1 NA19065.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.112-778_112-777dup others(2): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64683989 | |||||
| chr12:64684001
|
AGAGAGAG others(13): Show |
A | 33 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(30): Show | 33 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.112-784_112-765del others(20): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684001 | |||||
| chr12:64684007
|
A | AGTGAGTG others(5): Show |
1 | a0001c0001t0003g0279 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.112-779_112-778ins others(12): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684007 | |||||
| chr12:64684009
|
A | AGAGTGAG others(5): Show |
11 | a0001c0001t0004g0363a0001c0001t0007g0352a0001c0001t0010g0364others(8): Show | 11 | HG02055.hp1 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.112-777_112-776ins others(12): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684009 | |||||
| chr12:64684009
|
A | AGAGTGAG others(7): Show |
18 | a0001c0001t0008g0222a0001c0001t0008g0223a0001c0001t0008g0247others(15): Show | 18 | HG01891.hp1 HG02615.hp1 HG03041.hp2 others(15): Show |
intron_variant | MODIFIER | c.112-777_112-776ins others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684009 | |||||
| chr12:64684009
|
A | AGAGTGAG others(9): Show |
10 | a0001c0001t0006g0278a0001c0001t0008g0214a0001c0001t0008g0224others(7): Show | 10 | HG02027.hp2 HG02723.hp1 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.112-777_112-776ins others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684009 | |||||
| chr12:64684009
|
A | T | 1 | a0001c0001t0003g0279 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.112-778A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64684009 | ||||||
| chr12:64684011
|
T | A | 1 | a0001c0001t0088g0361 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-776T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64684011 | ||||||
| chr12:64684013
|
A | AGT | 13 | a0001c0001t0001g0062a0001c0001t0007g0346a0001c0002t0004g0015others(10): Show | 13 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.112-751_112-750dup others(2): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684013 | |||||
| chr12:64684013
|
A | AGTGT | 54 | a0001c0001t0004g0088a0001c0001t0004g0091a0001c0001t0004g0102others(51): Show | 54 | HG00280.hp1 HG00280.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.112-753_112-750dup others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684013 | |||||
| chr12:64684013
|
A | AGTGTGT | 19 | a0001c0001t0004g0215a0001c0001t0004g0293a0001c0001t0005g0201others(16): Show | 19 | HG00140.hp2 HG01256.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.112-755_112-750dup others(6): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684013 | |||||
| chr12:64684013
|
A | AGTGTGTG others(1): Show |
5 | a0001c0001t0027g0351a0001c0001t0027g0354a0001c0001t0027g0356others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-757_112-750dup others(8): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684013 | |||||
| chr12:64684013
|
A | AGTGTGTG others(3): Show |
1 | a0001c0001t0086g0362 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.112-759_112-750dup others(10): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684013 | |||||
| chr12:64684013
|
A | AGTGTGTG others(5): Show |
1 | a0001c0001t0085g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.112-761_112-750dup others(12): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684013 | |||||
| chr12:64684013
|
A | AGTGTGTG others(7): Show |
1 | a0001c0001t0028g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.112-763_112-750dup others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684013 | |||||
| chr12:64684013
|
A | T | 40 | a0001c0001t0003g0279a0001c0001t0004g0363a0001c0001t0006g0278others(37): Show | 40 | HG01891.hp1 HG02027.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.112-774A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64684013 | ||||||
| chr12:64684013
|
AGTGT | A | 79 | a0001c0001t0001g0234a0001c0001t0001g0333a0001c0001t0001g0340others(76): Show | 79 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.112-753_112-750del others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684013 | |||||
| chr12:64684036
|
G | GTGTGTGT others(8): Show |
1 | a0001c0001t0008g0276 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.112-750_112-749ins others(15): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684036 | |||||
| chr12:64684085
|
A | AT | 17 | a0001c0001t0001g0124a0001c0001t0002g0192a0001c0001t0003g0264others(14): Show | 17 | HG00597.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.112-683dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684085 | |||||
| chr12:64684085
|
AT | A | 45 | a0001c0001t0001g0072a0001c0001t0001g0212a0001c0001t0001g0234others(42): Show | 46 | HG00280.hp1 HG00323.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.112-683delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684085 | |||||
| chr12:64684138
|
G | C | 58 | a0001c0001t0004g0088a0001c0001t0004g0091a0001c0001t0004g0102others(55): Show | 58 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.112-649G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64684138 | ||||||
| chr12:64684242
|
T | C | 268 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(265): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.112-545T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64684242 | ||||||
| chr12:64684337
|
G | A | 1 | a0001c0001t0009g0097 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.112-450G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64684337 | ||||||
| chr12:64684431
|
G | GT | 30 | a0001c0001t0001g0234a0001c0001t0007g0346a0001c0001t0009g0244others(27): Show | 31 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.112-353dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684431 | |||||
| chr12:64684431
|
G | GTT | 120 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(117): Show | 120 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.112-354_112-353dup others(2): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684431 | |||||
| chr12:64684431
|
G | GTTT | 5 | a0001c0001t0002g0350a0001c0001t0006g0324a0001c0001t0032g0145others(2): Show | 5 | HG02080.hp2 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-355_112-353dup others(3): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684431 | |||||
| chr12:64684431
|
G | GTTTT | 27 | a0001c0001t0003g0279a0001c0001t0006g0278a0001c0001t0008g0214others(24): Show | 27 | HG01891.hp1 HG02027.hp2 HG02615.hp1 others(24): Show |
intron_variant | MODIFIER | c.112-353_112-352ins others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684431 | |||||
| chr12:64684431
|
G | T | 2 | a0001c0001t0046g0044a0002c0004t0011g0326 | 2 | HG02895.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.112-356G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64684431 | ||||||
| chr12:64684435
|
G | GT | 68 | a0001c0001t0003g0265a0001c0001t0004g0088a0001c0001t0004g0091others(65): Show | 68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.112-340dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 64684435 | |||||
| chr12:64684435
|
G | T | 192 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(189): Show | 193 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.112-352G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64684435 | ||||||
| chr12:64684439
|
T | G | 1 | a0001c0002t0081g0005 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.112-348T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64684439 | ||||||
| chr12:64684524
|
A | C | 14 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.112-263A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64684524 | ||||||
| chr12:64684735
|
C | T | 1 | a0001c0001t0008g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.112-52C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 1/4 | chr12 | 64684735 | ||||||
| chr12:64684944
|
T | C | 1 | a0001c0002t0028g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.219+50T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64684944 | ||||||
| chr12:64685310
|
A | G | 15 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(12): Show | 16 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.219+416A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64685310 | ||||||
| chr12:64685316
|
G | A | 1 | a0001c0001t0004g0363 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.219+422G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64685316 | ||||||
| chr12:64685374
|
A | G | 12 | a0001c0001t0007g0346a0001c0001t0071g0360a0001c0002t0004g0015others(9): Show | 12 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.219+480A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64685374 | ||||||
| chr12:64685412
|
T | G | 6 | a0001c0001t0057g0177a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+518T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64685412 | ||||||
| chr12:64685608
|
T | C | 12 | a0001c0001t0007g0346a0001c0001t0071g0360a0001c0002t0004g0015others(9): Show | 12 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.219+714T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64685608 | ||||||
| chr12:64685639
|
C | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0078others(6): Show | 9 | HG02015.hp2 HG02080.hp1 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.219+745C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64685639 | ||||||
| chr12:64685644
|
G | A | 1 | a0002c0003t0030g0001 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.219+750G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64685644 | ||||||
| chr12:64685774
|
T | C | 256 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(253): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.219+880T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64685774 | ||||||
| chr12:64685793
|
C | T | 1 | a0001c0001t0004g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.219+899C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64685793 | ||||||
| chr12:64685921
|
G | A | 2 | a0001c0002t0016g0033a0001c0002t0016g0035 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.219+1027G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64685921 | ||||||
| chr12:64685938
|
C | T | 1 | a0001c0002t0007g0011 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.219+1044C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64685938 | ||||||
| chr12:64685996
|
G | A | 10 | a0001c0001t0004g0363a0001c0001t0007g0352a0001c0001t0010g0364others(7): Show | 10 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.219+1102G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64685996 | ||||||
| chr12:64686009
|
T | C | 3 | a0001c0001t0036g0314a0001c0001t0036g0315a0001c0001t0075g0106 | 3 | HG03130.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.219+1115T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686009 | ||||||
| chr12:64686061
|
T | A | 1 | a0001c0001t0003g0309 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.219+1167T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686061 | ||||||
| chr12:64686063
|
G | A | 1 | a0001c0001t0061g0139 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.219+1169G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686063 | ||||||
| chr12:64686130
|
A | G | 50 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(47): Show | 50 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.219+1236A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686130 | ||||||
| chr12:64686182
|
GT | G | 27 | a0001c0001t0003g0279a0001c0001t0006g0278a0001c0001t0008g0214others(24): Show | 27 | HG01891.hp1 HG02027.hp2 HG02615.hp1 others(24): Show |
intron_variant | MODIFIER | c.219+1300delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 64686182 | |||||
| chr12:64686351
|
C | T | 28 | a0001c0001t0003g0279a0001c0001t0006g0278a0001c0001t0008g0214others(25): Show | 28 | HG01891.hp1 HG02027.hp2 HG02615.hp1 others(25): Show |
intron_variant | MODIFIER | c.219+1457C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686351 | ||||||
| chr12:64686388
|
A | G | 1 | a0001c0001t0026g0239 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.219+1494A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686388 | ||||||
| chr12:64686395
|
G | T | 6 | a0001c0001t0057g0177a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+1501G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686395 | ||||||
| chr12:64686483
|
C | T | 15 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(12): Show | 16 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.219+1589C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686483 | ||||||
| chr12:64686503
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.219+1609C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686503 | ||||||
| chr12:64686533
|
C | T | 15 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(12): Show | 16 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.219+1639C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686533 | ||||||
| chr12:64686639
|
C | T | 1 | a0001c0001t0053g0188 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.220-1577C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686639 | ||||||
| chr12:64686700
|
G | A | 45 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(42): Show | 45 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.220-1516G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686700 | ||||||
| chr12:64686755
|
A | G | 3 | a0001c0001t0036g0314a0001c0001t0036g0315a0001c0001t0075g0106 | 3 | HG03130.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.220-1461A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686755 | ||||||
| chr12:64686895
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.220-1321A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686895 | ||||||
| chr12:64686922
|
T | A | 10 | a0001c0001t0004g0363a0001c0001t0007g0352a0001c0001t0010g0364others(7): Show | 10 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.220-1294T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64686922 | ||||||
| chr12:64687026
|
G | A | 1 | a0001c0001t0002g0181 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.220-1190G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687026 | ||||||
| chr12:64687076
|
C | T | 1 | a0001c0001t0090g0369 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.220-1140C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687076 | ||||||
| chr12:64687080
|
C | T | 22 | a0001c0001t0004g0363a0001c0001t0007g0346a0001c0001t0007g0352others(19): Show | 22 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.220-1136C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687080 | ||||||
| chr12:64687101
|
C | G | 8 | a0001c0001t0012g0125a0001c0001t0012g0167a0001c0001t0012g0182others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.220-1115C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687101 | ||||||
| chr12:64687169
|
T | A | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.220-1047T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687169 | ||||||
| chr12:64687221
|
C | T | 50 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0192others(47): Show | 50 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.220-995C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687221 | ||||||
| chr12:64687222
|
G | A | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.220-994G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687222 | ||||||
| chr12:64687253
|
C | T | 1 | a0001c0001t0005g0205 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.220-963C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687253 | ||||||
| chr12:64687297
|
T | G | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.220-919T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687297 | ||||||
| chr12:64687433
|
T | A | 59 | a0001c0001t0004g0088a0001c0001t0004g0091a0001c0001t0004g0102others(56): Show | 59 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.220-783T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687433 | ||||||
| chr12:64687448
|
G | GT | 7 | a0001c0001t0001g0085a0001c0001t0001g0337a0001c0001t0006g0054others(4): Show | 7 | HG03942.hp2 NA18944.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.220-759dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 64687448 | |||||
| chr12:64687449
|
T | G | 69 | a0001c0001t0001g0234a0001c0001t0001g0333a0001c0001t0001g0340others(66): Show | 69 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.220-767T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687449 | ||||||
| chr12:64687481
|
G | GT | 9 | a0001c0001t0006g0336a0001c0001t0026g0239a0001c0001t0057g0177others(6): Show | 9 | HG00597.hp2 HG01433.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-724dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 64687481 | |||||
| chr12:64687549
|
A | G | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.220-667A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687549 | ||||||
| chr12:64687594
|
A | T | 3 | a0001c0001t0001g0232a0001c0001t0002g0153a0001c0001t0090g0369 | 3 | HG00609.hp1 HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.220-622A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687594 | ||||||
| chr12:64687659
|
T | C | 29 | a0001c0001t0003g0279a0001c0001t0006g0278a0001c0001t0008g0214others(26): Show | 29 | HG01891.hp1 HG02027.hp2 HG02615.hp1 others(26): Show |
intron_variant | MODIFIER | c.220-557T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687659 | ||||||
| chr12:64687901
|
C | G | 6 | a0001c0001t0057g0177a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.220-315C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687901 | ||||||
| chr12:64687958
|
GCAGTCAG others(3): Show |
G | 12 | a0001c0001t0007g0346a0001c0001t0071g0360a0001c0002t0004g0015others(9): Show | 12 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.220-254_220-245del others(10): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 64687958 | |||||
| chr12:64687978
|
G | A | 1 | a0001c0001t0065g0318 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.220-238G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64687978 | ||||||
| chr12:64688198
|
C | T | 6 | a0001c0001t0057g0177a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.220-18C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 2/4 | chr12 | 64688198 | ||||||
| chr12:64688550
|
G | A | 118 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.457+97G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64688550 | ||||||
| chr12:64688695
|
T | G | 10 | a0001c0001t0005g0126a0001c0001t0005g0141a0001c0001t0005g0193others(7): Show | 10 | HG01099.hp2 HG01934.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.457+242T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64688695 | ||||||
| chr12:64688704
|
G | T | 118 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.457+251G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64688704 | ||||||
| chr12:64688813
|
A | G | 2 | a0001c0001t0004g0293a0001c0001t0077g0292 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.457+360A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64688813 | ||||||
| chr12:64688837
|
C | T | 3 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109 | 3 | HG02055.hp2 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.457+384C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64688837 | ||||||
| chr12:64688864
|
T | C | 118 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.457+411T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64688864 | ||||||
| chr12:64688907
|
A | T | 2 | a0001c0001t0004g0303a0001c0001t0079g0225 | 2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.457+454A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64688907 | ||||||
| chr12:64688958
|
G | T | 259 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(256): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.457+505G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64688958 | ||||||
| chr12:64688985
|
G | A | 33 | a0001c0001t0004g0088a0001c0001t0004g0091a0001c0001t0004g0102others(30): Show | 33 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.457+532G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64688985 | ||||||
| chr12:64688987
|
C | T | 2 | a0001c0001t0003g0309a0001c0001t0040g0098 | 2 | HG02486.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.457+534C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64688987 | ||||||
| chr12:64689019
|
T | C | 1 | a0001c0001t0004g0305 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.457+566T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689019 | ||||||
| chr12:64689083
|
G | A | 3 | a0001c0001t0036g0314a0001c0001t0036g0315a0001c0001t0075g0106 | 3 | HG03130.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.457+630G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689083 | ||||||
| chr12:64689100
|
T | G | 1 | a0001c0002t0029g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.457+647T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689100 | ||||||
| chr12:64689109
|
A | G | 1 | a0001c0001t0050g0199 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.457+656A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689109 | ||||||
| chr12:64689207
|
G | A | 3 | a0001c0001t0018g0236a0001c0001t0018g0237a0001c0001t0073g0238 | 3 | NA18943.hp2 NA18953.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.457+754G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689207 | ||||||
| chr12:64689220
|
G | GGT | 37 | a0001c0001t0007g0346a0001c0001t0008g0246a0001c0001t0008g0247others(34): Show | 38 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.457+792_457+793dup others(2): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689220 | |||||
| chr12:64689220
|
G | GGTGT | 6 | a0001c0001t0057g0177a0001c0002t0021g0023a0001c0002t0028g0025others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.457+790_457+793dup others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689220 | |||||
| chr12:64689220
|
G | GGTGTGTG others(3): Show |
97 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.457+784_457+793dup others(10): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689220 | |||||
| chr12:64689220
|
G | GGTGTGTG others(5): Show |
17 | a0001c0001t0002g0147a0001c0001t0002g0152a0001c0001t0002g0155others(14): Show | 17 | HG01069.hp2 HG01099.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.457+782_457+793dup others(12): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689220 | |||||
| chr12:64689220
|
G | GGTGTGTG others(7): Show |
1 | a0001c0001t0085g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.457+780_457+793dup others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689220 | |||||
| chr12:64689248
|
C | T | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.457+795C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689248 | ||||||
| chr12:64689336
|
A | G | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.457+883A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689336 | ||||||
| chr12:64689388
|
A | G | 1 | a0001c0001t0012g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.457+935A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689388 | ||||||
| chr12:64689493
|
T | A | 1 | a0001c0001t0061g0139 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.457+1040T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689493 | ||||||
| chr12:64689630
|
C | T | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.457+1177C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689630 | ||||||
| chr12:64689777
|
C | G | 118 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.457+1324C>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689777 | ||||||
| chr12:64689791
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0009g0244a0001c0001t0009g0273a0001c0001t0032g0145others(1): Show | 4 | HG02647.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+1342_457+1351d others(12): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689791 | |||||
| chr12:64689791
|
C | CTTTTTTT others(4): Show |
30 | a0001c0001t0004g0289a0001c0001t0004g0363a0001c0001t0007g0352others(27): Show | 31 | HG01069.hp1 HG01167.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.457+1341_457+1351d others(13): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689791 | |||||
| chr12:64689791
|
C | CTTTTTTT others(5): Show |
73 | a0001c0001t0004g0088a0001c0001t0004g0091a0001c0001t0004g0102others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.457+1340_457+1351d others(14): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689791 | |||||
| chr12:64689791
|
C | CTTTTTTT others(6): Show |
24 | a0001c0001t0004g0299a0001c0001t0005g0198a0001c0001t0005g0205others(21): Show | 24 | HG00140.hp1 HG01891.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.457+1339_457+1351d others(15): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689791 | |||||
| chr12:64689791
|
C | CTTTTTTT others(7): Show |
7 | a0001c0001t0003g0279a0001c0001t0008g0248a0001c0001t0008g0249others(4): Show | 7 | HG02615.hp1 HG06807.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.457+1351_457+1352i others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689791 | |||||
| chr12:64689791
|
C | CTTTTTTT others(8): Show |
4 | a0001c0001t0001g0234a0001c0001t0006g0278a0001c0001t0014g0149others(1): Show | 4 | HG01169.hp2 HG02027.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+1351_457+1352i others(17): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689791 | |||||
| chr12:64689791
|
C | CTTTTTTT others(9): Show |
89 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0333others(86): Show | 89 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.457+1351_457+1352i others(18): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689791 | |||||
| chr12:64689791
|
C | CTTTTTTT others(10): Show |
19 | a0001c0001t0001g0340a0001c0001t0002g0140a0001c0001t0002g0144others(16): Show | 19 | HG01256.hp1 HG01358.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.457+1351_457+1352i others(19): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689791 | |||||
| chr12:64689791
|
C | CTTTTTTT others(11): Show |
4 | a0001c0001t0002g0146a0001c0001t0002g0156a0001c0001t0002g0162others(1): Show | 4 | HG01106.hp1 HG01175.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+1351_457+1352i others(20): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64689791 | |||||
| chr12:64689810
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.457+1357G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689810 | ||||||
| chr12:64689856
|
T | C | 241 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(238): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.457+1403T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689856 | ||||||
| chr12:64689946
|
G | T | 1 | a0001c0001t0005g0126 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.457+1493G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689946 | ||||||
| chr12:64689979
|
C | T | 3 | a0001c0001t0036g0314a0001c0001t0036g0315a0001c0001t0075g0106 | 3 | HG03130.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.458-1491C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689979 | ||||||
| chr12:64689980
|
G | A | 1 | a0001c0001t0005g0193 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.458-1490G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64689980 | ||||||
| chr12:64690057
|
G | T | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.458-1413G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690057 | ||||||
| chr12:64690091
|
G | A | 10 | a0001c0001t0004g0363a0001c0001t0007g0352a0001c0001t0010g0364others(7): Show | 10 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-1379G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690091 | ||||||
| chr12:64690205
|
G | A | 1 | a0001c0001t0003g0316 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.458-1265G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690205 | ||||||
| chr12:64690234
|
T | G | 10 | a0001c0001t0004g0363a0001c0001t0007g0352a0001c0001t0010g0364others(7): Show | 10 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-1236T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690234 | ||||||
| chr12:64690250
|
C | T | 1 | a0001c0002t0047g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.458-1220C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690250 | ||||||
| chr12:64690274
|
T | A | 10 | a0001c0001t0004g0363a0001c0001t0007g0352a0001c0001t0010g0364others(7): Show | 10 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-1196T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690274 | ||||||
| chr12:64690275
|
G | T | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.458-1195G>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690275 | ||||||
| chr12:64690332
|
C | T | 118 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.458-1138C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690332 | ||||||
| chr12:64690477
|
G | A | 15 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(12): Show | 16 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.458-993G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690477 | ||||||
| chr12:64690509
|
T | C | 1 | a0001c0001t0088g0361 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.458-961T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690509 | ||||||
| chr12:64690625
|
C | A | 118 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.458-845C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690625 | ||||||
| chr12:64690655
|
A | T | 1 | a0001c0001t0046g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.458-815A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690655 | ||||||
| chr12:64690714
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.458-756G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690714 | ||||||
| chr12:64690839
|
C | CT | 8 | a0001c0001t0013g0168a0001c0001t0057g0177a0001c0001t0060g0134others(5): Show | 8 | HG00280.hp2 HG02109.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-621dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 64690839 | |||||
| chr12:64690862
|
A | T | 2 | a0001c0002t0021g0217a0001c0002t0021g0218 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.458-608A>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690862 | ||||||
| chr12:64690863
|
T | A | 28 | a0001c0001t0003g0279a0001c0001t0006g0278a0001c0001t0008g0214others(25): Show | 28 | HG01891.hp1 HG02027.hp2 HG02615.hp1 others(25): Show |
intron_variant | MODIFIER | c.458-607T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690863 | ||||||
| chr12:64690914
|
G | A | 1 | a0001c0002t0047g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.458-556G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690914 | ||||||
| chr12:64690938
|
C | A | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.458-532C>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690938 | ||||||
| chr12:64690944
|
T | C | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.458-526T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690944 | ||||||
| chr12:64690963
|
T | C | 118 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.458-507T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690963 | ||||||
| chr12:64690968
|
C | T | 3 | a0001c0001t0032g0145a0001c0001t0041g0312a0001c0001t0063g0170 | 3 | HG02647.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.458-502C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64690968 | ||||||
| chr12:64691017
|
C | T | 118 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.458-453C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64691017 | ||||||
| chr12:64691021
|
C | T | 1 | a0001c0001t0031g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.458-449C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64691021 | ||||||
| chr12:64691029
|
T | G | 118 | a0001c0001t0001g0234a0001c0001t0001g0260a0001c0001t0001g0261others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.458-441T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64691029 | ||||||
| chr12:64691032
|
T | C | 1 | a0001c0001t0002g0328 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.458-438T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64691032 | ||||||
| chr12:64691320
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.458-150T>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64691320 | ||||||
| chr12:64691344
|
G | A | 1 | a0001c0001t0008g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.458-126G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64691344 | ||||||
| chr12:64691377
|
G | A | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.458-93G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64691377 | ||||||
| chr12:64691453
|
C | T | 2 | a0001c0001t0003g0209a0001c0001t0067g0210 | 2 | HG01109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.458-17C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 3/4 | chr12 | 64691453 | ||||||
| chr12:64691664
|
T | TGGGGGAT others(25): Show |
71 | a0001c0001t0002g0159a0001c0001t0002g0321a0001c0001t0003g0316others(68): Show | 72 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.567+121_567+152dup others(32): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64691664 | |||||
| chr12:64691664
|
T | TGGGGGAT others(57): Show |
135 | a0001c0001t0001g0039a0001c0001t0001g0057a0001c0001t0001g0260others(132): Show | 135 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.567+89_567+152dupG others(63): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64691664 | |||||
| chr12:64691664
|
T | TGGGGGAT others(89): Show |
4 | a0001c0001t0004g0215a0001c0001t0066g0220a0001c0001t0087g0353others(1): Show | 4 | HG00140.hp1 HG00140.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+152_567+153ins others(96): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64691664 | |||||
| chr12:64691664
|
T | TGGGGGAT others(121): Show |
1 | a0001c0001t0002g0206 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.567+152_567+153ins others(128): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64691664 | |||||
| chr12:64691664
|
TGGGGGAT others(25): Show |
T | 4 | a0001c0001t0001g0121a0001c0001t0009g0076a0001c0001t0025g0075others(1): Show | 4 | NA18978.hp1 NA19068.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.567+121_567+152del others(32): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64691664 | |||||
| chr12:64691668
|
G | GGATGGGA others(57): Show |
1 | a0001c0001t0008g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.567+92_567+155dupT others(63): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64691668 | |||||
| chr12:64691668
|
G | GGATGGGA others(89): Show |
2 | a0001c0001t0005g0195a0001c0001t0034g0204 | 2 | HG00735.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.567+152_567+153ins others(96): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64691668 | |||||
| chr12:64691670
|
A | ATGGGAAG others(57): Show |
1 | a0001c0001t0078g0345 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.567+152_567+153ins others(64): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64691670 | |||||
| chr12:64691704
|
G | GGGAAGAG others(56): Show |
1 | a0001c0001t0073g0238 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.567+152_567+153ins others(63): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64691704 | |||||
| chr12:64691723
|
A | AGGGCAGG others(58): Show |
1 | a0001c0001t0008g0276 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.567+152_567+153ins others(65): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64691723 | |||||
| chr12:64691970
|
G | C | 1 | a0001c0001t0071g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.567+391G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64691970 | ||||||
| chr12:64692037
|
C | T | 10 | a0001c0001t0012g0125a0001c0001t0012g0167a0001c0001t0012g0182others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.567+458C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64692037 | ||||||
| chr12:64692291
|
G | C | 3 | a0001c0001t0028g0048a0001c0001t0057g0177a0001c0002t0028g0025 | 3 | HG01361.hp2 HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.567+712G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64692291 | ||||||
| chr12:64692380
|
A | G | 6 | a0002c0003t0010g0116a0002c0003t0010g0119a0002c0003t0011g0114others(3): Show | 7 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.567+801A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64692380 | ||||||
| chr12:64692878
|
T | C | 1 | a0001c0001t0086g0362 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.567+1299T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64692878 | ||||||
| chr12:64692933
|
C | T | 9 | a0002c0003t0010g0116a0002c0003t0010g0119a0002c0003t0011g0111others(6): Show | 10 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.567+1354C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64692933 | ||||||
| chr12:64693144
|
C | CT | 23 | a0001c0001t0001g0077a0001c0001t0001g0122a0001c0001t0002g0144others(20): Show | 24 | HG01106.hp1 HG01192.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.567+1585dupT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64693144 | |||||
| chr12:64693144
|
C | CTT | 45 | a0001c0001t0004g0028a0001c0001t0004g0088a0001c0001t0004g0091others(42): Show | 45 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.567+1584_567+1585d others(4): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64693144 | |||||
| chr12:64693144
|
CT | C | 25 | a0001c0001t0001g0052a0001c0001t0001g0124a0001c0001t0001g0221others(22): Show | 25 | HG00323.hp2 HG01167.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.567+1585delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64693144 | |||||
| chr12:64693164
|
T | A | 25 | a0001c0001t0005g0126a0001c0001t0005g0128a0001c0001t0005g0141others(22): Show | 25 | HG00280.hp1 HG00735.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.567+1585T>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64693164 | ||||||
| chr12:64693414
|
AT | A | 81 | a0001c0001t0001g0212a0001c0001t0002g0192a0001c0001t0003g0043others(78): Show | 81 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.568-1336delT | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64693414 | |||||
| chr12:64693492
|
C | T | 2 | a0001c0001t0041g0312a0001c0001t0063g0170 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.568-1271C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64693492 | ||||||
| chr12:64693541
|
C | T | 9 | a0002c0003t0010g0116a0002c0003t0010g0119a0002c0003t0011g0111others(6): Show | 10 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.568-1222C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64693541 | ||||||
| chr12:64693604
|
C | T | 46 | a0001c0001t0004g0028a0001c0001t0004g0088a0001c0001t0004g0091others(43): Show | 46 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.568-1159C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64693604 | ||||||
| chr12:64693638
|
CGAACTTC others(7): Show |
C | 1 | a0001c0001t0049g0049 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.568-1114_568-1101d others(16): Show |
RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 64693638 | |||||
| chr12:64693749
|
G | C | 2 | a0001c0001t0002g0140a0001c0001t0002g0156 | 2 | HG01175.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.568-1014G>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64693749 | ||||||
| chr12:64693761
|
A | C | 9 | a0002c0003t0010g0116a0002c0003t0010g0119a0002c0003t0011g0111others(6): Show | 10 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.568-1002A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64693761 | ||||||
| chr12:64693874
|
T | C | 1 | a0001c0001t0053g0188 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.568-889T>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64693874 | ||||||
| chr12:64693946
|
C | T | 4 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.568-817C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64693946 | ||||||
| chr12:64694065
|
G | A | 16 | a0001c0001t0007g0053a0001c0001t0007g0100a0001c0001t0007g0304others(13): Show | 16 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.568-698G>A | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64694065 | ||||||
| chr12:64694138
|
A | C | 4 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0020g0109others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.568-625A>C | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64694138 | ||||||
| chr12:64694154
|
A | G | 6 | a0001c0001t0028g0048a0001c0001t0057g0177a0001c0002t0028g0025others(3): Show | 6 | HG01361.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.568-609A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64694154 | ||||||
| chr12:64694375
|
A | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02258.hp1 NA20905.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.568-388A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64694375 | ||||||
| chr12:64694381
|
C | T | 1 | a0001c0001t0037g0300 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.568-382C>T | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64694381 | ||||||
| chr12:64694403
|
A | G | 1 | a0001c0001t0090g0369 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.568-360A>G | RASSF3 | ENSG00000153179.14 | transcript | ENST00000542104.6 | protein_coding | 4/4 | chr12 | 64694403 |